U.S. patent application number 16/775192 was filed with the patent office on 2020-07-30 for chemokine receptor modulators and uses thereof.
The applicant listed for this patent is RAPT THERAPEUTICS, INC.. Invention is credited to Hilary Plake Beck, Berenger Biannic, Minna Hue Thanh Bui, Dennis X. Hu, Jeffrey J. Jackson, John Michael Ketcham, Jay Patrick Powers, Maureen Kay Reilly, Omar Robles-Resendiz, Hunter Paul Shunatona, James Ross Walker, David Juergen Wustrow, Ashkaan Younai, Mikhail Zibinsky.
Application Number | 20200239480 16/775192 |
Document ID | 20200239480 / US20200239480 |
Family ID | 1000004765400 |
Filed Date | 2020-07-30 |
Patent Application | download [pdf] |
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United States Patent
Application |
20200239480 |
Kind Code |
A1 |
Beck; Hilary Plake ; et
al. |
July 30, 2020 |
CHEMOKINE RECEPTOR MODULATORS AND USES THEREOF
Abstract
Disclosed herein, inter alia, are compounds and methods of use
thereof for the modulation of CCR4 activity.
Inventors: |
Beck; Hilary Plake; (Emerald
Hills, CA) ; Biannic; Berenger; (San Mateo, CA)
; Bui; Minna Hue Thanh; (Oakland, CA) ; Hu; Dennis
X.; (San Mateo, CA) ; Ketcham; John Michael;
(San Mateo, CA) ; Powers; Jay Patrick; (Pacifica,
CA) ; Reilly; Maureen Kay; (San Francisco, CA)
; Robles-Resendiz; Omar; (Redwood City, CA) ;
Shunatona; Hunter Paul; (San Francisco, CA) ; Walker;
James Ross; (Verona, WI) ; Wustrow; David
Juergen; (Los Gatos, CA) ; Younai; Ashkaan;
(San Francisco, CA) ; Zibinsky; Mikhail; (Redwood
City, CA) ; Jackson; Jeffrey J.; (San Bruno,
CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
RAPT THERAPEUTICS, INC. |
South San Francisco |
CA |
US |
|
|
Family ID: |
1000004765400 |
Appl. No.: |
16/775192 |
Filed: |
January 28, 2020 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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16195506 |
Nov 19, 2018 |
10604526 |
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16775192 |
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15662861 |
Jul 28, 2017 |
10179787 |
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16195506 |
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62426087 |
Nov 23, 2016 |
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62368848 |
Jul 29, 2016 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61K 31/198 20130101;
A61K 31/454 20130101; A61K 31/4985 20130101; A61K 45/06 20130101;
C07D 487/04 20130101; A61K 31/122 20130101; A61K 31/7135 20130101;
A61K 31/4706 20130101; A61K 31/728 20130101; A61K 31/5377 20130101;
A61K 31/593 20130101; A61K 31/519 20130101; A61K 31/42 20130101;
A61K 31/235 20130101 |
International
Class: |
C07D 487/04 20060101
C07D487/04; A61K 31/5377 20060101 A61K031/5377; A61K 31/122
20060101 A61K031/122; A61K 31/4985 20060101 A61K031/4985; A61K
31/593 20060101 A61K031/593; A61K 31/4706 20060101 A61K031/4706;
A61K 31/198 20060101 A61K031/198; A61K 31/519 20060101 A61K031/519;
A61K 31/7135 20060101 A61K031/7135; A61K 31/454 20060101
A61K031/454; A61K 45/06 20060101 A61K045/06; A61K 31/42 20060101
A61K031/42; A61K 31/728 20060101 A61K031/728; A61K 31/235 20060101
A61K031/235 |
Claims
1. A compound having structural Formula (I): ##STR00310## or a
pharmaceutically acceptable salt thereof, wherein: X.sup.1 is
CR.sup.8 or N; X.sup.2 is CR.sup.9 or N; X.sup.3 is CR.sup.10 or N;
n1, n2, n3, n4, n5, n6, n7, n8, n9 and n10 are independently an
integer from 0 to 4; m1, m2, m3, m4, m5, m6, m7, m8, m9, ml0, v1,
v2, v3, v4, v5, v6, v7, v8, v9 and v10 are independently 1 or 2; z1
is an integer from 0 to 5; z2 is an integer from 0 to 2; z3 is an
integer from 0 to 11; z4 is an integer from 0 to 2; L.sup.7 is a
bond, --O--, --S--, --NR.sup.72B--, --C(O)--, --C(O)O--, --S(O)--,
--S(O).sub.2--, substituted or unsubstituted alkylene, substituted
or unsubstituted heteroalkylene, substituted or unsubstituted
cycloalkylene, substituted or unsubstituted heterocycloalkylene,
substituted or unsubstituted arylene, or substituted or
unsubstituted heteroarylene; R.sup.1 is hydrogen, halogen,
--CX.sup.1.1.sub.3, --CHX.sup.1.1.sub.2, --CH.sub.2X.sup.1.1, --CN,
--N.sub.3, --SO.sub.n1R.sup.1A, --SO.sub.v1NR.sup.1BR.sup.1C,
--NHNR.sup.1BR.sup.1C, --ONR.sup.1BR.sup.1C,
--NHC(O)NHNR.sup.1BR.sup.1C, --NHC(O)NR.sup.1BR.sup.1C,
--N(O).sub.m1, --NR.sup.1BR.sup.1C, --C(O)R.sup.1D,
--C(O)OR.sup.1D, --C(O)NR.sup.1BR.sup.1C, --OR.sup.1A,
--NR.sup.1BSO.sub.2R.sup.1A, --NR.sup.1BC(O)R.sup.1D,
--NR.sup.1BC(O)OR.sup.1D, --NR.sup.1BOR.sup.1D,
--OCX.sup.1.1.sub.3, --OCHX.sup.1.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.2 is hydrogen,
halogen, --CX.sup.2.1.sub.3, --CHX.sup.2.1.sub.2,
--CH.sub.2X.sup.2.1, --CN, --N.sub.3, --SO.sub.n2R.sup.2A,
--SO.sub.v2NR.sup.2BR.sup.2C, --NHNR.sup.2BR.sup.2C,
--ONR.sup.2BR.sup.2C, --NHC(O)NHNR.sup.2BR.sup.2C,
--NHC(O)NR.sup.2BR.sup.2C, --N(O).sub.m2, --NR.sup.2BR.sup.2C,
--C(O)R.sup.2D, --C(O)OR.sup.2D, --C(O)NR.sup.2BR.sup.2C,
--OR.sup.2A, --NR.sup.2BSO.sub.2R.sup.2A, --NR.sup.2BC(O)R.sup.2D,
--NR.sup.2BC(O)OR.sup.2D, --NR.sup.2BOR.sup.2D,
--OCX.sup.2.1.sub.3, --OCHX.sup.2.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3 is
independently hydrogen, halogen, --CX.sup.3.1.sub.3,
--CHX.sup.3.1.sub.2, --CH.sub.2X.sup.3.1, --CN, --N.sub.3,
--SO.sub.n3R.sup.3A, --SO.sub.v3NR.sup.3BR.sup.3C,
--NHNR.sup.3BR.sup.3C, --ONR.sup.3BR.sup.3C,
--NHC(O)NHNR.sup.3BR.sup.3C, --NHC(O)NR.sup.3BR.sup.3C,
--N(O).sub.m3, --NR.sup.3BR.sup.3C, --C(O)R.sup.3D,
--C(O)OR.sup.3D, --C(O)NR.sup.3BR.sup.3C, --OR.sup.3A,
--NR.sup.3BSO.sub.2R.sup.3A, --NR.sup.3BC(O)R.sup.3D,
--NR.sup.3BC(O)OR.sup.3D, --NR.sup.3BOR.sup.3D,
--OCX.sup.3.1.sub.3, --OCHX.sup.3.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.4 is hydrogen,
halogen, --CX.sup.4.1.sub.3, --CHX.sup.4.1.sub.2,
--CH.sub.2X.sup.4.1, --CN, --N.sub.3, --SO.sub.n4R.sup.4A,
--SO.sub.v4NR.sup.4BR.sup.4C, --NHNR.sup.4BR.sup.4C,
--ONR.sup.4BR.sup.4B, --NHC(O)NHNR.sup.4BR.sup.4C,
--NHC(O)NR.sup.4BR.sup.4C, --N(O).sub.m4, --NR.sup.4BR.sup.4C,
--C(O)R.sup.4D, --C(O)OR.sup.4D, --C(O)NR.sup.4BR.sup.4C,
--OR.sup.4A, --NR.sup.4BSO.sub.2R.sup.4A, --NR.sup.4BC(O)R.sup.4D,
--NR.sup.4BC(O)OR.sup.4D, --NR.sup.4BOR.sup.4D,
--OCX.sup.4.1.sub.3, --OCHX.sup.4.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.5 is
independently hydrogen, halogen, oxo, --CX.sup.5.1.sub.3,
--CHX.sup.5.1.sub.2, --CH.sub.2X.sup.5.1, --CN, --N.sub.3,
--SO.sub.n5R.sup.5A, --SO.sub.v5NR.sup.5BR.sup.5C,
--NHNR.sup.5BR.sup.5C, --ONR.sup.5BR.sup.5C,
--NHC(O)NHNR.sup.5BR.sup.5C, --NHC(O)NR.sup.5BR.sup.5C,
--N(O).sub.m5, --NR.sup.5BR.sup.5C, --C(O)R.sup.5D,
--C(O)OR.sup.5D, --C(O)NR.sup.5BR.sup.5C, --OR.sup.5A,
--NR.sup.5BSO.sub.2R.sup.5A, --NR.sup.5BC(O)R.sup.5D,
--NR.sup.5BC(O)OR.sup.5D, --NR.sup.5BOR.sup.5D,
--OCX.sup.5.1.sub.3, --OCHX.sup.5.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.6 is
independently hydrogen, halogen, oxo, --CX.sup.6.1.sub.3,
--CHX.sup.6.1.sub.2, --CH.sub.2X.sup.6.1, --CN, --N.sub.3,
--SO.sub.n6R.sup.6A, --SO.sub.v6NR.sup.6BR.sup.6C,
--NHNR.sup.6BR.sup.6C, --ONR.sup.6BR.sup.6C,
--NHC(O)NHNR.sup.6BR.sup.6C, --NHC(O)NR.sup.6BR.sup.6C,
--N(O).sub.m6, --NR.sup.6BR.sup.6C, --C(O)R.sup.6D,
--C(O)OR.sup.6D, --C(O)NR.sup.6BR.sup.6C, --OR.sup.6A,
--NR.sup.6BSO.sub.2R.sup.6A, --NR.sup.6BC(O)R.sup.6D,
--NR.sup.6BC(O)OR.sup.6D, --NR.sup.6BOR.sup.6D,
--OCX.sup.6.1.sub.3, --OCHX.sup.6.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.7 is hydrogen,
halogen, --CX.sup.7.1.sub.3, --CHX.sup.7.1.sub.2,
--CH.sub.2X.sup.7.1, --CN, --N.sub.3, --SO.sub.n7R.sup.7A,
--SO.sub.v7NR.sup.7BNR.sup.7C, --NHNR.sup.7BR.sup.7C,
--ONR.sup.7BR.sup.7C, --NHC(O)NHNR.sup.7BR.sup.7C,
--NHC(O)NR.sup.7BR.sup.7C, --N(O).sub.m7, --NR.sup.7BR.sup.7C,
--C(O)R.sup.7D, --C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C,
--OR.sup.7A, --NR.sup.7BSO.sub.2R.sup.7A, --NR.sup.7BC(O)R.sup.7D,
--NR.sup.7BC(O)OR.sup.7D, --NR.sup.7BOR.sup.7D,
--OCX.sup.7.1.sub.3, --OCHX.sup.7.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.8 is hydrogen,
halogen, --CX.sup.8.1.sub.3, --CHX.sup.8.1.sub.2,
--CH.sub.2X.sup.8.1, --CN, --N.sub.3, --SO.sub.n8R.sup.8A,
--SO.sub.v8NR.sup.8BR.sup.8C, --NHNR.sup.8BR.sup.8C,
--ONR.sup.8BR.sup.8C, --NHC(O)NHNR.sup.8BR.sup.8C,
--NHC(O)NR.sup.8BR.sup.8C, --N(O).sub.m8, --NR.sup.8BR.sup.8C,
--C(O)R.sup.8D, --C(O)OR.sup.8D, --C(O)NR.sup.8BR.sup.8C,
--OR.sup.8A, --NR.sup.8BSO.sub.2R.sup.8A, --NR.sup.8BC(O)R.sup.8D,
--NR.sup.8BC(O)OR.sup.8D, --NR.sup.8BOR.sup.8D,
--OCX.sup.8.1.sub.3, --OCHX.sup.8.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.9 is hydrogen,
halogen, --CX.sup.9.1.sub.3, --CHX.sup.9.1.sub.2,
--CH.sub.2X.sup.9.1, --CN, --N.sub.3, --SO.sub.n9R.sup.9A,
--SO.sub.v9NR.sup.9BR.sup.9C, --NHNR.sup.9BR.sup.9C,
--ONR.sup.9BR.sup.9C, --NHC(O)NHNR.sup.9BR.sup.9C,
--NHC(O)NR.sup.9BR.sup.9C, --N(O).sub.m9, --NR.sup.9BR.sup.9C,
--C(O)R.sup.9D, --C(O)OR.sup.9D, --C(O)NR.sup.9BR.sup.9C,
--OR.sup.9A, --NR.sup.9BSO.sub.2R.sup.9A, --NR.sup.9BC(O)R.sup.9D,
--NR.sup.9BC(O)OR.sup.9D, --NR.sup.9BOR.sup.9D,
--OCX.sup.9.1.sub.3, --OCHX.sup.9.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.10 is hydrogen,
halogen, --CX.sup.10.1.sub.3, --CHX.sup.10.1.sub.2,
--CH.sub.2X.sup.10.1, --CN, --N.sub.3, --SO.sub.n10R.sup.10A,
--SO.sub.v10NR.sup.10BR.sup.10C, --NHNR.sup.10BR.sup.10C,
--ONR.sup.10BR.sup.10C, --NHC(O)NHNR.sup.10BR.sup.10C,
--NHC(O)NR.sup.10BR.sup.10C, --N(O).sub.m10, --NR.sup.10BR.sup.10C,
--C(O)R.sup.10D, --C(O)OR.sup.10D, --C(O)NR.sup.10BR.sup.10C,
--OR.sup.10A, --NR.sup.10BSO.sub.2R.sup.10A,
--NR.sup.10BC(O)R.sup.10D, --NR.sup.10BC(O)OR.sup.10D,
--NR.sup.10BOR.sup.10D, --OCX.sup.10.1.sub.3,
--OCHX.sup.10.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl; R.sup.1A, R.sup.1B, R.sup.1C,
R.sup.1D, R.sup.2A, R.sup.2B, R.sup.2C, R.sup.2D, R.sup.3A,
R.sup.3B, R.sup.3C, R.sup.3D, R.sup.4A, R.sup.4B, R.sup.4C,
R.sup.4D, R.sup.5A, R.sup.5B, R.sup.5C, R.sup.5D, R.sup.6A,
R.sup.6B, R.sup.6C, R.sup.6D, R.sup.7A, R.sup.7B, R.sup.7C,
R.sup.7D, R.sup.8A, R.sup.8B, R.sup.8C, R.sup.8D, R.sup.9A,
R.sup.9B, R.sup.9C, R.sup.9D, R.sup.10A, R.sup.10B, R.sup.10C and
R.sup.10D are independently hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, or substituted or unsubstituted heteroaryl; R.sup.1B,
R.sup.1C, R.sup.2B, R.sup.2C, R.sup.3B, R.sup.3C, R.sup.4B,
R.sup.4C, R.sup.5B, R.sup.5C, R.sup.6B, R.sup.6C, R.sup.7B,
R.sup.7C, R.sup.8B, R.sup.8C, R.sup.9B, R.sup.9C, R.sup.10B and
R.sup.10C substituents bonded to the same nitrogen atom may
optionally be joined to form a substituted or unsubstituted
heterocycloalkyl or substituted or unsubstituted heteroaryl; and
X.sup.1.1, X.sup.2.1, X.sup.3.1, X.sup.4.1, X.sup.5.1, X.sup.6.1,
X.sup.7.1, X.sup.8.1, X.sup.9.1 and X.sup.10.1 are independently
--Cl, --Br, --I or --F, wherein at least one of X.sup.1, X.sup.2
and X.sup.3 is N.
2.-3. (canceled)
4. The compound of claim 1, or a pharmaceutically acceptable salt
thereof, wherein the compound has structural Formula (II):
##STR00311## wherein: n3.2, and n3.3 are independently an integer
from 0 to 4; m3.2, m3.3, v3.2 and v3.3 are independently 1 or 2
R.sup.4 is hydrogen, --CX.sup.4.1.sub.3, --CN,
--C(O)NR.sup.4BR.sup.4C, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl; R.sup.3.2 is hydrogen, halogen,
--CX.sup.3.2.sub.3, --CHX.sup.3.2.sub.2, --CH.sub.2X.sup.3.2, --CN,
--N.sub.3, --SO.sub.n3.2R.sup.3.2A,
--SO.sub.v3.2NR.sup.3.2BR.sup.3.2C, --NHNR.sup.3.2BR.sup.3.2C,
--ONR.sup.3.2BR.sup.3.2C, --NHC(O)NHNR.sup.3.2BR.sup.3.2C,
--NHC(O)NR.sup.3.2BR.sup.3.2C, --N(O).sub.m3.2,
--NR.sup.3.2BR.sup.3.2C, --C(O)R.sup.3.2D, --C(O)OR.sup.3.2D,
--C(O)NR.sup.3.2BR.sup.3.2C, --OR.sup.3.2A,
--NR.sup.3.2BSO.sub.2R.sup.3.2A, --NR.sup.3.2BC(O)R.sup.3.2D,
--NR.sup.3.2BC(O)OR.sup.3.2D, --NR.sup.3.2BOR.sup.3.2D,
--OCX.sup.3.2.sub.3, --OCHX.sup.3.2.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3.3 is hydrogen,
halogen, --CX.sup.3.3.sub.3, --CHX.sup.3.3.sub.2,
--CH.sub.2X.sup.3.3, --CN, --N.sub.3, --SO.sub.n3.3R.sup.3.3A,
--SO.sub.v3.3NR.sup.3.3BR.sup.3.3C, --NHNR.sup.3.3BR.sup.3.3C,
--ONR.sup.3.3BR.sup.3.3C, --NHC(O)NHNR.sup.3.3BR.sup.3.3C,
--NHC(O)NR.sup.3.3BR.sup.3.3C, --N(O).sub.m3.3,
--NR.sup.3.3BR.sup.3.3C, --C(O)R.sup.3.3D, --C(O)OR.sup.3.3D,
--C(O)NR.sup.3.3BR.sup.3.3C, --OR.sup.3.3A,
--NR.sup.3.3BSO.sub.2R.sup.3.3A, --NR.sup.3.3BC(O)R.sup.3.3D,
--NR.sup.3.3BC(O)OR.sup.3.3D, --NR.sup.3.3BOR.sup.3.3D,
--OCX.sup.3.3.sub.3, --OCHX.sup.3.3.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3.2A, R.sup.3.2B,
R.sup.3.2C, R.sup.3.2D, R.sup.3.3A, R.sup.3.3B, R.sup.3.3C and
R.sup.3.3D are independently hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, or substituted or unsubstituted heteroaryl; R.sup.3.2B,
R.sup.3.2C, R.sup.3.3B and R.sup.3.3C substituents bonded to the
same nitrogen atom may optionally be joined to form a substituted
or unsubstituted heterocycloalkyl or substituted or unsubstituted
heteroaryl; and X.sup.3.2 and X.sup.3.3 are independently --Cl,
--Br, --I or --F.
5. The compound of claim 4, or a pharmaceutically acceptable salt
thereof, wherein the compound has structural Formula (IIa):
##STR00312##
6. (canceled)
7. The compound of claim 5, or a pharmaceutically acceptable salt
thereof, wherein the compound has structural Formula (IIc):
##STR00313##
8.-19. (canceled)
20. The compound of claim 1, or a pharmaceutically acceptable salt
thereof, wherein the compound has structural Formula (III):
##STR00314##
21. The compound of claim 1, or a pharmaceutically acceptable salt
thereof, wherein the compound has structural Formula (IV):
##STR00315##
22. The compound of claim 1, or a pharmaceutically acceptable salt
thereof, wherein the compound has structural Formula (V):
##STR00316##
23.-27. (canceled)
28. A pharmaceutical composition, comprising a compound having
structural Formula (I) and a pharmaceutically acceptable excipient:
##STR00317## or a pharmaceutically acceptable salt thereof,
wherein: X.sup.1 is CR.sup.8 or N; X.sup.2 is CR.sup.9 or N;
X.sup.3 is CR.sup.10 or N; n1, n2, n3, n4, n5, n6, n7, n8, n9 and
n10 are independently an integer from 0 to 4; m1, m2, m3, m4, m5,
m6, m7, m8, m9, m10, v1, v2, v3, v4, v5, v6, v7, v8, v9 and v10 are
independently 1 or 2; z1 is an integer from 0 to 5; z2 is an
integer from 0 to 2; z3 is an integer from 0 to 11; z4 is an
integer from 0 to 2; L.sup.7 is a bond, --O--, --S--,
--NR.sup.72B--, --C(O)--, --C(O)O--, --S(O)--, --S(O).sub.2--,
substituted or unsubstituted alkylene, substituted or unsubstituted
heteroalkylene, substituted or unsubstituted cycloalkylene,
substituted or unsubstituted heterocycloalkylene, substituted or
unsubstituted arylene, or substituted or unsubstituted
heteroarylene; R.sup.1 is hydrogen, halogen, --CX.sup.1.1.sub.3,
--CHX.sup.1.1.sub.2, --CH.sub.2X.sup.1.1, --CN, --N.sub.3,
--SO.sub.n1R.sup.1A, --SO.sub.v1NR.sup.1BR.sup.1C,
--NHNR.sup.1BR.sup.1C, --ONR.sup.1BR.sup.1C,
--NHC(O)NHNR.sup.1BR.sup.1C, --NHC(O)NR.sup.1BR.sup.1C,
--N(O).sub.m1, --NR.sup.1BR.sup.1C, --C(O)R.sup.1D,
--C(O)OR.sup.1D, --C(O)NR.sup.1BR.sup.1C, --OR.sup.1A,
--NR.sup.1BSO.sub.2R.sup.1A, --NR.sup.1BC(O)R.sup.1D,
--NR.sup.1BC(O)OR.sup.1D, --NR.sup.1BOR.sup.1D,
--OCX.sup.1.1.sub.3, --OCHX.sup.1.2, substituted or unsubstituted
alkyl, substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl; R.sup.2 is hydrogen, halogen,
--CX.sup.2.1.sub.3, --CHX.sup.2.1.sub.2, --CH.sub.2X.sup.2.1, --CN,
--N.sub.3, --SO.sub.n2R.sup.2A, --SO.sub.v2NR.sup.2BR.sup.2C,
--NHNR.sup.2BR.sup.2C, --ONR.sup.2BR.sup.2C,
--NHC(O)NHNR.sup.2BR.sup.2C, --NHC(O)NR.sup.2BR.sup.2C,
--N(O).sub.m2, --NR.sup.2BR.sup.2C, --C(O)R.sup.2D,
--C(O)OR.sup.2D, --C(O)NR.sup.2BR.sup.2C, --OR.sup.2A,
--NR.sup.2BSO.sub.2R.sup.2A, --NR.sup.2BC(O)R.sup.2D,
--NR.sup.2BC(O)OR.sup.2D, --NR.sup.2BOR.sup.2D,
--OCX.sup.2.1.sub.3, --OCHX.sup.2.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3 is
independently hydrogen, halogen, --CX.sup.3.1.sub.3,
--CHX.sup.3.1.sub.2, --CH.sub.2X.sup.3.1, --CN, --N.sub.3,
--SO.sub.n3R.sup.3A, --SO.sub.v3NR.sup.3BR.sup.3C,
--NHNR.sup.3BR.sup.3C, --ONR.sup.3BR.sup.3C,
--NHC(O)NHNR.sup.3BR.sup.3C, --NHC(O)NR.sup.3BR.sup.3C,
--N(O).sub.m3, --NR.sup.3BR.sup.3C, --C(O)R.sup.3D,
--C(O)OR.sup.3D, --C(O)NR.sup.3BR.sup.3C, --OR.sup.3A,
--NR.sup.3BSO.sub.2R.sup.3A, --NR.sup.3BC(O)R.sup.3D,
--NR.sup.3BC(O)OR.sup.3D, --NR.sup.3BOR.sup.3D,
--OCX.sup.3.1.sub.3, --OCHX.sup.3.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.4 is hydrogen,
halogen, --CX.sup.4.1.sub.3, --CHX.sup.4.1.sub.2,
--CH.sub.2X.sup.4.1, --CN, --N.sub.3, --SO.sub.n4R.sup.4A,
--SO.sub.v4NR.sup.4BR.sup.4C, --NHNR.sup.4BR.sup.4C,
--ONR.sup.4BR.sup.4B, --NHC(O)NHNR.sup.4BR.sup.4C,
--NHC(O)NR.sup.4BR.sup.4C, --N(O).sub.m4, --NR.sup.4BR.sup.4C,
--C(O)R.sup.4D, --C(O)OR.sup.4D, --C(O)NR.sup.4BR.sup.4C,
--OR.sup.4A, --NR.sup.4BSO.sub.2R.sup.4A, --NR.sup.4BC(O)R.sup.4D,
--NR.sup.4BC(O)OR.sup.4D, --NR.sup.4BOR.sup.4D,
--OCX.sup.4.1.sub.3, --OCHX.sup.4.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.5 is
independently hydrogen, halogen, oxo, --CX.sup.5.1.sub.3,
--CHX.sup.5.1.sub.2, --CH.sub.2X.sup.5.1, --CN, --N.sub.3,
--SO.sub.n5R.sup.5A, --SO.sub.v5NR.sup.5BR.sup.5C,
--NHNR.sup.5BR.sup.5C, --ONR.sup.5BR.sup.5C,
--NHC(O)NHNR.sup.5BR.sup.5C, --NHC(O)NR.sup.5BR.sup.5C,
--N(O).sub.m5, --NR.sup.5BR.sup.5C, --C(O)R.sup.5D,
--C(O)OR.sup.5D, --C(O)NR.sup.5BR.sup.5C, --OR.sup.5A,
--NR.sup.5BSO.sub.2R.sup.5A, --NRBC(O)R.sup.5D,
--NR.sup.5BC(O)OR.sup.5D, --NR.sup.5BOR.sup.5D,
--OCX.sup.5.1.sub.3, --OCHX.sup.5.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.6 is
independently hydrogen, halogen, oxo, --CX.sup.6.1.sub.3,
--CHX.sup.6.1.sub.2, --CH.sub.2X.sup.6.1, --CN, --N.sub.3,
--SO.sub.n6R.sup.6A, --SO.sub.v6NR.sup.6BR.sup.6C,
--NHNR.sup.6BR.sup.6C, --OR.sup.6BR.sup.6C,
--NHC(O)NHNR.sup.6BR.sup.6C, --NHC(O)NR.sup.6BR.sup.6C,
--N(O).sub.m6, --NR.sup.6BR.sup.6C, --C(O)R.sup.6D,
--C(O)OR.sup.6D, --C(O)NR.sup.6BR.sup.6C, --OR.sup.6A,
--NR.sup.6BSO.sub.2R.sup.6A, --NR.sup.6BC(O)R.sup.6D,
--NR.sup.6BC(O)OR.sup.6D, --NR.sup.6BOR.sup.6D,
--OCX.sup.6.1.sub.3, --OCHX.sup.6.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.7 is hydrogen,
halogen, --CX.sup.7.1.sub.3, --CHX.sup.7.1.sub.2,
--CH.sub.2X.sup.7.1, --CN, --N.sub.3, --SO.sub.n7R.sup.7A,
--SO.sub.v7NR.sup.7BR.sup.7C, R.sup.7BR.sup.7C,
--ONR.sup.7BR.sup.7C, --NHC(O)NHNR.sup.7BR.sup.7C,
--NHC(O)NR.sup.7BR.sup.7C, --N(O).sub.m7, --NR.sup.7BR.sup.7C,
--C(O)R.sup.7D, --C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C,
--OR.sup.7A, --NR.sup.7BSO.sub.2R.sup.7A, --NR.sup.7BC(O)R.sup.7D,
--NR.sup.7BC(O)OR.sup.7D, --NR.sup.7BOR.sup.7D,
--OCX.sup.7.1.sub.3, --OCHX.sup.7.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.8 is hydrogen,
halogen, --CX.sup.8.1.sub.3, --CHX.sup.8.1.sub.2,
--CH.sub.2X.sup.8.1, --CN, --N.sub.3, --SO.sub.n8R.sup.8A,
--SO.sub.v8NR.sup.8BR.sup.8C, --NHNR.sup.8BR.sup.8C,
--ONR.sup.8BR.sup.8C, --NHC(O)NHNR.sup.8BR.sup.8C,
--NHC(O)NR.sup.8BR.sup.8C, --N(O).sub.m8, --NR.sup.8BR.sup.8C,
--C(O)R.sup.8D, --C(O)OR.sup.8D, --C(O)NR.sup.8BR.sup.8C,
--OR.sup.8A, --NR.sup.8BSO.sub.2R.sup.8A, --NR.sup.8BC(O)R.sup.8D,
--NR.sup.8BC(O)OR.sup.8D, --NR.sup.8BOR.sup.8D,
--OCX.sup.8.1.sub.3, --OCHX.sup.8.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.9 is hydrogen,
halogen, --CX.sup.9.1.sub.3, --CHX.sup.9.1.sub.2,
--CH.sub.2X.sup.9.1, --CN, --N.sub.3, --SO.sub.n9R.sup.9A,
--SO.sub.v9NR.sup.9BR.sup.9C, --NHNR.sup.9BR.sup.9C,
--ONR.sup.9BR.sup.9C, --NHC(O)NHNR.sup.9BR.sup.9C,
--NHC(O)NR.sup.9BR.sup.9C, --N(O).sub.m9, --NR.sup.9BR.sup.9C,
--C(O)R.sup.9D, --C(O)OR.sup.9D, --C(O)NR.sup.9BR.sup.9C,
--OR.sup.9A, --NR.sup.9BSO.sub.2R.sup.9A, --NR.sup.9BC(O)R.sup.9D,
--NR.sup.9BC(O)OR.sup.9D, --NR.sup.9BOR.sup.9D,
--OCX.sup.9.1.sub.3, --OCHX.sup.9.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.10 is hydrogen,
halogen, --CX.sup.10.1.sub.3, --CHX.sup.10.1.sub.2,
--CH.sub.2X.sup.10.1, --CN, --N.sub.3, --SO.sub.n10R.sup.10A,
--SO.sub.v10NR.sup.10BR.sup.10C, --NHNR.sup.10BR.sup.10C,
--ONR.sup.10BR.sup.10C, --NHC(O)NHNR.sup.10BR.sup.10C,
--NHC(O)NR.sup.10BR.sup.10C, --N(O).sub.m10, --NR.sup.10BR.sup.10C,
--C(O)R.sup.10D, --C(O)OR.sup.10D, --C(O)NR.sup.10BR.sup.10C,
--OR.sup.10A, --NR.sup.10BSO.sub.2R.sup.10A,
--NR.sup.10BC(O)R.sup.10D, --NR.sup.10BC(O)OR.sup.10D,
--NR.sup.10BOR.sup.10D, --OCX.sup.10.1.sub.3,
--OCHX.sup.10.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl; R.sup.1A, R.sup.1B, R.sup.1C,
R.sup.1D, R.sup.2A, R.sup.2B, R.sup.2C, R.sup.2D, R.sup.3A,
R.sup.3B, R.sup.3C, R.sup.3D, R.sup.4A, R.sup.4B, R.sup.4C,
R.sup.4D, R.sup.5A, R.sup.5B, R.sup.5C, R.sup.5D, R.sup.6A,
R.sup.6B, R.sup.6C, R.sup.6D, R.sup.7A, R.sup.7B, R.sup.7C,
R.sup.7D, R.sup.8A, R.sup.8B, R.sup.8C, R.sup.8D, R.sup.9A,
R.sup.9B, R.sup.9C, R.sup.9D, R.sup.10A, R.sup.10B, R.sup.10C and
R.sup.10D are independently hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, or substituted or unsubstituted heteroaryl; R.sup.1B,
R.sup.1C, R.sup.2B, R.sup.2C, R.sup.3B, R.sup.3C, R.sup.4B,
R.sup.4C, R.sup.5B, R.sup.5C, R.sup.6B, R.sup.6C, R.sup.7B,
R.sup.7C, R.sup.8B, R.sup.8C, R.sup.9B, R.sup.9C, R.sup.10B and
R.sup.10C substituents bonded to the same nitrogen atom may
optionally be joined to form a substituted or unsubstituted
heterocycloalkyl or substituted or unsubstituted heteroaryl; and
X.sup.1.1, X.sup.2.1, X.sup.3.1, X.sup.4.1, X.sup.5.1, X.sup.6.1,
X.sup.7.1, X.sup.8.1, X.sup.9.1 and X.sup.10.1 are independently
--Cl, --Br, --I or --F, wherein at least one of X.sup.1, X.sup.2
and X.sup.3 is N.
29. A method of treating or preventing a disease or disorder
mediated by C--C chemokine receptor type 4 (CCR4), comprising
administering to a subject in need thereof a therapeutically
effective amount of the pharmaceutical composition of claim 28.
30. A method of inhibiting CCR4, comprising contacting CCR4 with
the compound of claim 1.
31. A method of treating or preventing a disease or disorder
mediated by CCR4, comprising administering to a subject in need
thereof a therapeutically effective amount of a compound having
structural Formula (I): ##STR00318## or a pharmaceutically
acceptable salt thereof, wherein: X.sup.1 is CR.sup.8 or N; X.sup.2
is CR.sup.9 or N; X.sup.3 is CR.sup.10 or N; n1, n2, n3, n4, n5,
n6, n7, n8, n9 and n10 are independently an integer from 0 to 4;
m1, m2, m3, m4, m5, m6, m7, m8, m9, m10, v1, v2, v3, v4, v5, v6,
v7, v8, v9 and v10 are independently 1 or 2; z1 is an integer from
0 to 5; z2 is an integer from 0 to 2; z3 is an integer from 0 to
11; z4 is an integer from 0 to 2; L.sup.7 is a bond, --O--, --S--,
--NR.sup.72B--, --C(O)--, --C(O)O--, --S(O)--, --S(O).sub.2--,
substituted or unsubstituted alkylene, substituted or unsubstituted
heteroalkylene, substituted or unsubstituted cycloalkylene,
substituted or unsubstituted heterocycloalkylene, substituted or
unsubstituted arylene, or substituted or unsubstituted
heteroarylene; R.sup.1 is hydrogen, halogen, --CX.sup.1.1.sub.3,
--CHX.sup.1.1.sub.2, --CH.sub.2X.sup.1.1, --CN, --N.sub.3,
--SO.sub.n1R.sup.1A, --SO.sub.v1NR.sup.1BR.sup.1C,
--NHNR.sup.1BR.sup.1C, --ONR.sup.1BR.sup.1C,
--NHC(O)NHNR.sup.1BR.sup.1C, --NHC(O)NR.sup.1BR.sup.1C,
--N(O).sub.m1, --NR.sup.1BR.sup.1C, --C(O)R.sup.1D,
--C(O)OR.sup.1D, --C(O)NR.sup.1BR.sup.1C, --OR.sup.1A,
--NR.sup.1BSO.sub.2R.sup.1A, --NR.sup.1BC(O)R.sup.1D,
--NR.sup.1BC(O)OR.sup.1D, --NR.sup.1BOR.sup.1D,
--OCX.sup.1.1.sub.3, --OCHX.sup.1.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.2 is hydrogen,
halogen, --CX.sup.2.1.sub.3, --CHX.sup.2.1.sub.2,
--CH.sub.2X.sup.2.1, --CN, --N.sub.3, --SO.sub.n2R.sup.2A,
--SO.sub.v2NR.sup.2BR.sup.2C, --NHNR.sup.2BR.sup.2C,
--ONR.sup.2BR.sup.2C, --NHC(O)NHNR.sup.2BR.sup.2C,
--NHC(O)NR.sup.2BR.sup.2C, --N(O).sub.m2, --NR.sup.2BR.sup.2C,
--C(O)R.sup.2D, --C(O)OR.sup.2D, --C(O)NR.sup.2BR.sup.2C,
--OR.sup.2A, --NR.sup.2BSO.sub.2R.sup.2A, --NR.sup.2BC(O)R.sup.2D,
--NR.sup.2BC(O)OR.sup.2D, --NR.sup.2BOR.sup.2D,
--OCX.sup.2.1.sub.3, --OCHX.sup.2.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3 is
independently hydrogen, halogen, --CX.sup.3.1.sub.3,
--CHX.sup.3.1.sub.2, --CH.sub.2X.sup.3.1, --CN, --N.sub.3,
--SO.sub.n3R.sup.3A, --SO.sub.v3NR.sup.3BR.sup.3C,
--NHNR.sup.3BR.sup.3C, --ONR.sup.3BR.sup.3C,
--NHC(O)NHNR.sup.3BR.sup.3C, --NHC(O)NR.sup.3BR.sup.3C,
--N(O).sub.m3, --NR.sup.3BR.sup.3C, --C(O)R.sup.3D,
--C(O)OR.sup.3D, --C(O)NR.sup.3BR.sup.3C, --OR.sup.3A,
--NR.sup.3BSO.sub.2R.sup.3A, --NR.sup.3BC(O)R.sup.3D,
--NR.sup.3BC(O)OR.sup.3D, --NR.sup.3BOR.sup.3D,
--OCX.sup.3.1.sub.3, --OCHX.sup.3.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.4 is hydrogen,
halogen, --CX.sup.4.1.sub.3, --CHX.sup.4.1.sub.2,
--CH.sub.2X.sup.4.1, --CN, --N.sub.3, --SO.sub.n4R.sup.4A,
--SO.sub.v4NR.sup.4BR.sup.4C, --NHNR.sup.4BR.sup.4C,
--ONR.sup.4BR.sup.4C, --NHC(O)NHNR.sup.4BR.sup.4C,
--NHC(O)NR.sup.4BR.sup.4C, --N(O).sub.m4, --NR.sup.4BR.sup.4C,
--C(O)R.sup.4D, --C(O)OR.sup.4D, --C(O)NR.sup.4BR.sup.4C,
--OR.sup.4A, --NR.sup.4BSO.sub.2R.sup.4A, --NR.sup.4BC(O)R.sup.4D,
--NR.sup.4BC(O)OR.sup.4D, --NR.sup.4BOR.sup.4D,
--OCX.sup.4.1.sub.3, --OCHX.sup.4.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.5 is
independently hydrogen, halogen, oxo, --CX.sup.5.1.sub.3,
--CHX.sup.5.1.sub.2, --CH.sub.2X.sup.5.1, --CN, --N.sub.3,
--SO.sub.n5R.sup.5A, --SO.sub.v5NR.sup.5BR.sup.5C,
--NHNR.sup.5BR.sup.5C, --ONR.sup.5BR.sup.5C,
--NHC(O)NHNR.sup.5BR.sup.5C, --NHC(O)NR.sup.5BR.sup.5C,
--N(O).sub.m5, --NR.sup.5BR.sup.5C, --C(O)R.sup.5D,
--C(O)OR.sup.5D, --C(O)NR.sup.5BR.sup.5C, --OR.sup.5A,
--NR.sup.5BSO.sub.2R.sup.5A, --NR.sup.5BC(O)R.sup.5D,
--NR.sup.5BC(O)OR.sup.5D, --NR.sup.5BOR.sup.5D,
--OCX.sup.5.1.sub.3, --OCHX.sup.5.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.6 is
independently hydrogen, halogen, oxo, --CX.sup.6.1.sub.3,
--CHX.sup.6.1.sub.2, --CH.sub.2X.sup.6.1, --CN, --N.sub.3,
--SO.sub.n6R.sup.6A, --SO.sub.v6NR.sup.6BR.sup.6C,
--NHNR.sup.6BR.sup.6C, --OR.sup.6BR.sup.6C,
--NHC(O)NHNR.sup.6BR.sup.6C, --NHC(O)NR.sup.6BR.sup.6C,
--N(O).sub.m6, --NR.sup.6BR.sup.6C, --C(O)R.sup.6D,
--C(O)OR.sup.6D, --C(O)NR.sup.6BR.sup.6C, --OR.sup.6A,
--NR.sup.6BSO.sub.2R.sup.6A, --NR.sup.6BC(O)R.sup.6D,
--NR.sup.6BC(O)OR.sup.6D, --NR.sup.6BOR.sup.6D,
--OCX.sup.6.1.sub.3, --OCHX.sup.6.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.7 is hydrogen,
halogen, --CX.sup.7.1.sub.3, --CHX.sup.7.1.sub.2,
--CH.sub.2X.sup.7.1, --CN, --N.sub.3, --SO.sub.n7R.sup.7A,
--SO.sub.v7NR.sup.7BR.sup.7C, --NHNR.sup.7BR.sup.7C,
--ONR.sup.7BR.sup.7C, --NHC(O)NHNR.sup.7BR.sup.7C,
--NHC(O)NR.sup.7BR.sup.7C, --N(O).sub.m7, --NR.sup.7BR.sup.7C,
--C(O)R.sup.7D, --C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C,
--OR.sup.7A, --NR.sup.7BSO.sub.2R.sup.7A, --NR.sup.7BC(O)R.sup.7D,
--NR.sup.7BC(O)OR.sup.7D, --NR.sup.7BOR.sup.7D,
--OCX.sup.7.1.sub.3, --OCHX.sup.7.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.8 is hydrogen,
halogen, --CX.sup.8.1.sub.3, --CHX.sup.8.1.sub.2,
--CH.sub.2X.sup.8.1, --CN, --N.sub.3, --SO.sub.n8R.sup.8A,
--SO.sub.v8NR.sup.8BR.sup.8C, --NHNR.sup.8BR.sup.8C,
--ONR.sup.8BR.sup.8C, --NHC(O)NHNR.sup.8BR.sup.8C,
--NHC(O)NR.sup.8BR.sup.8C, --N(O).sub.m8, --NR.sup.8BR.sup.8C,
--C(O)R.sup.8D, --C(O)OR.sup.8D, --C(O)NR.sup.8BR.sup.8C,
--OR.sup.8A, --NR.sup.8BSO.sub.2R.sup.8A, --NR.sup.8BC(O)R.sup.8D,
--NR.sup.8BC(O)OR.sup.8D, --NR.sup.8BOR.sup.8D,
--OCX.sup.8.1.sub.3, --OCHX.sup.8.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.9 is hydrogen,
halogen, --CX.sup.9.1.sub.3, --CHX.sup.9.1.sub.2,
--CH.sub.2X.sup.9.1, --CN, --N.sub.3, --SO.sub.n9R.sup.9A,
--SO.sub.v9NR.sup.9BR.sup.9C, --NHNR.sup.9BR.sup.9C,
--ONR.sup.9BR.sup.9C, --NHC(O)NHNR.sup.9BR.sup.9C,
--NHC(O)NR.sup.9BR.sup.9C, --N(O).sub.m9, --NR.sup.9BR.sup.9C,
--C(O)R.sup.9D, --C(O)OR.sup.9D, --C(O)NR.sup.9BR.sup.9C,
--OR.sup.9A, --NR.sup.9BSO.sub.2R.sup.9A, --NR.sup.9BC(O)R.sup.9D,
--NR.sup.9BC(O)OR.sup.9D, --NR.sup.9BOR.sup.9D,
--OCX.sup.9.1.sub.3, --OCHX.sup.9.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.10 is hydrogen,
halogen, --CX.sup.10.1.sub.3, --CHX.sup.10.1.sub.2,
--CH.sub.2X.sup.10.1, --CN, --N.sub.3, --SO.sub.n10R.sup.10A,
--SO.sub.v10NR.sup.10BR.sup.10C, --NHNR.sup.10BR.sup.10C,
--ONR.sup.10BR.sup.10C, --NHC(O)NHNR.sup.10BR.sup.10C,
--NHC(O)NR.sup.10BR.sup.10C, --N(O).sub.m10, --NR.sup.10BR.sup.10C,
--C(O)R.sup.10D, --C(O)OR.sup.10D, --C(O)NR.sup.10BR.sup.10C,
--OR.sup.10A, --R.sup.10BSO.sub.2R.sup.10A,
--NR.sup.10BC(O)R.sup.10D, --NR.sup.10BC(O)OR.sup.10D,
--NR.sup.10BOR.sup.10D, --OCX.sup.10.1.sub.3,
--OCHX.sup.10.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl; R.sup.1A, R.sup.1B, R.sup.1C,
R.sup.1D, R.sup.2A, R.sup.2B, R.sup.2C, R.sup.2D, R.sup.3A,
R.sup.3B, R.sup.3C, R.sup.3D, R.sup.4A, R.sup.4B, R.sup.4C,
R.sup.4D, R.sup.5A, R.sup.5B, R.sup.5C, R.sup.5D, R.sup.6A,
R.sup.6B, R.sup.6C, R.sup.6D, R.sup.7A, R.sup.7B, R.sup.7C,
R.sup.7D, R.sup.8A, R.sup.8B, R.sup.8C, R.sup.8D, R.sup.9A,
R.sup.9B, R.sup.9C, R.sup.9D, R.sup.10A, R.sup.10B, R.sup.10C and
R.sup.10D are independently hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, or substituted or unsubstituted heteroaryl; R.sup.1B,
R.sup.1C, R.sup.2B, R.sup.2C, R.sup.3B, R.sup.3C, R.sup.4B,
R.sup.4C, R.sup.5B, R.sup.5C, R.sup.6B, R.sup.6C, R.sup.7B,
R.sup.7C, R.sup.8B, R.sup.8C, R.sup.9B, R.sup.9C, R.sup.10B and
R.sup.10C substituents bonded to the same nitrogen atom may
optionally be joined to form a substituted or unsubstituted
heterocycloalkyl or substituted or unsubstituted heteroaryl; and
X.sup.1.1, X.sup.2.1, X.sup.3.1, X.sup.4.1, X.sup.5.1, X.sup.6.1,
X.sup.7.1, X.sup.8.1, X.sup.9.1 and X.sup.10.1 are independently
--Cl, --Br, --I or --F, wherein at least one of X.sup.1, X.sup.2
and X.sup.3 is N.
32.-33. (canceled)
34. The method of claim 31, wherein the compound has structural
Formula (II): ##STR00319## or a pharmaceutically acceptable salt
thereof, wherein: n3.2, and n3.3 are independently an integer from
0 to 4; m3.2, m3.3, v3.2 and v3.3 are independently 1 or 2 R.sup.4
is hydrogen, --CX.sup.4.1.sub.3, --CN, --C(O)NR.sup.4BR.sup.4C,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, or substituted or unsubstituted heteroaryl; R.sup.3.2 is
hydrogen, halogen, --CX.sup.3.2.sub.3, --CHX.sup.3.2.sub.2,
--CH.sub.2X.sup.3.2, --CN, --N.sub.3, --SO.sub.n3.2R.sup.3.2A,
--SO.sub.v3.2NR.sup.3.2BR.sup.3.2C, --NHNR.sup.3.2BR.sup.3.2C,
--ONR.sup.3.2BR.sup.3.2C, --NHC(O)NHNR.sup.3.2BR.sup.3.2C,
--NHC(O)NR.sup.3.2BR.sup.3.2C, --N(O).sub.m3.2,
--NR.sup.3.2BR.sup.3.2C, --C(O)R.sup.3.2D, --C(O)OR.sup.3.2D,
--C(O)NR.sup.3.2BR.sup.3.2C, --OR.sup.3.2A,
--NR.sup.3.2BSO.sub.2R.sup.3.2A, --NR.sup.3.2BC(O)R.sup.3.2D,
--NR.sup.3.2BC(O)OR.sup.3.2D, --NR.sup.3.2BOR.sup.3.2D,
--OCX.sup.3.2.sub.3, --OCHX.sup.3.2.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3.3 is hydrogen,
halogen, --CX.sup.3.3.sub.3, --CHX.sup.3.3.sub.2,
--CH.sub.2X.sup.3.3, --CN, --N.sub.3, --SO.sub.n3.3R.sup.3.3A,
--SO.sub.v3.3NR.sup.3.3BR.sup.3.3C, --NHNR.sup.3.3BR.sup.3.3C,
--ONR.sup.3.3BR.sup.3.3C, --NHC(O)NHNR.sup.3.3BR.sup.3.3C,
--NHC(O)NR.sup.3.3BR.sup.3.3C, --N(O).sub.m3.3,
--NR.sup.3.3BR.sup.3.3C, --C(O)R.sup.3.3D, --C(O)OR.sup.3.3D,
--C(O)NR.sup.3.3BR.sup.3.3C, --OR.sup.3.3A,
--NR.sup.3.3BSO.sub.2R.sup.3.3A, --NR.sup.3.3BC(O)R.sup.3.3D,
--NR.sup.3.3BC(O)OR.sup.3.3D, --NR.sup.3.3BOR.sup.3.3D,
--OCX.sup.3.3.sub.3, --OCHX.sup.3.3.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3.2A, R.sup.3.2B,
R.sup.3.2C, R.sup.3.2D, R.sup.3.3A, R.sup.3.3B, R.sup.3.3C and
R.sup.3.3D are independently hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, or substituted or unsubstituted heteroaryl; R.sup.3.2B,
R.sup.3.2C, R.sup.3.2B and R.sup.3.2C substituents bonded to the
same nitrogen atom may optionally be joined to form a substituted
or unsubstituted heterocycloalkyl or substituted or unsubstituted
heteroaryl; and X.sup.3.2 and X.sup.3.3 are independently --Cl,
--Br, --I or --F.
35. The method of claim 34, wherein the compound has structural
Formula (IIa): ##STR00320## or a pharmaceutically acceptable salt
thereof.
36. The method of claim 34, wherein the compound has structural
Formula (IIb): ##STR00321## or a pharmaceutically acceptable salt
thereof.
37. The method of claim 35, wherein the compound has structural
Formula (IIc): ##STR00322## or a pharmaceutically acceptable salt
thereof.
38. The method of claim 36, wherein the compound has structural
Formula (IId): ##STR00323## or a pharmaceutically acceptable salt
thereof.
39.-56. (canceled)
57. The method of claim 31, wherein the disease or disorder is an
immune, inflammatory, or cardiovascular or metabolic disease or
disorder.
58.-62. (canceled)
63. The method of claim 31, wherein the disease or disorder is
cancer.
64. The method of claim 63, further comprising co-administering a
chemotherapeutic agent or anticancer agent in combination with a
compound of structural Formula (I).
65.-67. (canceled)
68. The method of claim 63, wherein the cancer is colon cancer or
pancreatic cancer.
Description
CROSS-REFERENCES TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 16/195,506, filed on Nov. 19, 2018, which is a
continuation of U.S. patent application Ser. No. 15/662,861 filed
Jul. 28, 2017, now U.S. Pat. No. 10,179,787, issued on Jan. 15,
2019, and claims the benefit of priority under 35 U.S.C. .sctn.
119(e) of U.S. Provisional Application No. 62/368,848, filed Jul.
29, 2016 and U.S. Provisional Application No. 62/426,087, filed
Nov. 23, 2016. The disclosure of each of the prior applications is
considered part of and is incorporated by reference in the
disclosure of this application in their entireties and for all
purposes.
BACKGROUND
Brief Summary of the Invention
[0002] In an aspect provided herein, is a compound having
structural Formula (I):
##STR00001##
or a pharmaceutically acceptable salt thereof. X.sup.1 is CR.sup.8
or N. X.sup.2 is CR.sup.9 or N. X.sup.3 is CR.sup.10 or N. The
symbols n1, n2, n3, n4, n5, n6, n7, n8, n9 and n10 are
independently an integer from 0 to 4. The symbol z3 is an integer
from 0 to 11. In embodiments, z3 is independently an integer from 0
to 4. The symbols m1, m2, m3, m4, m5, m6, m7, m8, m9, m10, v1, v2,
v3, v4, v5, v6, v7, v8, v9 and v10 are independently 1 or 2. The
symbol z1 is an integer from 0 to 5. The symbol z2 is an integer
from 0 to 4. In embodiments, z2 is an integer from 0 to 2. The
symbol z4 is an integer from 0 to 2. L.sup.7 is a bond, --O--,
--S--, --NR.sup.7.2B--, --C(O)--, --C(O)O--, --S(O)--,
--S(O).sub.2--, substituted or unsubstituted alkylene, substituted
or unsubstituted heteroalkylene, substituted or unsubstituted
cycloalkylene, substituted or unsubstituted heterocycloalkylene,
substituted or unsubstituted arylene, or substituted or
unsubstituted heteroarylene. R.sup.1 is hydrogen, halogen,
--CX.sup.1.1.sub.3, --CHX.sup.1.1.sub.2, --CH.sub.2X.sup.1.1, --CN,
--N.sub.3, --SO.sub.n1R.sup.1A, --SO.sub.v1NR.sup.1BR.sup.1C,
--NHNR.sup.1BR.sup.1C, --ONR.sup.1BR.sup.1C,
--NHC(O)NHNR.sup.1BR.sup.1C, --NHC(O)NR.sup.1BR.sup.1C,
--N(O).sub.m1, --NR.sup.1BR.sup.1C, --C(O)R.sup.1D,
--C(O)OR.sup.1D, --C(O)NR.sup.1BR.sup.1C, --OR.sup.1A,
--NR.sup.1BSO.sub.2R.sup.1A, --NR.sup.1BC(O)R.sup.1D,
--NR.sup.1BC(O)OR.sup.1D, --NR.sup.1BOR.sup.1D,
--OCX.sup.1.1.sub.3, --OCHX.sup.1.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. R.sup.2 is hydrogen,
halogen, --CX.sup.2.1.sub.3, --CHX.sup.2.1.sub.2,
--CH.sub.2X.sup.2.1, --CN, --N.sub.3, --SO.sub.n2R.sup.2A,
--SO.sub.v2NR.sup.2BR.sup.2C, --NHNR.sup.2BR.sup.2C,
--ONR.sup.2BR.sup.2C, --OR.sup.2BR.sup.2C,
--NHC(O)NHNR.sup.2BR.sup.2C, --NHC(O)NR.sup.2BR.sup.2C,
--N(O).sub.m2, --NR.sup.2BR.sup.2C, --C(O)R.sup.2D,
--C(O)OR.sup.2D, --C(O)NR.sup.2BR.sup.2C, --OR.sup.2A,
--NR.sup.2BSO.sub.2R.sup.2A, --NR.sup.2BC(O)R.sup.2D,
--NR.sup.2BC(O)OR.sup.2D, --NR.sup.2BOR.sup.2D,
--OCX.sup.2.1.sub.3, --OCHX.sup.2.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. R.sup.3 is
independently hydrogen, halogen, --CX.sup.3.1.sub.3,
--CHX.sup.3.1.sub.2, --CH.sub.2X.sup.3.1, --CN, --N.sub.3,
--SO.sub.n3R.sup.3A, --SO.sub.v3NR.sup.3BR.sup.3C,
--NHNR.sup.3BR.sup.3C, --ONR.sup.3BR.sup.3C,
--NHC(O)NHNR.sup.3BR.sup.3C, --NHC(O)NR.sup.3BR.sup.3C,
--N(O).sub.m3, --NR.sup.3BR.sup.3C, --C(O)R.sup.3D,
--C(O)OR.sup.3D, --C(O)NR.sup.3BR.sup.3C, --OR.sup.3A,
--NR.sup.3BSO.sub.2R.sup.3A, --NR.sup.3BC(O)R.sup.3D,
--NR.sup.3BC(O)OR.sup.3D, --NR.sup.3BOR.sup.3D,
--OCX.sup.3.1.sub.3, --OCHX.sup.3.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. R.sup.4 is hydrogen,
halogen, --CX.sup.4.1.sub.3, --CHX.sup.4.1.sub.2,
--CH.sub.2X.sup.4.1, --CN, --N.sub.3, --SO.sub.n4R.sup.4A,
--SO.sub.v4NR.sup.4BR.sup.4C, --NHNR.sup.4BR.sup.4C,
--ONR.sup.4BR.sup.4C, --NHC(O)NHNR.sup.4BR.sup.4C,
--NHC(O)NR.sup.4BR.sup.4C, --N(O).sub.m4, --NR.sup.4BR.sup.4C,
--C(O)R.sup.4D, --C(O)OR.sup.4D, --C(O)NR.sup.4BR.sup.4C,
--OR.sup.4A, --NR.sup.4BSO.sub.2R.sup.4A, --NR.sup.4BC(O)R.sup.4D,
--NR.sup.4BC(O)OR.sup.4D, --NR.sup.4BOR.sup.4D,
--OCX.sup.4.1.sub.3, --OCHX.sup.4.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. R.sup.5 is
independently hydrogen, halogen, oxo, --CX.sup.5.1.sub.3,
--CHX.sup.5.1.sub.2, --CH.sub.2X.sup.5.1, --CN, --N.sub.3,
--SO.sub.n5R.sup.5A, --SO.sub.v5NR.sup.5BR.sup.5C,
--NHNR.sup.5BR.sup.5C, --ONR.sup.5BR.sup.5C,
--NHC(O)NHNR.sup.5BR.sup.5C, --NHC(O)NR.sup.5BR.sup.5C,
--N(O).sub.m5, --NR.sup.5BR.sup.5C, --C(O)R.sup.5D,
--C(O)OR.sup.5D, --C(O)NR.sup.5BR.sup.5C, --OR.sup.5A,
--NR.sup.5BSO.sub.2R.sup.5A, --NR.sup.5BC(O)R.sup.5D,
--NR.sup.5BC(O)OR.sup.5D, --NR.sup.5BOR.sup.5D,
--OCX.sup.5.1.sub.3, --OCHX.sup.5.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. R.sup.6 is
independently hydrogen, halogen, oxo, --CX.sup.6.1.sub.3,
--CHX.sup.6.1.sub.2, --CH.sub.2X.sup.6.1, --CN, --N.sub.3,
--SO.sub.n6R.sup.6A, --SO.sub.v6NR.sup.6BR.sup.6C,
--NHNR.sup.6BR.sup.6C, --ONR.sup.6BR.sup.6C,
--NHC(O)NHNR.sup.6BR.sup.6C, --NHC(O)NR.sup.6BR.sup.6C,
--N(O).sub.m6, --NR.sup.6BR.sup.6C, --C(O)R.sup.6D,
--C(O)OR.sup.6D, --C(O)NR.sup.6BR.sup.6C, --OR.sup.6A,
--NR.sup.6BSO.sub.2R.sup.6A, --NR.sup.6BC(O)R.sup.6D,
--NR.sup.6BC(O)OR.sup.6D, --NR.sup.6BOR.sup.6D,
--OCX.sup.6.1.sub.3, --OCHX.sup.6.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. R.sup.7 is hydrogen,
halogen, --CX.sup.7.1.sub.3, --CHX.sup.7.1.sub.2,
--CH.sub.2X.sup.7.1, --CN, --N.sub.3, --SO.sub.n7R.sup.7A,
--SO.sub.v7NR.sup.7BR.sup.7C, --NHNR.sup.7BR.sup.7C,
--ONR.sup.7BR.sup.7C, --NHC(O)NHNR.sup.7BR.sup.7C,
--NHC(O)NR.sup.7BR.sup.7C, --N(O).sub.m7, --NR.sup.7BR.sup.7C,
--C(O)R.sup.7D, --C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C,
--OR.sup.7A, --NR.sup.7BSO.sub.2R.sup.7A, --NR.sup.7BC(O)R.sup.7D,
--NR.sup.7BC(O)OR.sup.7D, --NR.sup.7BOR.sup.7D,
--OCX.sup.7.1.sub.3, --OCHX.sup.7.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. R.sup.8 is hydrogen,
halogen, --CX.sup.8.1.sub.3, --CHX.sup.8.1.sub.2,
--CH.sub.2X.sup.8.1, --CN, --N.sub.3, --SO.sub.n8R.sup.8A,
--SO.sub.v8NR.sup.8BR.sup.8C, --NHNR.sup.8BR.sup.8C,
--ONR.sup.8BR.sup.8C, --NHC(O)NHNR.sup.8BR.sup.8C,
--NHC(O)NR.sup.8BR.sup.8C, --N(O).sub.m8, --NR.sup.8BR.sup.8C,
--C(O)R.sup.8D, --C(O)OR.sup.8D, --C(O)NR.sup.8BR.sup.8C,
--OR.sup.8A, --NR.sup.8BSO.sub.2R.sup.8A, --NR.sup.8BC(O)R.sup.8D,
--NR.sup.8BC(O)OR.sup.8D, --NR.sup.8BOR.sup.8D,
--OCX.sup.8.1.sub.3, --OCHX.sup.8.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. R.sup.9 is hydrogen,
halogen, --CX.sup.9.1.sub.3, --CHX.sup.9.1.sub.2,
--CH.sub.2X.sup.9.1, --CN, --N.sub.3, --SO.sub.n9R.sup.9A,
--SO.sub.v9NR.sup.9BR.sup.9C, --NHNR.sup.9BR.sup.9C,
--ONR.sup.9BR.sup.9C, --NHC(O)NHNR.sup.9BR.sup.9C,
--NHC(O)NR.sup.9BR.sup.9C, --N(O).sub.m9, --NR.sup.9BR.sup.9C,
--C(O)R.sup.9D, --C(O)OR.sup.9D, --C(O)NR.sup.9BR.sup.9C,
--OR.sup.9A, --NR.sup.9BSO.sub.2R.sup.9A, --NR.sup.9BC(O)R.sup.9D,
--NR.sup.9BC(O)OR.sup.9D, --NR.sup.9BOR.sup.9D,
--OCX.sup.9.1.sub.3, --OCHX.sup.9.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. R.sup.10 is hydrogen,
halogen, --CX.sup.10.1.sub.3, --CHX.sup.10.1.sub.2,
--CH.sub.2X.sup.10.1, --CN, --N.sub.3, --SO.sub.n10R.sup.10A,
--SO.sub.v10NR.sup.10BR.sup.10C, --NHNR.sup.10BR.sup.10C,
--ONR.sup.10BR.sup.10C, --NHC(O)NHNR.sup.10BR.sup.10C,
--NHC(O)NR.sup.10BR.sup.10C, --N(O).sub.m10, --NR.sup.10BR.sup.10C,
--C(O)R.sup.10D, --C(O)OR.sup.10D, --C(O)NR.sup.10BR.sup.10C,
--OR.sup.10A, --NR.sup.10BSO.sub.2R.sup.10A,
--NR.sup.10BC(O)R.sup.10D, --NR.sup.10BC(O)OR.sup.10D,
--NR.sup.10BOR.sup.10D, --OCX.sup.10.1.sub.3,
--OCHX.sup.10.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl. R.sup.1A, R.sup.1B, R.sup.1C,
R.sup.1D, R.sup.2A, R.sup.2B, R.sup.2D, R.sup.2D, R.sup.3A,
R.sup.3B, R.sup.3D, R.sup.3D, R.sup.4A, R.sup.4B, R.sup.4D,
R.sup.4D, R.sup.5A, R.sup.5B, R.sup.5D, R.sup.5D, R.sup.6A,
R.sup.6B, R.sup.6D, R.sup.6D, R.sup.7A, R.sup.7B, R.sup.7D,
R.sup.7D, R.sup.7.2B, R.sup.8A, R.sup.8B, R.sup.8D, R.sup.8D,
R.sup.9A, R.sup.9B, R.sup.9D, R.sup.9D, R.sup.10A, R.sup.10B,
R.sup.10C and R.sup.10D are independently hydrogen, halogen,
--CF.sub.3, --CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH,
--CONH.sub.2, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, or substituted or unsubstituted heteroaryl;
R.sup.1B, R.sup.1C, R.sup.2B, R.sup.2C, R.sup.3B, R.sup.3C,
R.sup.4B, R.sup.4C, R.sup.5B, R.sup.5C, R.sup.6B, R.sup.6C,
R.sup.7B, R.sup.7C, R.sup.8B, R.sup.8C, R.sup.9B, R.sup.9C,
R.sup.10B and R.sup.10C substituents bonded to the same nitrogen
atom may optionally be joined to form a substituted or
unsubstituted heterocycloalkyl or substituted or unsubstituted
heteroaryl. X.sup.1.1, X.sup.2.1, X.sup.3.1, X.sup.4.1, X.sup.5.1,
X.sup.6.1, X.sup.7.1, X.sup.8.1, X.sup.9.1 and X.sup.10.1 are
independently --Cl, --Br, --I or --F. At least one of X.sup.1,
X.sup.2 and X.sup.3 is N.
[0003] In an aspect is provided a pharmaceutical composition,
including a compound as described herein, including embodiments, or
the structural Formula (I), (II), (IIa), (IIb), (IIc), (IId),
(III), (IV), (V), (VI), or (VII), and a pharmaceutically acceptable
excipient.
[0004] In another aspect is provided a method of inhibiting C--C
chemokine receptor type 4 (CCR4), the method comprising contacting
CCR4 with a compound as described herein, including embodiments, or
the structural Formula (I), (II), (IIa), (IIb), (IIc), (IId),
(III), (IV), (V), (VI), or (VII) or a pharmaceutically acceptable
salt thereof.
[0005] In an aspect, is provided a method of treating or preventing
a disease or disorder mediated by CCR4, comprising administering to
a subject in need thereof a therapeutically effective amount of a
compound as described herein, including embodiments, or the
structural Formula (I), (II), (IIa), (IIb), (IIc), (IId), (III),
(IV), (V), (VI), or (VII) or a pharmaceutically acceptable salt
thereof.
[0006] In another aspect, provided herein is a kit including a
compound described herein (e.g., a CCR4 inhibitor) or
pharmaceutical compositions thereof. The kits are generally in the
form of a physical structure housing various components, as
described below, and may be utilized, for example, in practicing
the methods described above.
DETAILED DESCRIPTION
[0007] Provided herein are, for example, compounds and compositions
for inhibition of C--C chemokine receptor type 4, and
pharmaceutical compositions comprising same. Also provided herein
are, for example, methods of treating or preventing a disease,
disorder or condition, or a symptom thereof, mediated by modulation
(e.g., inhibition) of CCR4.
I. Definitions
[0008] The abbreviations used herein have their conventional
meaning within the chemical and biological arts. The chemical
structures and formulae set forth herein are constructed according
to the standard rules of chemical valency known in the chemical
arts.
[0009] Where substituent groups are specified by their conventional
chemical formulae, written from left to right, they equally
encompass the chemically identical substituents that would result
from writing the structure from right to left, e.g., --CH.sub.2O--
is equivalent to --OCH.sub.2--.
[0010] The term "alkyl," by itself or as part of another
substituent, means, unless otherwise stated, a straight (i.e.,
unbranched) or branched carbon chain (or carbon), or combination
thereof, which may be fully saturated, mono- or polyunsaturated and
can include mono-, di- and multivalent radicals, having the number
of carbon atoms designated (i.e., C.sub.1-C.sub.10 means one to ten
carbons).
[0011] Alkyl is an uncyclized chain. Examples of saturated
hydrocarbon radicals include, but are not limited to, groups such
as methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, isobutyl,
sec-butyl, (cyclohexyl)methyl, homologs and isomers of, for
example, n-pentyl, n-hexyl, n-heptyl, n-octyl, and the like. An
unsaturated alkyl group is one having one or more double bonds or
triple bonds.
[0012] Examples of unsaturated alkyl groups include, but are not
limited to, vinyl, 2-propenyl, crotyl, 2-isopentenyl,
2-(butadienyl), 2,4-pentadienyl, 3-(1,4-pentadienyl), ethynyl, 1-
and 3-propynyl, 3-butynyl, and the higher homologs and isomers. An
alkoxy is an alkyl attached to the remainder of the molecule via an
oxygen linker (--O--).
[0013] The term "alkylene," by itself or as part of another
substituent, means, unless otherwise stated, a divalent radical
derived from an alkyl, as exemplified, but not limited by,
--CH.sub.2CH.sub.2CH.sub.2CH.sub.2--. Typically, an alkyl (or
alkylene) group will have from 1 to 24 carbon atoms, with those
groups having 10 or fewer carbon atoms being preferred herein. A
"lower alkyl" or "lower alkylene" is a shorter chain alkyl or
alkylene group, generally having eight or fewer carbon atoms.
[0014] The term "alkenylene," by itself or as part of another
substituent, means, unless otherwise stated, a divalent radical
derived from an alkene.
[0015] The term "heteroalkyl," by itself or in combination with
another term, means, unless otherwise stated, a stable straight or
branched chain, or combinations thereof, including at least one
carbon atom and at least one heteroatom (e.g., O, N, P, Si, and S),
and wherein the nitrogen and sulfur atoms may optionally be
oxidized, and the nitrogen heteroatom may optionally be
quaternized. The heteroatom(s) (e.g., N, S, Si, or P) may be placed
at any interior position of the heteroalkyl group or at the
position at which the alkyl group is attached to the remainder of
the molecule. Heteroalkyl is an uncyclized chain. Examples include,
but are not limited to: --CH.sub.2--CH.sub.2--O--CH.sub.3,
--CH.sub.2--CH.sub.2--NH--CH.sub.3,
--CH.sub.2--CH.sub.2--N(CH.sub.3)--CH.sub.3,
--CH.sub.2--S--CH.sub.2--CH.sub.3, --CH.sub.2--CH.sub.2,
--S(O)--CH.sub.3, --CH.sub.2--CH.sub.2--S(O).sub.2--CH.sub.3,
--CH.dbd.CH--O--CH.sub.3, --Si(CH.sub.3).sub.3,
--CH.sub.2--CH.dbd.N--OCH.sub.3,
--CH.dbd.CH--N(CH.sub.3)--CH.sub.3, --O--CH.sub.3,
--O--CH.sub.2--CH.sub.3, and --CN. Up to two or three heteroatoms
may be consecutive, such as, for example, --CH.sub.2--NH--OCH.sub.3
and --CH.sub.2--O--Si(CH.sub.3).sub.3. A heteroalkyl moiety may
include one heteroatom (e.g., O, N, S, Si, or P). A heteroalkyl
moiety may include two optionally different heteroatoms (e.g., O,
N, S, Si, or P). A heteroalkyl moiety may include three optionally
different heteroatoms (e.g., O, N, S, Si, or P). A heteroalkyl
moiety may include four optionally different heteroatoms (e.g., O,
N, S, Si, or P). A heteroalkyl moiety may include five optionally
different heteroatoms (e.g., O, N, S, Si, or P). A heteroalkyl
moiety may include up to 8 optionally different heteroatoms (e.g.,
O, N, S, Si, or P).
[0016] Similarly, the term "heteroalkylene," by itself or as part
of another substituent, means, unless otherwise stated, a divalent
radical derived from heteroalkyl, as exemplified, but not limited
by, --CH.sub.2--CH.sub.2--S--CH.sub.2--CH.sub.2-- and
--CH.sub.2--S--CH.sub.2--CH.sub.2--NH--CH.sub.2--. For
heteroalkylene groups, heteroatoms can also occupy either or both
of the chain termini (e.g., alkyleneoxy, alkylenedioxy,
alkyleneamino, alkylenediamino, and the like). Still further, for
alkylene and heteroalkylene linking groups, no orientation of the
linking group is implied by the direction in which the formula of
the linking group is written. For example, the formula
--C(O).sub.2R'-- represents both --C(O).sub.2R'-- and
--R'C(O).sub.2--. As described above, heteroalkyl groups, as used
herein, include those groups that are attached to the remainder of
the molecule through a heteroatom, such as --C(O)R', --C(O)NR',
--NR'R'', --OR', --SR', and/or --SO.sub.2R'. Where "heteroalkyl" is
recited, followed by recitations of specific heteroalkyl groups,
such as --NR'R'' or the like, it will be understood that the terms
heteroalkyl and --NR'R'' are not redundant or mutually exclusive.
Rather, the specific heteroalkyl groups are recited to add clarity.
Thus, the term "heteroalkyl" should not be interpreted herein as
excluding specific heteroalkyl groups, such as --NR'R'' or the
like.
[0017] The terms "cycloalkyl" and "heterocycloalkyl," by themselves
or in combination with other terms, mean, unless otherwise stated,
cyclic versions of"alkyl" and "heteroalkyl," respectively.
Cycloalkyl and heterocycloalkyl are not aromatic. Additionally, for
heterocycloalkyl, a heteroatom can occupy the position at which the
heterocycle is attached to the remainder of the molecule. Examples
of cycloalkyl include, but are not limited to, cyclopropyl,
cyclobutyl, cyclopentyl, cyclohexyl, 1-cyclohexenyl,
3-cyclohexenyl, cycloheptyl, and the like. Examples of
heterocycloalkyl include, but are not limited to,
1-(1,2,5,6-tetrahydropyridyl), 1-piperidinyl, 2-piperidinyl,
3-piperidinyl, 4-morpholinyl, 3-morpholinyl, tetrahydrofuran-2-yl,
tetrahydrofuran-3-yl, tetrahydrothien-2-yl, tetrahydrothien-3-yl,
1-piperazinyl, 2-piperazinyl, and the like. A "cycloalkylene" and a
"heterocycloalkylene," alone or as part of another substituent,
means a divalent radical derived from a cycloalkyl and
heterocycloalkyl, respectively. "Cycloalkyl" is also meant to refer
to bicyclic and polycyclic hydrocarbon rings such as, for example,
bicyclo[2.2.1]heptane, bicyclo[2.2.2]octane, etc.
[0018] The terms "halo" or "halogen," by themselves or as part of
another substituent, mean, unless otherwise stated, a fluorine,
chlorine, bromine, or iodine atom. Additionally, terms such as
"haloalkyl" are meant to include monohaloalkyl and polyhaloalkyl.
For example, the term "halo(C.sub.1-C.sub.4)alkyl" includes, but is
not limited to, fluoromethyl, difluoromethyl, trifluoromethyl,
2,2,2-trifluoroethyl, 4-chlorobutyl, 3-bromopropyl, and the
like.
[0019] The term "acyl" means, unless otherwise stated, --C(O)R
where R is a substituted or unsubstituted alkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, or substituted or unsubstituted heteroaryl.
[0020] The term "aryl" means, unless otherwise stated, a
polyunsaturated, aromatic, hydrocarbon substituent, which can be a
single ring or multiple rings (preferably from 1 to 3 rings) that
are fused together (i.e., a fused ring aryl) or linked covalently.
A fused ring aryl refers to multiple rings fused together wherein
at least one of the fused rings is an aryl ring. The term
"heteroaryl" refers to aryl groups (or rings) that contain at least
one heteroatom such as N, O, or S, wherein the nitrogen and sulfur
atoms are optionally oxidized, and the nitrogen atom(s) are
optionally quaternized. Thus, the term "heteroaryl" includes fused
ring heteroaryl groups (i.e., multiple rings fused together wherein
at least one of the fused rings is a heteroaromatic ring). A
5,6-fused ring heteroarylene refers to two rings fused together,
wherein one ring has 5 members and the other ring has 6 members,
and wherein at least one ring is a heteroaryl ring. Likewise, a
6,6-fused ring heteroarylene refers to two rings fused together,
wherein one ring has 6 members and the other ring has 6 members,
and wherein at least one ring is a heteroaryl ring. And a 6,5-fused
ring heteroarylene refers to two rings fused together, wherein one
ring has 6 members and the other ring has 5 members, and wherein at
least one ring is a heteroaryl ring. A heteroaryl group can be
attached to the remainder of the molecule through a carbon or
heteroatom. Non-limiting examples of aryl and heteroaryl groups
include phenyl, naphthyl, pyrrolyl, pyrazolyl, pyridazinyl,
triazinyl, pyrimidinyl, imidazolyl, pyrazinyl, purinyl, oxazolyl,
isoxazolyl, thiazolyl, furyl, thienyl, pyridyl, pyrimidyl,
benzothiazolyl, benzoxazoyl benzimidazolyl, benzofuran,
isobenzofuranyl, indolyl, isoindolyl, benzothiophenyl, isoquinolyl,
quinoxalinyl, quinolyl, 1-naphthyl, 2-naphthyl, 4-biphenyl,
1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 3-pyrazolyl, 2-imidazolyl,
4-imidazolyl, pyrazinyl, 2-oxazolyl, 4-oxazolyl,
2-phenyl-4-oxazolyl, 5-oxazolyl, 3-isoxazolyl, 4-isoxazolyl,
5-isoxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-furyl,
3-furyl, 2-thienyl, 3-thienyl, 2-pyridyl, 3-pyridyl, 4-pyridyl,
2-pyrimidyl, 4-pyrimidyl, 5-benzothiazolyl, purinyl,
2-benzimidazolyl, 5-indolyl, 1-isoquinolyl, 5-isoquinolyl,
2-quinoxalinyl, 5-quinoxalinyl, 3-quinolyl, and 6-quinolyl.
Substituents for each of the above noted aryl and heteroaryl ring
systems are selected from the group of acceptable substituents
described below. An "arylene" and a "heteroarylene," alone or as
part of another substituent, mean a divalent radical derived from
an aryl and heteroaryl, respectively. A heteroaryl group
substituent may be --O-- bonded to a ring heteroatom nitrogen.
[0021] Spirocyclic rings are two or more rings wherein adjacent
rings are attached through a single atom. The individual rings
within spirocyclic rings may be identical or different. Individual
rings in spirocyclic rings may be substituted or unsubstituted and
may have different substituents from other individual rings within
a set of spirocyclic rings. Possible substituents for individual
rings within spirocyclic rings are the possible substituents for
the same ring when not part of spirocyclic rings (e.g. substituents
for cycloalkyl or heterocycloalkyl rings). Spirocylic rings may be
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted cycloalkylene, substituted or unsubstituted
heterocycloalkyl or substituted or unsubstituted
heterocycloalkylene and individual rings within a spirocyclic ring
group may be any of the immediately previous list, including having
all rings of one type (e.g. all rings being substituted
heterocycloalkylene wherein each ring may be the same or different
substituted heterocycloalkylene). When referring to a spirocyclic
ring system, heterocyclic spirocyclic rings means a spirocyclic
rings wherein at least one ring is a heterocyclic ring and wherein
each ring may be a different ring. When referring to a spirocyclic
ring system, substituted spirocyclic rings means that at least one
ring is substituted and each substituent may optionally be
different.
[0022] The symbol "" denotes the point of attachment of a chemical
moiety to the remainder of a molecule or chemical formula.
[0023] The term "oxo," as used herein, means an oxygen that is
double bonded to a carbon atom.
[0024] The term "alkylarylene" as an arylene moiety covalently
bonded to an alkylene moiety (also referred to herein as an
alkylene linker). In embodiments, the alkylarylene group has the
formula:
##STR00002##
[0025] An alkylarylene moiety may be substituted (e.g. with a
substituent group) on the alkylene moiety or the arylene linker
(e.g. at carbons 2, 3, 4, or 6) with halogen, oxo, --N.sub.3,
--CF.sub.3, --CCl.sub.3, --CBr.sub.3, --CI.sub.3, --CN, --CHO,
--OH, --NH.sub.2, --COOH, --CONH.sub.2, --NO.sub.2, --SH,
--SO.sub.2CH.sub.3--SO.sub.3H, --OSO.sub.3H, --SO.sub.2NH.sub.2,
--NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2, substituted or
unsubstituted C.sub.1-C.sub.5 alkyl or substituted or unsubstituted
2 to 5 membered heteroalkyl). In embodiments, the alkylarylene is
unsubstituted.
[0026] Each of the above terms (e.g., "alkyl," "heteroalkyl,"
"cycloalkyl," "heterocycloalkyl," "aryl," and "heteroaryl")
includes both substituted and unsubstituted forms of the indicated
radical. Preferred substituents for each type of radical are
provided below.
[0027] Substituents for the alkyl and heteroalkyl radicals
(including those groups often referred to as alkylene, alkenyl,
heteroalkylene, heteroalkenyl, alkynyl, cycloalkyl,
heterocycloalkyl, cycloalkenyl, and heterocycloalkenyl) can be one
or more of a variety of groups selected from, but not limited to,
--OR', .dbd.O, .dbd.NR', .dbd.N--OR', --NR'R'', --SR', -halogen,
--SiR'R''R''', --OC(O)R', --C(O)R', --CO.sub.2R', --CONR'R'',
--OC(O)NR'R'', --NR''C(O)R', --NR'--C(O)NR''R''',
--NR''C(O).sub.2R', --NR--C(NR'R''R''').dbd.NR'''',
--NR--C(NR'R'').dbd.NR''', --S(O)R', --S(O).sub.2R',
--S(O).sub.2NR'R'', --NRSO.sub.2R', --NR'NR''R''', --ONR'R'',
--NR'C(O)NR''NR'''R'''', --CN, --NO.sub.2, --NR'SO.sub.2R'',
--NR'C(O)R'', --NR'C(O)--OR'', --NR'OR'', in a number ranging from
zero to (2m'+1), where m' is the total number of carbon atoms in
such radical. R, R', R'', R''', and R'''' each preferably
independently refer to hydrogen, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl (e.g., aryl substituted with 1-3 halogens), substituted or
unsubstituted heteroaryl, substituted or unsubstituted alkyl,
alkoxy, or thioalkoxy groups, or arylalkyl groups. When a compound
described herein includes more than one R group, for example, each
of the R groups is independently selected as are each R', R'',
R''', and R'''' group when more than one of these groups is
present. When R' and R'' are attached to the same nitrogen atom,
they can be combined with the nitrogen atom to form a 4-, 5-, 6-,
or 7-membered ring. For example, --NR'R'' includes, but is not
limited to, 1-pyrrolidinyl and 4-morpholinyl. From the above
discussion of substituents, one of skill in the art will understand
that the term "alkyl" is meant to include groups including carbon
atoms bound to groups other than hydrogen groups, such as haloalkyl
(e.g., --CF.sub.3 and --CH.sub.2CF.sub.3) and acyl (e.g.,
--C(O)CH.sub.3, --C(O)CF.sub.3, --C(O)CH.sub.2OCH.sub.3, and the
like).
[0028] Similar to the substituents described for the alkyl radical,
substituents for the aryl and heteroaryl groups are varied and are
selected from, for example: --OR', --NR'R'', --SR', -halogen,
--SiR'R''R''', --OC(O)R', --C(O)R', --CO.sub.2R', --CONR'R'',
--OC(O)NR'R'', --NR''C(O)R', --NR'--C(O)NR''R''',
--NR''C(O).sub.2R', --NR--C(NR'R''R''').dbd.NR'''',
--NR--C(NR'R'').dbd.NR''', --S(O)R', --S(O).sub.2R',
--S(O).sub.2NR'R'', --NRSO.sub.2R', --NR'NR''R''', --ONR'R'',
--NR'C(O)NR''NR'''R'''', --CN, --NO.sub.2, --R', --N.sub.3,
--CH(Ph).sub.2, fluoro(C.sub.1-C.sub.4)alkoxy, and
fluoro(C.sub.1-C.sub.4)alkyl, --NR'SO.sub.2R'', --NR'C(O)R'',
--NR'C(O)--OR'', --NR'OR'', in a number ranging from zero to the
total number of open valences on the aromatic ring system; and
where R', R'', R''', and R'''' are preferably independently
selected from hydrogen, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, and
substituted or unsubstituted heteroaryl. When a compound described
herein includes more than one R group, for example, each of the R
groups is independently selected as are each R', R'', R''', and
R'''' groups when more than one of these groups is present.
[0029] Substituents for rings (e.g. cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, cycloalkylene, heterocycloalkylene, arylene, or
heteroarylene) may be depicted as substituents on the ring rather
than on a specific atom of a ring (commonly referred to as a
floating substituent). In such a case, the substituent may be
attached to any of the ring atoms (obeying the rules of chemical
valency) and in the case of fused rings or spirocyclic rings, a
substituent depicted as associated with one member of the fused
rings or spirocyclic rings (a floating substituent on a single
ring), may be a substituent on any of the fused rings or
spirocyclic rings (a floating substituent on multiple rings). When
a substituent is attached to a ring, but not a specific atom (a
floating substituent), and a subscript for the substituent is an
integer greater than one, the multiple substituents may be on the
same atom, same ring, different atoms, different fused rings,
different spirocyclic rings, and each substituent may optionally be
different. Where a point of attachment of a ring to the remainder
of a molecule is not limited to a single atom (a floating
substituent), the attachment point may be any atom of the ring and
in the case of a fused ring or spirocyclic ring, any atom of any of
the fused rings or spirocyclic rings while obeying the rules of
chemical valency. Where a ring, fused rings, or spirocyclic rings
contain one or more ring heteroatoms and the ring, fused rings, or
spirocyclic rings are shown with one more floating substituents
(including, but not limited to, points of attachment to the
remainder of the molecule), the floating substituents may be bonded
to the heteroatoms. Where the ring heteroatoms are shown bound to
one or more hydrogens (e.g. a ring nitrogen with two bonds to ring
atoms and a third bond to a hydrogen) in the structure or formula
with the floating substituent, when the heteroatom is bonded to the
floating substituent, the substituent will be understood to replace
the hydrogen, while obeying the rules of chemical valency.
[0030] Two or more substituents may optionally be joined to form
aryl, heteroaryl, cycloalkyl, or heterocycloalkyl groups. Such
so-called ring-forming substituents are typically, though not
necessarily, found attached to a cyclic base structure. In one
embodiment, the ring-forming substituents are attached to adjacent
members of the base structure. For example, two ring-forming
substituents attached to adjacent members of a cyclic base
structure create a fused ring structure. In another embodiment, the
ring-forming substituents are attached to a single member of the
base structure. For example, two ring-forming substituents attached
to a single member of a cyclic base structure create a spirocyclic
structure. In yet another embodiment, the ring-forming substituents
are attached to non-adjacent members of the base structure.
[0031] Two of the substituents on adjacent atoms of the aryl or
heteroaryl ring may optionally form a ring of the formula
-T-C(O)--(CRR').sub.q--U--, wherein T and U are independently
--NR--, --O--, --CRR'--, or a single bond, and q is an integer of
from 0 to 3. Alternatively, two of the substituents on adjacent
atoms of the aryl or heteroaryl ring may optionally be replaced
with a substituent of the formula -A-(CH.sub.2).sub.r--B--, wherein
A and B are independently --CRR'--, --O--, --NR--, --S--, --S(O)--,
--S(O).sub.2--, --S(O).sub.2NR'--, or a single bond, and r is an
integer of from 1 to 4. One of the single bonds of the new ring so
formed may optionally be replaced with a double bond.
Alternatively, two of the substituents on adjacent atoms of the
aryl or heteroaryl ring may optionally be replaced with a
substituent of the formula --(CRR').sub.s--X'--
(C''R''R''').sub.d--, where s and d are independently integers of
from 0 to 3, and X' is --O--, --NR'--, --S--, --S(O)--,
--S(O).sub.2--, or --S(O).sub.2NR'--. The substituents R, R', R'',
and R''' are preferably independently selected from hydrogen,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, and substituted or unsubstituted heteroaryl.
[0032] As used herein, the terms "heteroatom" or "ring heteroatom"
are meant to include oxygen (O), nitrogen (N), sulfur (S),
phosphorus (P), and silicon (Si).
[0033] A "substituent group," as used herein, means a group
selected from the following moieties:
(A) oxo, halogen, --CF.sub.3, --CN, --OH, --NH.sub.2, --COOH,
--CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2,
--NHC.dbd.(O)NHNH.sub.2, --NHC.dbd.(O) NH.sub.2, --NHSO.sub.2H,
--NHC.dbd.(O)H, --NHC(O)--OH, --NHOH, --OCF.sub.3, --OCHF.sub.2,
unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted
cycloalkyl, unsubstituted heterocycloalkyl, unsubstituted aryl,
unsubstituted heteroaryl, and (B) alkyl, heteroalkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, substituted with at least one
substituent selected from: (i) oxo, halogen, --CF.sub.3, --CN,
--OH, --NH.sub.2, --COOH, --CONH.sub.2, --NO.sub.2, --SH,
--SO.sub.3H, --SO.sub.4H, --SO.sub.2NH.sub.2, --NHNH.sub.2,
--ONH.sub.2, --NHC.dbd.(O)NHNH.sub.2, --NHC.dbd.(O) NH.sub.2,
--NHSO.sub.2H, --NHC.dbd.(O)H, --NHC(O)--OH, --NHOH, --OCF.sub.3,
--OCHF.sub.2, unsubstituted alkyl, unsubstituted heteroalkyl,
unsubstituted cycloalkyl, unsubstituted heterocycloalkyl,
unsubstituted aryl, unsubstituted heteroaryl, and (ii) alkyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
substituted with at least one substituent selected from: (a) oxo,
halogen, --CF.sub.3, --CN, --OH, --NH.sub.2, --COOH, --CONH.sub.2,
--NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H, --SO.sub.2NH.sub.2,
--NHNH.sub.2, --ONH.sub.2, --NHC.dbd.(O)NHNH.sub.2, --NHC.dbd.(O)
NH.sub.2, --NHSO.sub.2H, --NHC.dbd.(O)H, --NHC(O)--OH, --NHOH,
--OCF.sub.3, --OCHF.sub.2, unsubstituted alkyl, unsubstituted
heteroalkyl, unsubstituted cycloalkyl, unsubstituted
heterocycloalkyl, unsubstituted aryl, unsubstituted heteroaryl, and
(b) alkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, substituted with at least one substituent selected
from: oxo, halogen, --CF.sub.3, --CN, --OH, --NH.sub.2, --COOH,
--CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2,
--NHC.dbd.(O)NHNH.sub.2, --NHC.dbd.(O) NH.sub.2, --NHSO.sub.2H,
--NHC.dbd.(O)H, --NHC(O)--OH, --NHOH, --OCF.sub.3, --OCHF.sub.2,
unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted
cycloalkyl, unsubstituted heterocycloalkyl, unsubstituted aryl,
unsubstituted heteroaryl.
[0034] A "size-limited substituent" or "size-limited substituent
group," as used herein, means a group selected from all of the
substituents described above for a "substituent group," wherein
each substituted or unsubstituted alkyl is a substituted or
unsubstituted C.sub.1-C.sub.20 alkyl, each substituted or
unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 20
membered heteroalkyl, each substituted or unsubstituted cycloalkyl
is a substituted or unsubstituted C.sub.3-C.sub.5 cycloalkyl, each
substituted or unsubstituted heterocycloalkyl is a substituted or
unsubstituted 3 to 8 membered heterocycloalkyl, each substituted or
unsubstituted aryl is a substituted or unsubstituted
C.sub.6-C.sub.10 aryl, and each substituted or unsubstituted
heteroaryl is a substituted or unsubstituted 5 to 10 membered
heteroaryl.
[0035] A "lower substituent" or "lower substituent group," as used
herein, means a group selected from all of the substituents
described above for a "substituent group," wherein each substituted
or unsubstituted alkyl is a substituted or unsubstituted
C.sub.1-C.sub.5 alkyl, each substituted or unsubstituted
heteroalkyl is a substituted or unsubstituted 2 to 8 membered
heteroalkyl, each substituted or unsubstituted cycloalkyl is a
substituted or unsubstituted C.sub.3-C.sub.7 cycloalkyl, each
substituted or unsubstituted heterocycloalkyl is a substituted or
unsubstituted 3 to 7 membered heterocycloalkyl, each substituted or
unsubstituted aryl is a substituted or unsubstituted
C.sub.6-C.sub.10 aryl, and each substituted or unsubstituted
heteroaryl is a substituted or unsubstituted 5 to 9 membered
heteroaryl.
[0036] In some embodiments, each substituted group described in the
compounds herein is substituted with at least one substituent
group. More specifically, in some embodiments, each substituted
alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted
heterocycloalkyl, substituted aryl, substituted heteroaryl,
substituted alkylene, substituted heteroalkylene, substituted
cycloalkylene, substituted heterocycloalkylene, substituted
arylene, and/or substituted heteroarylene described in the
compounds herein are substituted with at least one substituent
group. In other embodiments, at least one or all of these groups
are substituted with at least one size-limited substituent group.
In other embodiments, at least one or all of these groups are
substituted with at least one lower substituent group.
[0037] In other embodiments of the compounds herein, each
substituted or unsubstituted alkyl may be a substituted or
unsubstituted C.sub.1-C.sub.20 alkyl, each substituted or
unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 20
membered heteroalkyl, each substituted or unsubstituted cycloalkyl
is a substituted or unsubstituted C.sub.3-C.sub.5 cycloalkyl, each
substituted or unsubstituted heterocycloalkyl is a substituted or
unsubstituted 3 to 8 membered heterocycloalkyl, each substituted or
unsubstituted aryl is a substituted or unsubstituted
C.sub.6-C.sub.10 aryl, and/or each substituted or unsubstituted
heteroaryl is a substituted or unsubstituted 5 to 10 membered
heteroaryl. In some embodiments of the compounds herein, each
substituted or unsubstituted alkylene is a substituted or
unsubstituted C.sub.1-C.sub.20 alkylene, each substituted or
unsubstituted heteroalkylene is a substituted or unsubstituted 2 to
20 membered heteroalkylene, each substituted or unsubstituted
cycloalkylene is a substituted or unsubstituted C.sub.3-C.sub.5
cycloalkylene, each substituted or unsubstituted
heterocycloalkylene is a substituted or unsubstituted 3 to 8
membered heterocycloalkylene, each substituted or unsubstituted
arylene is a substituted or unsubstituted C.sub.6-C.sub.10 arylene,
and/or each substituted or unsubstituted heteroarylene is a
substituted or unsubstituted 5 to 10 membered heteroarylene.
[0038] In some embodiments, each substituted or unsubstituted alkyl
is a substituted or unsubstituted C.sub.1-C.sub.5 alkyl, each
substituted or unsubstituted heteroalkyl is a substituted or
unsubstituted 2 to 8 membered heteroalkyl, each substituted or
unsubstituted cycloalkyl is a substituted or unsubstituted
C.sub.3-C.sub.7 cycloalkyl, each substituted or unsubstituted
heterocycloalkyl is a substituted or unsubstituted 3 to 7 membered
heterocycloalkyl, each substituted or unsubstituted aryl is a
substituted or unsubstituted C.sub.6-C.sub.10 aryl, and/or each
substituted or unsubstituted heteroaryl is a substituted or
unsubstituted 5 to 9 membered heteroaryl. In some embodiments, each
substituted or unsubstituted alkylene is a substituted or
unsubstituted C.sub.1-C.sub.5 alkylene, each substituted or
unsubstituted heteroalkylene is a substituted or unsubstituted 2 to
8 membered heteroalkylene, each substituted or unsubstituted
cycloalkylene is a substituted or unsubstituted C.sub.3-C.sub.7
cycloalkylene, each substituted or unsubstituted
heterocycloalkylene is a substituted or unsubstituted 3 to 7
membered heterocycloalkylene, each substituted or unsubstituted
arylene is a substituted or unsubstituted C.sub.6-C.sub.10 arylene,
and/or each substituted or unsubstituted heteroarylene is a
substituted or unsubstituted 5 to 9 membered heteroarylene. In some
embodiments, the compound is a chemical species set forth in the
Examples section, figures, or tables below.
[0039] Certain compounds of the present invention possess
asymmetric carbon atoms (optical or chiral centers) or double
bonds; the enantiomers, racemates, diastereomers, tautomers,
geometric isomers, stereoisometric forms that may be defined, in
terms of absolute stereochemistry, as (R)- or (S)- or, as (D)- or
(L)-for amino acids, and individual isomers are encompassed within
the scope of the present invention. The compounds of the present
invention do not include those that are known in art to be too
unstable to synthesize and/or isolate. The present invention is
meant to include compounds in racemic and optically pure forms.
Optically active (R)- and (S)-, or (D)- and (L)-isomers may be
prepared using chiral synthons or chiral reagents, or resolved
using conventional techniques. When the compounds described herein
contain olefinic bonds or other centers of geometric asymmetry, and
unless specified otherwise, it is intended that the compounds
include both E and Z geometric isomers.
[0040] As used herein, the term "isomers" refers to compounds
having the same number and kind of atoms, and hence the same
molecular weight, but differing in respect to the structural
arrangement or configuration of the atoms.
[0041] The term "tautomer," as used herein, refers to one of two or
more structural isomers which exist in equilibrium and which are
readily converted from one isomeric form to another.
[0042] It will be apparent to one skilled in the art that certain
compounds of this invention may exist in tautomeric forms, all such
tautomeric forms of the compounds being within the scope of the
invention.
[0043] Unless otherwise stated, structures depicted herein are also
meant to include all stereochemical forms of the structure; i.e.,
the R and S configurations for each asymmetric center.
[0044] Therefore, single stereochemical isomers as well as
enantiomeric and diastereomeric mixtures of the present compounds
are within the scope of the invention.
[0045] Unless otherwise stated, structures depicted herein are also
meant to include compounds which differ only in the presence of one
or more isotopically enriched atoms. For example, compounds having
the present structures except for the replacement of a hydrogen by
a deuterium or tritium, or the replacement of a carbon by .sup.13C-
or .sup.14C-enriched carbon are within the scope of this
invention.
[0046] The compounds of the present invention may also contain
unnatural proportions of atomic isotopes at one or more of the
atoms that constitute such compounds. For example, the compounds
may be radiolabeled with radioactive isotopes, such as for example
tritium (.sup.3H), iodine-125 (.sup.125I), or carbon-14 (.sup.14C).
All isotopic variations of the compounds of the present invention,
whether radioactive or not, are encompassed within the scope of the
present invention.
[0047] It should be noted that throughout the application that
alternatives are written in Markush groups, for example, each amino
acid position that contains more than one possible amino acid. It
is specifically contemplated that each member of the Markush group
should be considered separately, thereby comprising another
embodiment, and the Markush group is not to be read as a single
unit.
[0048] "Analog," or "analogue" is used in accordance with its plain
ordinary meaning within Chemistry and Biology and refers to a
chemical compound that is structurally similar to another compound
(i.e., a so-called "reference" compound) but differs in
composition, e.g., in the replacement of one atom by an atom of a
different element, or in the presence of a particular functional
group, or the replacement of one functional group by another
functional group, or the absolute stereochemistry of one or more
chiral centers of the reference compound. Accordingly, an analog is
a compound that is similar or comparable in function and appearance
but not in structure or origin to a reference compound.
[0049] The terms "a" or "an," as used in herein means one or more.
In addition, the phrase "substituted with a[n]," as used herein,
means the specified group may be substituted with one or more of
any or all of the named substituents. For example, where a group,
such as an alkyl or heteroaryl group, is "substituted with an
unsubstituted C.sub.1-C.sub.20 alkyl, or unsubstituted 2 to 20
membered heteroalkyl," the group may contain one or more
unsubstituted C.sub.1-C.sub.20 alkyls, and/or one or more
unsubstituted 2 to 20 membered heteroalkyls.
[0050] Moreover, where a moiety is substituted with an R
substituent, the group may be referred to as "R-substituted." Where
a moiety is R-substituted, the moiety is substituted with at least
one R substituent and each R substituent is optionally different.
Where a particular R group is present in the description of a
chemical genus (such as Formula (I)), a Roman alphabetic symbol may
be used to distinguish each appearance of that particular R group.
For example, where multiple R.sup.13 substituents are present, each
R.sup.13 substituent may be distinguished as R.sup.13A, R.sup.13B,
R.sup.13C, R.sup.13D, etc., wherein each of R.sup.13A, R.sup.13B,
R.sup.13C, R.sup.13D, etc. is defined within the scope of the
definition of R.sup.13 and optionally differently.
[0051] A "detectable moiety" as used herein refers to a moiety that
can be covalently or noncovalently attached to a compound or
biomolecule that can be detected for instance, using techniques
known in the art. In embodiments, the detectable moiety is
covalently attached. The detectable moiety may provide for imaging
of the attached compound or biomolecule. The detectable moiety may
indicate the contacting between two compounds. Exemplary detectable
moieties are fluorophores, antibodies, reactive dies, radio-labeled
moieties, magnetic contrast agents, and quantum dots. Exemplary
fluorophores include fluorescein, rhodamine, GFP, coumarin, FITC,
Alexa fluor, Cy3, Cy5, BODIPY, and cyanine dyes. Exemplary
radionuclides include Fluorine-18, Gallium-68, and Copper-64.
Exemplary magnetic contrast agents include gadolinium, iron oxide
and iron platinum, and manganese.
[0052] Descriptions of compounds of the present invention are
limited by principles of chemical bonding known to those skilled in
the art. Accordingly, where a group may be substituted by one or
more of a number of substituents, such substitutions are selected
so as to comply with principles of chemical bonding and to give
compounds which are not inherently unstable and/or would be known
to one of ordinary skill in the art as likely to be unstable under
ambient conditions, such as aqueous, neutral, and several known
physiological conditions. For example, a heterocycloalkyl or
heteroaryl is attached to the remainder of the molecule via a ring
heteroatom in compliance with principles of chemical bonding known
to those skilled in the art thereby avoiding inherently unstable
compounds.
[0053] The term "pharmaceutically acceptable salts" is meant to
include salts of the active compounds that are prepared with
relatively nontoxic acids or bases, depending on the particular
substituents found on the compounds described herein. When
compounds of the present invention contain relatively acidic
functionalities, base addition salts can be obtained by contacting
the neutral form of such compounds with a sufficient amount of the
desired base, either neat or in a suitable inert solvent. Examples
of pharmaceutically acceptable base addition salts include sodium,
potassium, calcium, ammonium, organic amino, or magnesium salt, or
a similar salt. When compounds of the present invention contain
relatively basic functionalities, acid addition salts can be
obtained by contacting the neutral form of such compounds with a
sufficient amount of the desired acid, either neat or in a suitable
inert solvent. Examples of pharmaceutically acceptable acid
addition salts include those derived from inorganic acids like
hydrochloric, hydrobromic, nitric, carbonic, monohydrogencarbonic,
phosphoric, monohydrogenphosphoric, dihydrogenphosphoric, sulfuric,
monohydrogensulfuric, hydriodic, or phosphorous acids and the like,
as well as the salts derived from relatively nontoxic organic acids
like acetic, propionic, isobutyric, maleic, malonic, benzoic,
succinic, suberic, fumaric, lactic, mandelic, phthalic,
benzenesulfonic, p-tolylsulfonic, citric, tartaric, oxalic,
methanesulfonic, and the like. Also included are salts of amino
acids such as arginate and the like, and salts of organic acids
like glucuronic or galactunoric acids and the like (see, for
example, Berge et al., "Pharmaceutical Salts", Journal of
Pharmaceutical Science, 1977, 66, 1-19). Certain specific compounds
of the present invention contain both basic and acidic
functionalities that allow the compounds to be converted into
either base or acid addition salts.
[0054] Thus, the compounds of the present invention may exist as
salts, such as with pharmaceutically acceptable acids. The present
invention includes such salts. Non-limiting examples of such salts
include hydrochlorides, hydrobromides, phosphates, sulfates,
methanesulfonates, nitrates, maleates, acetates, citrates,
fumarates, proprionates, tartrates (e.g., (+)-tartrates,
(-)-tartrates, or mixtures thereof including racemic mixtures),
succinates, benzoates, and salts with amino acids such as glutamic
acid, and quaternary ammonium salts (e.g. methyl iodide, ethyl
iodide, and the like). These salts may be prepared by methods known
to those skilled in the art.
[0055] The neutral forms of the compounds are preferably
regenerated by contacting the salt with a base or acid and
isolating the parent compound in the conventional manner. The
parent form of the compound may differ from the various salt forms
in certain physical properties, such as solubility in polar
solvents. In embodiments, compounds of the present invention
contain both basic and acidic functionalities that allow the
compounds to be converted into either base or acid addition salts.
The neutral forms of the compounds may be regenerated by contacting
the salt with a base or acid and isolating the parent compound in a
conventional manner. The parent form of the compounds differs from
the various salt forms in certain physical properties, such as
solubility in polar solvents, but, unless specifically indicated,
the salts disclosed herein are equivalent to the parent form of the
compound for the purposes of the present invention.
[0056] In addition to salt forms, the present invention provides
compounds, which are in a prodrug form. Prodrugs of the compounds
described herein are those compounds that readily undergo chemical
changes under physiological conditions to provide the compounds of
the present invention. Prodrugs of the compounds described herein
may be converted in vivo after administration. Additionally,
prodrugs can be converted to the compounds of the present invention
by chemical or biochemical methods in an ex vivo environment, such
as, for example, when contacted with a suitable enzyme or chemical
reagent.
[0057] Certain compounds of the present invention can exist in
unsolvated forms as well as solvated forms, including hydrated
forms. In general, the solvated forms are equivalent to unsolvated
forms and are encompassed within the scope of the present
invention. Certain compounds of the present invention may exist in
multiple crystalline or amorphous forms. In general, all physical
forms are equivalent for the uses contemplated by the present
invention and are intended to be within the scope of the present
invention.
[0058] "Pharmaceutically acceptable excipient" and
"pharmaceutically acceptable carrier" refer to a substance that
aids the administration of a compound to and absorption by a
subject and can be included in the compositions of the present
invention without causing a significant adverse toxicological
effect on the patient. Non-limiting examples of pharmaceutically
acceptable excipients include water, NaCl, normal saline solutions,
lactated Ringer's, normal sucrose, normal glucose, binders,
fillers, disintegrants, lubricants, coatings, sweeteners, flavors,
salt solutions (such as Ringer's solution), alcohols, oils,
gelatins, carbohydrates such as lactose, amylose or starch, fatty
acid esters, hydroxymethycellulose, polyvinyl pyrrolidine, and
colors, and the like. Such preparations can be sterilized and, if
desired, mixed with auxiliary agents such as lubricants,
preservatives, stabilizers, wetting agents, emulsifiers, salts for
influencing osmotic pressure, buffers, coloring, and/or aromatic
substances and the like that do not deleteriously react with the
compounds of the invention. One of skill in the art will recognize
that other pharmaceutical excipients are useful in the present
invention.
[0059] The term "preparation" is intended to include the
formulation of the active compound with encapsulating material as a
carrier providing a capsule in which the active component with or
without other carriers, is surrounded by a carrier, which is thus
in association with it. Similarly, cachets and lozenges are
included. Tablets, powders, capsules, pills, cachets, and lozenges
can be used as solid dosage forms suitable for oral
administration.
[0060] A "CCR4 inhibitor" refers to a compound (e.g., compounds
described herein) that reduces the activity of CCR4 when compared
to a control, such as absence of the compound or a compound with
known inactivity.
[0061] The terms "polypeptide," "peptide" and "protein" are used
interchangeably herein to refer to a polymer of amino acid
residues, wherein the polymer may optionally be conjugated to a
moiety that does not consist of amino acids. The terms apply to
amino acid polymers in which one or more amino acid residue is an
artificial chemical mimetic of a corresponding naturally occurring
amino acid, as well as to naturally occurring amino acid polymers
and non-naturally occurring amino acid polymer. In embodiments, the
terms "polypeptide," "peptide," and "protein", used interchangeably
herein, refer to a polymeric form of amino acids of any length,
which can include genetically coded and non-genetically coded amino
acids, chemically or biochemically modified or derivatized amino
acids, and polypeptides having modified polypeptide backbones. The
terms include fusion proteins, including, but not limited to,
fusion proteins with a heterologous amino acid sequence; fusion
proteins with heterologous and homologous leader sequences, with or
without N-terminus methionine residues; immunologically tagged
proteins; and the like.
[0062] A polypeptide, or a cell is "recombinant" when it is
artificial or engineered, or derived from or contains an artificial
or engineered protein or nucleic acid (e.g. non-natural or not wild
type). For example, a polynucleotide that is inserted into a vector
or any other heterologous location, e.g., in a genome of a
recombinant organism, such that it is not associated with
nucleotide sequences that normally flank the polynucleotide as it
is found in nature is a recombinant polynucleotide. A protein
expressed in vitro or in vivo from a recombinant polynucleotide is
an example of a recombinant polypeptide. Likewise, a polynucleotide
sequence that does not appear in nature, for example a variant of a
naturally occurring gene, is recombinant.
[0063] "Contacting" is used in accordance with its plain ordinary
meaning and refers to the process of allowing at least two distinct
species (e.g. chemical compounds including biomolecules or cells)
to become sufficiently proximal to react, interact or physically
touch. It should be appreciated; however, the resulting reaction
product can be produced directly from a reaction between the added
reagents or from an intermediate from one or more of the added
reagents that can be produced in the reaction mixture.
[0064] The term "contacting" may include allowing two species to
react, interact, or physically touch, wherein the two species may
be a compound as described herein and a protein or enzyme. In some
embodiments contacting includes allowing a compound described
herein to interact with a protein or enzyme that is involved in a
signaling pathway (e.g., MAP kinase pathway).
[0065] As defined herein, the term "activation", "activate",
"activating" and the like in reference to a protein refers to
conversion of a protein into a biologically active derivative from
an initial inactive or deactivated state. The terms reference
activation, or activating, sensitizing, or up-regulating signal
transduction or enzymatic activity or the amount of a protein
decreased in a disease.
[0066] The terms "agonist," "activator," "upregulator," etc. refer
to a substance capable of detectably increasing the expression or
activity of a given gene or protein. The agonist can increase
expression or activity 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%
or more in comparison to a control in the absence of the agonist.
In certain instances, expression or activity is 1.5-fold, 2-fold,
3-fold, 4-fold, 5-fold, 10-fold or higher than the expression or
activity in the absence of the agonist.
[0067] In embodiments, an agonist is a molecule that interacts with
a target to cause or promote an increase in the activation of the
target. In embodiments, activators are molecules that increase,
activate, facilitate, enhance activation, sensitize, or
up-regulate, e.g., a gene, protein, ligand, receptor, or cell.
[0068] As defined herein, the term "inhibition," "inhibit,",
"inhibiting," and the like, in reference to a protein-inhibitor
interaction means negatively affecting (e.g. decreasing) the
activity or function of the protein relative to the activity or
function of the protein in the absence of the inhibitor. In
embodiments inhibition means negatively affecting (e.g. decreasing)
the concentration or levels of the protein relative to the
concentration or level of the protein in the absence of the
inhibitor. In embodiments inhibition refers to reduction of a
disease or symptoms of disease. In embodiments, inhibition refers
to a reduction in the activity of a particular protein target.
Thus, inhibition includes, at least in part, partially or totally
blocking stimulation, decreasing, preventing, or delaying
activation, or inactivating, desensitizing, or down-regulating
signal transduction or enzymatic activity or the amount of a
protein. In embodiments, inhibition refers to a reduction of
activity of a target protein resulting from a direct interaction
(e.g. an inhibitor binds to the target protein). In embodiments,
inhibition refers to a reduction of activity of a target protein
from an indirect interaction (e.g. an inhibitor binds to a protein
that activates the target protein, thereby preventing target
protein activation).
[0069] The terms "inhibitor," "repressor" or "antagonist" or
"downregulator" interchangeably refer to a substance capable of
detectably decreasing the expression or activity of a given gene or
protein. The antagonist can decrease expression or activity 10%,
20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or more in comparison to a
control in the absence of the antagonist. In certain instances,
expression or activity is 1.5-fold, 2-fold, 3-fold, 4-fold, 5-fold,
10-fold or lower than the expression or activity in the absence of
the antagonist. An antagonist prevents, reduces, inhibits, or
neutralizes the activity of an agonist, and an antagonist can also
prevent, inhibit, or reduce constitutive activity of a target,
e.g., a target receptor, even where there is no identified agonist.
In embodiments, inhibitors are molecules that decrease, block,
prevent, delay activation, inactivate, desensitize, or
down-regulate, e.g., a gene, protein, ligand, receptor, or cell. An
inhibitor may also be defined as a molecule that reduces, blocks,
or inactivates a constitutive activity. An "antagonist" is a
molecule that opposes the action(s) of an agonist.
[0070] The terms "C--C chemokine receptor type 4" and "CCR4" refer
to a protein (including homologs, isoforms, and functional
fragments thereof) and is a high affinity receptor for the
C--C-type chemokines (e.g., CCL2 (MCP-1), CCL4 (MIP-1), CCL5
(RANTES), CCL17 (TARC), and CCL22 (MDC)). It is referred to by a
number of different names in the scientific literature, including
"CC-CKR-4", "C--C CKR-4", "K5-5", "CD194", "CMKBR4", "ChemR13",
"HGCN", and "14099".
[0071] The term includes any recombinant or naturally-occurring
form of CCR4 variants thereof that maintain CCR4 activity (e.g.
within at least 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 100%
activity compared to wildtype CCR4). The term includes any mutant
form of CCR4 variants (e.g., frameshift mutations) thereof that
maintain CCR4 activity (e.g. within at least 30%, 40%, 50%, 60%,
70%, 80%, 90%, 95%, or 100% activity compared to wildtype CCR4). In
embodiments, the CCR4 protein encoded by the CCR4 gene has the
amino acid sequence set forth in or corresponding to Entrez 1233,
UniProt P51679, or RefSeq (protein) NP_005499.1. In embodiments,
the CCR4 gene has the nucleic acid sequence set forth in RefSeq
(mRNA) NM_005508. In embodiments, the amino acid sequence or
nucleic acid sequence is the sequence known at the time of filing
of the present application. In embodiments, the sequence
corresponds to GI:5031627. In embodiments, the sequence corresponds
to NP_005499.1. In embodiments, the sequence corresponds to
NM_005508.4. In embodiments, the sequence corresponds to
GI:48762930. In embodiments, the CCR4 is a human CCR4, such as a
human cancer causing CCR4. Though frequently found on dendritic
cells, macrophages, NK cells, platelets, and basophils, CCR4 is
predominantly associated with T cells. It plays a role in the
progression of multiple inflammation-related disorders, and, as
described herein, has also been implicated in a number of other
conditions. The genomic sequence of CCR4 is present on chromosome 3
(NC_000003.12), and the CCR4 gene is conserved in a number of
species, including chimpanzee, Rhesus monkey, dog, cow, mouse, rat,
chicken, and zebrafish. The CCR4 polypeptide comprises 360 amino
acid residues (NP_005499.1), and, like other chemokine receptors,
CCR4 is a G protein-coupled receptor found on the surface of
leukocytes (see Horuk (1994) Trends Pharm. Sci. 15:159-165).
[0072] The term "expression" includes any step involved in the
production of the polypeptide including, but not limited to,
transcription, post-transcriptional modification, translation,
post-translational modification, and secretion. Expression can be
detected using conventional techniques for detecting protein (e.g.,
ELISA, Western blotting, flow cytometry, immunofluorescence,
immunohistochemistry, etc.).
[0073] The terms "disease" or "condition" refer to a state of being
or health status of a patient or subject capable of being treated
with the compounds or methods provided herein. The disease may be a
cancer. The disease may be an autoimmune disease. The disease may
be an inflammatory disease. The disease may be an infectious
disease. In some further instances, "cancer" refers to human
cancers and carcinomas, sarcomas, adenocarcinomas, lymphomas,
leukemias, etc., including solid and lymphoid cancers, kidney,
breast, lung, bladder, colon, ovarian, prostate, pancreas, stomach,
brain, head and neck, skin, uterine, testicular, glioma, esophagus,
and liver cancer, including hepatocarcinoma, lymphoma, including
B-acute lymphoblastic lymphoma, non-Hodgkin's lymphomas (e.g.,
Burkitt's, Small Cell, and Large Cell lymphomas), Hodgkin's
lymphoma, leukemia (including MDS, AML, ALL, ATLL and CML), or
multiple myeloma.
[0074] As used herein, the term "inflammatory disease" refers to a
disease or condition characterized by aberrant inflammation (e.g.
an increased level of inflammation compared to a control such as a
healthy person not suffering from a disease). Examples of
inflammatory diseases include autoimmune diseases, arthritis,
rheumatoid arthritis, psoriatic arthritis, juvenile idiopathic
arthritis, multiple sclerosis, systemic lupus erythematosus (SLE),
myasthenia gravis, juvenile onset diabetes, diabetes mellitus type
1, Guillain-Barre syndrome, Hashimoto's encephalitis, Hashimoto's
thyroiditis, ankylosing spondylitis, psoriasis, Sjogren's syndrome,
vasculitis, glomerulonephritis, auto-immune thyroiditis, Behcet's
disease, Crohn's disease, ulcerative colitis, bullous pemphigoid,
sarcoidosis, ichthyosis, Graves ophthalmopathy, inflammatory bowel
disease, Addison's disease, Vitiligo, asthma, allergic asthma, acne
vulgaris, celiac disease, chronic prostatitis, inflammatory bowel
disease, pelvic inflammatory disease, reperfusion injury, ischemia
reperfusion injury, stroke, sarcoidosis, transplant rejection,
interstitial cystitis, atherosclerosis, scleroderma, and atopic
dermatitis. Such conditions are frequently inextricably intertwined
with other diseases, disorders and conditions. A non-limiting list
of inflammatory-related diseases, disorders and conditions which
may, for example, be caused by inflammatory cytokines, include,
arthritis, kidney failure, lupus, asthma, psoriasis, colitis,
pancreatitis, allergies, fibrosis, surgical complications (e.g.,
where inflammatory cytokines prevent healing), anemia, and
fibromyalgia. Other diseases and disorders which may be associated
with chronic inflammation include Alzheimer's disease, congestive
heart failure, stroke, aortic valve stenosis, arteriosclerosis,
osteoporosis, Parkinson's disease, infections, inflammatory bowel
disease (IBD), allergic contact dermatitis and other eczemas,
systemic sclerosis, transplantation and multiple sclerosis. Some of
the aforementioned diseases, disorders and conditions for which a
compound (e.g., CCR4 inhibitor) of the present invention may be
particularly efficacious (due to, for example, limitations of
current therapies) are described in more detail hereafter.
[0075] As used herein, the term "cancer" refers to all types of
cancer, neoplasm or malignant tumors found in mammals (e.g.
humans), including leukemia, carcinomas and sarcomas. Exemplary
cancers that may be treated with a compound or method provided
herein include brain cancer, glioma, glioblastoma, neuroblastoma,
prostate cancer, colorectal cancer, pancreatic cancer, cervical
cancer, gastric cancer, ovarian cancer, lung cancer, and cancer of
the head. Exemplary cancers that may be treated with a compound or
method provided herein include cancer of the thyroid, endocrine
system, brain, breast, cervix, colon, head & neck, liver,
kidney, lung, non-small cell lung, melanoma, mesothelioma, ovary,
sarcoma, stomach, uterus, Medulloblastoma, colorectal cancer,
pancreatic cancer. Additional examples include, thyroid carcinoma,
cholangiocarcinoma, pancreatic adenocarcinoma, skin cutaneous
melanoma, colon adenocarcinoma, rectum adenocarcinoma, stomach
adenocarcinoma, esophageal carcinoma, head and neck squamous cell
carcinoma, breast invasive carcinoma, lung adenocarcinoma, lung
squamous cell carcinoma, Hodgkin's Disease, Non-Hodgkin's Lymphoma,
multiple myeloma, neuroblastoma, glioma, glioblastoma multiforme,
ovarian cancer, rhabdomyosarcoma, primary thrombocytosis, primary
macroglobulinemia, primary brain tumors, cancer, malignant
pancreatic insulanoma, malignant carcinoid, urinary bladder cancer,
premalignant skin lesions, testicular cancer, lymphomas, thyroid
cancer, neuroblastoma, esophageal cancer, genitourinary tract
cancer, malignant hypercalcemia, endometrial cancer, adrenal
cortical cancer, neoplasms of the endocrine or exocrine pancreas,
medullary thyroid cancer, medullary thyroid carcinoma, melanoma,
colorectal cancer, papillary thyroid cancer, hepatocellular
carcinoma, or prostate cancer.
[0076] The term "leukemia" refers broadly to progressive, malignant
diseases of the blood-forming organs and is generally characterized
by a distorted proliferation and development of leukocytes and
their precursors in the blood and bone marrow. Leukemia is
generally clinically classified on the basis of (1) the duration
and character of the disease-acute or chronic; (2) the type of cell
involved; myeloid (myelogenous), lymphoid (lymphogenous), or
monocytic; and (3) the increase or non-increase in the number
abnormal cells in the blood-leukemic or aleukemic (subleukemic).
Exemplary leukemias that may be treated with a compound or method
provided herein include, for example, acute nonlymphocytic
leukemia, chronic lymphocytic leukemia, acute granulocytic
leukemia, chronic granulocytic leukemia, acute promyelocytic
leukemia, adult T-cell leukemia, aleukemic leukemia, a
leukocythemic leukemia, basophylic leukemia, blast cell leukemia,
bovine leukemia, chronic myelocytic leukemia, leukemia cutis,
embryonal leukemia, eosinophilic leukemia, Gross' leukemia,
hairy-cell leukemia, hemoblastic leukemia, hemocytoblastic
leukemia, histiocytic leukemia, stem cell leukemia, acute monocytic
leukemia, leukopenic leukemia, lymphatic leukemia, lymphoblastic
leukemia, lymphocytic leukemia, lymphogenous leukemia, lymphoid
leukemia, lymphosarcoma cell leukemia, mast cell leukemia,
megakaryocytic leukemia, micromyeloblastic leukemia, monocytic
leukemia, myeloblastic leukemia, myelocytic leukemia, myeloid
granulocytic leukemia, myelomonocytic leukemia, Naegeli leukemia,
plasma cell leukemia, multiple myeloma, plasmacytic leukemia,
promyelocytic leukemia, Rieder cell leukemia, Schilling's leukemia,
stem cell leukemia, subleukemic leukemia, or undifferentiated cell
leukemia.
[0077] The term "sarcoma" generally refers to a tumor which is made
up of a substance like the embryonic connective tissue and is
generally composed of closely packed cells embedded in a fibrillar
or homogeneous substance. Sarcomas that may be treated with a
compound or method provided herein include a chondrosarcoma,
fibrosarcoma, lymphosarcoma, melanosarcoma, myxosarcoma,
osteosarcoma, Abemethy's sarcoma, adipose sarcoma, liposarcoma,
alveolar soft part sarcoma, ameloblastic sarcoma, botryoid sarcoma,
chloroma sarcoma, chorio carcinoma, embryonal sarcoma, Wilms' tumor
sarcoma, endometrial sarcoma, stromal sarcoma, Ewing's sarcoma,
fascial sarcoma, fibroblastic sarcoma, giant cell sarcoma,
granulocytic sarcoma, Hodgkin's sarcoma, idiopathic multiple
pigmented hemorrhagic sarcoma, immunoblastic sarcoma of B cells,
lymphoma, immunoblastic sarcoma of T-cells, Jensen's sarcoma,
Kaposi's sarcoma, Kupffer cell sarcoma, angiosarcoma, leukosarcoma,
malignant mesenchymoma sarcoma, parosteal sarcoma, reticulocytic
sarcoma, Rous sarcoma, serocystic sarcoma, synovial sarcoma, or
telangiectaltic sarcoma.
[0078] The term "melanoma" is taken to mean a tumor arising from
the melanocytic system of the skin and other organs. Melanomas that
may be treated with a compound or method provided herein include,
for example, acral-lentiginous melanoma, amelanotic melanoma,
benign juvenile melanoma, Cloudman's melanoma, S91 melanoma,
Harding-Passey melanoma, juvenile melanoma, lentigo maligna
melanoma, malignant melanoma, nodular melanoma, subungal melanoma,
or superficial spreading melanoma.
[0079] The term "carcinoma" refers to a malignant new growth made
up of epithelial cells tending to infiltrate the surrounding
tissues and give rise to metastases. Exemplary carcinomas that may
be treated with a compound or method provided herein include, for
example, thyroid carcinoma, cholangiocarcinoma, pancreatic
adenocarcinoma, skin cutaneous melanoma, colon adenocarcinoma,
rectum adenocarcinoma, stomach adenocarcinoma, esophageal
carcinoma, head and neck squamous cell carcinoma, breast invasive
carcinoma, lung adenocarcinoma, lung squamous cell carcinoma,
medullary thyroid carcinoma, familial medullary thyroid carcinoma,
acinar carcinoma, acinous carcinoma, adenocystic carcinoma, adenoid
cystic carcinoma, carcinoma adenomatosum, carcinoma of adrenal
cortex, alveolar carcinoma, alveolar cell carcinoma, basal cell
carcinoma, carcinoma basocellulare, basaloid carcinoma,
basosquamous cell carcinoma, bronchioalveolar carcinoma,
bronchiolar carcinoma, bronchogenic carcinoma, cerebriform
carcinoma, cholangiocellular carcinoma, chorionic carcinoma,
colloid carcinoma, comedo carcinoma, corpus carcinoma, cribriform
carcinoma, carcinoma en cuirasse, carcinoma cutaneum, cylindrical
carcinoma, cylindrical cell carcinoma, duct carcinoma, carcinoma
durum, embryonal carcinoma, encephaloid carcinoma, epiermoid
carcinoma, carcinoma epitheliale adenoides, exophytic carcinoma,
carcinoma ex ulcere, carcinoma fibrosum, gelatiniforni carcinoma,
gelatinous carcinoma, giant cell carcinoma, carcinoma
gigantocellulare, glandular carcinoma, granulosa cell carcinoma,
hair-matrix carcinoma, hematoid carcinoma, hepatocellular
carcinoma, Hurthle cell carcinoma, hyaline carcinoma, hypernephroid
carcinoma, infantile embryonal carcinoma, carcinoma in situ,
intraepidermal carcinoma, intraepithelial carcinoma, Krompecher's
carcinoma, Kulchitzky-cell carcinoma, large-cell carcinoma,
lenticular carcinoma, carcinoma lenticulare, lipomatous carcinoma,
lymphoepithelial carcinoma, carcinoma medullare, medullary
carcinoma, melanotic carcinoma, carcinoma molle, mucinous
carcinoma, carcinoma muciparum, carcinoma mucocellulare,
mucoepidermoid carcinoma, carcinoma mucosum, mucous carcinoma,
carcinoma myxomatodes, nasopharyngeal carcinoma, oat cell
carcinoma, carcinoma ossificans, osteoid carcinoma, papillary
carcinoma, periportal carcinoma, preinvasive carcinoma, prickle
cell carcinoma, pultaceous carcinoma, renal cell carcinoma of
kidney, reserve cell carcinoma, carcinoma sarcomatodes,
schneiderian carcinoma, scirrhous carcinoma, carcinoma scroti,
signet-ring cell carcinoma, carcinoma simplex, small-cell
carcinoma, solanoid carcinoma, spheroidal cell carcinoma, spindle
cell carcinoma, carcinoma spongiosum, squamous carcinoma, squamous
cell carcinoma, string carcinoma, carcinoma telangiectaticum,
carcinoma telangiectodes, transitional cell carcinoma, carcinoma
tuberosum, tuberous carcinoma, verrucous carcinoma, or carcinoma
villosum.
[0080] As used herein, the term "autoimmune disease" refers to a
disease or condition in which a subject's immune system has an
aberrant immune response against a substance that does not normally
elicit an immune response in a healthy subject. Examples of
autoimmune diseases that may be treated with a compound,
pharmaceutical composition, or method described herein include
Acute Disseminated Encephalomyelitis (ADEM), Acute necrotizing
hemorrhagic leukoencephalitis, Addison's disease,
Agammaglobulinemia, Alopecia areata, Amyloidosis, Ankylosing
spondylitis, Anti-GBM/Anti-TBM nephritis, Antiphospholipid syndrome
(APS), Autoimmune angioedema, Autoimmune aplastic anemia,
Autoimmune dysautonomia, Autoimmune hepatitis, Autoimmune
hyperlipidemia, Autoimmune immunodeficiency, Autoimmune inner ear
disease (AIED), Autoimmune myocarditis, Autoimmune oophoritis,
Autoimmune pancreatitis, Autoimmune retinopathy, Autoimmune
thrombocytopenic purpura (ATP), Autoimmune thyroid disease,
Autoimmune urticaria, Axonal or neuronal neuropathies, Balo
disease, Behcet's disease, Bullous pemphigoid, Cardiomyopathy,
Castleman disease, Celiac disease, Chagas disease, Chronic fatigue
syndrome, Chronic inflammatory demyelinating polyneuropathy (CIDP),
Chronic recurrent multifocal ostomyelitis (CRMO), Churg-Strauss
syndrome, Cicatricial pemphigoid/benign mucosal pemphigoid, Crohn's
disease, Cogans syndrome, Cold agglutinin disease, Congenital heart
block, Coxsackie myocarditis, CREST disease, Essential mixed
cryoglobulinemia, Demyelinating neuropathies, Dermatitis
herpetiformis, Dermatomyositis, Devic's disease (neuromyelitis
optica), Discoid lupus, Dressler's syndrome, Endometriosis,
Eosinophilic esophagitis, Eosinophilic fasciitis, Erythema nodosum,
Experimental allergic encephalomyelitis, Evans syndrome,
Fibromyalgia, Fibrosing alveolitis, Giant cell arteritis (temporal
arteritis), Giant cell myocarditis, Glomerulonephritis,
Goodpasture's syndrome, Granulomatosis with Polyangiitis (GPA)
(formerly called Wegener's Granulomatosis), Graves' disease,
Guillain-Barre syndrome, Hashimoto's encephalitis, Hashimoto's
thyroiditis, Hemolytic anemia, Henoch-Schonlein purpura, Herpes
gestationis, Hypogammaglobulinemia, Idiopathic thrombocytopenic
purpura (ITP), IgA nephropathy, IgG4-related sclerosing disease,
Immunoregulatory lipoproteins, Inclusion body myositis,
Interstitial cystitis, Juvenile arthritis, Juvenile diabetes (Type
1 diabetes), Juvenile myositis, Kawasaki syndrome, Lambert-Eaton
syndrome, Leukocytoclastic vasculitis, Lichen planus, Lichen
sclerosus, Ligneous conjunctivitis, Linear IgA disease (LAD), Lupus
(SLE), Lyme disease, chronic, Meniere's disease, Microscopic
polyangiitis, Mixed connective tissue disease (MCTD), Mooren's
ulcer, Mucha-Habermann disease, Multiple sclerosis, Myasthenia
gravis, Myositis, Narcolepsy, Neuromyelitis optica (Devic's),
Neutropenia, Ocular cicatricial pemphigoid, Optic neuritis,
Palindromic rheumatism, PANDAS (Pediatric Autoimmune
Neuropsychiatric Disorders Associated with Streptococcus),
Paraneoplastic cerebellar degeneration, Paroxysmal nocturnal
hemoglobinuria (PNH), Parry Romberg syndrome, Parsonnage-Turner
syndrome, Pars planitis (peripheral uveitis), Pemphigus, Peripheral
neuropathy, Perivenous encephalomyelitis, Pernicious anemia, POEMS
syndrome, Polyarteritis nodosa, Type I, II, & III autoimmune
polyglandular syndromes, Polymyalgia rheumatica, Polymyositis,
Postmyocardial infarction syndrome, Postpericardiotomy syndrome,
Progesterone dermatitis, Primary biliary cirrhosis, Primary
sclerosing cholangitis, Psoriasis, Psoriatic arthritis, Idiopathic
pulmonary fibrosis, Pyoderma gangrenosum, Pure red cell aplasia,
Raynauds phenomenon, Reactive Arthritis, Reflex sympathetic
dystrophy, Reiter's syndrome, Relapsing polychondritis, Restless
legs syndrome, Retroperitoneal fibrosis, Rheumatic fever,
Rheumatoid arthritis, Sarcoidosis, Schmidt syndrome, Scleritis,
Scleroderma, Sjogren's syndrome, Sperm & testicular
autoimmunity, Stiff person syndrome, Subacute bacterial
endocarditis (SBE), Susac's syndrome, Sympathetic ophthalmia,
Takayasu's arteritis, Temporal arteritis/Giant cell arteritis,
Thrombocytopenic purpura (TTP), Tolosa-Hunt syndrome, Transverse
myelitis, Type 1 diabetes, Ulcerative colitis, Undifferentiated
connective tissue disease (UCTD), Uveitis, Vasculitis,
Vesiculobullous dermatosis, Vitiligo, or Wegener's granulomatosis
(i.e., Granulomatosis with Polyangiitis (GPA).
[0081] As used herein, the term "inflammatory disease" refers to a
disease or condition characterized by aberrant inflammation (e.g.
an increased level of inflammation compared to a control such as a
healthy person not suffering from a disease). Examples of
inflammatory diseases include traumatic brain injury, arthritis,
rheumatoid arthritis, psoriatic arthritis, juvenile idiopathic
arthritis, multiple sclerosis, systemic lupus erythematosus (SLE),
myasthenia gravis, juvenile onset diabetes, diabetes mellitus type
1, Guillain-Barre syndrome, Hashimoto's encephalitis, Hashimoto's
thyroiditis, ankylosing spondylitis, psoriasis, Sjogren's syndrome,
vasculitis, glomerulonephritis, auto-immune thyroiditis, Behcet's
disease, Crohn's disease, ulcerative colitis, bullous pemphigoid,
sarcoidosis, ichthyosis, Graves ophthalmopathy, inflammatory bowel
disease, Addison's disease, Vitiligo, asthma, asthma, allergic
asthma, acne vulgaris, celiac disease, chronic prostatitis,
inflammatory bowel disease, pelvic inflammatory disease,
reperfusion injury, sarcoidosis, transplant rejection, interstitial
cystitis, atherosclerosis, and atopic dermatitis.
[0082] The terms "treating", or "treatment" refer to any indicia of
success in the therapy or amelioration of an injury, disease,
pathology or condition, including any objective or subjective
parameter such as abatement; remission; diminishing of symptoms or
making the injury, pathology or condition more tolerable to the
patient; slowing in the rate of degeneration or decline; making the
final point of degeneration less debilitating; improving a
patient's physical or mental well-being.
[0083] The treatment or amelioration of symptoms can be based on
objective or subjective parameters; including the results of a
physical examination, neuropsychiatric exams, and/or a psychiatric
evaluation. The term "treating" and conjugations thereof, may
include prevention of an injury, pathology, condition, or disease.
In embodiments, treating is preventing. In embodiments, treating
does not include preventing.
[0084] "Treating" or "treatment" as used herein (and as
well-understood in the art) also broadly includes any approach for
obtaining beneficial or desired results in a subject's condition,
including clinical results. Beneficial or desired clinical results
can include, but are not limited to, alleviation or amelioration of
one or more symptoms or conditions, diminishment of the extent of a
disease, stabilizing (i.e., not worsening) the state of disease,
prevention of a disease's transmission or spread, delay or slowing
of disease progression, amelioration or palliation of the disease
state, diminishment of the reoccurrence of disease, and remission,
whether partial or total and whether detectable or undetectable. In
other words, "treatment" as used herein includes any cure,
amelioration, or prevention of a disease. Treatment may prevent the
disease from occurring; inhibit the disease's spread; relieve the
disease's symptoms (e.g., ocular pain, seeing halos around lights,
red eye, very high intraocular pressure), fully or partially remove
the disease's underlying cause, shorten a disease's duration, or do
a combination of these things.
[0085] "Treating" and "treatment" as used herein include
prophylactic treatment. Treatment methods include administering to
a subject a therapeutically effective amount of a compound
described herein. The administering step may consist of a single
administration or may include a series of administrations. The
length of the treatment period depends on a variety of factors,
such as the severity of the condition, the age of the patient, the
concentration of the compound, the activity of the compositions
used in the treatment, or a combination thereof. It will also be
appreciated that the effective dosage of an agent used for the
treatment or prophylaxis may increase or decrease over the course
of a particular treatment or prophylaxis regime. Changes in dosage
may result and become apparent by standard diagnostic assays known
in the art. In some instances, chronic administration may be
required. For example, the compositions are administered to the
subject in an amount and for a duration sufficient to treat the
patient.
[0086] The term "prevent" refers to a decrease in the occurrence of
disease symptoms in a patient. As indicated above, the prevention
may be complete (no detectable symptoms) or partial, such that
fewer symptoms are observed than would likely occur absent
treatment. In embodiments, prevent refers to slowing the
progression of the disease, disorder or condition or inhibiting
progression thereof to a harmful or otherwise undesired state.
[0087] "Patient" or "subject in need thereof" refers to a living
organism suffering from or prone to a disease or condition that can
be treated by administration of a pharmaceutical composition as
provided herein. Non-limiting examples include humans, other
mammals, bovines, rats, mice, dogs, monkeys, goat, sheep, cows,
deer, and other non-mammalian animals. In some embodiments, a
patient is human.
[0088] An "effective amount" is an amount sufficient for a compound
to accomplish a stated purpose relative to the absence of the
compound (e.g. achieve the effect for which it is administered,
treat a disease, reduce enzyme activity, increase enzyme activity,
reduce a signaling pathway, or reduce one or more symptoms of a
disease or condition). An example of an "effective amount" is an
amount sufficient to contribute to the treatment, prevention, or
reduction of a symptom or symptoms of a disease, which could also
be referred to as a "therapeutically effective amount." A
"reduction" of a symptom or symptoms (and grammatical equivalents
of this phrase) means decreasing of the severity or frequency of
the symptom(s), or elimination of the symptom(s). A
"prophylactically effective amount" of a drug is an amount of a
drug that, when administered to a subject, will have the intended
prophylactic effect, e.g., preventing or delaying the onset (or
reoccurrence) of an injury, disease, pathology or condition, or
reducing the likelihood of the onset (or reoccurrence) of an
injury, disease, pathology, or condition, or their symptoms. The
full prophylactic effect does not necessarily occur by
administration of one dose, and may occur only after administration
of a series of doses. Thus, a prophylactically effective amount may
be administered in one or more administrations. An "activity
decreasing amount," as used herein, refers to an amount of
antagonist required to decrease the activity of an enzyme relative
to the absence of the antagonist. A "function disrupting amount,"
as used herein, refers to the amount of antagonist required to
disrupt the function of an enzyme or protein relative to the
absence of the antagonist. The exact amounts will depend on the
purpose of the treatment, and will be ascertainable by one skilled
in the art using known techniques (see, e.g., Lieberman,
Pharmaceutical Dosage Forms (vols. 1-3, 1992); Lloyd, The Art,
Science and Technology of Pharmaceutical Compounding (1999);
Pickar, Dosage Calculations (1999); and Remington: The Science and
Practice of Pharmacy, 20th Edition, 2003, Gennaro, Ed., Lippincott,
Williams & Wilkins). The therapeutically effective amount can
be ascertained by measuring relevant physiological effects, and it
can be adjusted in connection with the dosing regimen and
diagnostic analysis of the subject's condition, and the like. By
way of example, measurement of the serum level of a CCR4 inhibitor
(or, e.g., a metabolite thereof) at a particular time
post-administration may be indicative of whether a therapeutically
effective amount has been administered.
[0089] For any compound described herein, the therapeutically
effective amount can be initially determined from cell culture
assays. Target concentrations will be those concentrations of
active compound(s) that are capable of achieving the methods
described herein, as measured using the methods described herein or
known in the art.
[0090] As is well known in the art, therapeutically effective
amounts for use in humans can also be determined from animal
models. For example, a dose for humans can be formulated to achieve
a concentration that has been found to be effective in animals. The
dosage in humans can be adjusted by monitoring compounds
effectiveness and adjusting the dosage upwards or downwards, as
described above. Adjusting the dose to achieve maximal efficacy in
humans based on the methods described above and other methods is
well within the capabilities of the ordinarily skilled artisan.
[0091] Adjusting the dose to achieve maximal therapeutic window
efficacy or toxicity in humans based on the methods described above
and other methods is well within the capabilities of the ordinarily
skilled artisan.
[0092] The term "therapeutically effective amount," as used herein,
refers to that amount of the therapeutic agent sufficient to
ameliorate the disorder, as described above. For example, for the
given parameter, a therapeutically effective amount will show an
increase or decrease of at least 5%, 10%, 15%, 20%, 25%, 40%, 50%,
60%, 75%, 80%, 90%, or at least 100%. Therapeutic efficacy can also
be expressed as "-fold" increase or decrease. For example, a
therapeutically effective amount can have at least a 1.2-fold,
1.5-fold, 2-fold, 5-fold, or more effect over a control.
[0093] Dosages may be varied depending upon the requirements of the
patient and the compound being employed. The dose administered to a
patient, in the context of the present invention should be
sufficient to effect a beneficial therapeutic response in the
patient over time. The size of the dose also will be determined by
the existence, nature, and extent of any adverse side-effects.
Determination of the proper dosage for a particular situation is
within the skill of the practitioner. Generally, treatment is
initiated with smaller dosages which are less than the optimum dose
of the compound. Thereafter, the dosage is increased by small
increments until the optimum effect under circumstances is reached.
Dosage amounts and intervals can be adjusted individually to
provide levels of the administered compound effective for the
particular clinical indication being treated. This will provide a
therapeutic regimen that is commensurate with the severity of the
individual's disease state.
[0094] As used herein, the term "administering" means oral
administration, administration as a suppository, topical contact,
intravenous, parenteral, intraperitoneal, intramuscular,
intralesional, intrathecal, intracranial, intranasal or
subcutaneous administration, or the implantation of a slow-release
device, e.g., a mini-osmotic pump, to a subject. Administration is
by any route, including parenteral and transmucosal (e.g., buccal,
sublingual, palatal, gingival, nasal, vaginal, rectal, or
transdermal). Parenteral administration includes, e.g.,
intravenous, intramuscular, intra-arteriole, intradermal,
subcutaneous, intraperitoneal, intraventricular, and intracranial.
Other modes of delivery include, but are not limited to, the use of
liposomal formulations, intravenous infusion, transdermal patches,
etc. By "co-administer" it is meant that a composition described
herein is administered at the same time, just prior to, or just
after the administration of one or more additional therapies (e.g.
anti-cancer agent, chemotherapeutic, or treatment for a
neurodegenerative disease). The compound of the invention can be
administered alone or can be coadministered to the patient.
Coadministration is meant to include simultaneous or sequential
administration of the compound individually or in combination (more
than one compound or agent). Thus, the preparations can also be
combined, when desired, with other active substances (e.g. to
reduce metabolic degradation). The compositions of the present
invention can be delivered by transdermally, by a topical route,
formulated as applicator sticks, solutions, suspensions, emulsions,
gels, creams, ointments, pastes, jellies, paints, powders, and
aerosols. Oral preparations include tablets, pills, powder,
dragees, capsules, liquids, lozenges, cachets, gels, syrups,
slurries, suspensions, etc., suitable for ingestion by the patient.
Solid form preparations include powders, tablets, pills, capsules,
cachets, suppositories, and dispersible granules. Liquid form
preparations include solutions, suspensions, and emulsions, for
example, water or water/propylene glycol solutions. The
compositions of the present invention may additionally include
components to provide sustained release and/or comfort. Such
components include high molecular weight, anionic mucomimetic
polymers, gelling polysaccharides and finely-divided drug carrier
substrates. These components are discussed in greater detail in
U.S. Pat. Nos. 4,911,920; 5,403,841; 5,212,162; and 4,861,760. The
entire contents of these patents are incorporated herein by
reference in their entirety for all purposes. The compositions of
the present invention can also be delivered as microspheres for
slow release in the body. For example, microspheres can be
administered via intradermal injection of drug-containing
microspheres, which slowly release subcutaneously (see Rao, J.
Biomater Sci. Polym. Ed. 7:623-645, 1995; as biodegradable and
injectable gel formulations (see, e.g., Gao Pharm. Res. 12:857-863,
1995); or, as microspheres for oral administration (see, e.g.,
Eyles, J. Pharm. Pharmacol. 49:669-674, 1997). In another
embodiment, the formulations of the compositions of the present
invention can be delivered by the use of liposomes which fuse with
the cellular membrane or are endocytosed, i.e., by employing
receptor ligands attached to the liposome, that bind to surface
membrane protein receptors of the cell resulting in endocytosis. By
using liposomes, particularly where the liposome surface carries
receptor ligands specific for target cells, or are otherwise
preferentially directed to a specific organ, one can focus the
delivery of the compositions of the present invention into the
target cells in vivo. (See, e.g., Al-Muhammed, J. Microencapsul.
13:293-306, 1996; Chonn, Curr. Opin. Biotechnol. 6:698-708, 1995;
Ostro, Am. J. Hosp. Pharm. 46:1576-1587, 1989). The compositions of
the present invention can also be delivered as nanoparticles.
[0095] By "co-administer" it is meant that a composition described
herein is administered at the same time, just prior to, or just
after the administration of one or more additional therapies. The
compounds of the invention can be administered alone or can be
coadministered to the patient. Coadministration is meant to include
simultaneous or sequential administration of the compounds
individually or in combination (more than one compound). The
compositions of the present invention can be delivered
transdermally, by a topical route, or formulated as applicator
sticks, solutions, suspensions, emulsions, gels, creams, ointments,
pastes, jellies, paints, powders, and aerosols.
[0096] For any compound described herein, the therapeutically
effective amount can be initially determined from cell culture
assays. Target concentrations will be those concentrations of
active compound(s) that are capable of achieving the methods
described herein, as measured using the methods described herein or
known in the art.
[0097] As is well known in the art, therapeutically effective
amounts for use in humans can also be determined from animal
models. For example, a dose for humans can be formulated to achieve
a concentration that has been found to be effective in animals. The
dosage in humans can be adjusted by monitoring compounds
effectiveness and adjusting the dosage upwards or downwards, as
described above. Adjusting the dose to achieve maximal efficacy in
humans based on the methods described above and other methods is
well within the capabilities of the ordinarily skilled artisan.
[0098] Dosages may be varied depending upon the requirements of the
patient and the compound being employed. The dose administered to a
patient, in the context of the present invention should be
sufficient to affect a beneficial therapeutic response in the
patient over time. The size of the dose also will be determined by
the existence, nature, and extent of any adverse side-effects.
Determination of the proper dosage for a particular situation is
within the skill of the practitioner. Generally, treatment is
initiated with smaller dosages which are less than the optimum dose
of the compound. Thereafter, the dosage is increased by small
increments until the optimum effect under circumstances is
reached.
[0099] Dosage amounts and intervals can be adjusted individually to
provide levels of the administered compound effective for the
particular clinical indication being treated. This will provide a
therapeutic regimen that is commensurate with the severity of the
individual's disease state.
[0100] Utilizing the teachings provided herein, an effective
prophylactic or therapeutic treatment regimen can be planned that
does not cause substantial toxicity and yet is effective to treat
the clinical symptoms demonstrated by the particular patient. This
planning should involve the careful choice of active compound by
considering factors such as compound potency, relative
bioavailability, patient body weight, presence and severity of
adverse side effects, preferred mode of administration and the
toxicity profile of the selected agent.
[0101] The compounds described herein can be used in combination
with one another, with other active agents known to be useful in
treating cancer (e.g. colon cancer), cardiovascular disease,
metabolic disease, immune or inflammatory disease or disorder.
[0102] In some embodiments, co-administration includes
administering one active agent within 0.5, 1, 2, 4, 6, 8, 10, 12,
16, 20, 24 hours, 2 days, 4 days, 1 week or 1 month of a second
active agent. Co-administration includes administering two active
agents simultaneously, approximately simultaneously (e.g., within
about 1, 5, 10, 15, 20, or 30 minutes of each other), or
sequentially in any order. In some embodiments, co-administration
can be accomplished by co-formulation, i.e., preparing a single
pharmaceutical composition including both active agents. In other
embodiments, the active agents can be formulated separately. In
another embodiment, the active and/or adjunctive agents may be
linked or conjugated to one another. In some embodiments, the
compounds described herein may be combined with treatments for
cancer (e.g. colon cancer), cardiovascular disease, metabolic
disease, immune or inflammatory disease or disorder.
[0103] "Cardiovascular agent" is used in accordance with its plain
ordinary meaning and refers to a composition (e.g. compound, drug,
antagonist, inhibitor, modulator) used in any way to treat
conditions of the heart or the circulatory or vascular system. In
some embodiments, a cardiovascular agent is an agent identified
herein having utility in methods of treating cardiovascular disease
or disorder. In some embodiments, a cardiovascular agent is an
agent approved by the FDA or similar regulatory agency of a country
other than the USA, for treating cardiovascular disease or
disorder.
[0104] "Anti-inflammatory agent" is used in accordance with its
plain ordinary meaning and refers to a composition (e.g. compound,
drug, antagonist, inhibitor, modulator) used in any way to reduce
inflammation or swelling. In some embodiments, an anti-inflammatory
agent is an agent identified herein having utility in methods of
treating an inflammatory disease or disorder. In some embodiments,
an anti-inflammatory agent is an agent approved by the FDA or
similar regulatory agency of a country other than the USA, for
reducing swelling and inflammation.
[0105] The compounds described herein can be administered to treat
an immune or inflammatory disease or disorder, a cardiovascular or
metabolic disease or disorder and/or cancer. In this regard, the
compounds disclosed herein may be administered either alone to
treat such diseases or disorders or may be co-administered with
another therapeutic agent to treat such diseases or disorders.
[0106] The compounds disclosed herein may be co-administered with a
cytokine or agonist or antagonist of cytokine function, (including
agents which act on cytokine signaling pathways such as modulators
of the SOCS system) including alpha-, beta-, and gamma-interferons;
insulin-like growth factor type I (IGF-1); interleukins (IL)
including IL1 to 17, and interleukin antagonists or inhibitors such
as analcinra; tumour necrosis factor alpha (TNF-.alpha.) inhibitors
such as anti-TNF monoclonal antibodies (for example infliximab;
adalimumab, and CDP-870) and TNF receptor antagonists including
immunoglobulin molecules (such as etanercept) and
low-molecular-weight agents such as pentoxyfylline.
[0107] The compounds disclosed herein may be co-administered with
an anti-inflammatory agent, such as thalidomide or a derivative
thereof, a retinoid, dithranol or calcipotriol, a non-steroidal
anti-inflammatory agent (hereinafter NSAID) including non-selective
cyclo-oxygenase COX-1/COX-2 inhibitors whether applied topically or
systemically (such as piroxicam, diclofenac, propionic acids such
as naproxen, flurbiprofen, fenoprofen, ketoprofen and ibuprofen,
fenamates such as mefenamic acid, indomethacin, sulindac,
azapropazone, pyrazolones such as phenylbutazone, salicylates such
as aspirin); selective COX-2 inhibitors (such as meloxicam,
celecoxib, rofecoxib, valdecoxib, lumarocoxib, parecoxib and
etoricoxib); cyclo-oxygenase inhibiting nitric oxide donors
(CINODs); glucocorticosteroids (whether administered by topical,
oral, intramuscular, intravenous, or intra-articular routes);
methotrexate; leflunomide; hydroxychloroquine; d-penicillamine;
auranofin or other parenteral or oral gold preparations;
analgesics; diacerein; intra-articular therapies such as hyaluronic
acid derivatives; and nutritional supplements such as
glucosamine.
[0108] The compounds disclosed herein may be co-administered with a
calcium channel blocker, a beta-adrenoceptor blocker, an
angiotensin-converting enzyme (ACE) inhibitor, an angiotensin-2
receptor antagonist; a lipid lowering agent such as a statin or a
fibrate; a modulator of blood cell morphology such as
pentoxyfylline; thrombolytic, or an anticoagulant such as a
platelet aggregation inhibitor.
[0109] "Anti-cancer agent" is used in accordance with its plain
ordinary meaning and refers to a composition (e.g. compound, drug,
antagonist, inhibitor, modulator) having antineoplastic properties
or the ability to inhibit the growth or proliferation of cells. In
some embodiments, an anti-cancer agent is a chemotherapeutic. In
some embodiments, an anti-cancer agent is an agent identified
herein having utility in methods of treating cancer. In some
embodiments, an anti-cancer agent is an agent approved by the FDA
or similar regulatory agency of a country other than the USA, for
treating cancer. Examples of anti-cancer agents include, but are
not limited to, MEK (e.g. MEK1, MEK2, or MEK1 and MEK2) inhibitors
(e.g. XL518, CI-1040, PD035901, selumetinib/AZD6244,
GSK1120212/trametinib, GDC-0973, ARRY-162, ARRY-300, AZD8330,
PD0325901, U0126, PD98059, TAK-733, PD318088, AS703026, BAY
869766), alkylating agents (e.g., cyclophosphamide, ifosfamide,
chlorambucil, busulfan, melphalan, mechlorethamine, uramustine,
thiotepa, nitrosoureas, nitrogen mustards (e.g., mechloroethamine,
cyclophosphamide, chlorambucil, meiphalan), ethylenimine and
methylmelamines (e.g., hexamethlymelamine, thiotepa), alkyl
sulfonates (e.g., busulfan), nitrosoureas (e.g., carmustine,
lomusitne, semustine, streptozocin), triazenes (decarbazine)),
anti-metabolites (e.g., 5-azathioprine, leucovorin, capecitabine,
fludarabine, gemcitabine, pemetrexed, raltitrexed, folic acid
analog (e.g., methotrexate), or pyrimidine analogs (e.g.,
fluorouracil, floxouridine, Cytarabine), purine analogs (e.g.,
mercaptopurine, thioguanine, pentostatin), etc.), plant alkaloids
(e.g., vincristine, vinblastine, vinorelbine, vindesine,
podophyllotoxin, paclitaxel, docetaxel, etc.), topoisomerase
inhibitors (e.g., irinotecan, topotecan, amsacrine, etoposide
(VP16), etoposide phosphate, teniposide, etc.), antitumor
antibiotics (e.g., doxorubicin, adriamycin, daunorubicin,
epirubicin, actinomycin, bleomycin, mitomycin, mitoxantrone,
plicamycin, etc.), platinum-based compounds (e.g. cisplatin,
oxaloplatin, carboplatin), anthracenedione (e.g., mitoxantrone),
substituted urea (e.g., hydroxyurea), methyl hydrazine derivative
(e.g., procarbazine), adrenocortical suppressant (e.g., mitotane,
aminoglutethimide), epipodophyllotoxins (e.g., etoposide),
antibiotics (e.g., daunorubicin, doxorubicin, bleomycin), enzymes
(e.g., L-asparaginase), inhibitors of mitogen-activated protein
kinase signaling (e.g. U0126, PD98059, PD184352, PD0325901,
ARRY-142886, SB239063, SP600125, BAY 43-9006, wortmannin, or
LY294002, Syk inhibitors, mTOR inhibitors, antibodies (e.g.,
rituxan), gossyphol, genasense, polyphenol E, Chlorofusin, all
trans-retinoic acid (ATRA), bryostatin, tumor necrosis
factor-related apoptosis-inducing ligand (TRAIL),
5-aza-2'-deoxycytidine, all trans retinoic acid, doxorubicin,
vincristine, etoposide, gemcitabine, imatinib (Gleevec.RTM.),
geldanamycin, 17-N-Allylamino-17-Demethoxygeldanamycin (17-AAG),
flavopiridol, LY294002, bortezomib, trastuzumab, BAY 11-7082,
PKC412, PD184352, 20-epi-1, 25 dihydroxyvitamin D3;
5-ethynyluracil; abiraterone; aclarubicin; acylfulvene; adecypenol;
adozelesin; aldesleukin; ALL-TK antagonists; altretamine;
ambamustine; amidox; amifostine; aminolevulinic acid; amrubicin;
amsacrine; anagrelide; anastrozole; andrographolide; angiogenesis
inhibitors; antagonist D; antagonist G; antarelix; anti-dorsalizing
morphogenetic protein-i; antiandrogen, prostatic carcinoma;
antiestrogen; antineoplaston; antisense oligonucleotides;
aphidicolin glycinate; apoptosis gene modulators; apoptosis
regulators; apurinic acid; ara-CDP-DL-PTBA; arginine deaminase;
asulacrine; atamestane; atrimustine; axinastatin 1; axinastatin 2;
axinastatin 3; azasetron; azatoxin; azatyrosine; baccatin III
derivatives; balanol; batimastat; BCR/ABL antagonists;
benzochlorins; benzoylstaurosporine; beta lactam derivatives;
beta-alethine; betaclamycin B; betulinic acid; bFGF inhibitor;
bicalutamide; bisantrene; bisaziridinylspermine; bisnafide;
bistratene A; bizelesin; breflate; bropirimine; budotitane;
buthionine sulfoximine; calcipotriol; calphostin C; camptothecin
derivatives; canarypox IL-2; capecitabine;
carboxamide-amino-triazole; carboxyamidotriazole; CaRest M3; CARN
700; cartilage derived inhibitor; carzelesin; casein kinase
inhibitors (ICOS); castanospermine; cecropin B; cetrorelix;
chlorins; chloroquinoxaline sulfonamide; cicaprost; cis-porphyrin;
cladribine; clomifene analogues; clotrimazole; collismycin A;
collismycin B; combretastatin A4; combretastatin analogue;
conagenin; crambescidin 816; crisnatol; cryptophycin 8;
cryptophycin A derivatives; curacin A; cyclopentanthraquinones;
cycloplatam; cypemycin; cytarabine ocfosfate; cytolytic factor;
cytostatin; dacliximab; decitabine; dehydrodidemnin B; deslorelin;
dexamethasone; dexifosfamide; dexrazoxane; dexverapamil;
diaziquone; didemnin B; didox; diethylnorspermine;
dihydro-5-azacytidine; 9-dioxamycin; diphenyl spiromustine;
docosanol; dolasetron; doxifluridine; droloxifene; dronabinol;
duocarmycin SA; ebselen; ecomustine; edelfosine; edrecolomab;
eflornithine; elemene; emitefur; epirubicin; epristeride;
estramustine analogue; estrogen agonists; estrogen antagonists;
etanidazole; etoposide phosphate; exemestane; fadrozole;
fazarabine; fenretinide; filgrastim; finasteride; flavopiridol;
flezelastine; fluasterone; fludarabine; fluorodaunorunicin
hydrochloride; forfenimex; formestane; fostriecin; fotemustine;
gadolinium texaphyrin; gallium nitrate; galocitabine; ganirelix;
gelatinase inhibitors; gemcitabine; glutathione inhibitors;
hepsulfam; heregulin; hexamethylene bisacetamide; hypericin;
ibandronic acid; idarubicin; idoxifene; idramantone; ilmofosine;
ilomastat; imidazoacridones; imiquimod; immunostimulant peptides;
insulin-like growth factor-1 receptor inhibitor; interferon
agonists; interferons; interleukins; iobenguane; iododoxorubicin;
ipomeanol, 4-; iroplact; irsogladine; isobengazole;
isohomohalicondrin B; itasetron; j asplakinolide; kahalalide F;
lamellarin-N triacetate; lanreotide; leinamycin; lenograstim;
lentinan sulfate; leptolstatin; letrozole; leukemia inhibiting
factor; leukocyte alpha interferon;
leuprolide+estrogen+progesterone; leuprorelin; levamisole;
liarozole; linear polyamine analogue; lipophilic disaccharide
peptide; lipophilic platinum compounds; lissoclinamide 7;
lobaplatin; lombricine; lometrexol; lonidamine; losoxantrone;
lovastatin; loxoribine; lurtotecan; lutetium texaphyrin;
lysofylline; lytic peptides; maitansine; mannostatin A; marimastat;
masoprocol; maspin; matrilysin inhibitors; matrix metalloproteinase
inhibitors; menogaril; merbarone; meterelin; methioninase;
metoclopramide; MIF inhibitor; mifepristone; miltefosine;
mirimostim; mismatched double stranded RNA; mitoguazone;
mitolactol; mitomycin analogues; mitonafide; mitotoxin fibroblast
growth factor-saporin; mitoxantrone; mofarotene; molgramostim;
monoclonal antibody, human chorionic gonadotrophin; monophosphoryl
lipid A+myobacterium cell wall sk; mopidamol; multiple drug
resistance gene inhibitor; multiple tumor suppressor 1-based
therapy; mustard anticancer agent; mycaperoxide B; mycobacterial
cell wall extract; myriaporone; N-acetyldinaline; N-substituted
benzamides; nafarelin; nagrestip; naloxone+pentazocine; napavin;
naphterpin; nartograstim; nedaplatin; nemorubicin; neridronic acid;
neutral endopeptidase; nilutamide; nisamycin; nitric oxide
modulators; nitroxide antioxidant; nitrullyn; 06-benzylguanine;
octreotide; okicenone; oligonucleotides; onapristone; ondansetron;
ondansetron; oracin; oral cytokine inducer; ormaplatin; osaterone;
oxaliplatin; oxaunomycin; palauamine; palmitoylrhizoxin; pamidronic
acid; panaxytriol; panomifene; parabactin; pazelliptine;
pegaspargase; peldesine; pentosan polysulfate sodium; pentostatin;
pentrozole; perflubron; perfosfamide; perillyl alcohol;
phenazinomycin; phenylacetate; phosphatase inhibitors; picibanil;
pilocarpine hydrochloride; pirarubicin; piritrexim; placetin A;
placetin B; plasminogen activator inhibitor; platinum complex;
platinum compounds; platinum-triamine complex; porfimer sodium;
porfiromycin; prednisone; propyl bis-acridone; prostaglandin J2;
proteasome inhibitors; protein A-based immune modulator; protein
kinase C inhibitor; protein kinase C inhibitors, microalgal;
protein tyrosine phosphatase inhibitors; purine nucleoside
phosphorylase inhibitors; purpurins; pyrazoloacridine;
pyridoxylated hemoglobin polyoxyethylerie conjugate; raf
antagonists; raltitrexed; ramosetron; ras farnesyl protein
transferase inhibitors; ras inhibitors; ras-GAP inhibitor;
retelliptine demethylated; rhenium Re 186 etidronate; rhizoxin;
ribozymes; RII retinamide; rogletimide; rohitukine; romurtide;
roquinimex; rubiginone B 1; ruboxyl; safingol; saintopin; SarCNU;
sarcophytol A; sargramostim; Sdi 1 mimetics; semustine; senescence
derived inhibitor 1; sense oligonucleotides; signal transduction
inhibitors; signal transduction modulators; single chain
antigen-binding protein; sizofuran; sobuzoxane; sodium borocaptate;
sodium phenylacetate; solverol; somatomedin binding protein;
sonermin; sparfosic acid; spicamycin D; spiromustine; splenopentin;
spongistatin 1; squalamine; stem cell inhibitor; stem-cell division
inhibitors; stipiamide; stromelysin inhibitors; sulfinosine;
superactive vasoactive intestinal peptide antagonist; suradista;
suramin; swainsonine; synthetic glycosaminoglycans; tallimustine;
tamoxifen methiodide; tauromustine; tazarotene; tecogalan sodium;
tegafur; tellurapyrylium; telomerase inhibitors; temoporfin;
temozolomide; teniposide; tetrachlorodecaoxide; tetrazomine;
thaliblastine; thiocoraline; thrombopoietin; thrombopoietin
mimetic; thymalfasin; thymopoietin receptor agonist; thymotrinan;
thyroid stimulating hormone; tin ethyl etiopurpurin; tirapazamine;
titanocene bichloride; topsentin; toremifene; totipotent stem cell
factor; translation inhibitors; tretinoin; triacetyluridine;
triciribine; trimetrexate; triptorelin; tropisetron; turosteride;
tyrosine kinase inhibitors; tyrphostins; UBC inhibitors; ubenimex;
urogenital sinus-derived growth inhibitory factor; urokinase
receptor antagonists; vapreotide; variolin B; vector system,
erythrocyte gene therapy; velaresol; veramine; verdins;
verteporfin; vinorelbine; vinxaltine; vitaxin; vorozole;
zanoterone; zeniplatin; zilascorb; zinostatin stimalamer,
Adriamycin, Dactinomycin, Bleomycin, Vinblastine, Cisplatin,
acivicin; aclarubicin; acodazole hydrochloride; acronine;
adozelesin; aldesleukin; altretamine; ambomycin; ametantrone
acetate; aminoglutethimide; amsacrine; anastrozole; anthramycin;
asparaginase; asperlin; azacitidine; azetepa; azotomycin;
batimastat; benzodepa; bicalutamide; bisantrene hydrochloride;
bisnafide dimesylate; bizelesin; bleomycin sulfate; brequinar
sodium; bropirimine; busulfan; cactinomycin; calusterone;
caracemide; carbetimer; carboplatin; carmustine; carubicin
hydrochloride; carzelesin; cedefingol; chlorambucil; cirolemycin;
cladribine; crisnatol mesylate; cyclophosphamide; cytarabine;
dacarbazine; daunorubicin hydrochloride; decitabine; dexormaplatin;
dezaguanine; dezaguanine mesylate; diaziquone; doxorubicin;
doxorubicin hydrochloride; droloxifene; droloxifene citrate;
dromostanolone propionate; duazomycin; edatrexate; eflornithine
hydrochloride; elsamitrucin; enloplatin; enpromate; epipropidine;
epirubicin hydrochloride; erbulozole; esorubicin hydrochloride;
estramustine; estramustine phosphate sodium; etanidazole;
etoposide; etoposide phosphate; etoprine; fadrozole hydrochloride;
fazarabine; fenretinide; floxuridine; fludarabine phosphate;
fluorouracil; fluorocitabine; fosquidone; fostriecin sodium;
gemcitabine; gemcitabine hydrochloride; hydroxyurea; idarubicin
hydrochloride; ifosfamide; iimofosine; interleukin I1 (including
recombinant interleukin II, or rlL.sub.2), interferon alfa-2a;
interferon alfa-2b; interferon alfa-n1; interferon alfa-n3;
interferon beta-1a; interferon gamma-1b; iproplatin; irinotecan
hydrochloride; lanreotide acetate; letrozole; leuprolide acetate;
liarozole hydrochloride; lometrexol sodium; lomustine; losoxantrone
hydrochloride; masoprocol; maytansine; mechlorethamine
hydrochloride; megestrol acetate; melengestrol acetate; melphalan;
menogaril; mercaptopurine; methotrexate; methotrexate sodium;
metoprine; meturedepa; mitindomide; mitocarcin; mitocromin;
mitogillin; mitomalcin; mitomycin; mitosper; mitotane; mitoxantrone
hydrochloride; mycophenolic acid; nocodazoie; nogalamycin;
ormaplatin; oxisuran; pegaspargase; peliomycin; pentamustine;
peplomycin sulfate; perfosfamide; pipobroman; piposulfan;
piroxantrone hydrochloride; plicamycin; plomestane; porfimer
sodium; porfiromycin; prednimustine; procarbazine hydrochloride;
puromycin; puromycin hydrochloride; pyrazofurin; riboprine;
rogletimide; safingol; safingol hydrochloride; semustine;
simtrazene; sparfosate sodium; sparsomycin; spirogermanium
hydrochloride; spiromustine; spiroplatin; streptonigrin;
streptozocin; sulofenur; talisomycin; tecogalan sodium; tegafur;
teloxantrone hydrochloride; temoporfin; teniposide; teroxirone;
testolactone; thiamiprine; thioguanine; thiotepa; tiazofurin;
tirapazamine; toremifene citrate; trestolone acetate; triciribine
phosphate; trimetrexate; trimetrexate glucuronate; triptorelin;
tubulozole hydrochloride; uracil mustard; uredepa; vapreotide;
verteporfin; vinblastine sulfate; vincristine sulfate; vindesine;
vindesine sulfate; vinepidine sulfate; vinglycinate sulfate;
vinleurosine sulfate; vinorelbine tartrate; vinrosidine sulfate;
vinzolidine sulfate; vorozole; zeniplatin; zinostatin; zorubicin
hydrochloride, agents that arrest cells in the G2-M phases and/or
modulate the formation or stability of microtubules, (e.g.
Taxol..TM. (i.e. paclitaxel), Taxotere..TM., compounds comprising
the taxane skeleton, Erbulozole (i.e. R-55104), Dolastatin 10 (i.e.
DLS-10 and NSC-376128), Mivobulin isethionate (i.e. as CI-980),
Vincristine, NSC-639829, Discodermolide (i.e. as NVP-XX-A-296),
ABT-751 (Abbott, i.e. E-7010), Altorhyrtins (e.g. Altorhyrtin A and
Altorhyrtin C), Spongistatins (e.g. Spongistatin 1, Spongistatin 2,
Spongistatin 3, Spongistatin 4, Spongistatin 5, Spongistatin 6,
Spongistatin 7, Spongistatin 8, and Spongistatin 9), Cemadotin
hydrochloride (i.e. LU-103793 and NSC-D-669356), Epothilones (e.g.
Epothilone A, Epothilone B, Epothilone C (i.e. desoxyepothilone A
or dEpoA), Epothilone D (i.e. KOS-862, dEpoB, and desoxyepothilone
B), Epothilone E, Epothilone F, Epothilone B N-oxide, Epothilone A
N-oxide, 16-aza-epothilone B, 21-aminoepothilone B (i.e.
BMS-310705), 21-hydroxyepothilone D (i.e. Desoxyepothilone F and
dEpoF), 26-fluoroepothilone, Auristatin PE (i.e. NSC-654663),
Soblidotin (i.e. TZT-1027), LS-4559-P (Pharmacia, i.e. LS-4577),
LS-4578 (Pharmacia, i.e. LS-477-P), LS-4477 (Pharmacia), LS-4559
(Pharmacia), RPR-112378 (Aventis), Vincristine sulfate, DZ-3358
(Daiichi), FR-182877 (Fujisawa, i.e. WS-9885B), GS-164 (Takeda),
GS-198 (Takeda), KAR-2 (Hungarian Academy of Sciences), BSF-223651
(BASF, i.e. ILX-651 and LU-223651), SAH-49960 (Lilly/Novartis),
SDZ-268970 (Lilly/Novartis), AM-97 (Armad/Kyowa Hakko), AM-132
(Armad), AM-138 (Armad/Kyowa Hakko), IDN-5005 (Indena),
Cryptophycin 52 (i.e. LY-355703), AC-7739 (Ajinomoto, i.e.
AVE-8063A and CS-39.HCl), AC-7700 (Ajinomoto, i.e. AVE-8062,
AVE-8062A, CS-39-L-Ser.HCl, and RPR-258062A), Vitilevuamide,
Tubulysin A, Canadensol, Centaureidin (i.e. NSC-106969), T-138067
(Tularik, i.e. T-67, TL-138067 and TI-138067), COBRA-1 (Parker
Hughes Institute, i.e. DDE-261 and WHI-261), H10 (Kansas State
University), H16 (Kansas State University), Oncocidin Al (i.e.
BTO-956 and DIME), DDE-313 (Parker Hughes Institute), Fijianolide
B, Laulimalide, SPA-2 (Parker Hughes Institute), SPA-1 (Parker
Hughes Institute, i.e. SPIKET-P), 3-IAABU (Cytoskeleton/Mt. Sinai
School of Medicine, i.e. MF-569), Narcosine (also known as
NSC-5366), Nascapine, D-24851 (Asta Medica), A-105972 (Abbott),
Hemiasterlin, 3-BAABU (Cytoskeleton/Mt. Sinai School of Medicine,
i.e. MF-191), TMPN (Arizona State University), Vanadocene
acetylacetonate, T-138026 (Tularik), Monsatrol, Inanocine (i.e.
NSC-698666), 3-IAABE (Cytoskeleton/Mt. Sinai School of Medicine),
A-204197 (Abbott), T-607 (Tuiarik, i.e. T-900607), RPR-115781
(Aventis), Eleutherobins (such as Desmethyleleutherobin,
Desaetyleleutherobin, lsoeleutherobin A, and Z-Eleutherobin),
Caribaeoside, Caribaeolin, Halichondrin B, D-64131 (Asta Medica),
D-68144 (Asta Medica), Diazonamide A, A-293620 (Abbott), NPI-2350
(Nereus), Taccalonolide A, TUB-245 (Aventis), A-259754 (Abbott),
Diozostatin, (
-)-Phenylahistin (i.e. NSCL-96F037), D-68838 (Asta Medica), D-68836
(Asta Medica), Myoseverin B, D-43411 (Zentaris, i.e. D-81862),
A-289099 (Abbott), A-318315 (Abbott), HTI-286 (i.e. SPA-110,
trifluoroacetate salt) (Wyeth), D-82317 (Zentaris), D-82318
(Zentaris), SC-12983 (NCI), Resverastatin phosphate sodium,
BPR-OY-007 (National Health Research Institutes), and SSR-250411
(Sanofi)), steroids (e.g., dexamethasone), finasteride, aromatase
inhibitors, gonadotropin-releasing hormone agonists (GnRH) such as
goserelin or leuprolide, adrenocorticosteroids (e.g., prednisone),
progestins (e.g., hydroxyprogesterone caproate, megestrol acetate,
medroxyprogesterone acetate), estrogens (e.g., diethlystilbestrol,
ethinyl estradiol), antiestrogen (e.g., tamoxifen), androgens
(e.g., testosterone propionate, fluoxymesterone), antiandrogen
(e.g., flutamide), immunostimulants (e.g., Bacillus Calmette-Guerin
(BCG), levamisole, interleukin-2, alpha-interferon, etc.),
monoclonal antibodies (e.g., anti-CD20, anti-HER2, anti-CD52,
anti-HLA-DR, and anti-VEGF monoclonal antibodies), immunotoxins
(e.g., anti-CD33 monoclonal antibody-calicheamicin conjugate,
anti-CD22 monoclonal antibody-pseudomonas exotoxin conjugate,
etc.), radioimmunotherapy (e.g., anti-CD20 monoclonal antibody
conjugated to .sup.111In, .sup.90Y, or .sup.131I, etc.),
triptolide, homoharringtonine, dactinomycin, doxorubicin,
epirubicin, topotecan, itraconazole, vindesine, cerivastatin,
vincristine, deoxyadenosine, sertraline, pitavastatin, irinotecan,
clofazimine, 5-nonyloxytryptamine, vemurafenib, dabrafenib,
erlotinib, gefitinib, EGFR inhibitors, epidermal growth factor
receptor (EGFR)-targeted therapy or therapeutic (e.g. gefitinib
(Iressa.TM.), erlotinib (Tarceva.TM.), cetuximab (Erbitux.TM.),
lapatinib (Tykerb.TM.), panitumumab (Vectibix.TM.), vandetanib
(Caprelsa.TM.), afatinib/BIBW2992, CI-1033/canertinib,
neratinib/HKI-272, CP-724714, TAK-285, AST-1306, ARRY334543,
ARRY-380, AG-1478, dacomitinib/PF299804, OSI-420/desmethyl
erlotinib, AZD8931, AEE788, pelitinib/EKB-569, CUDC-101, WZ8040,
WZ4002, WZ3146, AG-490, XL647, PD153035, BMS-599626), sorafenib,
imatinib, sunitinib, dasatinib, or the like.
[0110] "Chemotherapeutic" or "chemotherapeutic agent" is used in
accordance with its plain ordinary meaning and refers to a chemical
composition or compound having antineoplastic properties or the
ability to inhibit the growth or proliferation of cells.
[0111] Additionally, the compounds described herein can be
co-administered with conventional immunotherapeutic agents
including, but not limited to, immunostimulants (e.g., Bacillus
Calmette-Guerin (BCG), levamisole, interleukin-2, alpha-interferon,
etc.), monoclonal antibodies (e.g., anti-CD20, anti-HER2,
anti-CD52, anti-HLA-DR, and anti-VEGF monoclonal antibodies),
immunotoxins (e.g., anti-CD33 monoclonal antibody-calicheamicin
conjugate, anti-CD22 monoclonal antibody-pseudomonas exotoxin
conjugate, etc.), and radioimmunotherapy (e.g., anti-CD20
monoclonal antibody conjugated to .sup.111In, .sup.90Y, or
.sup.131I, etc.).
[0112] The compounds disclosed herein may be co-administered with
an antiproliferative/antineoplastic drug or a combination thereof,
as used in medical oncology, such as an alkylating agent (for
example cis-platin, carboplatin, cyclophosphamide, nitrogen
mustard, melphalan, chlorambucil, busulphan or a nitrosourea); an
antimetabolite (for example an antifolate such as a
fluoropyrimidine like 5-fluorouracil or tegafur, raltitrexed,
methotrexate, cytosine arabinoside, hydroxyurea, gemcitabine or
paclitaxel); an antitumour antibiotic (for example an anthracycline
such as adriamycin, bleomycin, doxorubicin, daunomycin, epirubicin,
idarubicin, mitomycin-C, dactinomycin or mithramycin); an
antimitotic agent (for example a vinca alkaloid such as
vincristine, vinblastine, vindesine or vinorelbine, or a taxoid
such as taxol or taxotere); or a topoisomerase inhibitor (for
example an epipodophyllotoxin such as etoposide, teniposide,
amsacrine, topotecan or a camptothecin); (ii) a cytostatic agent
such as an antioestrogen (for example tamoxifen, toremifene,
raloxifene, droloxifene or iodoxyfene), an oestrogen receptor down
regulator (for example fulvestrant), an antiandrogen (for example
bicalutamide, flutamide, nilutamide or cyproterone acetate), a LHRH
antagonist or LHRH agonist (for example goserelin, leuprorelin or
buserelin), a progestogen (for example megestrol acetate), an
aromatase inhibitor (for example as anastrozole, letrozole,
vorazole or exemestane) or an inhibitor of 5.alpha.-reductase such
as finasteride; (iii) an agent which inhibits cancer cell invasion
(for example a metalloproteinase inhibitor like marimastat or an
inhibitor of urokinase plasminogen activator receptor function);
(iv) an inhibitor of growth factor function, for example: a growth
factor antibody (for example the anti-erbb2 antibody trastuzumab,
or the anti-erbb 1 antibody cetuximab [C225]), a farnesyl
transferase inhibitor, a tyrosine kinase inhibitor or a
serine/threonine kinase inhibitor, an inhibitor of the epidermal
growth factor family (for example an EGFR family tyrosine kinase
inhibitor such as
N-(3-chloro-4-fluorophenyl)-7-methoxy-6-(3-morpholinopropoxy)quinazoli-
-n-4-amine (gefitinib, AZD 1839),
N-(3-ethynylphenyl)-6,7-bis(2-methoxyethoxy)quinazolin-4-amine
(erlotinib, OSI-774) or
6-acrylamido-N-(3-chloro-4-fluorophenyl)-7-(3-morpholinopropoxy)quinazoli-
-n-4-amine (CI 1033)), an inhibitor of the platelet-derived growth
factor family, or an inhibitor of the hepatocyte growth factor
family; (v) an antiangiogenic agent such as one which inhibits the
effects of vascular endothelial growth factor (for example the
anti-vascular endothelial cell growth factor antibody bevacizumab,
a compound disclosed in WO 97/22596, WO 97/30035, WO 97/32856 or WO
98/13354), or a compound that works by another mechanism (for
example linomide, an inhibitor of integrin.alpha.v.beta.3 function
or an angiostatin); (vi) a vascular damaging agent such as
combretastatin A4, or a compound disclosed in WO 99/02166, WO
00/40529, WO 00/41669, WO 01/92224, WO 02/04434 or WO 02/08213;
(vii) an agent used in antisense therapy, for example one directed
to one of the targets listed above, such as ISIS 2503, an anti-ras
antisense; (viii) an agent used in a gene therapy approach, for
example approaches to replace aberrant genes such as aberrant p53
or aberrant BRCA1 or BRCA2, GDEPT (gene-directed enzyme pro-drug
therapy) approaches such as those using cytosine deaminase,
thymidine kinase or a bacterial nitroreductase enzyme and
approaches to increase patient tolerance to chemotherapy or
radiotherapy such as multi-drug resistance gene therapy; or (ix) an
agent used in an immunotherapeutic approach, for example ex-vivo
and in-vivo approaches to increase the immunogenicity of patient
tumour cells, such as transfection with cytokines such as
interleukin 2, interleukin 4 or granulocyte-macrophage colony
stimulating factor, approaches to decrease T-cell anergy,
approaches using transfected immune cells such as
cytokine-transfected dendritic cells, approaches using
cytokine-transfected tumour cell lines and approaches using
anti-idiotypic antibodies.
[0113] In embodiments, the compounds disclosed herein can be
co-administered with an antibody, such as a monoclonal antibody
targeting B-Lymphocytes (such as CD20 (rituximab), MRA-aTL16R and
T-Lymphocytes, CTLA4-Ig, HuMax 11-15) or antibody modulating Ig
function such as anti-IgE (for example omalizumab).
[0114] In embodiments, treatment of cancer includes administration
of an effective amount of at least two of the following: a CCR4
inhibitor, an inhibitor of the PD-L1/PD-1 pathway, an inhibitor of
CTLA-4, an agonistic antibody of CD137 (4-1BB). In some
embodiments, the method may comprise the use of two or more
combinations.
[0115] In embodiments, treatment of cancer includes an effective
amount of at least two or more of the following: a CCR4 inhibitor
and any combination of agent that may be an immune modulator such
as, but not limited to, those listed in Table 1. These immune
modulators can be depleting antibodies, neutralizing antibodies,
blocking antibodies, agonistic antibodies, small molecule
modulators (inhibitors or stimulators) or small molecule
analogs.
TABLE-US-00001 TABLE 1 Target or Regulatory Therapy Examples of
Agents Mechanism TIM-3 TSR-022, MGB453 Checkpoint-receptor LAG-3
BMS-986016, IMP321 Checkpoint-receptor B7-H3 MGA271, MGD-009
Checkpoint-receptor TIGIT RG-6058 Checkpoint-receptor BTLA
Checkpoint-receptor CD28 AMG 557, Checkpoint-receptor CD40
SEA-CD40, dacetuzumab, CP- Checkpoint-receptor 870,893, Chi Lob
7/4, lucatumumab CD80 galiximab Checkpoint-receptor GITR
INCAGN1876, TRX518, Checkpoint-receptor ICOS MEDI-570
Checkpoint-receptor OX40 MEDI-6469, INCAGN1949, Checkpoint-receptor
(CD134) huMab OX40L, NKG2A monalizumab Checkpoint-receptor TGF-beta
Galunisertib, luspatercept, YH- Cytokines 14618, dalantercept,
BG-00011, trabedersen, isth-0036,, ace-083, IL2 NKTR-214,
recombinant IL2, Cytokines aldesleukin IL12 EGEN-001, NHS-IL12
Cytokines IL7 Recombinant IL-7, Cytokines IL15 NIZ-985, ALT-803,
Cytokines IL21 Recombinant IL-21, anti- Cytokines CD20.IL21, IL13
Tralokinumab, dupilumab CSF1R cabiralizumab Cytokine PI3K delta
INCB50465, idealisib, TGR- Kinase 1202, AMG319, PI3K gamma IPI-549
Kinase DNMT (DNA Azacytidine, decitabine, Epigenetic Regulator
methyl guadecitabine, transferase inhibitor) HDAC Vorinostat,
Panobinostat, Epigenetic Regulator (histone belinostat, entinostat,
mocetinostat, deacetylase) givinostat, chidamide, quisinostat,
abexinostat, chr-3996, ar-42, Brd4 INCN54329, INCB57643,
Transcription birabresib, apabetalone, alvocidib, regulator
PLX-51107, FT-1101, RG-6146, AZD-8186, CPI-0610, JQ1 HMT (histone
Epigenetic Regulator methyl transferases) LSD1 INCB59872, IMG-7289,
RG-6016, Epigenetic Regulator CC-90011, GSK-2879552, ORY- 2001,
4SC-202, ORY-3001, TNFa Recombinant TNFa, MEDI-1873, Cytokine
FPA-154, LKZ-145 IL1 Recombinant IL1 Cytokine IFNa Recombinant
interferon alpha-n1, Cytokine Recombinant interferon alpha-2b,
Recombinant interferon alpha-n3 IFNb Recombinant IFN beta-1a,
Cytokine IFNg actimmune Cytokine STING Cyclic di-nucleotides
Signaling Molecule TLR Poly I:C, IMO-2055, TMX-101, Pathogen
imiquimod, CpG, MGN1703, Recognition glucopyranosyl lipid A,
CBLB502, Receptor BCG, HILTONOL, AMPLIGEN, MOTOLIMOD, DUK-CPG-001,
AS15 IL10 Recombinant IL-10 Cytokine CCR2 CCX140, CCX872,
BMS-813160, Chemokine CENICRIVIROC, CNTX-6970. PF-4136309,
plozalizumab, INCB- 9471, PF-04634817 CCR5 Maraviroc, PRO-140, BMS-
Chemokine 813160, NIFEVIROC, OHR-118 CXCR4 Ulocuplumab, plerixafor,
x4p-001, Chemokine us1-311, ly-2510924, APH-0812, BL-8040,
BURIXAFOR, BALIXAFORTIDE, PTX-9908, GMI-1359, F-50067 LFA1 Adhesion
Molecule MICA/B IPH-4301 Immune Receptor Ligand VISTA CA-170
Checkpoint-Ligand Adenosine ISTRADEFYLLINE, Nucleoside TOZADENANT,
PBF-509, PBF- 999, CPI-444 CD39 OREG-103. Anti-CD39 antibodies,
Ecto-enzyme CD73 Oleclumab, PBF-1662, anti-CD73 Ecto-Enzyme
antibodies PD1 Pembrolizumab, nivolumab, Checkpoint-receptor
INCSHR1210, CT-011, AMP224 PD-L1 Atezolizumab, avelumab
Checkpoint-Ligand PD-L2 Checkpoint-Ligand CTLA4 Tremelimumab
Checkpoint-receptor CD137 Urelumab, utomilumab, BMS- 663513,
PF-05082566 AXL BGB-324, BPI-9016M, S-49076 Kinase MERTK BGB-324,
BPI-9016M, S-49076 Kinase TYRO BGB-324, BPI-9016M, S-49076 BTK
ibrutinib Kinase ITK ibrutinib Kinase LCK Kinase TET2 Enzyme
Arginase Cb-1158 Endo/ecto enzyme GCN2 Kinase B7-H4 MDX-1140,
AMP-110 Checkpoint-receptor HIF1alpha PT2385 Transcription Factor
LIGHT TNF Superfamily (TNFSF14) FLT3 CDX-301, FLX925, quizartinib,
Kinase gilteritinib, PKC412, midostaurin, crenolanib CD158
Lirlumab, IPH-2101 CD47 Anti-CD47, TTI-621, NI-1701, SRF-231,
Effi-DEM, RCT-1938 IDO Epacadostat, F287, BMS983205, GDC-0919,
indoximod, RORgamma
[0116] In a further embodiment, the compounds described herein can
be co-administered with conventional radiotherapeutic agents
including, but not limited to, radionuclides such as .sup.47Sc,
.sup.64Cu, .sup.67Cu, .sup.89Sr, .sup.86Y, .sup.87Y, .sup.90Y,
.sup.105Rh, .sup.111Ag, .sup.111In, .sup.117mSn, .sup.149Pm,
.sup.153Sm, .sup.166Ho, .sup.177Lu, .sup.186Re, .sup.188Re,
.sup.211At, and .sup.212Bi, optionally conjugated to antibodies
directed against tumor antigens.
[0117] In addition, a CCR4 inhibitor may be combined with the
therapeutic administration of immune cells, sometimes referred to
as adoptive cell transfer. These cells may be cells from the
patient, a genetically related or unrelated donor, they may be
genetically modified (e.g. CAR-T cells, NK cells, etc), cell lines,
genetically modified cell lines and live or dead versions of the
above. CCR4 inhibitors may also be combined with vaccines of any
kind (e.g. protein/peptide, viral, bacterial, cellular) to
stimulate immune responses to cancer.
[0118] In embodiments, treatment is administration of an effective
amount of a CCR4 inhibitor in combination with an inhibitor of the
PD-L1/PD-1 pathway, an inhibitor of CTLA-4, an agonistic antibody
of CD137 (4-1BB) or in combination with another immune modulator as
listed in Table 1.
[0119] In embodiments, treatment is therapeutic administration of
an effective amount of a CCR4 inhibitor in combination with an
inhibitor of the PD-L1/PD-1 pathway, an inhibitor of CTLA-4, an
agonistic antibody of CD 137 (4-1BB) or in combination with another
immune modulator as listed in Table 1. Here, treatment starts when
tumors reach a size of 40-70 mm.sup.3.
[0120] The CCR4 inhibitors disclosed herein can be administered by
any acceptable route, such oral, intraadiposal, intraarterial,
intraarticular, intracranial, intradermal, intralesional,
intramusculay, intranasal, intraocularal, intrapericardial,
intraperitoneal, intrapleural, intraprostatical, intrarectal,
intrathecal, intratracheal, intratumoral, intraumbilical,
intravaginal, intravenousl, intravesicullar, intravitreal,
liposomal, local, mucosal, parenteral, rectal, subconjunctival,
subcutaneous, sublingual, topical, transbuccal, transdermal,
vaginal, in cremes, in lipid compositions, via a catheter, via a
lavage, via continuous infusion, via infusion, via inhalation, via
injection, via local delivery, via localized perfusion, bathing
target cells directly, or any combination thereof.
[0121] The immune modulators disclosed herein can be administered
by any acceptable route, such oral, intraadiposal, intraarterial,
intraarticular, intracranial, intradermal, intralesional,
intramusculay, intranasal, intraocularal, intrapericardial,
intraperitoneal, intrapleural, intraprostatical, intrarectal,
intrathecal, intratracheal, intratumoral, intraumbilical,
intravaginal, intravenousl, intravesicullar, intravitreal,
liposomal, local, mucosal, parenteral, rectal, subconjunctival,
subcutaneous, sublingual, topical, transbuccal, transdermal,
vaginal, in cremes, in lipid compositions, via a catheter, via a
lavage, via continuous infusion, via infusion, via inhalation, via
injection, via local delivery, via localized perfusion, bathing
target cells directly, or any combination thereof.
[0122] The CCR4 inhibitors disclosed herein may be administered
once daily until study reached endpoint. The immune modulator
disclosed herein may be administered at least three times but in
some studies four or more times depending on the length of the
study and/or the design of the study.
[0123] The methods disclosed herein may be used in combination with
additional cancer therapy. In some embodiments, the distinct cancer
therapy comprises surgery, radiotherapy, chemotherapy, toxin
therapy, immunotherapy, cryotherapy or gene therapy. In some
embodiments, the cancer is a chemotherapy-resistant or
radio-resistant cancer.
[0124] A "cell" as used herein, refers to a cell carrying out
metabolic or other function sufficient to preserve or replicate its
genomic DNA. A cell can be identified by well-known methods in the
art including, for example, presence of an intact membrane,
staining by a particular dye, ability to produce progeny or, in the
case of a gamete, ability to combine with a second gamete to
produce a viable offspring. Cells may include prokaryotic and
eukaroytic cells. Prokaryotic cells include but are not limited to
bacteria. Eukaryotic cells include but are not limited to yeast
cells and cells derived from plants and animals, for example
mammalian, insect (e.g., spodoptera) and human cells. Cells may be
useful when they are naturally nonadherent or have been treated not
to adhere to surfaces, for example by trypsinization.
[0125] "Control" or "control experiment" is used in accordance with
its plain ordinary meaning and refers to an experiment in which the
subjects or reagents of the experiment are treated as in a parallel
experiment except for omission of a procedure, reagent, or variable
of the experiment. In some instances, the control is used as a
standard of comparison in evaluating experimental effects. In some
embodiments, a control is the measurement of the activity of a
protein in the absence of a compound as described herein (including
embodiments and examples).
[0126] The term "modulator" refers to a composition that increases
or decreases the level of a target molecule or the function of a
target molecule or the physical state of the target of the
molecule. In some embodiments, a CCR4 associated disease modulator
is a compound that reduces the severity of one or more symptoms of
a disease associated with CCR4 (e.g. cancer, inflammatory disease,
autoimmune disease, or infectious disease). A CCR4 modulator is a
compound that increases or decreases the activity or function or
level of activity or level of function of CCR4. A modulator may act
alone, or it may use a cofactor, e.g., a protein, metal ion, or
small molecule. Examples of modulators include small molecule
compounds and other bioorganic molecules. Numerous libraries of
small molecule compounds (e.g., combinatorial libraries) are
commercially available and can serve as a starting point for
identifying a modulator. The skilled artisan is able to develop one
or more assays (e.g., biochemical or cell-based assays) in which
such compound libraries can be screened in order to identify one or
more compounds having the desired properties; thereafter, the
skilled medicinal chemist is able to optimize such one or more
compounds by, for example, synthesizing and evaluating analogs and
derivatives thereof. Synthetic and/or molecular modeling studies
can also be utilized in the identification of an activator
[0127] The term "modulate" is used in accordance with its plain
ordinary meaning and refers to the act of changing or varying one
or more properties. "Modulation" refers to the process of changing
or varying one or more properties. For example, as applied to the
effects of a modulator on a target protein, to modulate means to
change by increasing or decreasing a property or function of the
target molecule or the amount of the target molecule. In
embodiments, the terms "modulate", "modulation" and the like refer
to the ability of a molecule (e.g., an activator or an inhibitor)
to increase or decrease the function or activity of CCR4, either
directly or indirectly, relative to the absence of the
molecule.
[0128] The term "associated" or "associated with" in the context of
a substance or substance activity or function associated with a
disease (e.g. a protein associated disease, a cancer associated
with CCR4 activity, CCR4 associated cancer, CCR4 associated disease
(e.g., cancer, inflammatory disease, autoimmune disease, or
infectious disease)) means that the disease (e.g. cancer,
inflammatory disease, autoimmune disease, or infectious disease) is
caused by (in whole or in part), or a symptom of the disease is
caused by (in whole or in part) the substance or substance activity
or function. For example, a cancer associated with CCR4 activity or
function may be a cancer that results (entirely or partially) from
aberrant CCR4 function (e.g. enzyme activity, protein-protein
interaction, signaling pathway) or a cancer wherein a particular
symptom of the disease is caused (entirely or partially) by
aberrant CCR4 activity or function. As used herein, what is
described as being associated with a disease, if a causative agent,
could be a target for treatment of the disease. For example, a
cancer associated with CCR4 activity or function or a CCR4
associated disease (e.g., cancer, inflammatory disease, autoimmune
disease, or infectious disease), may be treated with a compound
described herein (e.g., CCR4 modulator or CCR4 inhibitor), in the
instance where increased CCR4 activity or function (e.g. signaling
pathway activity) causes the disease (e.g., cancer, inflammatory
disease, autoimmune disease, or infectious disease). For example,
an inflammatory disease associated with CCR4 activity or function
or an CCR4 associated inflammatory disease, may be treated with an
CCR4 modulator or CCR4 inhibitor, in the instance where increased
CCR4 activity or function (e.g. signaling pathway activity) causes
the disease.
[0129] The term "aberrant" as used herein refers to different from
normal. When used to describe enzymatic activity or protein
function, aberrant refers to activity or function that is greater
or less than a normal control or the average of normal non-diseased
control samples. Aberrant activity may refer to an amount of
activity that results in a disease, wherein returning the aberrant
activity to a normal or non-disease-associated amount (e.g. by
administering a compound or using a method as described herein),
results in reduction of the disease or one or more disease
symptoms.
[0130] The term "signaling pathway" as used herein refers to a
series of interactions between cellular and optionally
extra-cellular components (e.g. proteins, nucleic acids, small
molecules, ions, lipids) that conveys a change in one component to
one or more other components, which in turn may convey a change to
additional components, which is optionally propogated to other
signaling pathway components. For example, binding of a CCR4 with a
compound as described herein may reduce the level of a product of
the CCR4 catalyzed reaction or the level of a downstream derivative
of the product or binding may reduce the interactions between the
CCR4 or a reaction product and downstream effectors or signaling
pathway components (e.g., MAP kinase pathway), resulting in changes
in cell growth, proliferation, or survival.
[0131] As used herein, the terms "CCR4 inhibitor", "CCR4
antagonist", "C--C chemokine receptor type 4 inhibitor", "C--C
chemokine receptor type 4 antagonist" and all other related
art-accepted terms, many of which are set forth below, refer to a
compound capable of modulating, either directly or indirectly, the
CCR4 receptor in an in vitro assay, an in vivo model, and/or other
means indicative of therapeutic efficacy. The terms also refer to a
compound that exhibits at least some therapeutic benefit in a human
subject.
[0132] The phrase "in a sufficient amount to effect a change" means
that there is a detectable difference between a level of an
indicator measured before (e.g., a baseline level) and after
administration of a particular therapy. Indicators include any
objective parameter (e.g., serum concentration) or subjective
parameter (e.g., a subject's feeling of well-being).
[0133] The "activity" of a molecule may describe or refer to the
binding of the molecule to a ligand or to a receptor; to catalytic
activity; to the ability to stimulate gene expression or cell
signaling, differentiation, or maturation; to antigenic activity;
to the modulation of activities of other molecules; and the like.
The term "proliferative activity" encompasses an activity that
promotes, that is necessary for, or that is specifically associated
with, for example, normal cell division, as well as cancer, tumors,
dysplasia, cell transformation, metastasis, and angiogenesis.
[0134] "Substantially pure" indicates that a component makes up
greater than about 50% of the total content of the composition, and
typically greater than about 60% of the total polypeptide content.
More typically, "substantially pure" refers to compositions in
which at least 75%, at least 85%, at least 90% or more of the total
composition is the component of interest. In some cases, the
polypeptide will make up greater than about 90%, or greater than
about 95% of the total content of the composition (percentage in a
weight per weight basis).
[0135] The terms "specifically binds" and "selectively binds," when
referring to a ligand/receptor, antibody/antigen, or other binding
pair, indicate a binding reaction which is determinative of the
presence of the protein in a heterogeneous population of proteins
and other biologics. Thus, under designated conditions, a specified
ligand binds to a particular receptor and does not bind in a
significant amount to other proteins present in the sample. The
antibody, or binding composition derived from the antigen-binding
site of an antibody, of the contemplated method binds to its
antigen, or a variant or mutein thereof, with an affinity that is
at least two-fold greater, at least 10-times greater, at least
20-times greater, or at least 100-times greater than the affinity
with any other antibody, or binding composition derived therefrom.
In embodiments, the antibody will have an affinity that is greater
than about 10.sup.9 liters/mol, as determined by, e.g., Scatchard
analysis (Munsen, et al. (1980) Analyt. Biochem. 107:220-239).
[0136] The terms "DNA," "nucleic acid," "nucleic acid molecule,"
"polynucleotide" and the like are used interchangeably herein to
refer to a polymeric form of nucleotides of any length, either
deoxyribonucleotides or ribonucleotides, or analogs thereof.
Non-limiting examples of polynucleotides include linear and
circular nucleic acids, messenger RNA (mRNA), complementary DNA
(cDNA), recombinant polynucleotides, vectors, probes, primers and
the like.
[0137] As used herein, the terms "variants" and "homologs" are used
interchangeably to refer to amino acid or nucleic acid sequences
that are similar to reference amino acid or nucleic acid sequences,
respectively. The term encompasses naturally-occurring variants and
non-naturally-occurring variants. Naturally-occurring variants
include homologs (polypeptides and nucleic acids that differ in
amino acid or nucleotide sequence, respectively, from one species
to another), and allelic variants (polypeptides and nucleic acids
that differ in amino acid or nucleotide sequence, respectively,
from one individual to another within a species). Thus, variants
and homologs encompass naturally occurring amino acid and nucleic
acid sequences encoded thereby and their isoforms, as well as
splice variants of a protein or gene. The terms also encompass
nucleic acid sequences that vary in one or more bases from a
naturally-occurring nucleic acid sequence but still translate into
an amino acid sequence that corresponds to the naturally-occurring
protein due to degeneracy of the genetic code.
Non-naturally-occurring variants and homologs include polypeptides
and nucleic acids that comprise a change in amino acid or
nucleotide sequence, respectively, where the change in sequence is
artificially introduced (e.g., muteins); for example, the change is
generated in the laboratory by human intervention ("hand of man").
Therefore, non-naturally occurring variants and homologs may also
refer to those that differ from the naturally occurring sequences
by one or more conservative substitutions and/or tags and/or
conjugates.
[0138] The term "muteins" as used herein refers broadly to mutated
recombinant proteins. These proteins usually carry single or
multiple amino acid substitutions and are frequently derived from
cloned genes that have been subjected to site-directed or random
mutagenesis, or from completely synthetic genes.
II. Compounds
[0139] In an aspect provided herein, is a compound having
structural Formula (I):
##STR00003##
or a pharmaceutically acceptable salt thereof. X.sup.1 is CR.sup.8
or N. X.sup.2 is CR.sup.9 or N. X.sup.3 is CR.sup.1 or N. The
symbols n1, n2, n3, n4, n5, n6, n7, n8, n9 and n10 are
independently an integer from 0 to 4. The symbols m1, m2, m3, m4,
m5, m6, m7, m8, m9, m10, v1, v2, v3, v4, v5, v6, v7, v8, v9 and v10
are independently 1 or 2. The symbol z1 is an integer from 0 to 5.
The symbol z2 is an integer from 0 to 5. In embodiments, z2 is an
integer from 0 to 2. The symbol z3 is an integer from 0 to 11. In
embodiments, the symbol z3 is an integer from 0 to 4. The symbol z4
is an integer from 0 to 2. L.sup.7 is a bond, --O--, --S--,
--NR.sup.7.2B--, --C(O)--, --C(O)O--, --S(O)--, --S(O).sub.2--,
substituted or unsubstituted alkylene, substituted or unsubstituted
heteroalkylene, substituted or unsubstituted cycloalkylene,
substituted or unsubstituted heterocycloalkylene, substituted or
unsubstituted arylene, or substituted or unsubstituted
heteroarylene. R.sup.1 is hydrogen, halogen, --CX.sup.1.1.sub.3,
--CHX.sup.1.1.sub.2, --CH.sub.2X.sup.1.1, --CN, --N.sub.3,
--SO.sub.n1R.sup.1A, --SO.sub.v1NR.sup.1BR.sup.1C,
--NHNR.sup.1BR.sup.1C, --ONR.sup.1BR.sup.1C,
--NHC(O)NHNR.sup.1BR.sup.1C, --NHC(O)NR.sup.1BR.sup.1C,
--N(O).sub.m1, --NR.sup.1BR.sup.1C, --C(O)R.sup.1D,
--C(O)OR.sup.1D, --C(O)NR.sup.1BR.sup.1C, --OR.sup.1A,
--NR.sup.1BSO.sub.2R.sup.1A--NR.sup.1BC(O)R.sup.1D,
--NR.sup.1BC(O)OR.sup.1D, --NR.sup.1BOR.sup.1D,
--OCX.sup.1.1.sub.3, --OCHX.sup.1.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. R.sup.2 is hydrogen,
halogen, --CX.sup.2.1.sub.3, --CHX.sup.2.1.sub.2,
--CH.sub.2X.sup.2.1, --CN, --N.sub.3, --SO.sub.n2R.sup.2A,
--SO.sub.v2NR.sup.2BR.sup.2C, --NHNR.sup.2BR.sup.2C,
--ONR.sup.2BR.sup.2C, --NHC(O)NHNR.sup.2BR.sup.2C,
--NHC(O)NR.sup.2BR.sup.2C, --N(O).sub.m2, --NR.sup.2BR.sup.2C,
--C(O)R.sup.2D, --C(O)OR.sup.2D, --C(O)NR.sup.2BR.sup.2C,
--OR.sup.2A, --NR.sup.2BSO.sub.2R.sup.2A--NR.sup.2BC(O)R.sup.2D,
--NR.sup.2BC(O)OR.sup.2D, --NR.sup.2BOR.sup.2D,
--OCX.sup.2.1.sub.3, --OCHX.sup.2.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. R.sup.3 is
independently hydrogen, halogen, --CX.sup.3.1.sub.3,
--CHX.sup.3.1.sub.2, --CH.sub.2X.sup.3.1, --CN, --N.sub.3,
--SO.sub.n3R.sup.3A, --SO.sub.v3NR.sup.3BR.sup.3C,
--NHNR.sup.3BR.sup.3C, --ONR.sup.3BR.sup.3C,
--NHC(O)NHNR.sup.3BR.sup.3C, --NHC(O)NR.sup.3BR.sup.3C,
--N(O).sub.m3, --NR.sup.3BR.sup.3C, --C(O)R.sup.3D,
--C(O)OR.sup.3D, --C(O)NR.sup.3BR.sup.3C, --OR.sup.3A,
--NR.sup.3BSO.sub.2R.sup.3A, --NR.sup.3BC(O)R.sup.3D,
--NR.sup.3BC(O)OR.sup.3D, --NR.sup.3BOR.sup.3D,
--OCX.sup.3.1.sub.3, --OCHX.sup.3.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. R.sup.4 is hydrogen,
halogen, --CX.sup.4.1.sub.3, --CHX.sup.4.1.sub.2,
--CH.sub.2X.sup.4.1, --CN, --N.sub.3, --SO.sub.n4R.sup.4A,
--SO.sub.v4NR.sup.4BR.sup.4C, --NHNR.sup.4BR.sup.4C,
--ONR.sup.4BR.sup.4C, --NHC(O)NHNR.sup.4BR.sup.4C,
--NHC(O)NR.sup.4BR.sup.4C, --N(O).sub.m4, --NR.sup.4BR.sup.4C,
--C(O)R.sup.4D, --C(O)OR.sup.4D, --C(O)NR.sup.4BR.sup.4C,
--OR.sup.4A, --NR.sup.4BSO.sub.2R.sup.4A, --NR.sup.4BC(O)R.sup.4D,
--NR.sup.4BC(O)OR.sup.4D, --NR.sup.4BOR.sup.4D,
--OCX.sup.4.1.sub.3, --OCHX.sup.4.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. R.sup.5 is
independently hydrogen, halogen, oxo, --CX.sup.5.1.sub.3,
--CHX.sup.5.1.sub.2, --CH.sub.2X.sup.5.1, --CN, --N.sub.3,
--SO.sub.n5R.sup.5A, --SO.sub.v5NR.sup.5BR.sup.5C,
--NHNR.sup.5BR.sup.5C, --ONR.sup.5BR.sup.5C,
--NHC(O)NHNR.sup.5BR.sup.5C, --NHC(O)NR.sup.5BR.sup.5C,
--N(O).sub.m5, --NR.sup.5BR.sup.5C, --C(O)R.sup.5D,
--C(O)OR.sup.5D, --C(O)NR.sup.5BR.sup.5C, --OR.sup.5A,
--NR.sup.5BSO.sub.2R.sup.5A, --NR.sup.5BC(O)R.sup.5D,
--NR.sup.5BC(O)OR.sup.5D, --NR.sup.5BOR.sup.5D,
--OCX.sup.5.1.sub.3, --OCHX.sup.5.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. R.sup.6 is
independently hydrogen, halogen, oxo, --CX.sup.6.1.sub.3,
--CHX.sup.6.1.sub.2, --CH.sub.2X.sup.6.1, --CN, --N.sub.3,
--SO.sub.n6R.sup.6A, --SO.sub.v6NR.sup.6BR.sup.6C,
--NHNR.sup.6BR.sup.6C, --ONR.sup.6BR.sup.6C,
--NHC(O)NHNR.sup.6BR.sup.6C, --NHC(O)NR.sup.6BR.sup.6C,
--N(O).sub.m6, --NR.sup.6BR.sup.6C, --C(O)R.sup.6D,
--C(O)OR.sup.6D, --C(O)NR.sup.6BR.sup.6C, --OR.sup.6A,
--NR.sup.6BSO.sub.2R.sup.6A, --NR.sup.6BC(O)R.sup.6D,
--NR.sup.6BC(O)OR.sup.6D, --NR.sup.6BOR.sup.6D,
--OCX.sup.6.1.sub.3, --OCHX.sup.6.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. R.sup.7 is hydrogen,
halogen, --CX.sup.7.1.sub.3, --CHX.sup.7.1.sub.2,
--CH.sub.2X.sup.7.1, --CN, --N.sub.3, --SO.sub.n7R.sup.7A,
--SO.sub.v7NR.sup.7BR.sup.7C, --NHNR.sup.7BR.sup.7C,
--ONR.sup.7BR.sup.7C, --NHC(O)NHNR.sup.7BR.sup.7C,
--NHC(O)NR.sup.7BR.sup.7C, --N(O).sub.m7, --NR.sup.7BR.sup.7C,
--C(O)R.sup.7D, --C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C,
--OR.sup.7A, --NR.sup.7BSO.sub.2R.sup.7A, --NR.sup.7BC(O)R.sup.7D,
--NR.sup.7BC(O)OR.sup.7D, --NR.sup.7BOR.sup.7D,
--OCX.sup.7.1.sub.3, --OCHX.sup.7.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. R.sup.8 is hydrogen,
halogen, --CX.sup.8.1.sub.3, --CHX.sup.8.1.sub.2,
--CH.sub.2X.sup.8.1, --CN, --N.sub.3, --SO.sub.n8R.sup.8A,
--SO.sub.v8NR.sup.8BR.sup.8C, --NHNR.sup.8BR.sup.8C,
--ONR.sup.8BR.sup.8C, --NHC(O)NHNR.sup.8BR.sup.8C,
--NHC(O)NR.sup.8BR.sup.8C, --N(O).sub.m8, --NR.sup.8BR.sup.8C,
--C(O)R.sup.8D, --C(O)OR.sup.8D, --C(O)NR.sup.8BR.sup.8C,
--OR.sup.8A, --NR.sup.8BSO.sub.2R.sup.8A, --NR.sup.8BC(O)R.sup.8D,
--NR.sup.8BC(O)OR.sup.8D, --NR.sup.8BOR.sup.8D,
--OCX.sup.8.1.sub.3, --OCHX.sup.8.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. R.sup.9 is hydrogen,
halogen, --CX.sup.9.1.sub.3, --CHX.sup.9.1.sub.2,
--CH.sub.2X.sup.9.1, --CN, --N.sub.3, --SO.sub.n9R.sup.9A,
--SO.sub.v9NR.sup.9BR.sup.9C, --NHNR.sup.9BR.sup.9C,
--ONR.sup.9BR.sup.9C, --NHC(O)NHNR.sup.9BR.sup.9C,
--NHC(O)NR.sup.9BR.sup.9C, --N(O).sub.m9, --NR.sup.9BR.sup.9C,
--C(O)R.sup.9D, --C(O)OR.sup.9D, --C(O)NR.sup.9BR.sup.9C,
--OR.sup.9A, --NR.sup.9BSO.sub.2R.sup.9A, --NR.sup.9BC(O)R.sup.9D,
--NR.sup.9BC(O)OR.sup.9D, --NR.sup.9BOR.sup.9D,
--OCX.sup.9.1.sub.3, --OCHX.sup.9.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. R.sup.10 is hydrogen,
halogen, --CX.sup.10.1.sub.3, --CHX.sup.10.1.sub.2,
--CH.sub.2X.sup.10.1, --CN, --N.sub.3, --SO.sub.n10R.sup.10A,
--SO.sub.v10NR.sup.10BR.sup.10C, --NHNR.sup.10BR.sup.10C,
--ONR.sup.10BR.sup.10C, --NHC(O)NHNR.sup.10BR.sup.10C,
--NHC(O)NR.sup.10BR.sup.10C, --N(O).sub.m10, --NR.sup.10BR.sup.10C,
--C(O)R.sup.10D, --C(O)OR.sup.10D, --C(O)NR.sup.10BR.sup.10C,
--OR.sup.10A, --NR.sup.10BSO.sub.2R.sup.10A,
--NR.sup.10BC(O)R.sup.10D, --NR.sup.10BC(O)OR.sup.10D,
--NR.sup.10BOR.sup.10D, --OCX.sup.10.1.sub.3,
--OCHX.sup.10.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl. R.sup.1A, R.sup.1B, R.sup.1C,
R.sup.1D, R.sup.2A, R.sup.2B, R.sup.2C, R.sup.2D, R.sup.3A,
R.sup.3B, R.sup.3C, R.sup.3D, R.sup.4A, R.sup.4B, R.sup.4C,
R.sup.4D, R.sup.5A, R.sup.5B, R.sup.5C, R.sup.5D, R.sup.6A,
R.sup.6B, R.sup.6C, R.sup.6D, R.sup.7A, R.sup.7B, R.sup.7C,
R.sup.7D, R.sup.7.2B, R.sup.8A, R.sup.8B, R.sup.8C, R.sup.8D,
R.sup.9A, R.sup.9B, R.sup.9C, R.sup.9D, R.sup.10A, R.sup.10B,
R.sup.10C and R.sup.10D are independently hydrogen, halogen,
--CF.sub.3, --CCl.sub.3, --CBr.sub.3, --Cl.sub.3, --COOH,
--CONH.sub.2, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, or substituted or unsubstituted heteroaryl;
R.sup.1B, R.sup.1C, R.sup.2B, R.sup.2C, R.sup.3B, R.sup.3C,
R.sup.4B, R.sup.4C, R.sup.5B, R.sup.5C, R.sup.6B, R.sup.6C,
R.sup.7B, R.sup.7C, R.sup.8B, R.sup.8C, R.sup.9B, R.sup.9C,
R.sup.10B and R.sup.10C substituents bonded to the same nitrogen
atom may optionally be joined to form a substituted or
unsubstituted heterocycloalkyl or substituted or unsubstituted
heteroaryl. X.sup.1.1, X.sup.2.1, X.sup.3.1, X.sup.4.1, X.sup.5.1,
X.sup.6.1, X.sup.7.1, X.sup.8.1, X.sup.9.1 and X.sup.10.1 are
independently --Cl, --Br, --I or --F, wherein at least one of
X.sup.1, X.sup.2 and X.sup.3 is N.
[0140] In embodiments, X.sup.1 is CR.sup.8. In embodiments, X.sup.2
is CR.sup.9. In embodiments, X.sup.3 is CR.sup.10. In embodiments,
X.sup.1 is N. In embodiments, X.sup.2 is N. In embodiments, X.sup.3
is N.
[0141] In embodiments, R.sup.1 is halogen, --CX.sup.1.1.sub.3,
--CHX.sup.1.1.sub.2, --CH.sub.2X.sup.1.1, --CN, --N.sub.3,
--SO.sub.n1R.sup.1A, --SO.sub.v1NR.sup.1BR.sup.1C,
--NHNR.sup.1BR.sup.1C, --ONR.sup.1BR.sup.1C,
--NHC(O)N.sup.1BNR.sup.1BR.sup.1C, --NHC(O)NR.sup.1BR.sup.1C,
--N(O).sub.m1, --NR.sup.1BR.sup.1C, --C(O)R.sup.1D,
--C(O)OR.sup.1D, --C(O)NR.sup.1BR.sup.1C, --OR.sup.1A,
--NR.sup.1BSO.sub.2R.sup.1A, --NR.sup.1BC(O)R.sup.1D,
--NR.sup.1BC(O)OR.sup.1D, --NR.sup.1BOR.sup.1D,
--OCX.sup.1.1.sub.3, --OCHX.sup.1.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. In embodiments, R.sup.1
is hydrogen.
[0142] In embodiments, R.sup.1 is hydrogen, halogen,
--CX.sup.1.1.sub.3, --CHX.sup.1.1.sub.2, --CH.sub.2X.sup.1.1, --CN,
--N.sub.3, --SO.sub.n1R.sup.1A, --SO.sub.v1NR.sup.1BR.sup.1C,
--NHNR.sup.1BR.sup.1C--ONR.sup.1BR.sup.1C,
--NHC(O)NHNR.sup.1BR.sup.1C, --NHC(O)NR.sup.1BR.sup.1C,
--N(O).sub.m1, --NR.sup.1BR.sup.1C, --C(O)R.sup.1D,
--C(O)OR.sup.1D, --C(O)NR.sup.1BR.sup.1C, --OR.sup.1A,
--NR.sup.1BSO.sub.2R.sup.1A, --NR.sup.1BC(O)R.sup.1D,
--NR.sup.1BC(O)OR.sup.1D, --NR.sup.1BOR.sup.1D,
--OCX.sup.1.1.sub.3, --OCHX.sup.1.1.sub.2, R.sup.11-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl), R.sup.11-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl),
R.sup.11-substituted or unsubstituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl), R.sup.11-substituted or unsubstituted
heterocycloalkyl (e.g., 3 to 8 membered heterocycloalkyl, 3 to 6
membered heterocycloalkyl, or 5 to 6 membered heterocycloalkyl),
R.sup.11-substituted or unsubstituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl), or R.sup.11-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0143] In embodiments, R.sup.1 is R.sup.11-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.1 is
R.sup.11-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.1 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0144] In embodiments, R.sup.1 is R.sup.11-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.1 is R.sup.11-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.1 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0145] In embodiments, R.sup.1 is R.sup.11-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.1 is R.sup.11-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.1 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0146] In embodiments, R.sup.1 is R.sup.11-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.1 is
R.sup.11-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.1 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0147] In embodiments, R.sup.1 is R.sup.11-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.1 is R.sup.11-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.1 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0148] In embodiments, R.sup.1 is R.sup.11-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.1 is R.sup.11-substituted heteroaryl (e.g., 5 to
10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.1 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0149] In embodiments, R.sup.2 is halogen, --CX.sup.2.1.sub.3,
--CHX.sup.2.1.sub.2, --CH.sub.2X.sup.2.1, --CN, --N.sub.3,
--SO.sub.n2R.sup.2A, --SO.sub.v2NR.sup.2BR.sup.2C,
--NHNR.sup.2BR.sup.2C, --ONR.sup.2BR.sup.2C,
--NHC(O)NHNR.sup.2BR.sup.2C, --NHC(O)NR.sup.2BR.sup.2C,
--N(O).sub.m2, --NR.sup.2BR.sup.2C, --C(O)R.sup.2D,
--C(O)OR.sup.2D, --C(O)NR.sup.2BR.sup.2C, --OR.sup.2A,
--NR.sup.2BSO.sub.2R.sup.2A--NR.sup.2BC(O)R.sup.2D,
--NR.sup.2BC(O)OR.sup.2D, --NR.sup.2BOR.sup.2D, --OCX.sup.2B,
--OCHX.sup.2.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl. In embodiments, R.sup.2 is
hydrogen.
[0150] In embodiments, R.sup.2 is halogen, --CX.sup.2.1.sub.3,
--CHX.sup.2.1.sub.2, --CH.sub.2X.sup.2.1, --CN, --N.sub.3,
--SO.sub.n2R.sup.2A, --SO.sub.v2NR.sup.2BR.sup.2C,
--NHNR.sup.2BR.sup.2C, --ONR.sup.2BR.sup.2C,
--NHC(O)NHNR.sup.2BR.sup.2C, --NHC(O)NR.sup.2BR.sup.2C,
--N(O).sub.m2, --NR.sup.2BR.sup.2C, --C(O)R.sup.2D,
--C(O)OR.sup.2D, --C(O)NR.sup.2BR.sup.2C, --OR.sup.2A,
--NR.sup.2BSO.sub.2R.sup.2A, --NR.sup.2BC(O)R.sup.2D,
--NR.sup.2BC(O)OR.sup.2D, --NR.sup.2BOR.sup.2D,
--OCX.sup.2.1.sub.3, --OCHX.sup.2.1.sub.2, R.sup.14-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl), R.sup.14-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl),
R.sup.14-substituted or unsubstituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl), R.sup.14-substituted or unsubstituted
heterocycloalkyl (e.g., 3 to 8 membered heterocycloalkyl, 3 to 6
membered heterocycloalkyl, or 5 to 6 membered heterocycloalkyl),
R.sup.14-substituted or unsubstituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl), or R.sup.14-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0151] In embodiments, R.sup.2 is R.sup.14-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.2 is
R.sup.14-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.2 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.2 is an unsubstituted ethyl. In embodiments, R.sup.2 is an
unsubstituted C.sub.3 alkyl. In embodiments, R.sup.2 is an
unsubstituted C.sub.4 alkyl.
[0152] In embodiments, R.sup.2 is R.sup.14-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.2 is R.sup.14-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.2 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0153] In embodiments, R.sup.2 is R.sup.14-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.2 is R.sup.14-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.2 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0154] In embodiments, R.sup.2 is R.sup.14-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.2 is
R.sup.14-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.2 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0155] In embodiments, R.sup.2 is R.sup.14-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.2 is R.sup.14-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.2 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0156] In embodiments, R.sup.2 is R.sup.14-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.2 is R.sup.14-substituted heteroaryl (e.g., 5 to
10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.2 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0157] In embodiments, R.sup.3 is independently halogen,
--CX.sup.3.1.sub.3, --CHX.sup.3.1.sub.2, --CH.sub.2X.sup.3.1, --CN,
--N.sub.3, --SO.sub.n3R.sup.3A, --SO.sub.v3NR.sup.3BR.sup.3,
--NHNR.sup.3BR.sup.3C, --ONR.sup.3BR.sup.3C,
--NHC(O)NHNR.sup.3BR.sup.3C, --NHC(O)NR.sup.3BR.sup.3,
--N(O).sub.m3, --NR.sup.3BR.sup.3C, --C(O)R.sup.3D,
--C(O)OR.sup.3D, --C(O)NR.sup.3BR.sup.3C, --OR.sup.3A,
--NR.sup.3BSO.sub.2R.sup.3A, --NR.sup.3BC(O)R.sup.3D,
--NR.sup.3BC(O)OR.sup.3D, --NR.sup.3BOR.sup.3D,
--OCX.sup.3.1.sub.3, --OCHX.sup.3.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. In embodiments, R.sup.3
is hydrogen.
[0158] In embodiments, R.sup.3 is independently halogen,
--CX.sup.3.1.sub.3, --CHX.sup.3.1.sub.2, --CH.sub.2X.sup.3.1, --CN,
--N.sub.3, --SO.sub.n3R.sup.3A, --SO.sub.v3NR.sup.3BR.sup.3,
--NHNR.sup.3BR.sup.3C, --ONR.sup.3BR.sup.3C,
--NHC(O)NHNR.sup.3BR.sup.3C, --NHC(O)NR.sup.3BR.sup.3C,
--N(O).sub.m3, --NR.sup.3BR.sup.3C, --C(O)R.sup.3D,
--C(O)OR.sup.3D, --C(O)NR.sup.3BR.sup.3C, --OR.sup.3A,
--NR.sup.3BSO.sub.2R.sup.3A, --NR.sup.3BC(O)R.sup.3D,
--NR.sup.3BC(O)OR.sup.3D, --NR.sup.3BOR.sup.3D,
--OCX.sup.3.1.sub.3, --OCHX.sup.3.1.sub.2, R.sup.17-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl), R.sup.17-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl),
R.sup.17-substituted or unsubstituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl), R.sup.17-substituted or unsubstituted
heterocycloalkyl (e.g., 3 to 8 membered heterocycloalkyl, 3 to 6
membered heterocycloalkyl, or 5 to 6 membered heterocycloalkyl),
R.sup.17-substituted or unsubstituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl), or R.sup.17-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0159] In embodiments, R.sup.3 is independently
R.sup.17-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In
embodiments, R.sup.3 is independently R.sup.17-substituted alkyl
(e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.3 is independently an
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl).
[0160] In embodiments, R.sup.3 is independently
R.sup.17-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.3 is independently
R.sup.17-substituted heteroalkyl (e.g., 2 to 8 membered
heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4 membered
heteroalkyl). In embodiments, R.sup.3 is independently an
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl).
[0161] In embodiments, R.sup.3 is independently
R.sup.17-substituted or unsubstituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.3 is
independently R.sup.17-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.3 is
independently an unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8
cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6
cycloalkyl).
[0162] In embodiments, R.sup.3 is independently
R.sup.17-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl). In embodiments, R.sup.3 is
independently R.sup.17-substituted heterocycloalkyl (e.g., 3 to 8
membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl). In embodiments, R.sup.3 is
independently an unsubstituted heterocycloalkyl (e.g., 3 to 8
membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl).
[0163] In embodiments, R.sup.3 is independently
R.sup.17-substituted or unsubstituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl). In embodiments, R.sup.3 is
independently R.sup.17-substituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl). In embodiments, R.sup.3 is
independently an unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl,
C.sub.10 aryl, or phenyl).
[0164] In embodiments, R.sup.3 is independently
R.sup.17-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.3 is independently
R.sup.17-substituted heteroaryl (e.g., 5 to 10 membered heteroaryl,
5 to 9 membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.3 is independently an unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0165] In embodiments, the definition of R.sup.3 is assumed by
(independently assigned to) R.sup.3.1, R.sup.3.2, R.sup.3.3,
R.sup.3.4, R.sup.3.5.
[0166] In embodiments, R.sup.3.2 is halogen, --CX.sup.3.2.sub.3,
--CHX.sup.3.2.sub.2, --CH.sub.2X.sup.3.2, --CN, --N.sub.3,
--SO.sub.n3.2R.sup.3.2A, --SO.sub.v3.2NR.sup.3.2BR.sup.3.2C,
--NHNR.sup.3.2BR.sup.3.2C, --ONR.sup.3.2BR.sup.3.2C,
--NHC(O)NHNR.sup.3.2BR.sup.3.2C, --NHC(O)NR.sup.3.2BR.sup.3.2C,
--N(O).sub.m3.2, --NR.sup.3.2BR.sup.3.2C, --C(O)R.sup.3.2D,
--C(O)OR.sup.3.2D, --C(O)NR.sup.3.2BR.sup.3.2C, --OR.sup.3.2A,
--NR.sup.3.2BSO.sub.2R.sup.3.2A, --NR.sup.3.2BC(O)R.sup.3.2D,
--NR.sup.3.2BC(O)OR.sup.3.2D, --NR.sup.3.2BOR.sup.3.2D,
--OCX.sup.3.2.sub.3, --OCHX.sup.3.2.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. X.sup.3.2 is halogen.
In embodiments, R.sup.3.2 is hydrogen. In embodiments, R.sup.3.2 is
halogen. In embodiments, R.sup.3.2 is chlorine.
[0167] In embodiments, R.sup.3.2 is hydrogen, halogen,
--CX.sup.3.2.sub.3, --CHX.sup.3.2.sub.2, --CH.sub.2X.sup.3.2, --CN,
--N.sub.3, --SO.sub.n3.2R.sup.3.2A,
--SO.sub.v3.2NR.sup.3.2BR.sup.3.2C, --NHNR.sup.3.2BNR.sup.3.2C,
--ONR.sup.3.2BR.sup.3.2C, --NHC(O)NHNR.sup.3.2BR.sup.3.2C,
--NHC(O)NR.sup.3.2BR.sup.3.2C, --N(O).sub.m3.2,
--NR.sup.3.2BR.sup.3.2C, --C(O)R.sup.3.2D, --C(O)OR.sup.3.2D,
--C(O)NR.sup.3.2BR.sup.3.2C, --OR.sup.3.2A,
--NR.sup.3.2BSO.sub.2R.sup.3.2A, --NR.sup.3.2BC(O)R.sup.3.2D,
--NR.sup.3.2BC(O)OR.sup.3.2D, --NR.sup.3.2BOR.sup.3.2D,
--OCX.sup.3.2.sub.3, --OCHX.sup.3.2.sub.2, R.sup.17.2-substituted
or unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.17.2-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17.2-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17.2-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17.2-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.17.2-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0168] In embodiments, R.sup.3.2 is R.sup.17.2-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.3.2 is
R.sup.17.2-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.3.2 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0169] In embodiments, R.sup.3.2 is R.sup.17.2-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.3.2 is R.sup.17.2-substituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.3.2 is an
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl).
[0170] In embodiments, R.sup.3.2 is R.sup.17.2-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.3.2 is R.sup.17.2-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.3.2 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0171] In embodiments, R.sup.3.2 is R.sup.17.2-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.3.2 is
R.sup.17.2-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.3.2 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0172] In embodiments, R.sup.3.2 is R.sup.17.2-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.3.2 is R.sup.17.2-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.3.2 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0173] In embodiments, R.sup.3.2 is R.sup.17.2-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.3.2 is R.sup.17.2-substituted heteroaryl (e.g.,
5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.3.2 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0174] In embodiments, R.sup.3.3 is, halogen, --CX.sup.3.3.sub.3,
--CHX.sup.3.3.sub.2, --CH.sub.2X.sup.3.3, --CN, --N.sub.3,
--SO.sub.n3.3R.sup.3.3A, SO.sub.v3.3NR.sup.3.3BR.sup.3.3C,
--NHNR.sup.3.3BR.sup.3.3C, --ONR.sup.3.3BR.sup.3.3C,
--NHC(O)NHNR.sup.3.3BR.sup.3.3C, --NHC(O)NR.sup.3.3BR.sup.3.3C,
--N(O).sub.m3.3, --NR.sup.3.3BR.sup.3.3C, --C(O)R.sup.3.3D,
--C(O)OR.sup.3.3D, --C(O)NR.sup.3.3BR.sup.3.3C, --OR.sup.3.3A,
--NR.sup.3.3BSO.sub.2R.sup.3.3A, --NR.sup.3.3BC(O)R.sup.3.3D,
--NR.sup.3.3BC(O)OR.sup.3.3D, --NR.sup.3.3BOR.sup.3.3D,
--OCX.sup.3.3.sub.3, --OCHX.sup.3.3.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. X.sup.3.3 is halogen.
In embodiments, R.sup.3.3 is hydrogen. In embodiments, R.sup.3.3 is
halogen. In embodiments, R.sup.3.3 is chlorine.
[0175] In embodiments, R.sup.3.3 is hydrogen, halogen,
--CX.sup.3.3.sub.3, --CHX.sup.3.3.sub.2, --CH.sub.2X.sup.3.3, --CN,
--N.sub.3, --SO.sub.n3.3R.sup.3.3A,
--SO.sub.v3.3NR.sup.3.3BR.sup.3.3C, --NHNR.sup.3.3BR.sup.3.3C,
--ONR.sup.3.3BR.sup.3.3C, --NHC(O)NHNR.sup.3.3BR.sup.3.3C,
--NHC(O)NR.sup.3.3BR.sup.3.3C, --N(O).sub.m3.3,
--NR.sup.3.3BR.sup.3.3C, --C(O)R.sup.3.3D, --C(O)OR.sup.3.3D,
--C(O)NR.sup.3.3BR.sup.3.3C, OR.sup.3.3A,
--NR.sup.3.3BSO.sub.2R.sup.3.3A, --NR.sup.3.3BC(O)R.sup.3.3D,
--NR.sup.3.3BC(O)OR.sup.3.3D, --NR.sup.3.3BOR.sup.3.3D,
--OCX.sup.3.3.sub.3, --OCHX.sup.3.3.sub.2, R.sup.17.3-substituted
or unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.17.3-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17.3-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17.3-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17.3-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.17.3-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0176] In embodiments, R.sup.3.3 is R.sup.17.3-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.3.3 is
R.sup.17.3-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.3.3 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0177] In embodiments, R.sup.3.3 is R.sup.17.3-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.3.3 is R.sup.17.3-substituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.3.3 is an
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl).
[0178] In embodiments, R.sup.3.3 is R.sup.17.3-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.3.3 is R.sup.17.3-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.3.3 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0179] In embodiments, R.sup.3.3 is R.sup.17.3-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.3.3 is
R.sup.17.3-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.3.3 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0180] In embodiments, R.sup.3.3 is R.sup.17.3-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.3.3 is R.sup.17.3-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.3.3 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0181] In embodiments, R.sup.3.3 is R.sup.17.3-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.3.3 is R.sup.17.3-substituted heteroaryl (e.g.,
5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.3.3 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0182] In embodiments, R.sup.4 is halogen, --CX.sup.4.1.sub.3,
--CHX.sup.4.1.sub.2, --CH.sub.2X.sup.4.1, --CN, --N.sub.3,
--SO.sub.n4R.sup.4A, --SO.sub.v4NR.sup.4BR.sup.4C,
--NHNR.sup.4BR.sup.4C, --ONR.sup.4BR.sup.4C,
--NHC(O)NHNR.sup.4BR.sup.4C, --NHC(O)NR.sup.4BR.sup.4C,
--N(O).sub.m4, --NR.sup.4BR.sup.4C, --C(O)R.sup.4D,
--C(O)OR.sup.4D, --C(O)NR.sup.4BR.sup.4C, --OR.sup.4A,
--NR.sup.4BSO.sub.2R.sup.4A, --NR.sup.4BC(O)R.sup.4D,
--NR.sup.4BC(O)OR.sup.4D, --NR.sup.4BOR.sup.4D,
--OCX.sup.4.1.sub.3, --OCHX.sup.4.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. In embodiments, R.sup.4
is hydrogen.
[0183] In embodiments, R.sup.4 is halogen, --CX.sup.4.1.sub.3,
--CHX.sup.4.1.sub.2, --CH.sub.2X.sup.4.1, --CN, --N.sub.3,
--SO.sub.n4R.sup.4A, --SO.sub.v4NR.sup.4BR.sup.4C,
--NHNR.sup.4BR.sup.4C, --ONR.sup.4BR.sup.4C,
--NHC(O)NHNR.sup.4BR.sup.4C, --NHC(O)NR.sup.4BR.sup.4C,
--N(O).sub.m4, --NR.sup.4BR.sup.4C, --C(O)R.sup.4D,
--C(O)OR.sup.4D, --C(O)NR.sup.4BR.sup.4C, --OR.sup.4A,
--NR.sup.4BSO.sub.2R.sup.4A, --NR.sup.4BC(O)R.sup.4D,
--NR.sup.4BC(O)OR.sup.4D, --NR.sup.4BOR.sup.4D,
--OCX.sup.4.1.sub.3, --OCHX.sup.4.1.sub.2, R.sup.20-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl), R.sup.20-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl),
R.sup.20-substituted or unsubstituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl), R.sup.20-substituted or unsubstituted
heterocycloalkyl (e.g., 3 to 8 membered heterocycloalkyl, 3 to 6
membered heterocycloalkyl, or 5 to 6 membered heterocycloalkyl),
R.sup.20-substituted or unsubstituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl), or R.sup.20-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.4 is --CN. In embodiments, R.sup.4 is
--C(O)NH.sub.2. In embodiments, R.sup.4 is --CF.sub.3. In
embodiments, R.sup.4 is --CH.sub.3.
[0184] In embodiments, R.sup.4 is R.sup.20-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.4 is
R.sup.20-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.4 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0185] In embodiments, R.sup.4 is an unsubstituted ethyl. In
embodiments, R.sup.4 is an unsubstituted C.sub.3 alkyl. In
embodiments, R.sup.4 is an unsubstituted C.sub.4 alkyl.
[0186] In embodiments, R.sup.4 is R.sup.20-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.4 is R.sup.20-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.4 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0187] In embodiments, R.sup.4 is R.sup.20-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.4 is R.sup.20-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.4 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0188] In embodiments, R.sup.4 is R.sup.20-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.4 is
R.sup.20-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.4 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0189] In embodiments, R.sup.4 is R.sup.20-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.4 is R.sup.20-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.4 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0190] In embodiments, R.sup.4 is R.sup.20-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.4 is R.sup.20-substituted heteroaryl (e.g., 5 to
10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.4 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0191] In embodiments, R.sup.5 is independently halogen, oxo,
--CX.sup.5.1.sub.3, --CHX.sup.5.1.sub.2, --CH.sub.2X.sup.5.1, --CN,
--N.sub.3, --SO.sub.n5R.sup.5A, --SO.sub.v5NR.sup.5BR.sup.5C,
--NHNR.sup.5BR.sup.5C, --ONR.sup.5BR.sup.5C,
--NHC(O)NHNR.sup.5BR.sup.5C, --NHC(O)NR.sup.5BR.sup.5C,
--N(O).sub.m5, --NR.sup.5BR.sup.5C, --C(O)R.sup.5D,
--C(O)OR.sup.5D, --C(O)NR.sup.5BR.sup.5C, --OR.sup.5A,
--NR.sup.5BSO.sub.2R.sup.5A, --NR.sup.5BC(O)R.sup.5D,
--NR.sup.5BC(O)OR.sup.5D, --NR.sup.5BOR.sup.5D,
--OCX.sup.5.1.sub.3, --OCHX.sup.5.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. In embodiments, R.sup.5
is hydrogen.
[0192] In embodiments, R.sup.5 is independently halogen,
--CX.sup.5.1.sub.3, --CHX.sup.5.1.sub.2, --CH.sub.2X.sup.5.1, --CN,
--N.sub.3, --SO.sub.n5R.sup.5A, --SO.sub.v5NR.sup.5BR.sup.5C,
--NHNR.sup.5BR.sup.5C, --ONR.sup.5BR.sup.5C,
--NHC(O)NHNR.sup.5BR.sup.5C, --NHC(O)NR.sup.5BR.sup.5C,
--N(O).sub.m5, --NR.sup.5BR.sup.5C, --C(O)R.sup.5D,
--C(O)OR.sup.5D, --C(O)NR.sup.5BR.sup.5C, --OR.sup.5A,
--NR.sup.5BSO.sub.2R.sup.5A, --NR.sup.5BC(O)R.sup.5D,
--NR.sup.5BC(O)OR.sup.5D, --NR.sup.5BOR.sup.5D,
--OCX.sup.5.1.sub.3, --OCHX.sup.5.1.sub.2, R.sup.23-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl), R.sup.23-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl),
R.sup.23-substituted or unsubstituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl), R.sup.23-substituted or unsubstituted
heterocycloalkyl (e.g., 3 to 8 membered heterocycloalkyl, 3 to 6
membered heterocycloalkyl, or 5 to 6 membered heterocycloalkyl),
R.sup.23-substituted or unsubstituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl), or R.sup.23-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0193] In embodiments, R.sup.5 is independently
R.sup.23-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In
embodiments, R.sup.5 is independently R.sup.23-substituted alkyl
(e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.5 is independently an
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl).
[0194] In embodiments, R.sup.5 is independently
R.sup.23-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.5 is independently
R.sup.23-substituted heteroalkyl (e.g., 2 to 8 membered
heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4 membered
heteroalkyl). In embodiments, R.sup.5 is independently an
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl).
[0195] In embodiments, R.sup.5 is independently
R.sup.23-substituted or unsubstituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.5 is
independently R.sup.23-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.5 is
independently an unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8
cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6
cycloalkyl).
[0196] In embodiments, R.sup.5 is independently
R.sup.23-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl). In embodiments, R.sup.5 is
independently R.sup.23-substituted heterocycloalkyl (e.g., 3 to 8
membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl). In embodiments, R.sup.5 is
independently an unsubstituted heterocycloalkyl (e.g., 3 to 8
membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl).
[0197] In embodiments, R.sup.5 is independently
R.sup.23-substituted or unsubstituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl). In embodiments, R.sup.5 is
independently R.sup.23-substituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl). In embodiments, R.sup.5 is
independently an unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl,
C.sub.10 aryl, or phenyl).
[0198] In embodiments, R.sup.5 is independently
R.sup.23-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.5 is independently
R.sup.23-substituted heteroaryl (e.g., 5 to 10 membered heteroaryl,
5 to 9 membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.5 is independently an unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0199] In embodiments, R.sup.6 is independently halogen, oxo,
--CX.sup.6.1.sub.3, --CHX.sup.6.1.sub.2, --CH.sub.2X.sup.6.1, --CN,
--N.sub.3, --SO.sub.n6R.sup.6A, --SO.sub.v6NR.sup.6BR.sup.6C,
--NHNR.sup.6BR.sup.6C, --ONR.sup.6BR.sup.6C,
--NHC(O)NHNR.sup.6BR.sup.6C, --NHC(O)NR.sup.6BR.sup.6C,
--N(O).sub.m6, --NR.sup.6BR.sup.6C, --C(O)R.sup.6D,
--C(O)OR.sup.6D, --C(O)NR.sup.6BR.sup.6C, --OR.sup.6A,
--NR.sup.6BSO.sub.2R.sup.6A, --NR.sup.6BC(O)R.sup.6D,
--NR.sup.6BC(O)OR.sup.6D, --NR.sup.6BOR.sup.6D,
--OCX.sup.6.1.sub.3, --OCHX.sup.6.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. In embodiments, R.sup.6
is hydrogen.
[0200] In embodiments, R.sup.6 is independently halogen,
--CX.sup.6.1.sub.3, --CHX.sup.6.1.sub.2, --CH.sub.2X.sup.6.1, --CN,
--N.sub.3, --SO.sub.n6R.sup.6A, --SO.sub.v6NR.sup.6BR.sup.6C,
--NHNR.sup.6BR.sup.6C, --ONR.sup.6BR.sup.6C,
--NHC(O)NHNR.sup.6BR.sup.6C, --NHC(O)NR.sup.6BR.sup.6C,
--N(O).sub.m6, --NR.sup.6BR.sup.6C, --C(O)R.sup.6D,
--C(O)OR.sup.6D, --C(O)NR.sup.6BR.sup.6C, --OR.sup.6A,
--NR.sup.6BSO.sub.2R.sup.6A, --NR.sup.6BC(O)R.sup.6D,
--NR.sup.6BC(O)OR.sup.6D, --NR.sup.6BOR.sup.6D,
--OCX.sup.6.1.sub.3, --OCHX.sup.6.1.sub.2, R.sup.26-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl), R.sup.26-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl),
R.sup.26-substituted or unsubstituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl), R.sup.26-substituted or unsubstituted
heterocycloalkyl (e.g., 3 to 8 membered heterocycloalkyl, 3 to 6
membered heterocycloalkyl, or 5 to 6 membered heterocycloalkyl),
R.sup.26-substituted or unsubstituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl), or R.sup.26-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0201] In embodiments, R.sup.6 is hydrogen. In embodiments, R.sup.6
is R.sup.26-substituted or unsubstituted alkyl. In embodiments,
R.sup.6 is unsubstituted phenyl. In embodiments, R.sup.6 is --F. In
embodiments, R.sup.6 is --OH. In embodiments, R.sup.6 is
--CH.sub.2OH. In embodiments, R.sup.6 is --(CH.sub.2).sub.2OH. In
embodiments, R.sup.6 is --(CH.sub.2).sub.3OH. In embodiments,
R.sup.6 is --C(CH.sub.3).sub.2OH. In embodiments, R.sup.6 is
--CH.sub.2SO.sub.2NH.sub.2. In embodiments, R.sup.6 is
--(CH.sub.2).sub.2SO.sub.2NH.sub.2. In embodiments, R.sup.6 is
--CH.sub.2C(O)NH.sub.2. In embodiments, R.sup.6 is
--(CH.sub.2).sub.2C(O)NH.sub.2. In embodiments, R.sup.6 is
--(CH.sub.2).sub.3C(O)NH.sub.2. In embodiments, R.sup.6 is
--CH.sub.2NHSO.sub.2CF.sub.3. In embodiments, R.sup.6 is
--(CH.sub.2).sub.2NHSO.sub.2CF.sub.3. In embodiments, R.sup.6 is
--(CH.sub.2).sub.3NHSO.sub.2CF.sub.3. In embodiments, R.sup.6 is
--CH.sub.2NHSO.sub.2CH.sub.3. In embodiments, R.sup.6 is
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3. In embodiments, R.sup.6 is
--(CH.sub.2).sub.3NHSO.sub.2CH.sub.3. In embodiments, R.sup.6 is
--CH.sub.2SO.sub.2CH.sub.3. In embodiments, R.sup.6 is
--(CH.sub.2).sub.2SO.sub.2CH.sub.3. In embodiments, R.sup.6 is
--CH.sub.2SO.sub.2NH.sub.2. In embodiments, R.sup.6 is
--(CH.sub.2).sub.2SO.sub.2NH.sub.2.
[0202] In embodiments, R.sup.6 is independently
R.sup.26-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.5
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In
embodiments, R.sup.6 is independently R.sup.26-substituted alkyl
(e.g., C.sub.1-C.sub.5 alkyl, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.6 is independently an
unsubstituted alkyl (e.g., C.sub.1-C.sub.5 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl).
[0203] In embodiments, R.sup.6 is independently
R.sup.26-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.6 is independently
R.sup.26-substituted heteroalkyl (e.g., 2 to 8 membered
heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4 membered
heteroalkyl). In embodiments, R.sup.6 is independently an
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl).
[0204] In embodiments, R.sup.6 is independently
R.sup.26-substituted or unsubstituted cycloalkyl (e.g.,
C.sub.3-C.sub.5 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.6 is
independently R.sup.26-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.6 is
independently an unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8
cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6
cycloalkyl).
[0205] In embodiments, R.sup.6 is independently
R.sup.26-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl). In embodiments, R.sup.6 is
independently R.sup.26-substituted heterocycloalkyl (e.g., 3 to 8
membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl). In embodiments, R.sup.6 is
independently an unsubstituted heterocycloalkyl (e.g., 3 to 8
membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl).
[0206] In embodiments, R.sup.6 is independently
R.sup.26-substituted or unsubstituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl). In embodiments, R.sup.6 is
independently R.sup.26-substituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl). In embodiments, R.sup.6 is
independently an unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl,
C.sub.10 aryl, or phenyl).
[0207] In embodiments, R.sup.6 is independently
R.sup.26-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.6 is independently
R.sup.26-substituted heteroaryl (e.g., 5 to 10 membered heteroaryl,
5 to 9 membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.6 is independently an unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0208] In embodiments, R.sup.7 is halogen, --CX.sup.7.1.sub.3,
--CHX.sup.7.1.sub.2, --CH.sub.2X.sup.7.1, --CN, --N.sub.3,
--SO.sub.n7R.sup.7A, --SO.sub.v7NR.sup.7BR.sup.7C,
--NHNR.sup.7BR.sup.7C, --ONR.sup.7BR.sup.7C,
--NHC(O)NHNR.sup.7BR.sup.7C, --NHC(O)NR.sup.7BR.sup.7C,
--N(O).sub.m7, --NR.sup.7BR.sup.7C, --C(O)R.sup.7D,
--C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C, --OR.sup.7A,
--NR.sup.7BSO.sub.2R.sup.7A, --NR.sup.7BC(O)R.sup.7D,
--NR.sup.7BC(O)OR.sup.7D, --NR.sup.7BOR.sup.7D,
--OCX.sup.7.1.sub.3, --OCHX.sup.7.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. In embodiments, R.sup.7
is hydrogen. In embodiments, R.sup.7 is --C(O)OH. In embodiments,
R.sup.7 is --OH. In embodiments, R.sup.7 is --NH.sub.2. In
embodiments, R.sup.7 is --C(O)NH.sub.2.
[0209] In embodiments, R.sup.7 is halogen, --CX.sup.7.1.sub.3,
--CHX.sup.7.1.sub.2, --CH.sub.2X.sup.7.1, --CN, --N.sub.3,
--SO.sub.n7R.sup.7A, --SO.sub.v7NR.sup.7BR.sup.7C,
--NHNR.sup.7BR.sup.7C, --ONR.sup.7BR.sup.7C,
--NHC(O)NHNR.sup.7BR.sup.7C, --NHC(O)NR.sup.7BR.sup.7C,
--N(O).sub.m7, --NR.sup.7BR.sup.7C, --C(O)R.sup.7D,
--C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C, --OR.sup.7A,
--NR.sup.7BSO.sub.2R.sup.7A, --NR.sup.7BC(O)R.sup.7D,
--NR.sup.7BC(O)OR.sup.7D, --NR.sup.7BOR.sup.7D,
--OCX.sup.7.1.sub.3, --OCHX.sup.7.1.sub.2, R.sup.29-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl), R.sup.29-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl),
R.sup.29-substituted or unsubstituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl), R.sup.29-substituted or unsubstituted
heterocycloalkyl (e.g., 3 to 8 membered heterocycloalkyl, 3 to 6
membered heterocycloalkyl, or 5 to 6 membered heterocycloalkyl),
R.sup.29-substituted or unsubstituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl), or R.sup.29-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0210] In embodiments, R.sup.7 is --(CH.sub.2).sub.3COOH. In
embodiments, R.sup.7 is --(CH.sub.2).sub.2COOH. In embodiments,
R.sup.7 is --(CH.sub.2).sub.1COOH. In embodiments, R.sup.7 is
--(CH.sub.2).sub.2CONH.sub.2. In embodiments, R.sup.7 is
--(CH.sub.2).sub.3CONH.sub.2. In embodiments, R.sup.7 is
--(CH.sub.2).sub.3OH. In embodiments, R.sup.7 is substituted
cyclobutyl.
[0211] In embodiments, R.sup.7 is
--(CH.sub.2).sub.2SO.sub.2CH.sub.3. In embodiments, R.sup.7 is
--CH.sub.2CH(CH.sub.3)OH. In embodiments, R.sup.7 is
--(CH.sub.2).sub.2OH. In embodiments, R.sup.7 is
--(CH.sub.2).sub.4OH. In embodiments, R.sup.7 is
--(CH.sub.2).sub.1OH. In embodiments, R.sup.7 is
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3. In embodiments, R.sup.7 is
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.2CH.sub.3. In embodiments,
R.sup.7 is --(CH.sub.2).sub.2NHSO.sub.2(CH.sub.2).sub.2CH.sub.3. In
embodiments, R.sup.7 is
--(CH.sub.2).sub.2NHSO.sub.2CH(CH.sub.3).sub.2.
[0212] In embodiments, R.sup.7 is
--(CH.sub.2).sub.2NHC(O)OCH.sub.3. In embodiments, R.sup.7 is
--(CH.sub.2).sub.3SO.sub.2CH.sub.3. In embodiments, R.sup.7 is
--(CH.sub.2).sub.2NHC(O)CH.sub.3. In embodiments, R.sup.7 is
--(CH.sub.2).sub.2NHC(O)H. In embodiments, R.sup.7 is
--CH.sub.2C(O)OCH.sub.3. In embodiments, R.sup.7 is
--CH.sub.2C(O)OCH.sub.2CH.sub.3. In embodiments, R.sup.7 is
--(CH.sub.2).sub.3SO.sub.2NH.sub.2. In embodiments, R.sup.7 is
--(CH.sub.2).sub.2SO.sub.2NH.sub.2. In embodiments, R.sup.7 is
--(CH.sub.2).sub.1SO.sub.2NH.sub.2. In embodiments, R.sup.7 is
--(CH.sub.2).sub.2NHC(O)CH.sub.2CH.sub.3. In embodiments, R.sup.7
is --(CH.sub.2).sub.2NHC(O)CH(CH.sub.3).sub.2.
[0213] In embodiments, R.sup.7 is hydrogen. In embodiments, R.sup.7
is R.sup.29-substituted or unsubstituted alkyl. In embodiments,
R.sup.7 is phenyl. In embodiments, R.sup.7 is --(CH.sub.2).sub.2OH.
In embodiments, R.sup.7 is --CH.sub.2C(CH.sub.3).sub.2OH. In
embodiments, R.sup.7 is --(CH.sub.2).sub.3OH. In embodiments,
R.sup.7 is --(CH.sub.2).sub.2CH(CH.sub.3).sub.2OH.
[0214] In embodiments, R.sup.7 is
--(CH.sub.2).sub.2SO.sub.2NH.sub.2. In embodiments, R.sup.7 is
--(CH.sub.2).sub.3SO.sub.2NH.sub.2. In embodiments, R.sup.7 is
--(CH.sub.2).sub.2CONH.sub.2. In embodiments, R.sup.7 is
--(CH.sub.2).sub.3CONH.sub.2. In embodiments, R.sup.7 is
--(CH.sub.2).sub.3CON(H)Me. In embodiments, R.sup.7 is
--(CH.sub.2).sub.3CON(Me).sub.2. In embodiments, R.sup.7 is
--(CH.sub.2).sub.2SO.sub.2Me. In embodiments, R.sup.7 is
--(CH.sub.2).sub.3SO.sub.2Me. In embodiments, R.sup.7 is
--CH.sub.2CH(OH)Me. In embodiments, R.sup.7 is --CH.sub.2CO.sub.2H.
In embodiments, R.sup.7 is --(CH.sub.2).sub.2CO.sub.2H. In
embodiments, R.sup.7 is --CH(CH.sub.3)CH.sub.2CO.sub.2H. In
embodiments, R.sup.7 is --(CH.sub.2).sub.3CO.sub.2H. In
embodiments, R.sup.7 is --(CH.sub.2).sub.2SO.sub.2NHCH.sub.3. In
embodiments, R.sup.7 is
--(CH.sub.2).sub.2SO.sub.2N(CH.sub.3).sub.2. In embodiments,
R.sup.7 is --(CH.sub.2).sub.2SO.sub.2--(N-morpholinyl). In
embodiments, R.sup.7 is --(CH.sub.2).sub.2NHCOCH.sub.3. In
embodiments, R.sup.7 is --(CH.sub.2).sub.2NHC(O)OCH.sub.3. In
embodiments, R.sup.7 is --(CH.sub.2).sub.3NHCOCH.sub.3. In
embodiments, R.sup.7 is --(CH.sub.2).sub.2NHCOCH(CH.sub.3).sub.2.
In embodiments, R.sup.7 is --(CH.sub.2).sub.2NHSO.sub.2CH.sub.3. In
embodiments, R.sup.7 is --(CH.sub.2).sub.2NHSO.sub.2CF.sub.3. In
embodiments, R.sup.7 is
--(CH.sub.2).sub.2NHSO.sub.2NHCH(CH.sub.3).sub.2. In embodiments,
R.sup.7 is --CH.sub.2CH(CH.sub.3)CH.sub.2OH (R and S). In
embodiments, R.sup.7 is --CH(CH.sub.3)(CH.sub.2).sub.2OH. In
embodiments, R.sup.7 is --CH.sub.2-(2-imidazoyl). In embodiments,
R.sup.7 is --CH.sub.2-(4-imidazoyl). In embodiments, R.sup.7 is
--CH.sub.2-(3-pyrazoyl). In embodiments, R.sup.7 is
4-tetrahydropyranyl. In embodiments, R.sup.7 is 3-oxetanyl. In
embodiments, R.sup.7 is --(CH.sub.2).sub.2NHCO.sub.2Me. In
embodiments, R.sup.7 is --(CH.sub.2).sub.3NHCO.sub.2Me.
[0215] In embodiments, R.sup.7 is hydrogen, R.sup.29-substituted or
unsubstituted alkyl, phenyl, --F, --OH, --CH.sub.2OH,
--(CH.sub.2).sub.2OH, --(CH.sub.2).sub.3OH, --C(CH.sub.3).sub.2OH,
--CH.sub.2SO.sub.2NH.sub.2, --(CH.sub.2).sub.2SO.sub.2NH.sub.2,
--CH.sub.2C(O)NH.sub.2, --(CH.sub.2).sub.2C(O)NH.sub.2,
--(CH.sub.2).sub.3C(O)NH.sub.2, --CH.sub.2NHSO.sub.2CF.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2CF.sub.3,
--(CH.sub.2).sub.3NHSO.sub.2CF.sub.3, --CH.sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.3NHSO.sub.2CH.sub.3, --CH.sub.2SO.sub.2CH.sub.3,
--(CH.sub.2).sub.2SO.sub.2CH.sub.3, --CH.sub.2SO.sub.2NH.sub.2 or
--(CH.sub.2).sub.2SO.sub.2NH.sub.2.
[0216] In embodiments, R.sup.7 is R.sup.29-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.7 is
R.sup.29-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.7 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0217] In embodiments, R.sup.7 is an unsubstituted C.sub.1-C.sub.4
alkyl. In embodiments, R.sup.7 is an unsubstituted C.sub.1-C.sub.3
alkyl. In embodiments, R.sup.7 is an unsubstituted C.sub.1-C.sub.2
alkyl. In embodiments, R.sup.7 is an unsubstituted C.sub.4 alkyl.
In embodiments, R.sup.7 is an unsubstituted C.sub.3 alkyl. In
embodiments, R.sup.7 is a R.sup.27-substituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl). In embodiments, R.sup.7 is a R.sup.27-substituted
C.sub.1-C.sub.4 alkyl. In embodiments, R.sup.7 is a
R.sup.27-substituted C.sub.1-C.sub.3 alkyl. In embodiments, R.sup.7
is a R.sup.27-substituted C.sub.1-C.sub.2 alkyl. In embodiments,
R.sup.7 is a R.sup.27-substituted C.sub.4 alkyl. In embodiments,
R.sup.7 is a R.sup.27-substituted C.sub.3 alkyl.
[0218] In embodiments, R.sup.7 is R.sup.29-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.7 is R.sup.29-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.7 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0219] In embodiments, R.sup.7 is R.sup.29-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.7 is R.sup.29-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.7 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.7 is an unsubstituted C.sub.3-C.sub.6
cycloalkyl. In embodiments, R.sup.7 is an unsubstituted
C.sub.3-C.sub.5 cycloalkyl. In embodiments, R.sup.7 is an
unsubstituted C.sub.3-C.sub.4 cycloalkyl. In embodiments, R.sup.7
is an unsubstituted C.sub.4 cycloalkyl. In embodiments, R.sup.7 is
a R.sup.29-substituted C.sub.3-C.sub.6 cycloalkyl. In embodiments,
R.sup.7 is a R.sup.29-substituted C.sub.3-C.sub.5 cycloalkyl. In
embodiments, R.sup.7 is a R.sup.29-substituted C.sub.3-C.sub.4
cycloalkyl. In embodiments, R.sup.7 is a R.sup.29-substituted
C.sub.4 cycloalkyl.
[0220] In embodiments, R.sup.7 is R.sup.29-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.7 is
R.sup.29-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.7 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0221] In embodiments, R.sup.7 is R.sup.29-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.7 is R.sup.29-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.7 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0222] In embodiments, R.sup.7 is R.sup.29-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.7 is R.sup.29-substituted heteroaryl (e.g., 5 to
10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.7 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0223] In embodiments, R.sup.8 is halogen, --CX.sup.8.1.sub.3,
--CHX.sup.8.1.sub.2, --CH.sub.2X.sup.8.1, --CN, --N.sub.3,
--SO.sub.n8R.sup.8A, --SO.sub.v8NR.sup.8BR.sup.8C,
--NHNR.sup.8BR.sup.8C, --ONR.sup.8BR.sup.8C,
--NHC(O)NHNR.sup.8BR.sup.8C, --NHC(O)NR.sup.8BR.sup.8C,
--N(O).sub.m8, --NR.sup.8BR.sup.8C, --C(O)R.sup.8D,
--C(O)OR.sup.8D, --C(O)NR.sup.8BR.sup.8C, --OR.sup.8A,
--NR.sup.8BSO.sub.2R.sup.8A, --NR.sup.8BC(O)R.sup.8D,
--NR.sup.8BC(O)OR.sup.8D, --NR.sup.8BOR.sup.8D,
--OCX.sup.8.1.sub.3, --OCHX.sup.8.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. In embodiments, R.sup.8
is hydrogen.
[0224] In embodiments, R.sup.8 is halogen, --CX.sup.8.1.sub.3,
--CHX.sup.8.1.sub.2, --CH.sub.2X.sup.8.1, --CN, --N.sub.3,
--SO.sub.n8R.sup.8A, --SO.sub.v8NR.sup.8BR.sup.8C,
--NHNR.sup.8BR.sup.8C, --ONR.sup.8BR.sup.8C,
--NHC(O)NHNR.sup.8BR.sup.8C, --NHC(O)NR.sup.8BR.sup.8C,
--N(O).sub.m8, --NR.sup.8BR.sup.8C, --C(O)R.sup.8D,
--C(O)OR.sup.8D, --C(O)NR.sup.8BR.sup.8C, --OR.sup.8A,
--NR.sup.8BSO.sub.2R.sup.8A, --NR.sup.8BC(O)R.sup.8D,
--NR.sup.8BC(O)OR.sup.8D, --NR.sup.8BOR.sup.8D,
--OCX.sup.8.1.sub.3, --OCHX.sup.8.1.sub.2, R.sup.32-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl), R.sup.32-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl),
R.sup.32-substituted or unsubstituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl), R.sup.32-substituted or unsubstituted
heterocycloalkyl (e.g., 3 to 8 membered heterocycloalkyl, 3 to 6
membered heterocycloalkyl, or 5 to 6 membered heterocycloalkyl),
R.sup.32-substituted or unsubstituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl), or R.sup.32-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0225] In embodiments, R.sup.8 is R.sup.32-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.8 is
R.sup.32-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.8 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0226] In embodiments, R.sup.8 is R.sup.32-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.8 is R.sup.32-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.8 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0227] In embodiments, R.sup.8 is R.sup.32-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.8 is R.sup.32-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.8 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0228] In embodiments, R.sup.8 is R.sup.32-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.8 is
R.sup.32-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.8 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0229] In embodiments, R.sup.8 is R.sup.32-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.8 is R.sup.32-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.8 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, Cio aryl, or phenyl).
[0230] In embodiments, R.sup.8 is R.sup.32-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.8 is R.sup.32-substituted heteroaryl (e.g., 5 to
10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.8 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0231] In embodiments, R.sup.9 is halogen, --CX.sup.9.1.sub.3,
--CHX.sup.9.1.sub.2, --CH.sub.2X.sup.9.1, --CN, --N.sub.3,
--SO.sub.n9R.sup.9A, --SO.sub.v9NR.sup.9BR.sup.9C,
--NHNR.sup.9BR.sup.9C, --ONR.sup.9BR.sup.9C,
--NHC(O)NHNR.sup.9BR.sup.9C, --NHC(O)NR.sup.9BR.sup.9C,
--N(O).sub.m9, --NR.sup.9BR.sup.9C, --C(O)R.sup.9D,
--C(O)OR.sup.9D, --C(O)NR.sup.9BR.sup.9C, --OR.sup.9A,
--NR.sup.9BSO.sub.2R.sup.9A, --NR.sup.9BC(O)R.sup.9D,
--NR.sup.9BC(O)OR.sup.9D, --NR.sup.9BOR.sup.9D,
--OCX.sup.9.1.sub.3, --OCHX.sup.9.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. In embodiments, R.sup.9
is hydrogen.
[0232] In embodiments, R.sup.9 is halogen, --CX.sup.9.1.sub.3,
--CHX.sup.9.1.sub.2, --CH.sub.2X.sup.9.1, --CN, --N.sub.3,
--SO.sub.n9R.sup.9A, --SO.sub.v9NR.sup.9BR.sup.9C,
--NHNR.sup.9BR.sup.9C, --ONR.sup.9BR.sup.9C,
--NHC(O)NHNR.sup.9BR.sup.9C, --NHC(O)NR.sup.9BR.sup.9C,
--N(O).sub.m9, --NR.sup.9BR.sup.9C, --C(O)R.sup.9D,
--C(O)OR.sup.9D, --C(O)NR.sup.9BR.sup.9C, --OR.sup.9A,
--NR.sup.9BSO.sub.2R.sup.9A, --NR.sup.9BC(O)R.sup.9D,
--NR.sup.9BC(O)OR.sup.9D, --NR.sup.9BOR.sup.9D,
--OCX.sup.9.1.sub.3, --OCHX.sup.9.1.sub.2, R.sup.35-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl), R.sup.35-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl),
R.sup.35-substituted or unsubstituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl), R.sup.35-substituted or unsubstituted
heterocycloalkyl (e.g., 3 to 8 membered heterocycloalkyl, 3 to 6
membered heterocycloalkyl, or 5 to 6 membered heterocycloalkyl),
R.sup.35-substituted or unsubstituted aryl (e.g., C.sub.6-C.sub.10
aryl, C.sub.10 aryl, or phenyl), or R.sup.35-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0233] In embodiments, R.sup.9 is R.sup.35-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.9 is
R.sup.35-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.9 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0234] In embodiments, R.sup.9 is R.sup.35-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.9 is R.sup.35-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.9 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0235] In embodiments, R.sup.9 is R.sup.35-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.9 is R.sup.35-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.9 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0236] In embodiments, R.sup.9 is R.sup.35-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.9 is
R.sup.35-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.9 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0237] In embodiments, R.sup.9 is R.sup.35-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.9 is R.sup.35-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.9 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0238] In embodiments, R.sup.9 is R.sup.35-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.9 is R.sup.35-substituted heteroaryl (e.g., 5 to
10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.9 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0239] In embodiments, R.sup.10 is halogen, --CX.sup.10.1.sub.3,
--CHX.sup.10.1.sub.2, --CH.sub.2X.sup.10.1, --CN, --N.sub.3,
--SO.sub.n10R.sup.10A, --SO.sub.v10NR.sup.10BR.sup.10C,
--NHNR.sup.10BR.sup.10C, --ONR.sup.10BR.sup.10C,
--NHC(O)NHNR.sup.10BR.sup.10C, --NHC(O)NR.sup.10BR.sup.10C,
--N(O).sub.m10, --NR.sup.10BR.sup.10C, --C(O)R.sup.10D,
--C(O)OR.sup.10D, --C(O)NR.sup.10BR.sup.10C, --OR.sup.10A,
--NR.sup.10BSO.sub.2R.sup.10A, --NR.sup.10BC(O)R.sup.10D,
--NR.sup.10BC(O)OR.sup.10D, --NR.sup.10BOR.sup.10D,
--OCX.sup.10.1.sub.3, --OCHX.sup.10.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. In embodiments,
R.sup.10 is hydrogen.
[0240] In embodiments, R.sup.10 is halogen, --CX.sup.10.1.sub.3,
--CHX.sup.10.1.sub.2, --CH.sub.2X.sup.10.1, --CN, --N.sub.3,
--SO.sub.n10R.sup.10A, --SO.sub.v10NR.sup.10BR.sup.10C,
--NHNR.sup.10BR.sup.10C, --ONR.sup.10BR.sup.10C,
--NHC(O)NHNR.sup.10BR.sup.10C, --NHC(O)NR.sup.10BR.sup.10C,
--N(O).sub.m10, --NR.sup.10BR.sup.10C, --C(O)R.sup.10D,
--C(O)OR.sup.10D, --C(O)NR.sup.10BR.sup.10C, --OR.sup.10A,
--NR.sup.10BSO.sub.2R.sup.10A, --NR.sup.10BC(O)R.sup.10D,
--NR.sup.10BC(O)OR.sup.10D, --NR.sup.10BOR.sup.10D,
--OCX.sup.10.1.sub.3, --OCHX.sup.10.1.sub.2, R.sup.38-substituted
or unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.38-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.38-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.38-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.38-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.38-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0241] In embodiments, R.sup.10 is R.sup.38-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.10 is
R.sup.38-substituted alkyl (e.g., C.sub.1-C.sub.5 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.10 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.5 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0242] In embodiments, R.sup.10 is R.sup.38-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.10 is R.sup.38-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.10 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0243] In embodiments, R.sup.10 is R.sup.38-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.5 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.10 is R.sup.38-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.10 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.5 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0244] In embodiments, R.sup.10 is R.sup.38-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.10 is
R.sup.38-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.10 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0245] In embodiments, R.sup.10 is R.sup.38-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.10 is R.sup.38-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.10 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, Cio.sub.0 aryl, or phenyl).
[0246] In embodiments, R.sup.10 is R.sup.38-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.10 is R.sup.38-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.10 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0247] In embodiments, L.sup.7 is a bond, --O--, --S--,
--NR.sup.7.2B--, --C(O)--, --C(O)O--, --S(O), --S(O)--, substituted
or unsubstituted alkylene (e.g., C.sub.1-C.sub.8 alkylene,
C.sub.1-C.sub.6 alkylene, or C.sub.1-C.sub.4 alkylene), substituted
or unsubstituted heteroalkylene (e.g., 2 to 8 membered
heteroalkylene, 2 to 6 membered heteroalkylene, or 2 to 4 membered
heteroalkylene), substituted or unsubstituted cycloalkylene (e.g.,
C.sub.3-C.sub.8 cycloalkylene, C.sub.3-C.sub.6 cycloalkylene, or
C.sub.5-C.sub.6 cycloalkylene), substituted or unsubstituted
heterocycloalkylene (e.g., 3 to 8 membered heterocycloalkylene, 3
to 6 membered heterocycloalkylene, or 5 to 6 membered
heterocycloalkylene), substituted or unsubstituted arylene (e.g.,
C.sub.6-C.sub.10 arylene, C.sub.10 arylene, or phenylene), or
substituted or unsubstituted heteroarylene (e.g., 5 to 10 membered
heteroarylene, 5 to 9 membered heteroarylene, or 5 to 6 membered
heteroarylene).
[0248] In embodiments, L.sup.7 is a bond, --O--, --S--,
--NR.sup.72B--, --C(O)--, --C(O)O--, --S(O), --S(O)--,
R.sup.41-substituted or unsubstituted alkylene (e.g.,
C.sub.1-C.sub.8 alkylene, C.sub.1-C.sub.6 alkylene, or
C.sub.1-C.sub.4 alkylene), R.sup.41-substituted or unsubstituted
heteroalkylene (e.g., 2 to 8 membered heteroalkylene, 2 to 6
membered heteroalkylene, or 2 to 4 membered heteroalkylene),
R.sup.41-substituted or unsubstituted cycloalkylene (e.g.,
C.sub.3-C.sub.8 cycloalkylene, C.sub.3-C.sub.6 cycloalkylene, or
C.sub.5-C.sub.6 cycloalkylene), R.sup.41-substituted or
unsubstituted heterocycloalkylene (e.g., 3 to 8 membered
heterocycloalkylene, 3 to 6 membered heterocycloalkylene, or 5 to 6
membered heterocycloalkylene), R.sup.41-substituted or
unsubstituted arylene (e.g., C.sub.6-C.sub.10 arylene, C.sub.10
arylene, or phenylene), or R.sup.41-substituted or unsubstituted
heteroarylene (e.g., 5 to 10 membered heteroarylene, 5 to 9
membered heteroarylene, or 5 to 6 membered heteroarylene). In
embodiments, L.sup.7 is a bond.
[0249] In embodiments, L.sup.7 is R.sup.41-substituted or
unsubstituted alkylene (e.g., C.sub.1-C.sub.8 alkylene,
C.sub.1-C.sub.6 alkylene, or C.sub.1-C.sub.4 alkylene). In
embodiments, L.sup.7 is R.sup.41-substituted alkylene (e.g.,
C.sub.1-C.sub.8 alkylene, C.sub.1-C.sub.6 alkylene, or
C.sub.1-C.sub.4 alkylene). In embodiments, L.sup.7 is an
unsubstituted alkylene (e.g., C.sub.1-C.sub.8 alkylene,
C.sub.1-C.sub.6 alkylene, or C.sub.1-C.sub.4 alkylene).
[0250] In embodiments, L.sup.7 is R.sup.41-substituted or
unsubstituted heteroalkylene (e.g., 2 to 8 membered heteroalkylene,
2 to 6 membered heteroalkylene, or 2 to 4 membered heteroalkylene).
In embodiments, L.sup.7 is R.sup.41-substituted heteroalkylene
(e.g., 2 to 8 membered heteroalkylene, 2 to 6 membered
heteroalkylene, or 2 to 4 membered heteroalkylene). In embodiments,
L.sup.7 is an unsubstituted heteroalkylene (e.g., 2 to 8 membered
heteroalkylene, 2 to 6 membered heteroalkylene, or 2 to 4 membered
heteroalkylene).
[0251] In embodiments, L.sup.7 is R.sup.41-substituted or
unsubstituted cycloalkylene (e.g., C.sub.3-C.sub.8 cycloalkylene,
C.sub.3-C.sub.6 cycloalkylene, or C.sub.5-C.sub.6 cycloalkylene).
In embodiments, L.sup.7 is R.sup.41-substituted cycloalkylene
(e.g., C.sub.3-C.sub.8 cycloalkylene, C.sub.3-C.sub.6
cycloalkylene, or C.sub.5-C.sub.6 cycloalkylene). In embodiments,
L.sup.7 is an unsubstituted cycloalkylene (e.g., C.sub.3-C.sub.8
cycloalkylene, C.sub.3-C.sub.6 cycloalkylene, or C.sub.5-C.sub.6
cycloalkylene).
[0252] In embodiments, L.sup.7 is R.sup.41-substituted or
unsubstituted heterocycloalkylene (e.g., 3 to 8 membered
heterocycloalkylene, 3 to 6 membered heterocycloalkylene, or 5 to 6
membered heterocycloalkylene). In embodiments, L.sup.7 is
R.sup.41-substituted heterocycloalkylene (e.g., 3 to 8 membered
heterocycloalkylene, 3 to 6 membered heterocycloalkylene, or 5 to 6
membered heterocycloalkylene). In embodiments, L.sup.7 is an
unsubstituted heterocycloalkylene (e.g., 3 to 8 membered
heterocycloalkylene, 3 to 6 membered heterocycloalkylene, or 5 to 6
membered heterocycloalkylene).
[0253] In embodiments, L.sup.7 is R.sup.41-substituted or
unsubstituted arylene (e.g., C.sub.6-C.sub.10 arylene, C.sub.10
arylene, or phenylene). In embodiments, L.sup.7 is
R.sup.41-substituted arylene (e.g., C.sub.6-C.sub.10 arylene,
C.sub.10 arylene, or phenylene). In embodiments, L.sup.7 is an
unsubstituted arylene (e.g., C.sub.6-C.sub.10 arylene, C.sub.10
arylene, or phenylene).
[0254] In embodiments, L.sup.7 is R.sup.41-substituted or
unsubstituted heteroarylene (e.g., 5 to 10 membered heteroarylene,
5 to 9 membered heteroarylene, or 5 to 6 membered heteroarylene).
In embodiments, L.sup.7 is R.sup.41-substituted heteroarylene
(e.g., 5 to 10 membered heteroarylene, 5 to 9 membered
heteroarylene, or 5 to 6 membered heteroarylene). In embodiments,
L.sup.7 is an unsubstituted heteroarylene (e.g., 5 to 10 membered
heteroarylene, 5 to 9 membered heteroarylene, or 5 to 6 membered
heteroarylene).
[0255] In embodiments, R.sup.1A is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.11A-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.11A-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.11A-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.11A-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.11A-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.11A-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0256] In embodiments, R.sup.2A is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.14A-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.14A-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.14A-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.14A-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.14A-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.14A-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0257] In embodiments, R.sup.3A is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.17A-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.17A-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17A-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17A-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17A-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.17A-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0258] In embodiments, R.sup.3.2A is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.17.2A-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.17.2A-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17.2A-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17.2A-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17.2A-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl), or R.sup.17.2A-substituted or unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0259] In embodiments, R.sup.3.3A is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.17.3A-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.17.3A-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17.3A-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17.3A-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17.3A-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl), or R.sup.17.3A-substituted or unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0260] In embodiments, R.sup.4A is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.20A-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.20A-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.20A-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.20A-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.20A-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.20A-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0261] In embodiments, R.sup.5A is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.23A-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.23A-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.23A-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.23A-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.23A-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.23A-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0262] In embodiments, R.sup.6A is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.26A-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.26A-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.26A-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.26A-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.26A-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.26A-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0263] In embodiments, R.sup.7A is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.29A-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.29A-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.29A-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.29A-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.29A-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.29A-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0264] In embodiments, R.sup.8A is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.32A-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.32A-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.32A-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.32A-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.32A-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.32A-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0265] In embodiments, R.sup.9A is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.35A-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.35A-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.35A-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.35A-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.35A-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.35A-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0266] In embodiments, R.sup.10A is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.38A-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.38A-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.38A-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.38A-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.38A-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.38A-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0267] In embodiments, R.sup.1B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.11B-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.11B-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.11B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.11B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.11B-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.11B-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.1B and R.sup.1C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.11B-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.11B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0268] In embodiments, R.sup.2B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.14B-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.14B-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.14B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.5 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.14B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.14B-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.14B-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.2B and R.sup.2C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.14B-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.14B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0269] In embodiments, R.sup.3B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.17B-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.17B-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17B-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.17B-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.3B and R.sup.3C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.17B-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.17B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0270] In embodiments, R.sup.3.2B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.17.2B-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.17.2B-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17.2B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17.2B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17.2B-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl), or R.sup.17.2B-substituted or unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0271] In embodiments, R.sup.3.3B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.17.3B-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.17.3B-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17.3B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17.3B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17.3B-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl), or R.sup.17.3B-substituted or unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0272] In embodiments, R.sup.4B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.20B-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.20B-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.20B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.20B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.20B-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.20B-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.4B and R.sup.4C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.20B-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.20B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0273] In embodiments, R.sup.5B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.23B-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.23B-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.23B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.23B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.23B-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.23B-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.5B and R.sup.5C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.23B-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.23B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0274] In embodiments, R.sup.6B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.26B-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.5
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.26B-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.26B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.26B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.26B-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.26B-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.6B and R.sup.6C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.26B-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.26B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0275] In embodiments, R.sup.7B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.29B-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.5
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.29B-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.29B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.29B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.29B-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.29B-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.7B and R.sup.7C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.29B-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.29B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0276] In embodiments, R.sup.8B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.32B-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.32B-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.32B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.32B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.32B-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.32B-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.8B and R.sup.8C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.32B-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.32B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0277] In embodiments, R.sup.9B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.35B-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.35B-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.35B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.35B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.35B-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.35B-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.9B and R.sup.9C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.35B-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.35B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0278] In embodiments, R.sup.10B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.38B-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.38B-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.38B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.38B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.38B-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.38B-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.10B and R.sup.10C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.38B-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.38B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0279] In embodiments, R.sup.1C is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.11C-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.11C-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.11C-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.11C-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.11C-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.11C-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.1B and R.sup.1C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.11C-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.11C-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0280] In embodiments, R.sup.2C is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.14C-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.14C-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.14C-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.14C-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.14C-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.14C-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.2B and R.sup.2C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.14C-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.14C-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0281] In embodiments, R.sup.3C is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.17C-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.17C-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17C-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17C-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17C-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.17C-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.3B and R.sup.3C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.17C-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.17C-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0282] In embodiments, R.sup.3.2C is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.17.2C-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.17.2C-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17.2C-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17.2C-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17.2C-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl), or R.sup.17.2C-substituted or unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0283] In embodiments, R.sup.3.3C is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.17.3C-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.17.3C-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17.3C-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17.3C-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17.3C-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl), or R.sup.17.3C-substituted or unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0284] In embodiments, R.sup.4C is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.20C-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.20C-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.20C-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.20C-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.20C-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.20C-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.4B and R.sup.4C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.20C-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.20C-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0285] In embodiments, R.sup.5C is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.23C-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.23C-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.23C-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.23C-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.23C-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.23C-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.5B and R.sup.5C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.23C-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.23C-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0286] In embodiments, R.sup.6C is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.26C-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.26C-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.26C-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.26C-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.26C-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.26C-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.6B and R.sup.6C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.26C-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.26C-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0287] In embodiments, R.sup.7C is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.29C-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.29C-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.29C-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.29C-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.29C-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.29C-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.7B and R.sup.7C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.29C-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.29C-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0288] In embodiments, R.sup.8c is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.32C-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.32C-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.32C-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.32C-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.32C-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.32C-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.8B and R.sup.8C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.32C-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.32C-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0289] In embodiments, R.sup.9C is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.35C-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.35C-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.35C-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.35C-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.35C-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.35C-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.9B and R.sup.9C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.35C-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.35C-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0290] In embodiments, R.sup.10C is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.38C-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.38C-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.38C-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.38C-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.38C-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.38C-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.10B and R.sup.10C substituents
bonded to the same nitrogen atom may optionally be joined to form a
R.sup.38B-substituted or unsubstituted heterocycloalkyl (e.g., 3 to
8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5
to 6 membered heterocycloalkyl) or R.sup.38B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0291] In embodiments, R.sup.1D is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.11D-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.11D-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.11D-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.11D-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.11D-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.11D-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0292] In embodiments, R.sup.2D is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.14D-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.14D-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.14D-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.14D-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.14D-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.14D-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0293] In embodiments, R.sup.3D is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.17D-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.17D-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17D-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17D-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17D-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.17D-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0294] In embodiments, R.sup.3.2D is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.17.2D-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.17.2D-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17.2D-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17.2D-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17.2D-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl), or R.sup.17.2D-substituted or unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0295] In embodiments, R.sup.3.3D is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.17.3D-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.17.3D-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.17.3D-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.17.3D-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.17.3D-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl), or R.sup.17.3D-substituted or unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0296] In embodiments, R.sup.4D is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.20D-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.20D-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.20D-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.20D-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.20D-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.20D-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0297] In embodiments, R.sup.5D is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.23D-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.23D-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.23D-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.23D-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.23D-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.23D-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0298] In embodiments, R.sup.6D is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.26D-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.26D-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.26D-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.26D-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.26D-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.26D-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0299] In embodiments, R.sup.7D is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.29D-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.29D-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.29D-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.29D-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.29D-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.29D-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.7D is hydrogen. In embodiments,
R.sup.7D is --NH.sub.2. In embodiments, R.sup.7D is --CH.sub.3. In
embodiments, R.sup.7D is unsubstituted C.sub.1-C.sub.3 alkyl.
[0300] In embodiments, R.sup.8D is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.32D-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.32D-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.32D-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.32D-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.32D-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.32D-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0301] In embodiments, R.sup.9D is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.35D-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.35D-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.35D-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.35D-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.35D-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.35D-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0302] In embodiments, R.sup.10D is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.38D-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.38D-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.38D-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.38D-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.38D-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.38D-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0303] In embodiments, R.sup.7.2B is hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
R.sup.41.2B-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.41.2B-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.41.2B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.41.2B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.41.2B-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl), or R.sup.41.2B-substituted or unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0304] R.sup.11 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.12-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.12-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.12-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.12-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.12-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.12-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0305] In embodiments, R.sup.11 is R.sup.12-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.11 is
R.sup.12-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.11 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0306] In embodiments, R.sup.11 is R.sup.12-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.11 is R.sup.12-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.11 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0307] In embodiments, R.sup.11 is R.sup.12-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.11 is R.sup.12-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.11 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0308] In embodiments, R.sup.11 is R.sup.12-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.11 is
R.sup.12-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.11 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0309] In embodiments, R.sup.11 is R.sup.12-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.11 is R.sup.12-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.11 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0310] In embodiments, R.sup.11 is R.sup.12-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.11 is R.sup.12-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.11 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0311] R.sup.12 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.13-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.13-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.13-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.13-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.13-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.13-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0312] In embodiments, R.sup.12 is R.sup.13-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.12 is
R.sup.13-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.12 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0313] In embodiments, R.sup.12 is R.sup.13-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.12 is R.sup.13-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.12 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0314] In embodiments, R.sup.12 is R.sup.13-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.12 is R.sup.13-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.12 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0315] In embodiments, R.sup.12 is R.sup.13-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.12 is
R.sup.13-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.12 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0316] In embodiments, R.sup.12 is R.sup.13-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.12 is R.sup.13-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.12 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0317] In embodiments, R.sup.12 is R.sup.13-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.12 is R.sup.13-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.12 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0318] R.sup.14 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.15-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.15-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.15-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.15-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.15-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.15-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0319] In embodiments, R.sup.14 is R.sup.15-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.14 is
R.sup.15-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.14 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0320] In embodiments, R.sup.14 is R.sup.15-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.14 is R.sup.15-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.14 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0321] In embodiments, R.sup.14 is R.sup.15-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.14 is R.sup.15-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.14 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0322] In embodiments, R.sup.14 is R.sup.15-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.14 is
R.sup.15-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.14 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0323] In embodiments, R.sup.14 is R.sup.15-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.14 is R.sup.15-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.14 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0324] In embodiments, R.sup.14 is R.sup.15-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.14 is R.sup.15-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.14 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0325] R.sup.15 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.16-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.16-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.16-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.16-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.16-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.16-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0326] In embodiments, R.sup.15 is R.sup.16-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.15 is
R.sup.16-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.15 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0327] In embodiments, R.sup.15 is R.sup.16-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.15 is R.sup.16-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.15 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0328] In embodiments, R.sup.15 is R.sup.16-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.15 is R.sup.16-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.5 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0329] In embodiments, R.sup.15 is R.sup.16-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.15 is
R.sup.16-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.5 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0330] In embodiments, R.sup.15 is R.sup.16-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.15 is R.sup.16-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.15 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0331] In embodiments, R.sup.15 is R.sup.16-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.15 is R.sup.16-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.15 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0332] R.sup.17 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.18-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.18-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.18-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.18-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.18-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.18-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0333] In embodiments, R.sup.17 is R.sup.18-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.17 is
R.sup.18-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.17 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0334] In embodiments, R.sup.17 is R.sup.18-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.17 is R.sup.18-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.17 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0335] In embodiments, R.sup.17 is R.sup.18-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.17 is R.sup.18-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.17 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0336] In embodiments, R.sup.17 is R.sup.18-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.17 is
R.sup.18-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.17 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0337] In embodiments, R.sup.17 is R.sup.18-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.17 is R.sup.18-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.17 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0338] In embodiments, R.sup.17 is R.sup.18-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.17 is R.sup.18-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.17 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0339] R.sup.18 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.19-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.19-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.19-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.19-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.19-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.19-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0340] In embodiments, R.sup.18 is R.sup.19-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.18 is
R.sup.19-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.18 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0341] In embodiments, R.sup.18 is R.sup.19-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.18 is R.sup.19-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.18 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0342] In embodiments, R.sup.18 is R.sup.19-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.18 is R.sup.19-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.8 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0343] In embodiments, R.sup.18 is R.sup.19-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.18 is
R.sup.19-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.8 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0344] In embodiments, R.sup.18 is R.sup.19-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.18 is R.sup.19-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.18 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0345] In embodiments, R.sup.18 is R.sup.19-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.18 is R.sup.19-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.18 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0346] R.sup.17.2 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.18.2-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.18.2-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.18.2-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.18.2-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.18.2-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.18.2-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0347] In embodiments, R.sup.17.2 is R.sup.18.2-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.17.2 is
R.sup.18.2-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.17.2 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0348] In embodiments, R.sup.17.2 is R.sup.18.2-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.17.2 is R.sup.18.2-substituted heteroalkyl
(e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or
2 to 4 membered heteroalkyl). In embodiments, R.sup.17.2 is an
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl).
[0349] In embodiments, R.sup.17.2 is R.sup.18.2-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.17.2 is R.sup.18.2-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.17.2 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0350] In embodiments, R.sup.17.2 is R.sup.18.2-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.17.2 is
R.sup.18.2-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.17.2 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0351] In embodiments, R.sup.17.2 is R.sup.18.2-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.17.2 is R.sup.18.2-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.17.2 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0352] In embodiments, R.sup.17.2 is R.sup.18.2-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.17.2 is R.sup.18.2-substituted heteroaryl (e.g.,
5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.17.2 is an
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0353] R.sup.18.2 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.19.2-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.19.2-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.19.2-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.19.2-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.19.2-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.19.2-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0354] In embodiments, R.sup.18.2 is R.sup.19.2-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.18.2 is
R.sup.19.2-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.18.2 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0355] In embodiments, R.sup.18.2 is R.sup.19.2-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.18.2 is R.sup.19.2-substituted heteroalkyl
(e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or
2 to 4 membered heteroalkyl). In embodiments, R.sup.18.2 is an
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl).
[0356] In embodiments, R.sup.18.2 is R.sup.19.2-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.18.2 is R.sup.19.2-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.18.2 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0357] In embodiments, R.sup.18.2 is R.sup.19.2-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.18.2 is
R.sup.19.2-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.18.2 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0358] In embodiments, R.sup.18.2 is R.sup.19.2-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.18.2 is R.sup.19.2-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.18.2 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0359] In embodiments, R.sup.18.2 is R.sup.19.2-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.18.2 is R.sup.19.2-substituted heteroaryl (e.g.,
5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.18.2 is an
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0360] R.sup.17.3 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.18.3-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.18.3-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.18.3-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.18.3-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.18.3-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.18.3-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0361] In embodiments, R.sup.17.3 is R.sup.18.3-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.17.3 is
R.sup.18.3-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.17.3 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0362] In embodiments, R.sup.17.3 is R.sup.18.3-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.17.3 is R.sup.18.3-substituted heteroalkyl
(e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or
2 to 4 membered heteroalkyl). In embodiments, R.sup.17.3 is an
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl).
[0363] In embodiments, R.sup.17.3 is R.sup.18.3-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.17.3 is R.sup.18.3-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.17.3 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0364] In embodiments, R.sup.17.3 is R.sup.18.3-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.17.3 is
R.sup.18.3-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.17.3 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0365] In embodiments, R.sup.17.3 is R.sup.18.3-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.17.3 is R.sup.18.3-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.17.3 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0366] In embodiments, R.sup.17.3 is R.sup.18.3-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.17.3 is R.sup.18.3-substituted heteroaryl (e.g.,
5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.17.3 is an
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0367] R.sup.18.3 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.19.3-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.19.3-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.19.3-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.19.3-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.19.3-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.19.3-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0368] In embodiments, R.sup.18.3 is R.sup.19.3-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.18.3 is
R.sup.19.3-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.18.3 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0369] In embodiments, R.sup.18.3 is R.sup.19.3-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.18.3 is R.sup.19.3-substituted heteroalkyl
(e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or
2 to 4 membered heteroalkyl). In embodiments, R.sup.18.3 is an
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl).
[0370] In embodiments, R.sup.18.3 is R.sup.19.3-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.18.3 is R.sup.19.3-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.18.3 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0371] In embodiments, R.sup.18.3 is R.sup.19.3-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.18.3 is
R.sup.19.3-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.18.3 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0372] In embodiments, R.sup.18.3 is R.sup.19.3-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.18.3 is R.sup.19.3-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.18.3 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0373] In embodiments, R.sup.18.3 is R.sup.19.3-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.18.3 is R.sup.19.3-substituted heteroaryl (e.g.,
5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.18.3 is an
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0374] R.sup.20 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.21-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.21-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.21-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.21-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.21-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.21-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0375] In embodiments, R.sup.20 is R.sup.21-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.20 is
R.sup.21-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.20 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0376] In embodiments, R.sup.20 is R.sup.21-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.20 is R.sup.21-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.20 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0377] In embodiments, R.sup.20 is R.sup.21-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.20 is R.sup.21-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.20 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0378] In embodiments, R.sup.20 is R.sup.21-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.20 is
R.sup.21-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.20 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0379] In embodiments, R.sup.20 is R.sup.21-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.20 is R.sup.21-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.20 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0380] In embodiments, R.sup.20 is R.sup.21-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.20 is R.sup.21-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.20 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0381] R.sup.21 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.22-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.22-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.22-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.22-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.22-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.22-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0382] In embodiments, R.sup.21 is R.sup.22-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.21 is
R.sup.22-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.21 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0383] In embodiments, R.sup.21 is R.sup.22-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.21 is R.sup.22-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.21 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0384] In embodiments, R.sup.21 is R.sup.22-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.21 is R.sup.22-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.21 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0385] In embodiments, R.sup.21 is R.sup.22-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.21 is
R.sup.22-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.21 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0386] In embodiments, R.sup.21 is R.sup.22-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.21 is R.sup.22-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.21 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0387] In embodiments, R.sup.21 is R.sup.22-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.21 is R.sup.22-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.21 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0388] R.sup.23 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.24-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.24-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.24-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.24-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.24-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.24-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0389] In embodiments, R.sup.23 is R.sup.24-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.23 is
R.sup.24-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.23 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0390] In embodiments, R.sup.23 is R.sup.24-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.23 is R.sup.24-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.23 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0391] In embodiments, R.sup.23 is R.sup.24-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.23 is R.sup.24-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.23 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0392] In embodiments, R.sup.23 is R.sup.24-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.23 is
R.sup.24-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.23 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0393] In embodiments, R.sup.23 is R.sup.24-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.23 is R.sup.24-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.23 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0394] In embodiments, R.sup.23 is R.sup.24-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.23 is R.sup.24-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.23 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0395] R.sup.24 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.25-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.25-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.25-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.25-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.25-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.25-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0396] In embodiments, R.sup.24 is R.sup.25-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.24 is
R.sup.25-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.24 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0397] In embodiments, R.sup.24 is R.sup.25-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.24 is R.sup.25-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.24 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0398] In embodiments, R.sup.24 is R.sup.25-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.24 is R.sup.25-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.24 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0399] In embodiments, R.sup.24 is R.sup.25-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.24 is
R.sup.25-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.24 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0400] In embodiments, R.sup.24 is R.sup.25-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.24 is R.sup.25-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.24 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0401] In embodiments, R.sup.24 is R.sup.25-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.24 is R.sup.25-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.24 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0402] R.sup.26 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.27-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.27-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.27-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.27-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.27-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.27-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0403] In embodiments, R.sup.26 is R.sup.27-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.26 is
R.sup.27-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.26 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0404] In embodiments, R.sup.26 is R.sup.27-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.26 is R.sup.27-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.26 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0405] In embodiments, R.sup.26 is R.sup.27-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.26 is R.sup.27-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.26 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0406] In embodiments, R.sup.26 is R.sup.27-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.26 is
R.sup.27-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.26 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0407] In embodiments, R.sup.26 is R.sup.27-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.26 is R.sup.27-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.26 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, Cio aryl, or phenyl).
[0408] In embodiments, R.sup.26 is R.sup.27-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.26 is R.sup.27-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.26 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0409] R.sup.27 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.28-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.28-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.28-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.28-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.28-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.28-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0410] In embodiments, R.sup.27 is R.sup.28-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.27 is
R.sup.28-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.27 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0411] In embodiments, R.sup.27 is R.sup.28-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.27 is R.sup.28-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.27 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0412] In embodiments, R.sup.27 is R.sup.28-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.27 is R.sup.28-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.27 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0413] In embodiments, R.sup.27 is R.sup.28-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.27 is
R.sup.28-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.27 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0414] In embodiments, R.sup.27 is R.sup.28-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.27 is R.sup.28-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.27 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0415] In embodiments, R.sup.27 is R.sup.28-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.27 is R.sup.28-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.27 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0416] R.sup.29 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.30-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.30-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.30-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.30-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.30-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.30-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl). In embodiments, R.sup.29 is oxo. In embodiments,
R.sup.29 is --CH.sub.3. In embodiments, R.sup.29 is --COOH. In
embodiments, R.sup.29 is --NHC(O)NH.sub.2. In embodiments, R.sup.29
is --OH. In embodiments, R.sup.29 is --NH.sub.2. In embodiments,
R.sup.29 is --CONH.sub.2. In embodiments, R.sup.29 is
--NHC(O)OH.
[0417] In embodiments, R.sup.29 is --SO.sub.2CH.sub.3. In
embodiments, R.sup.29 is --NHSO.sub.2CH.sub.3. In embodiments,
R.sup.29 is --SO.sub.2CH.sub.2CH.sub.3. In embodiments, R.sup.29 is
--SO.sub.2R.sup.30. In embodiments, R.sup.29 is
--SO.sub.2CH(CH.sub.3).sub.2.
[0418] In embodiments, R.sup.29 is R.sup.30-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.29 is
R.sup.30-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.29 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0419] In embodiments, R.sup.29 is R.sup.30-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.29 is R.sup.30-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.29 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0420] In embodiments, R.sup.29 is R.sup.30-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.29 is R.sup.30-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.29 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0421] In embodiments, R.sup.29 is R.sup.30-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.29 is
R.sup.30-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.29 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0422] In embodiments, R.sup.29 is R.sup.30-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.29 is R.sup.30-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.29 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0423] In embodiments, R.sup.29 is R.sup.30-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.29 is R.sup.30-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.29 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0424] R.sup.30 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.31-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.31-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.31-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.31-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.31-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.31-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0425] In embodiments, R.sup.30 is R.sup.31-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.30 is
R.sup.31-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.30 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0426] In embodiments, R.sup.30 is R.sup.31-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.30 is R.sup.31-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.30 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0427] In embodiments, R.sup.30 is R.sup.31-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.30 is R.sup.31-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.30 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0428] In embodiments, R.sup.30 is R.sup.31-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.30 is
R.sup.31-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.30 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0429] In embodiments, R.sup.30 is R.sup.31-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.30 is R.sup.31-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.30 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0430] In embodiments, R.sup.30 is R.sup.31-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.30 is R.sup.31-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.30 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0431] R.sup.32 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.3.3-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.3.3-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.3.3-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.3.3-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.3.3-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.3.3-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0432] In embodiments, R.sup.32 is R.sup.33-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.32 is
R.sup.33-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.32 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0433] In embodiments, R.sup.32 is R.sup.33-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.32 is R.sup.3.3-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.32 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0434] In embodiments, R.sup.32 is R.sup.33-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.32 is R.sup.33-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.32 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0435] In embodiments, R.sup.32 is R.sup.33-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.32 is
R.sup.33-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.32 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0436] In embodiments, R.sup.32 is R.sup.33-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.32 is R.sup.33-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.32 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0437] In embodiments, R.sup.32 is R.sup.33-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.32 is R.sup.33-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.32 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0438] R.sup.33 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.34-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.34-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.34-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.34-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.34-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.34-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0439] In embodiments, R.sup.33 is R.sup.34-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.33 is
R.sup.34-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.3.3 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0440] In embodiments, R.sup.33 is R.sup.34-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.3.3 is R.sup.34-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.3.3 is an
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl).
[0441] In embodiments, R.sup.33 is R.sup.34-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.33 is R.sup.34-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.3.3 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0442] In embodiments, R.sup.33 is R.sup.34-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.33 is
R.sup.34-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.33 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0443] In embodiments, R.sup.33 is R.sup.34-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.33 is R.sup.34-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.3.3 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0444] In embodiments, R.sup.33 is R.sup.34-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.3.3 is R.sup.34-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.33 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0445] R.sup.35 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.36-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.36-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.36-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.36-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.36-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.36-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0446] In embodiments, R.sup.35 is R.sup.36-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.35 is
R.sup.36-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.35 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0447] In embodiments, R.sup.35 is R.sup.36-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.35 is R.sup.36-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.35 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0448] In embodiments, R.sup.35 is R.sup.36-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.35 is R.sup.36-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.35 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0449] In embodiments, R.sup.35 is R.sup.36-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.35 is
R.sup.36-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.35 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0450] In embodiments, R.sup.35 is R.sup.36-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.35 is R.sup.36-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.35 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0451] In embodiments, R.sup.35 is R.sup.36-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.35 is R.sup.36-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.35 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0452] R.sup.36 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.37-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.37-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.37-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.37-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.37-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.37-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0453] In embodiments, R.sup.36 is R.sup.37-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.36 is
R.sup.37-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.36 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0454] In embodiments, R.sup.36 is R.sup.37-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.36 is R.sup.37-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.36 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0455] In embodiments, R.sup.36 is R.sup.37-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.36 is R.sup.37-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.36 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0456] In embodiments, R.sup.36 is R.sup.37-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.36 is
R.sup.37-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.36 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0457] In embodiments, R.sup.36 is R.sup.37-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.36 is R.sup.37-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.36 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0458] In embodiments, R.sup.36 is R.sup.37-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.36 is R.sup.37-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.36 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0459] R.sup.38 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.39-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.39-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.39-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.39-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.39-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.39-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0460] In embodiments, R.sup.38 is R.sup.39-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.38 is
R.sup.39-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.38 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.5 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0461] In embodiments, R.sup.38 is R.sup.39-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.38 is R.sup.39-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.38 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0462] In embodiments, R.sup.38 is R.sup.39-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.38 is R.sup.39-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.38 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0463] In embodiments, R.sup.38 is R.sup.39-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.38 is
R.sup.39-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.38 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0464] In embodiments, R.sup.38 is R.sup.39-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.38 is R.sup.39-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.38 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0465] In embodiments, R.sup.38 is R.sup.39-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.38 is R.sup.39-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.38 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0466] R.sup.39 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.40-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.40-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.40-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.40-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.40-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.40-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0467] In embodiments, R.sup.39 is R.sup.40-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.39 is
R.sup.40-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.39 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0468] In embodiments, R.sup.39 is R.sup.40-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.39 is R.sup.40-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.39 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0469] In embodiments, R.sup.39 is R.sup.40-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.39 is R.sup.40-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.39 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0470] In embodiments, R.sup.39 is R.sup.40-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.39 is
R.sup.40-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.39 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0471] In embodiments, R.sup.39 is R.sup.40-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.39 is R.sup.40-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.39 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0472] In embodiments, R.sup.39 is R.sup.40-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.39 is R.sup.40-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.39 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0473] R.sup.41 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.42-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.42-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.42-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.42-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.42-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.42-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0474] In embodiments, R.sup.41 is R.sup.42-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.41 is
R.sup.42-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.41 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0475] In embodiments, R.sup.41 is R.sup.42-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.41 is R.sup.42-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.41 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0476] In embodiments, R.sup.41 is R.sup.42-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.41 is R.sup.42-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.41 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0477] In embodiments, R.sup.41 is R.sup.42-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.41 is
R.sup.42-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.41 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0478] In embodiments, R.sup.41 is R.sup.42-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.41 is R.sup.42-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.41 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0479] In embodiments, R.sup.41 is R.sup.42-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.41 is R.sup.42-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.41 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0480] R.sup.42 is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.43-substituted or unsubstituted alkyl (e.g., C.sub.1-C.sub.8
alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl),
R.sup.43-substituted or unsubstituted heteroalkyl (e.g., 2 to 8
membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.43-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.43-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.43-substituted or unsubstituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or
R.sup.43-substituted or unsubstituted heteroaryl (e.g., 5 to 10
membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6 membered
heteroaryl).
[0481] In embodiments, R.sup.42 is R.sup.43-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.42 is
R.sup.43-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.42 is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0482] In embodiments, R.sup.42 is R.sup.43-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.42 is R.sup.43-substituted heteroalkyl (e.g., 2
to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl). In embodiments, R.sup.42 is an unsubstituted
heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered
heteroalkyl, or 2 to 4 membered heteroalkyl).
[0483] In embodiments, R.sup.42 is R.sup.43-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.42 is R.sup.43-substituted cycloalkyl (e.g.,
C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.42 is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0484] In embodiments, R.sup.42 is R.sup.43-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.42 is
R.sup.43-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.42 is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0485] In embodiments, R.sup.42 is R.sup.43-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.42 is R.sup.43-substituted aryl
(e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.42 is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0486] In embodiments, R.sup.42 is R.sup.43-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.42 is R.sup.43-substituted heteroaryl (e.g., 5
to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to 6
membered heteroaryl). In embodiments, R.sup.42 is an unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0487] R.sup.41.2B is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.42.2B-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.42.2B-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.42.2B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.42.2B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.42.2B-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl), or R.sup.42.2B-substituted or unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0488] In embodiments, R.sup.41.2B is R.sup.42.2B-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.41.2B is
R.sup.42.2B-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.41.2B is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0489] In embodiments, R.sup.41.2B is R.sup.42.2B-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.41.2B is R.sup.42.2B-substituted heteroalkyl
(e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or
2 to 4 membered heteroalkyl). In embodiments, R.sup.41.2B is an
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl).
[0490] In embodiments, R.sup.41.2B is R.sup.42.2B-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.41.2B is R.sup.42.2B-substituted cycloalkyl
(e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.41.2B is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0491] In embodiments, R.sup.41.2B is R.sup.42.2B-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.41.2B is
R.sup.42.2B-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.41.2B is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0492] In embodiments, R.sup.41.2B is R.sup.42.2B-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.41.2B is R.sup.42.2B-substituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.41.2B is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0493] In embodiments, R.sup.41.2B is R.sup.42.2B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.41.2B is R.sup.42.2B-substituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl). In embodiments, R.sup.41.2B is an
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0494] R.sup.42.2B is independently oxo, halogen, --CCl.sub.3,
--CBr.sub.3, --CF.sub.3, --CI.sub.3, --CN, --OH, --NH.sub.2,
--COOH, --CONH.sub.2, --NO.sub.2, --SH, --SO.sub.3H, --SO.sub.4H,
--SO.sub.2NH.sub.2, --NHNH.sub.2, --ONH.sub.2, --NHC(O)NHNH.sub.2,
--NHC(O)NH.sub.2, --NHSO.sub.2H, --NHC(O)H, --NHC(O)OH, --NHOH,
--OCCl.sub.3, --OCF.sub.3, --OCBr.sub.3, --OCI.sub.3,
--OCHCl.sub.2, --OCHBr.sub.2, --OCHI.sub.2, --OCHF.sub.2,
R.sup.43.2B-substituted or unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), R.sup.43.2B-substituted or unsubstituted heteroalkyl (e.g.,
2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4
membered heteroalkyl), R.sup.43.2B-substituted or unsubstituted
cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6
cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl), R.sup.43.2B-substituted
or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), R.sup.43.2B-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl), or R.sup.43.2B-substituted or unsubstituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl).
[0495] In embodiments, R.sup.42.2B is R.sup.43.2B-substituted or
unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments, R.sup.42.2B is
R.sup.43.2B-substituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl). In embodiments,
R.sup.42.2B is an unsubstituted alkyl (e.g., C.sub.1-C.sub.8 alkyl,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4 alkyl).
[0496] In embodiments, R.sup.42.2B is R.sup.43.2B-substituted or
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl). In
embodiments, R.sup.42.2B is R.sup.43.2B-substituted heteroalkyl
(e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or
2 to 4 membered heteroalkyl). In embodiments, R.sup.42.2B is an
unsubstituted heteroalkyl (e.g., 2 to 8 membered heteroalkyl, 2 to
6 membered heteroalkyl, or 2 to 4 membered heteroalkyl).
[0497] In embodiments, R.sup.42.2B is R.sup.43.2B-substituted or
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl). In
embodiments, R.sup.42.2B is R.sup.43.2B-substituted cycloalkyl
(e.g., C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or
C.sub.5-C.sub.6 cycloalkyl). In embodiments, R.sup.42.2B is an
unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6 cycloalkyl).
[0498] In embodiments, R.sup.42.2B is R.sup.43.2B-substituted or
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.42.2B is
R.sup.43.2B-substituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl). In embodiments, R.sup.42.2B is an
unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl).
[0499] In embodiments, R.sup.42.2B is R.sup.43.2B-substituted or
unsubstituted aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or
phenyl). In embodiments, R.sup.42.2B is R.sup.43.2B-substituted
aryl (e.g., C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl). In
embodiments, R.sup.42.2B is an unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl).
[0500] In embodiments, R.sup.42.2B is R.sup.43.2B-substituted or
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl). In
embodiments, R.sup.42.2B is R.sup.43.2B-substituted heteroaryl
(e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or
5 to 6 membered heteroaryl). In embodiments, R.sup.42.2B is an
unsubstituted heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9
membered heteroaryl, or 5 to 6 membered heteroaryl).
[0501] R.sup.13, R.sup.16, R.sup.19, R.sup.19.2, R.sup.19.3,
R.sup.22, R.sup.25, R.sup.28, R.sup.31, R.sup.34, R.sup.37,
R.sup.40, R.sup.43, and R.sup.43.2B are independently hydrogen,
oxo, halogen, --CCl.sub.3, --CBr.sub.3, --CF.sub.3, --CI.sub.3,
--CN, --OH, --NH.sub.2, --COOH, --CONH.sub.2, --NO.sub.2, --SH,
--SO.sub.3H, --SO.sub.4H, --SO.sub.2NH.sub.2, --NHNH.sub.2,
--ONH.sub.2, --NHC(O)NHNH.sub.2, --NHC(O)NH.sub.2, --NHSO.sub.2H,
--NHC(O)H, --NHC(O)OH, --NHOH, --OCCl.sub.3, --OCF.sub.3,
--OCBr.sub.3, --OCI.sub.3, --OCHCl.sub.2, --OCHBr.sub.2,
--OCHI.sub.2, --OCHF.sub.2, unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), unsubstituted heteroalkyl (e.g., 2 to 8 membered
heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4 membered
heteroalkyl), unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8
cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6
cycloalkyl), unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0502] R.sup.11A, R.sup.11B, R.sup.11C, R.sup.11D, R.sup.14A,
R.sup.14B, R.sup.14C, R.sup.14D, R.sup.17A, R.sup.17B, R.sup.17C,
R.sup.17D, R.sup.17.2A, R.sup.17.2B, R.sup.17.2C, R.sup.17.2D,
R.sup.17.3A, R.sup.17.3B, R.sup.17.3C, R.sup.17.3D, R.sup.20A,
R.sup.20B, R.sup.20C, R.sup.20D, R.sup.23A, R.sup.23B, R.sup.23C,
R.sup.23D, R.sup.26A, R.sup.26B, R.sup.26C, R.sup.26D, R.sup.29A,
R.sup.29B, R.sup.29C, R.sup.29D, R.sup.32A, R.sup.32B, R.sup.32C,
R.sup.32D, R.sup.35A, R.sup.35B, R.sup.35C, R.sup.35D, R.sup.38A,
R.sup.38B, R.sup.38C, and R.sup.38D are independently hydrogen,
oxo, halogen, --CCl.sub.3, --CBr.sub.3, --CF.sub.3, --CI.sub.3,
--CN, --OH, --NH.sub.2, --COOH, --CONH.sub.2, --NO.sub.2, --SH,
--SO.sub.3H, --SO.sub.4H, --SO.sub.2NH.sub.2, --NHNH.sub.2,
--ONH.sub.2, --NHC(O)NHNH.sub.2, --NHC(O)NH.sub.2, --NHSO.sub.2H,
--NHC(O)H, --NHC(O)OH, --NHOH, --OCCl.sub.3, --OCF.sub.3,
--OCBr.sub.3, --OCI.sub.3, --OCHCl.sub.2, --OCHBr.sub.2,
--OCHI.sub.2, --OCHF.sub.2, unsubstituted alkyl (e.g.,
C.sub.1-C.sub.8 alkyl, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.4
alkyl), unsubstituted heteroalkyl (e.g., 2 to 8 membered
heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4 membered
heteroalkyl), unsubstituted cycloalkyl (e.g., C.sub.3-C.sub.8
cycloalkyl, C.sub.3-C.sub.6 cycloalkyl, or C.sub.5-C.sub.6
cycloalkyl), unsubstituted heterocycloalkyl (e.g., 3 to 8 membered
heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6
membered heterocycloalkyl), unsubstituted aryl (e.g.,
C.sub.6-C.sub.10 aryl, C.sub.10 aryl, or phenyl), or unsubstituted
heteroaryl (e.g., 5 to 10 membered heteroaryl, 5 to 9 membered
heteroaryl, or 5 to 6 membered heteroaryl).
[0503] In embodiments, X.sup.11 is --Cl. In embodiments, X.sup.1.1
is --F. In embodiments, X.sup.1.1 is --Br. In embodiments,
X.sup.1.1 is --I. In embodiments, X.sup.2.1 is --Cl. In
embodiments, X.sup.2.1 is --F. In embodiments, X.sup.2.1 is --Br.
In embodiments, X.sup.2.1 is --I. In embodiments, X.sup.3.1 is
--Cl. In embodiments, X.sup.3.1 is --F. In embodiments, X.sup.3.1
is --Br. In embodiments, X.sup.3.1 is --I. In embodiments,
X.sup.3.2 is --Cl. In embodiments, X.sup.3.2 is --F. In
embodiments, X.sup.3.2 is --Br. In embodiments, X.sup.3.2 is --I.
In embodiments, X.sup.3.3 is --Cl. In embodiments, X.sup.3.3 is
--F. In embodiments, X.sup.3.3 is --Br. In embodiments, X.sup.3.3
is --I. In embodiments, X.sup.4.1 is --Cl. In embodiments,
X.sup.4.1 is --F. In embodiments, X.sup.4.1 is --Br. In
embodiments, X.sup.4.1 is --I. In embodiments, X.sup.5.1 is --Cl.
In embodiments, X.sup.5.1 is --F. In embodiments, X.sup.5.1 is
--Br. In embodiments, X.sup.5.1 is --I. In embodiments, X.sup.6.1
is --Cl. In embodiments, X.sup.6.1 is --F. In embodiments,
X.sup.6.1 is --Br. In embodiments, X.sup.6.1 is --I. In
embodiments, X.sup.7.1 is --Cl. In embodiments, X.sup.7.1 is --F.
In embodiments, X.sup.7.1 is --Br. In embodiments, X.sup.7.1 is
--I. In embodiments, X.sup.8.1 is --Cl. In embodiments, X.sup.8.1
is --F. In embodiments, X.sup.8.1 is --Br. In embodiments,
X.sup.8.1 is --I. In embodiments, X.sup.9.1 is --Cl. In
embodiments, X.sup.9.1 is --F. In embodiments, X.sup.9.1 is --Br.
In embodiments, X.sup.9.1 is --I. In embodiments, X.sup.10.1 is
--Cl. In embodiments, X.sup.10.1 is --F. In embodiments, X.sup.10.1
is --Br. In embodiments, X.sup.10.1 is --I.
[0504] In embodiments, X.sup.1.1 is --Cl, and X.sup.1 is N. In
embodiments, X.sup.1.1 is --F, and X.sup.1.1 is N. In embodiments,
X.sup.1.1 is --Br, and X.sup.1 is N. In embodiments, X.sup.1.1 is
--I, and X.sup.1 is N. In embodiments, X.sup.2.1 is --Cl, and
X.sup.1 is N. In embodiments, X.sup.2.1 is --F, and X.sup.1 is N.
In embodiments, X.sup.2.1 is --Br, and X.sup.1 is N. In
embodiments, X.sup.2.1 is --I, and X.sup.1 is N. In embodiments,
X.sup.3.1 is --Cl, and X.sup.1 is N. In embodiments, X.sup.3.1 is
--F, and X.sup.1 is N. In embodiments, X.sup.3.1 is --Br, and
X.sup.1 is N. In embodiments, X.sup.3.1 is --I, and X.sup.1 is N.
In embodiments, X.sup.4.1 is --Cl, and X.sup.1 is N. In
embodiments, X.sup.4.1 is --F, and X.sup.1 is N. In embodiments,
X.sup.4.1 is --Br, and X.sup.1 is N. In embodiments, X.sup.4.1 is
--I, and X.sup.1 is N. In embodiments, X.sup.5.1 is --Cl, and
X.sup.1 is N. In embodiments, X.sup.5.1 is --F, and X.sup.1 is N.
In embodiments, X.sup.5.1 is --Br, and X.sup.1 is N. In
embodiments, X.sup.5.1 is --I, and X.sup.1 is N. In embodiments,
X.sup.6.1 is --Cl, and X.sup.1 is N. In embodiments, X.sup.6.1 is
--F, and X.sup.1 is N. In embodiments, X.sup.6.1 is --Br, and
X.sup.1 is N. In embodiments, X.sup.6.1 is --I, and X.sup.1 is N.
In embodiments, X.sup.7.1 is --Cl, and X.sup.1 is N. In
embodiments, X.sup.7.1 is --F, and X.sup.1 is N. In embodiments,
X.sup.7.1 is --Br, and X.sup.1 is N. In embodiments, X.sup.7.1 is
--I, and X.sup.1 is N. In embodiments, X.sup.8.1 is --Cl, and
X.sup.1 is N. In embodiments, X.sup.8.1 is --F, and X.sup.1 is N.
In embodiments, X.sup.8.1 is --Br, and X.sup.1 is N. In
embodiments, X.sup.8.1 is --I, and X.sup.1 is N. In embodiments,
X.sup.9.1 is --Cl, and X.sup.1 is N. In embodiments, X.sup.9.1 is
--F, and X.sup.1 is N. In embodiments, X.sup.9.1 is --Br, and
X.sup.1 is N. In embodiments, X.sup.9.1 is --I, and X.sup.1 is N.
In embodiments, X.sup.10.1 is --C.sub.1, and X.sup.1 is N. In
embodiments, X.sup.10.1 is --F, and X.sup.1 is N. In embodiments,
X.sup.10.1 is --Br, and X.sup.1 is N. In embodiments, X.sup.101 is
--I, and X.sup.1 is N.
[0505] In embodiments, X.sup.1.1 is --Cl, and X.sup.2 is N. In
embodiments, X.sup.1.1 is --F, and X.sup.2 is N. In embodiments,
X.sup.1.1 is --Br, and X.sup.2 is N. In embodiments, X.sup.1.1 is
--I, and X.sup.2 is N. In embodiments, X.sup.2.1 is --Cl, and
X.sup.2 is N. In embodiments, X.sup.2.1 is --F, and X.sup.2 is N.
In embodiments, X.sup.2.1 is --Br, and X.sup.2 is N. In
embodiments, X.sup.2.1 is --I, and X.sup.2 is N. In embodiments,
X.sup.3.1 is --Cl, and X.sup.2 is N. In embodiments, X.sup.3.1 is
--F, and X.sup.2 is N. In embodiments, X.sup.3.1 is --Br, and
X.sup.2 is N. In embodiments, X.sup.3.1 is --I, and X.sup.2 is N.
In embodiments, X.sup.4.1 is --Cl, and X.sup.2 is N. In
embodiments, X.sup.4.1 is --F, and X.sup.2 is N. In embodiments,
X.sup.4.1 is --Br, and X.sup.2 is N. In embodiments, X.sup.4.1 is
--I, and X.sup.2 is N. In embodiments, X.sup.5.1 is --Cl, and
X.sup.2 is N. In embodiments, X.sup.5.1 is --F, and X.sup.2 is N.
In embodiments, X.sup.5.1 is --Br, and X.sup.2 is N. In
embodiments, X.sup.5.1 is --I, and X.sup.2 is N. In embodiments,
X.sup.6.1 is --Cl, and X.sup.2 is N. In embodiments, X.sup.6.1 is
--F, and X.sup.2 is N. In embodiments, X.sup.6.1 is --Br, and
X.sup.2 is N. In embodiments, X.sup.6.1 is --I, and X.sup.2 is N.
In embodiments, X.sup.7.1 is --Cl, and X.sup.2 is N. In
embodiments, X.sup.7.1 is --F, and X.sup.2 is N. In embodiments,
X.sup.7.1 is --Br, and X.sup.2 is N. In embodiments, X.sup.7.1 is
--I, and X.sup.2 is N. In embodiments, X.sup.8.1 is --Cl, and
X.sup.2 is N. In embodiments, X.sup.8.1 is --F, and X.sup.2 is N.
In embodiments, X.sup.8.1 is --Br, and X.sup.2 is N. In
embodiments, X.sup.8.1 is --I, and X.sup.2 is N. In embodiments,
X.sup.9.1 is --Cl, and X.sup.2 is N. In embodiments, X.sup.9.1 is
--F, and X.sup.2 is N. In embodiments, X.sup.9.1 is --Br, and
X.sup.2 is N. In embodiments, X.sup.9.1 is --I, and X.sup.2 is N.
In embodiments, X.sup.10.1 is --C.sub.1, and X.sup.2 is N. In
embodiments, X.sup.10.1 is --F, and X.sup.2 is N. In embodiments,
X.sup.10.1 is --Br, and X.sup.2 is N. In embodiments, X.sup.10.1 is
--I, and X.sup.2 is N.
[0506] In embodiments, X.sup.1.1 is --Cl, and X.sup.3 is N. In
embodiments, X.sup.1.1 is --F, and X.sup.3 is N. In embodiments,
X.sup.1.1 is --Br, and X.sup.3 is N. In embodiments, X.sup.1.1 is
--I, and X.sup.3 is N. In embodiments, X.sup.2.1 is --Cl, and
X.sup.3 is N. In embodiments, X.sup.2.1 is --F, and X.sup.3 is N.
In embodiments, X.sup.2.1 is --Br, and X.sup.3 is N. In
embodiments, X.sup.2.1 is --I, and X.sup.3 is N. In embodiments,
X.sup.3.1 is --C.sub.1, and X.sup.3 is N. In embodiments, X.sup.3.1
is --F, and X.sup.3 is N. In embodiments, X.sup.3.1 is --Br, and
X.sup.3 is N. In embodiments, X.sup.3.1 is --I, and X.sup.3 is N.
In embodiments, X.sup.4.1 is --Cl, and X.sup.3 is N. In
embodiments, X.sup.4.1 is --F, and X.sup.3 is N. In embodiments,
X.sup.4.1 is --Br, and X.sup.3 is N. In embodiments, X.sup.4.1 is
--I, and X.sup.3 is N. In embodiments, X.sup.5.1 is --Cl, and
X.sup.3 is N. In embodiments, X.sup.5.1 is --F, and X.sup.3 is N.
In embodiments, X.sup.51 is --Br, and X.sup.3 is N. In embodiments,
X.sup.5.1 is --I, and X.sup.3 is N. In embodiments, X.sup.6.1 is
--Cl, and X.sup.3 is N. In embodiments, X.sup.6.1 is --F, and
X.sup.3 is N. In embodiments, X.sup.6.1 is --Br, and X.sup.3 is N.
In embodiments, X.sup.6.1 is --I, and X.sup.3 is N. In embodiments,
X.sup.7.1 is --Cl, and X.sup.3 is N. In embodiments, X.sup.7.1 is
--F, and X.sup.3 is N. In embodiments, X.sup.7.1 is --Br, and
X.sup.3 is N. In embodiments, X.sup.7.1 is --I, and X.sup.3 is N.
In embodiments, X.sup.8.1 is --Cl, and X.sup.3 is N. In
embodiments, X.sup.8.1 is --F, and X.sup.3 is N. In embodiments,
X.sup.8.1 is --Br, and X.sup.3 is N. In embodiments, X.sup.8.1 is
--I, and X.sup.3 is N. In embodiments, X.sup.9.1 is --Cl, and
X.sup.3 is N. In embodiments, X.sup.9.1 is --F, and X.sup.3 is N.
In embodiments, X.sup.9.1 is --Br, and X.sup.3 is N. In
embodiments, X.sup.9.1 is --I, and X.sup.3 is N. In embodiments,
X.sup.10.1 is --Cl, and X.sup.3 is N. In embodiments, X.sup.10.1 is
--F, and X.sup.3 is N. In embodiments, X.sup.10.1 is --Br, and
X.sup.3 is N. In embodiments, X.sup.10.1 is --I, and X.sup.3 is
N.
[0507] In embodiments, n1 is 0. In embodiments, n1 is 1. In
embodiments, n1 is 2. In embodiments, n1 is 3. In embodiments, n1
is 4. In embodiments, n2 is 0. In embodiments, n2 is 1. In
embodiments, n2 is 2. In embodiments, n2 is 3. In embodiments, n2
is 4. In embodiments, n3 is 0. In embodiments, n3 is 1. In
embodiments, n3 is 2. In embodiments, n3 is 3. In embodiments, n3
is 4. In embodiments, n3.2 is 0. In embodiments, n3.2 is 1. In
embodiments, n3.2 is 2. In embodiments, n3.2 is 3. In embodiments,
n3.2 is 4. In embodiments, n3.3 is 0. In embodiments, n3.3 is 1. In
embodiments, n3.3 is 2. In embodiments, n3.3 is 3. In embodiments,
n3.3 is 4. In embodiments, n4 is 0. In embodiments, n4 is 1. In
embodiments, n4 is 2. In embodiments, n4 is 3. In embodiments, n4
is 4. In embodiments, n5 is 0. In embodiments, n5 is 1. In
embodiments, n5 is 2. In embodiments, n5 is 3. In embodiments, n5
is 4. In embodiments, n6 is 0. In embodiments, n6 is 1. In
embodiments, n6 is 2. In embodiments, n6 is 3. In embodiments, n6
is 4. In embodiments, n7 is 0. In embodiments, n7 is 1. In
embodiments, n7 is 2. In embodiments, n7 is 3. In embodiments, n7
is 4. In embodiments, n8 is 0. In embodiments, n8 is 1. In
embodiments, n8 is 2. In embodiments, n8 is 3. In embodiments, n8
is 4. In embodiments, n8 is 0. In embodiments, n8 is 1. In
embodiments, n8 is 2. In embodiments, n8 is 3. In embodiments, n8
is 4. In embodiments, n9 is 0. In embodiments, n9 is 1. In
embodiments, n9 is 2. In embodiments, n9 is 3. In embodiments, n9
is 4. In embodiments, n10 is 0. In embodiments, n10 is 1. In
embodiments, n10 is 2. In embodiments, n10 is 3. In embodiments,
n10 is 4.
[0508] In embodiments, m1 is 1. In embodiments, m1 is 2. In
embodiments, v1 is 1. In embodiments, v1 is 2. In embodiments, m2
is 1. In embodiments, m2 is 2. In embodiments, v2 is 1. In
embodiments, v2 is 2. In embodiments, m3 is 1. In embodiments, m3
is 2. In embodiments, v3 is 1. In embodiments, v3 is 2. In
embodiments, m3.2 is 1. In embodiments, m3.2 is 2. In embodiments,
v3.2 is 1. In embodiments, v3.2 is 2. In embodiments, m3.3 is 1. In
embodiments, m3.3 is 2. In embodiments, v3.3 is 1. In embodiments,
v3.3 is 2. In embodiments, m4 is 1. In embodiments, m4 is 2. In
embodiments, v4 is 1. In embodiments, v4 is 2. In embodiments, m5
is 1. In embodiments, m5 is 2. In embodiments, v5 is 1. In
embodiments, v5 is 2. In embodiments, m6 is 1. In embodiments, m6
is 2. In embodiments, v6 is 1. In embodiments, v6 is 2. In
embodiments, m7 is 1. In embodiments, m7 is 2. In embodiments, v7
is 1. In embodiments, v7 is 2. In embodiments, m8 is 1. In
embodiments, m8 is 2. In embodiments, v8 is 1. In embodiments, v8
is 2. In embodiments, m9 is 1. In embodiments, m9 is 2. In
embodiments, v9 is 1. In embodiments, v9 is 2. In embodiments, m10
is 1. In embodiments, m10 is 2. In embodiments, v10 is 1. In
embodiments, v10 is 2.
[0509] In embodiments, z1 is 0. In embodiments, z1 is 1. In
embodiments, z1 is 2. In embodiments, z1 is 3. In embodiments, z1
is 4. In embodiments, z1 is 5.
[0510] In embodiments, z2 is 0. In embodiments, z2 is 1. In
embodiments, z2 is 2. In embodiments, z2 is 3. In embodiments, z2
is 4. In embodiments, z2 is 5.
[0511] In embodiments, z3 is 0. In embodiments, z3 is 1. In
embodiments, z3 is 2. In embodiments, z3 is 3. In embodiments, z3
is 4. In embodiments, z3 is 5. In embodiments, z3 is 6. In
embodiments, z3 is 7. In embodiments, z3 is 8. In embodiments, z3
is 9. In embodiments, z3 is 10. In embodiments, z3 is 11.
[0512] In embodiments, z4 is 0. In embodiments, z4 is 1. In
embodiments, z4 is 2.
[0513] In embodiments, z1 is 2, z2 is 0, z4 is 1, and R.sup.7 is
hydrogen, substituted or unsubstituted alkyl, phenyl, --F, --OH,
--CH.sub.2OH, --(CH.sub.2).sub.2OH, --(CH.sub.2).sub.3OH,
--C(CH.sub.3).sub.2OH, --CH.sub.2SO.sub.2NH.sub.2,
--(CH.sub.2).sub.2SO.sub.2NH.sub.2, --CH.sub.2C(O)NH.sub.2,
--(CH.sub.2).sub.2C(O)NH.sub.2, --(CH.sub.2).sub.3C(O)NH.sub.2,
--CH.sub.2NHSO.sub.2CF.sub.3, --(CH.sub.2).sub.2NHSO.sub.2CF.sub.3,
--(CH.sub.2).sub.3NHSO.sub.2CF.sub.3, --CH.sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.3NHSO.sub.2CH.sub.3, --CH.sub.2SO.sub.2CH.sub.3,
--(CH.sub.2).sub.2SO.sub.2CH.sub.3, --CH.sub.2SO.sub.2NH.sub.2 or
--(CH.sub.2).sub.2SO.sub.2NH.sub.2.
[0514] In embodiments, R.sup.1 and R.sup.2 are independently
hydrogen, substituted or unsubstituted alkyl or substituted or
unsubstituted heteroalkyl. In embodiments, R.sup.1 and R.sup.2 are
independently hydrogen, R.sup.1-substituted or unsubstituted alkyl
or R.sup.11-substituted or unsubstituted heteroalkyl. In
embodiments, R.sup.1 and R.sup.2 are hydrogen.
[0515] In embodiments, the compound has structural Formula
(II):
##STR00004##
or a pharmaceutically acceptable salt thereof, wherein R.sup.1,
R.sup.2, R.sup.4, X.sup.2, X.sup.3, z4, L.sup.7, and R.sup.7 as
described herein, including embodiments. R.sup.3.2 and R.sup.3.3
may be are substituents encompassed by the definitions of R.sup.3.
In embodiments, R.sup.3.2 is hydrogen, halogen, --CX.sup.3.2.sub.3,
--CHX.sup.3.2.sub.2, --CH.sub.2X.sup.3.2, --CN, --N.sub.3,
--SO.sub.n3.2R.sup.3.2A, --SO.sub.v3.2NR.sup.3.2BR.sup.3.2C,
--NHNR.sup.3.2BR.sup.3.2C, --ONR.sup.3.2BR.sup.3.2C,
--NHC(O)NHNR.sup.3.2BR.sup.3.2C, --NHC(O)NR.sup.3.2BR.sup.3.2C,
--N(O).sub.m3.2, --NR.sup.3.2BR.sup.3.2C, --C(O)R.sup.3.2D,
--C(O)OR.sup.3.2D, --C(O)NR.sup.3.2BR.sup.3.2C, --OR.sup.3.2A,
--NR.sup.3.2BSO.sub.2R.sup.3.2A, --NR.sup.3.2BC(O)R.sup.3.2D,
--NR.sup.3.2BC(O)OR.sup.3.2D, --NR.sup.3.2BOR.sup.3.2D,
--OCX.sup.3.2.sub.3, --OCHX.sup.3.2.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. R.sup.3.3 is hydrogen,
halogen, --CX.sup.3.3.sub.3, --CHX.sup.3.3.sub.2,
--CH.sub.2X.sup.3.3, --CN, --N.sub.3, --SO.sub.n3.3R.sup.3.3A,
--SO.sub.v3.3NR.sup.3.3BR.sup.3.3C, --NHNR.sup.3.3BR.sup.3.3C,
--ONR.sup.3.3BR.sup.3.3C, --NHC(O)NHNR.sup.3.3BR.sup.3.3C,
--NHC(O)NR.sup.3.3BR.sup.3.3C, --N(O).sub.m3.3,
--NR.sup.3.3BR.sup.3.3C, --C(O)R.sup.3.3D, --C(O)OR.sup.3.3D,
--C(O)NR.sup.3.3BR.sup.3.3C, --OR.sup.3.3A,
--NR.sup.3.3BSO.sub.2R.sup.3.3A, --NR.sup.3.3BC(O)R.sup.3.3D,
--NR.sup.3.3BC(O)OR.sup.3.3D, --NR.sup.3.3BOR.sup.3.3D,
--OCX.sup.3.3.sub.3, --OCHX.sup.3.3.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl. The symbols n3.2, and
n3.3 are independently an integer from 0 to 4. The symbols m3.2,
m3.3, v3.2 and v3.3 are independently 1 or 2. In embodiments,
R.sup.4 is hydrogen, --CX.sup.4.1.sub.3, --CN,
--C(O)NR.sup.4BR.sup.4C, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl.
[0516] R.sup.3.2A, R.sup.3.2B, R.sup.3.2C, R.sup.3.2D, R.sup.3.3A,
R.sup.3.3B, R.sup.3.3C and R.sup.3.3D are independently hydrogen,
halogen, --CF.sub.3, --CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH,
--CONH.sub.2, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, or substituted or unsubstituted heteroaryl.
R.sup.3.2BR.sup.3.2C, R.sup.3.2B and R.sup.3.2C substituents bonded
to the same nitrogen atom may optionally be joined to form a
substituted or unsubstituted heterocycloalkyl or substituted or
unsubstituted heteroaryl; and X.sup.3.3 and X.sup.3.3 are
independently --Cl, --Br, --I or --F.
[0517] In embodiments, the compound has structural Formula
(IIa):
##STR00005##
or a pharmaceutically acceptable salt thereof, wherein R.sup.1,
R.sup.2, R.sup.4, X.sup.3, z4, L.sup.7, and R.sup.7 as described
herein, including embodiments.
[0518] In embodiments, wherein the compound has structural Formula
(IIb):
##STR00006##
or a pharmaceutically acceptable salt thereof, wherein R.sup.1,
R.sup.2, R.sup.4, X.sup.2, z4, L.sup.7, and R.sup.7 as described
herein, including embodiments.
[0519] In embodiments, the compound has structural Formula
(IIc):
##STR00007##
or a pharmaceutically acceptable salt thereof wherein R.sup.1,
R.sup.2, R.sup.4, z4, L.sup.7, and R.sup.7 as described herein,
including embodiments. In embodiments, z4 is 1. In embodiments,
R.sup.1 and R.sup.2 are independently hydrogen, substituted or
unsubstituted alkyl or substituted or unsubstituted heteroalkyl. In
embodiments, R.sup.1 is hydrogen. In embodiments, R.sup.2 is
substituted or unsubstituted alkyl. In embodiments, R.sup.4 is
hydrogen, --CN, --C(O)NH.sub.2, --CX.sup.413 or substituted or
unsubstituted alkyl. In embodiments, R.sup.3.2 and R.sup.3.3 are
independently halogen. In embodiments, R.sup.3.2 and R.sup.3.3 are
independently chlorine. In embodiments, R.sup.7 is --OR.sup.7A,
--C(O)R.sup.7D, --C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C,
--SO.sub.n1R.sup.7A, --SO.sub.v1NR.sup.7BR.sup.7C, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl. In embodiments, L.sup.7
is a bond or substituted or unsubstituted alkylene. In embodiments,
L.sup.7 is a bond. In embodiments, L.sup.7 is a bond; and R.sup.7
is hydrogen, substituted or unsubstituted alkyl, phenyl,
--(CH.sub.2).sub.2OH, --CH.sub.2C(CH.sub.3).sub.2OH,
--(CH.sub.2).sub.3OH, --(CH.sub.2).sub.2CH(CH.sub.3).sub.2OH,
--(CH.sub.2).sub.2SO.sub.2NH.sub.2,
--(CH.sub.2).sub.3SO.sub.2NH.sub.2, --(CH.sub.2).sub.2CONH.sub.2,
--(CH.sub.2).sub.3CONH.sub.2--(CH.sub.2).sub.3CON(H)Me,
--(CH.sub.2).sub.3CON(Me).sub.2, --(CH.sub.2).sub.2SO.sub.2Me,
--(CH.sub.2).sub.3SO.sub.2Me, --CH.sub.2CH(OH)Me,
--CH.sub.2CO.sub.2H, --(CH.sub.2).sub.2CO.sub.2H,
--CH(CH.sub.3)CH.sub.2CO.sub.2H, --(CH.sub.2).sub.3CO.sub.2H,
--(CH.sub.2).sub.2SO.sub.2NHCH.sub.3,
--(CH.sub.2).sub.2SO.sub.2N(CH.sub.3).sub.2,
--(CH.sub.2).sub.2SO.sub.2--(N- morpholinyl),
--(CH.sub.2).sub.2NHCOCH.sub.3, --(CH.sub.2).sub.3NHCOCH.sub.3,
--(CH.sub.2).sub.2NHCOCH(CH.sub.3).sub.2,
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2CF.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2NHCH(CH.sub.3).sub.2,
--CH.sub.2CH(CH.sub.3)CH.sub.2OH (R and S),
--CH(CH.sub.3)(CH.sub.2).sub.2OH, --CH.sub.2-(2-imidazoyl),
--CH.sub.2-(4-imidazoyl), --CH.sub.2-(3-pyrazoyl),
4-tetrahydropyranyl, 3-oxetanyl, --(CH.sub.2).sub.2NHCO.sub.2Me,
--(CH.sub.2).sub.3NHCO.sub.2Me.
[0520] In embodiments, the compound has structural Formula
(IId):
##STR00008##
or a pharmaceutically acceptable salt thereof, wherein R.sup.1,
R.sup.2, R.sup.4, z4, L.sup.7, and R.sup.7 as described herein,
including embodiments. In embodiments, z4 is 1. In embodiments,
R.sup.1 and R.sup.2 are independently hydrogen, substituted or
unsubstituted alkyl or substituted or unsubstituted heteroalkyl. In
embodiments, R.sup.1 is hydrogen. In embodiments, R.sup.2 is
substituted or unsubstituted alkyl. In embodiments, R.sup.4 is
hydrogen, --CN, --C(O)NH.sub.2, --CX.sup.4.1.sub.3 or substituted
or unsubstituted alkyl. In embodiments, R.sup.4 is --CN,
--C(O)NH.sub.2, --CF.sub.3 or --CH.sub.3. In embodiments, R.sup.3.2
and R.sup.3.3 are independently halogen. In embodiments, R.sup.3.2
and R.sup.3.3 are independently chlorine. In embodiments, R.sup.7
is --OR.sup.7A, --C(O)R.sup.7D, --C(O)OR.sup.7D,
--C(O)NR.sup.7BR.sup.7C, --SO.sub.n1R.sup.7A,
--SO.sub.v1NR.sup.7BR.sup.7C, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl or substituted
or unsubstituted heteroaryl. In embodiments, L.sup.7 is a bond or
substituted or unsubstituted alkylene. In embodiments, L.sup.7 is a
bond. In embodiments, L.sup.7 is a bond; and R.sup.7 is hydrogen,
substituted or unsubstituted alkyl, phenyl, --(CH.sub.2).sub.2OH,
--CH.sub.2C(CH.sub.3).sub.2OH, --(CH.sub.2).sub.3OH,
--(CH.sub.2).sub.2CH(CH.sub.3).sub.2OH,
--(CH.sub.2).sub.2SO.sub.2NH.sub.2,
--(CH.sub.2).sub.3SO.sub.2NH.sub.2, --(CH.sub.2).sub.2CONH.sub.2,
--(CH.sub.2).sub.3CONH.sub.2--(CH.sub.2).sub.3CON(H)Me,
--(CH.sub.2).sub.3CON(Me).sub.2, --(CH.sub.2).sub.2SO.sub.2Me,
--(CH.sub.2).sub.3SO.sub.2Me, --CH.sub.2CH(OH)Me,
--CH.sub.2CO.sub.2H, --(CH.sub.2).sub.2CO.sub.2H,
--CH(CH.sub.3)CH.sub.2CO.sub.2H, --(CH.sub.2).sub.3CO.sub.2H,
--(CH.sub.2).sub.2SO.sub.2NHCH.sub.3,
--(CH.sub.2).sub.2SO.sub.2N(CH.sub.3).sub.2,
--(CH.sub.2).sub.2SO.sub.2--(N-morpholinyl),
--(CH.sub.2).sub.2NHCOCH.sub.3, --(CH.sub.2).sub.3NHCOCH.sub.3,
--(CH.sub.2).sub.2NHCOCH(CH.sub.3).sub.2,
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2CF.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2NHCH(CH.sub.3).sub.2,
--CH.sub.2CH(CH.sub.3)CH.sub.2OH (R and S),
--CH(CH.sub.3)(CH.sub.2).sub.2OH, --CH.sub.2-(2-imidazoyl),
--CH.sub.2-(4-imidazoyl), --CH.sub.2-(3-pyrazoyl),
4-tetrahydropyranyl, 3-oxetanyl, --(CH.sub.2).sub.2NHCO.sub.2Me,
--(CH.sub.2).sub.3NHCO.sub.2Me.
[0521] In embodiments, the compound has structural Formula
(III):
##STR00009##
or a pharmaceutically acceptable salt thereof, wherein R.sup.1,
R.sup.2, R.sup.4, R.sup.3, z1, X.sup.1, X.sup.2, X.sup.3, R.sup.5,
z2, R.sup.6, z.sup.3, z4, L.sup.7, and R.sup.7 as described herein,
including embodiments. In embodiments, R.sup.2 is hydrogen. In
embodiments, R.sup.1 is hydrogen. In embodiments, R.sup.1 is
--CH.sub.3.
[0522] In embodiments, the compound has structural Formula
(IV):
##STR00010##
or a pharmaceutically acceptable salt thereof, wherein R.sup.1,
R.sup.2, R.sup.4, R.sup.32, R.sup.3.3, X.sup.2, X.sup.3, z4,
L.sup.7, and R.sup.7 as described herein, including embodiments. In
embodiments, R.sup.2 is hydrogen. In embodiments, R.sup.1 is
hydrogen. In embodiments, R.sup.1 is --CH.sub.3.
[0523] In embodiments, the compound has structural Formula (V):
##STR00011##
or a pharmaceutically acceptable salt thereof, wherein R.sup.1,
R.sup.2, R.sup.4, R.sup.32, R.sup.3.3, X.sup.2, X.sup.3, z4,
L.sup.7, and R.sup.7 as described herein, including embodiments. In
embodiments, R.sup.2 is hydrogen. In embodiments, R.sup.1 is
hydrogen. In embodiments, R.sup.1 is --CH.sub.3.
[0524] In embodiments, the compound has structural Formula
(VI):
##STR00012##
or a pharmaceutically acceptable salt thereof, wherein R.sup.1,
R.sup.2, R.sup.4, X.sup.2, X.sup.3, L.sup.7, and R.sup.7 as
described herein, including embodiments.
[0525] In embodiments, the compound has structural Formula
(VII):
##STR00013##
or a pharmaceutically acceptable salt thereof, wherein R.sup.4,
R.sup.3.2, R.sup.3.3, X.sup.2, X.sup.3, L.sup.7, and R.sup.7 as
described herein, including embodiments.
[0526] In embodiments, the compound has the structure:
##STR00014## ##STR00015## ##STR00016## ##STR00017## ##STR00018##
##STR00019## ##STR00020##
or a pharmaceutically acceptable salt thereof.
[0527] In embodiments, the compound has the structure:
##STR00021## ##STR00022## ##STR00023## ##STR00024## ##STR00025##
##STR00026## ##STR00027## ##STR00028## ##STR00029## ##STR00030##
##STR00031## ##STR00032## ##STR00033## ##STR00034##
or a pharmaceutically acceptable salt thereof.
[0528] In embodiments, the compound has the structure:
##STR00035## ##STR00036## ##STR00037## ##STR00038## ##STR00039##
##STR00040## ##STR00041## ##STR00042## ##STR00043##
##STR00044##
or a pharmaceutically acceptable salt thereof.
[0529] In embodiments, the compound has the structure:
##STR00045## ##STR00046## ##STR00047## ##STR00048## ##STR00049##
##STR00050## ##STR00051## ##STR00052## ##STR00053## ##STR00054##
##STR00055## ##STR00056## ##STR00057## ##STR00058## ##STR00059##
##STR00060## ##STR00061## ##STR00062## ##STR00063##
##STR00064##
or a pharmaceutically acceptable salt thereof.
[0530] In some embodiments, a compound as described herein may
include multiple instances of a substituent (e.g., R.sup.3,
R.sup.5, or R.sup.6 and/or other variables). In such embodiments,
each variable may optional be different and be appropriately
labeled to distinguish each group for greater clarity. For example,
where each R.sup.3, R.sup.5, R.sup.6 is different, they may be
referred to, for example, as R.sup.3.1, R.sup.3.2, R.sup.3.3,
R.sup.3.4, R.sup.3.5, R.sup.5.1, R.sup.5.2, R.sup.5.3, R.sup.5.4,
or R.sup.6.1, R.sup.6.2, R.sup.6.3, R.sup.6.4, R.sup.6.5,
R.sup.6.6, R.sup.6.7, R.sup.6.8, R.sup.6.9, or R.sup.6.10,
respectively, wherein the definition of R.sup.3 is assumed by
(independently assigned to) R.sup.3.1, R.sup.3.2, R.sup.3.3,
R.sup.3.4, R.sup.3.5; R.sup.5 is assumed by (independently assigned
to) R.sup.5.1, R.sup.5.2, R.sup.5.3, R.sup.5.4; or R.sup.6 is
assumed by (independently assigned to) R.sup.6.1, R.sup.6.2,
R.sup.6.3, R.sup.6.4, R.sup.6.5, R.sup.6.6, R.sup.6.7, R.sup.6.8,
R.sup.6.9, or R.sup.6.10. The variables used within a definition of
R.sup.3, R.sup.5, or R.sup.6, and/or other variables that appear at
multiple instances and are different may similarly be appropriately
labeled to distinguish each group for greater clarity.
[0531] In embodiments, unless otherwise indicated, a compound
described herein is a racemic mixture of all stereoisomers. In
embodiments, unless otherwise indicated, a compound described
herein is a racemic mixture of all enantiomers. In embodiments,
unless otherwise indicated, a compound described herein is a
racemic mixture of two opposite stereoisomers. In embodiments,
unless otherwise indicated, a compound described herein is a
racemic mixture of two opposite enantiomers. In embodiments, unless
otherwise indicated, a compound described herein is a single
stereoisomer. In embodiments, unless otherwise indicated, a
compound described herein is a single enantiomer. In embodiments,
the compound is a compound described herein (e.g., in an aspect,
embodiment, example, figure, table, scheme, or claim).
III. Pharmaceutical Compositions
[0532] In an aspect is provided a pharmaceutical composition,
including a compound as described herein, including embodiments, or
the structural Formula (I), (II), (IIa), (IIb), (IIc), (IId),
(III), (IV), (V), (VI), or (VII), and a pharmaceutically acceptable
excipient.
[0533] The compounds (e.g., CCR4 inhibitors) of the present
invention may be in the form of compositions suitable for
administration to a subject. In general, such compositions are
"pharmaceutical compositions" comprising a compound (e.g., CCR4
inhibitor(s)) and one or more pharmaceutically acceptable or
physiologically acceptable diluents, carriers or excipients. In
certain embodiments, the compound (e.g., CCR4 inhibitor) are
present in a therapeutically acceptable amount. The pharmaceutical
compositions may be used in the methods of the present invention;
thus, for example, the pharmaceutical compositions can be
administered ex vivo or in vivo to a subject in order to practice
the therapeutic and prophylactic methods and uses described
herein.
[0534] The pharmaceutical compositions of the present invention can
be formulated to be compatible with the intended method or route of
administration; exemplary routes of administration are set forth
herein.
[0535] The pharmaceutical compositions containing the active
ingredient (e.g., an inhibitor of CCR4 function) may be in a form
suitable for oral use, for example, as tablets, capsules, troches,
lozenges, aqueous or oily suspensions, dispersible powders or
granules, emulsions, hard or soft capsules, or syrups, solutions,
microbeads or elixirs. Pharmaceutical compositions intended for
oral use may be prepared according to any method known to the art
for the manufacture of pharmaceutical compositions, and such
compositions may contain one or more agents such as, for example,
sweetening agents, flavoring agents, coloring agents and preserving
agents in order to provide pharmaceutically elegant and palatable
preparations. Tablets, capsules and the like contain the active
ingredient in admixture with non-toxic pharmaceutically acceptable
excipients which are suitable for the manufacture thereof. These
excipients may be, for example, diluents, such as calcium
carbonate, sodium carbonate, lactose, calcium phosphate or sodium
phosphate; granulating and disintegrating agents, for example, corn
starch, or alginic acid; binding agents, for example starch,
gelatin or acacia, and lubricating agents, for example magnesium
stearate, stearic acid or talc.
[0536] The tablets, capsules and the like suitable for oral
administration may be uncoated or coated by known techniques to
delay disintegration and absorption in the gastrointestinal tract
and thereby provide a sustained action. For example, a time-delay
material such as glyceryl monostearate or glyceryl distearate may
be employed. They may also be coated by techniques known in the art
to form osmotic therapeutic tablets for controlled release.
Additional agents include biodegradable or biocompatible particles
or a polymeric substance such as polyesters, polyamine acids,
hydrogel, polyvinyl pyrrolidone, polyanhydrides, polyglycolic acid,
ethylene-vinylacetate, methylcellulose, carboxymethylcellulose,
protamine sulfate, or lactide/glycolide copolymers,
polylactide/glycolide copolymers, or ethylenevinylacetate
copolymers in order to control delivery of an administered
composition. For example, the oral agent can be entrapped in
microcapsules prepared by coacervation techniques or by interfacial
polymerization, by the use of hydroxymethylcellulose or
gelatin-microcapsules or poly(methylmethacrolate) microcapsules,
respectively, or in a colloid drug delivery system. Colloidal
dispersion systems include macromolecule complexes, nano-capsules,
microspheres, microbeads, and lipid-based systems, including
oil-in-water emulsions, micelles, mixed micelles, and liposomes.
Methods for the preparation of the above-mentioned formulations
will be apparent to those skilled in the art.
[0537] Formulations for oral use may also be presented as hard
gelatin capsules wherein the active ingredient is mixed with an
inert solid diluent, for example, calcium carbonate, calcium
phosphate, kaolin or microcrystalline cellulose, or as soft gelatin
capsules wherein the active ingredient is mixed with water or an
oil medium, for example peanut oil, liquid paraffin, or olive
oil.
[0538] Aqueous suspensions contain the active materials in
admixture with excipients suitable for the manufacture thereof.
Such excipients can be suspending agents, for example sodium
carboxymethylcellulose, methylcellulose,
hydroxy-propylmethylcellulose, sodium alginate,
polyvinyl-pyrrolidone, gum tragacanth and gum acacia; dispersing or
wetting agents, for example a naturally-occurring phosphatide
(e.g., lecithin), or condensation products of an alkylene oxide
with fatty acids (e.g., polyoxy-ethylene stearate), or condensation
products of ethylene oxide with long chain aliphatic alcohols
(e.g., for heptadecaethyleneoxycetanol), or condensation products
of ethylene oxide with partial esters derived from fatty acids and
a hexitol (e.g., polyoxyethylene sorbitol monooleate), or
condensation products of ethylene oxide with partial esters derived
from fatty acids and hexitol anhydrides (e.g., polyethylene
sorbitan monooleate). The aqueous suspensions may also contain one
or more preservatives.
[0539] Oily suspensions may be formulated by suspending the active
ingredient in a vegetable oil, for example arachis oil, olive oil,
sesame oil or coconut oil, or in a mineral oil such as liquid
paraffin. The oily suspensions may contain a thickening agent, for
example beeswax, hard paraffin or cetyl alcohol. Sweetening agents,
such as those set forth above, and flavoring agents may be added to
provide a palatable oral preparation.
[0540] Dispersible powders and granules suitable for preparation of
an aqueous suspension by the addition of water provide the active
ingredient in admixture with a dispersing or wetting agent, and
optionally one or more suspending agents and/or preservatives.
Suitable dispersing or wetting agents and suspending agents are
exemplified herein.
[0541] The pharmaceutical compositions of the present invention may
also be in the form of oil-in-water emulsions. The oily phase may
be a vegetable oil, for example olive oil or arachis oil, or a
mineral oil, for example, liquid paraffin, or mixtures of these.
Suitable emulsifying agents may be naturally occurring gums, for
example, gum acacia or gum tragacanth; naturally occurring
phosphatides, for example, soy bean, lecithin, and esters or
partial esters derived from fatty acids; hexitol anhydrides, for
example, sorbitan monooleate; and condensation products of partial
esters with ethylene oxide, for example, polyoxyethylene sorbitan
monooleate.
[0542] The pharmaceutical compositions typically comprise a
therapeutically effective amount of a CCR4 inhibitor contemplated
by the present invention and one or more pharmaceutically and
physiologically acceptable formulation agents. Suitable
pharmaceutically acceptable or physiologically acceptable diluents,
carriers or excipients include, but are not limited to,
antioxidants (e.g., ascorbic acid and sodium bisulfate),
preservatives (e.g., benzyl alcohol, methyl parabens, ethyl or
n-propyl, p-hydroxybenzoate), emulsifying agents, suspending
agents, dispersing agents, solvents, fillers, bulking agents,
detergents, buffers, vehicles, diluents, and/or adjuvants. For
example, a suitable vehicle may be physiological saline solution or
citrate-buffered saline, possibly supplemented with other materials
common in pharmaceutical compositions for parenteral
administration. Neutral buffered saline or saline mixed with serum
albumin are further exemplary vehicles. Those skilled in the art
will readily recognize a variety of buffers that can be used in the
pharmaceutical compositions and dosage forms contemplated herein.
Typical buffers include, but are not limited to, pharmaceutically
acceptable weak acids, weak bases, or mixtures thereof. As an
example, the buffer components can be water soluble materials such
as phosphoric acid, tartaric acids, lactic acid, succinic acid,
citric acid, acetic acid, ascorbic acid, aspartic acid, glutamic
acid, and salts thereof. Acceptable buffering agents include, for
example, a Tris buffer;
N-(2-Hydroxyethyl)piperazine-N'-(2-ethanesulfonic acid) (HEPES);
2-(N-Morpholino)ethanesulfonic acid (MES);
2-(N-Morpholino)ethanesulfonic acid sodium salt (MES);
3-(N-Morpholino)propanesulfonic acid (MOPS); and
N-tris[Hydroxymethyl]methyl-3-aminopropanesulfonic acid (TAPS).
[0543] After a pharmaceutical composition has been formulated, it
may be stored in sterile vials as a solution, suspension, gel,
emulsion, solid, or dehydrated or lyophilized powder. Such
formulations may be stored either in a ready-to-use form, a
lyophilized form requiring reconstitution prior to use, a liquid
form requiring dilution prior to use, or other acceptable form. In
some embodiments, the pharmaceutical composition is provided in a
single-use container (e.g., a single-use vial, ampule, syringe, or
autoinjector (similar to, e.g., an EpiPen.RTM.)), whereas a
multi-use container (e.g., a multi-use vial) is provided in other
embodiments.
[0544] Formulations can also include carriers to protect the
composition against rapid degradation or elimination from the body,
such as a controlled release formulation, including liposomes,
hydrogels, prodrugs and microencapsulated delivery systems. For
example, a time-delay material such as glyceryl monostearate or
glyceryl stearate alone, or in combination with a wax, may be
employed. Any drug delivery apparatus may be used to deliver a CCR4
inhibitor, including implants (e.g., implantable pumps) and
catheter systems, slow injection pumps and devices, all of which
are well known to the skilled artisan.
[0545] Depot injections, which are generally administered
subcutaneously or intramuscularly, may also be utilized to release
the compound (e.g., CCR4 inhibitor) disclosed herein over a defined
period of time. Depot injections are usually either solid- or
oil-based and generally comprise at least one of the formulation
components set forth herein. One of ordinary skill in the art is
familiar with possible formulations and uses of depot
injections.
[0546] The pharmaceutical compositions may be in the form of a
sterile injectable aqueous or oleagenous suspension. This
suspension may be formulated according to the known art using those
suitable dispersing or wetting agents and suspending agents
mentioned herein. The sterile injectable preparation may also be a
sterile injectable solution or suspension in a non-toxic
parenterally-acceptable diluent or solvent, for example, as a
solution in 1,3-butane diol. Acceptable diluents, solvents and
dispersion media that may be employed include water, Ringer's
solution, isotonic sodium chloride solution, Cremophor.RTM. EL
(BASF, Parsippany, N.J.) or phosphate buffered saline (PBS),
ethanol, polyol (e.g., glycerol, propylene glycol, and liquid
polyethylene glycol), and suitable mixtures thereof. In addition,
sterile fixed oils are conventionally employed as a solvent or
suspending medium; for this purpose, any bland fixed oil may be
employed, including synthetic mono- or diglycerides. Moreover,
fatty acids, such as oleic acid, find use in the preparation of
injectables. Prolonged absorption of particular injectable
formulations can be achieved by including an agent that delays
absorption (e.g., aluminum monostearate or gelatin).
[0547] The present invention contemplates the administration of the
compound (e.g., CCR4 inhibitor) in the form of suppositories for
rectal administration. The suppositories can be prepared by mixing
the drug with a suitable non-irritating excipient, which is solid
at ordinary temperatures but liquid at the rectal temperature and
will therefore melt in the rectum to release the drug. Such
materials include, but are not limited to, cocoa butter and
polyethylene glycols.
[0548] The compound (e.g., CCR4 inhibitor) contemplated by the
present invention may be in the form of any other suitable
pharmaceutical composition (e.g., sprays for nasal or inhalation
use) currently known or developed in the future.
IV. Methods of Use
[0549] In another aspect is provided a method of inhibiting C--C
chemokine receptor type 4 (CCR4), the method comprising contacting
CCR4 with a compound as described herein, including embodiments, or
the structural Formula (I), (II), (IIa), (IIb), (IIc), (IId),
(III), (IV), (V), (VI), or (VII) or a pharmaceutically acceptable
salt thereof.
[0550] In an aspect, is provided a method of treating or preventing
a disease or disorder mediated by CCR4, comprising administering to
a subject in need thereof a therapeutically effective amount of a
compound as described herein, including embodiments, or the
structural Formula (I), (II), (IIa), (IIb), (IIc), (IId), (III),
(IV), (V), (VI), or (VII) or a pharmaceutically acceptable salt
thereof.
[0551] In embodiments, the method further includes administering a
therapeutically effective amount of a compound as described herein,
including embodiments, or the structural Formula (I), (II), (IIa),
(IIb), (IIc), (IId), (III), (IV), (V), (VI), or (VII) or a
pharmaceutically acceptable salt thereof.
[0552] In embodiments, the method further includes administering a
therapeutically effective amount of a compound as described herein,
including embodiments, or the structural Formulae (I), (II), (IIa),
(IIb), (IIc), (IId), (III), (IV), (V), (VI), or (VII) or a
pharmaceutically acceptable salt thereof.
[0553] In embodiments, the disease or disorder is an immune or
inflammatory disease or disorder. In embodiments, the methods of
treating an immune or inflammatory disease or disorder disclosed
herein further include co-administering an anti-inflammatory agent
in combination with a compound of structural Formula (I), (II),
(IIa), (IIb), (IIc), (IId), (III), (IV), (V), (VI), or (VII), or a
pharmaceutically acceptable salt thereof. In embodiments, the
anti-inflammatory is thalidomide or a derivative thereof, a
retinoid, dithranol or calcipotriol, a non-steroidal
anti-inflammatory agent (NSAID), cyclo-oxygenase inhibiting nitric
oxide donors (CINODs), glucocorticosteroids, methotrexate,
leflunomide, hydroxychloroquine, d-penicillamine, auranofin,
analgesics; diacerein, hyaluronic acid derivatives or nutritional
supplements.
[0554] In embodiments, the disease or disorder is a cardiovascular
or metabolic disease or disorder. In embodiments, the methods of
treating a cardiovascular or metabolic disease or disorder
disclosed herein further include co-administering a cardiovascular
agent or a metabolic disorder agent in combination with a compound
of structural Formula (I), (II), (IIa), (IIb), (IIc), (IId), (III),
(IV), (V), (VI), or (VII), or a pharmaceutically acceptable salt
thereof. In embodiments, the cardiovascular agent is a calcium
channel blocker, a beta-adrenoceptor blocker, an
angiotensin-converting enzyme (ACE) inhibitor, an angiotensin-2
receptor antagonist, a lipid lowering agent, a modulator of blood
cell morphology, a thrombolytic or an anticoagulant.
[0555] In embodiments, the disease or disorder is cancer. In
embodiments, the methods of treating cancer disclosed herein
further include co-administering a chemotherapeutic agent or
anticancer agent in combination with a compound of structural
Formula (I), (II), (IIa), (IIb), (IIc), (IId), (III), (IV), (V),
(VI), or (VII), or a pharmaceutically acceptable salt thereof. In
embodiments, the chemotherapeutic agent or anticancer agent is an
antiproliferative/antineoplastic drug, an antimetabolite, an
antitumour antibiotic, an antimitotic agent, a topoisomerase
inhibitor, a cytostatic agent, an oestrogen receptor down
regulator, an antiandrogen, a LHRH antagonist or LHRH agonist, a
progestogen, an aromatase inhibitor, an inhibitor of
5.alpha.-reductase, an agent which inhibits cancer cell invasion,
an inhibitor of growth factor function, a farnesyl transferase
inhibitor, a tyrosine kinase inhibitor, a serine/threonine kinase
inhibitor, an inhibitor of the epidermal growth factor family, an
inhibitor of the platelet-derived growth factor family, an
inhibitor of the hepatocyte growth factor family; an antiangiogenic
agent, a vascular damaging agent, an agent used in antisense
therapy, an anti-ras antisense, an agent used in a gene therapy, an
immunotherapeutic agent, or an antibody. In embodiments, the
methods of treating cancer disclosed herein further include
co-administering a chemotherapeutic agent or anticancer agent in
combination with a compound of structural Formula (I), (II), (IIa),
(IIb), (IIc), (IId), (III), (IV), (V), (VI), or (VII), or a
pharmaceutically acceptable salt thereof and a therapeutically
effective amount of at least two of: a CCR4 inhibitor, an inhibitor
of the PD-L1/PD-1 pathway, an inhibitor of CTLA-4 or an agonistic
antibody of CD137 (4-1BB). In embodiments, the methods of treating
cancer disclosed herein further include co-administering a
chemotherapeutic agent or anticancer agent in combination with a
compound of structural Formula (I), (II), (IIa), (IIb), (IIc),
(IId), (III), (IV), (V), (VI), or (VII), or a pharmaceutically
acceptable salt thereof and a therapeutically effective amount of
at least two of: a CCR4 inhibitor, an immune modulator agent or an
agent from Table 1, or any combination thereof.
[0556] In embodiments, the disease or disorder is inflammatory
bowel disease. In embodiments, the disease or disorder is
rheumatoid arthritis. In embodiments, the disease or disorder is
psoriasis. In embodiments, the disease or disorder includes
allergy-related disorders (e.g., hypersensitivity and anaphylactic
responses); gastrointestinal disorders (e.g., Crohn's disease,
ulcerative colitis, ileitis and enteritis); psoriasis and
inflammatory dermatoses (e.g., dermatitis, eczema, atopic
dermatitis, allergic contact dermatitis, dermatomyositis, urticaria
and pruritus); vasculitis; scleroderma; asthma, COPD, and
respiratory allergic diseases (e.g., allergic rhinitis and
hypersensitivity lung diseases); autoimmune diseases, including
arthritis (e.g., rheumatoid and psoriatic), multiple sclerosis,
systemic lupus erythematosus, type I diabetes and
glomerulonephritis; graft rejection (e.g., allograft rejection);
transplant rejection (e.g., solid organ); cancers, such as
leukemias, lymphomas and metastatic cancers, particularly solid
tumors (e.g., gastric cancers); and other diseases in which
inhibition of undesired inflammatory and/or immune responses is
desired, such as atherosclerosis, neurodegenerative diseases (e.g.,
Alzheimer's disease), encephalitis, meningitis, hepatitis,
nephritis, sepsis, sarcoidosis, allergic conjunctivitis, otitis,
and sinusitis. In particular embodiments, the CCR4-mediated
disease, disorder or condition is asthma, COPD, rhinitis,
idiopathic pulmonary fibrosis, psoriasis and contact dermatitis. In
embodiments the disease or disorder is including pulmonary
fibrosis, hepatic inflammation, asthma, atopic dermatitis, cancer
(e.g., thyroid carcinoma, cholangiocarcinoma, pancreatic
adenocarcinoma, skin cutaneous melanoma, colon adenocarcinoma,
rectum adenocarcinoma, stomach adenocarcinoma, esophageal
carcinoma, head and neck squamous cell carcinoma, breast invasive
carcinoma, lung adenocarcinoma, lung squamous cell carcinoma), or
granuloma development.
[0557] In embodiments, the method further includes administering a
therapeutically effective amount of a compound as described herein,
including embodiments, or the structural Formula (I), (II), (IIa),
(IIb), (IIc), (IId), (III), (IV), (V), (VI), or (VII) or a
pharmaceutically acceptable salt thereof.
[0558] In embodiments, the administration of the compounds
disclosed herein for the treatment or prevention of immune-,
inflammatory-, or cancer-related diseases, disorders and
conditions. Such diseases, disorders and conditions are described
in detail elsewhere, as are other maladies that may be treated or
prevented with compounds (e.g., CCR4 inhibitor) described
herein.
[0559] It is frequently beneficial to improve one of more physical
properties of the treatment modalities disclosed herein and/or the
manner in which they are administered. Improvements of physical
properties include, for example, methods of increasing water
solubility, bioavailability, serum half-life, and/or therapeutic
half-life; and/or modulating biological activity. Modifications
known in the art include pegylation, Fc-fusion and albumin fusion.
Although generally associated with large molecule agents (e.g.,
polypeptides), such modifications have recently been evaluated with
particular small molecules. By way of example, Chiang, M. et al.
(J. Am. Chem. Soc., 2014, 136(9):3370-73) describe a small molecule
agonist of the adenosine 2a receptor conjugated to the
immunoglobulin Fc domain. The small molecule-Fc conjugate retained
potent Fc receptor and adenosine 2a receptor interactions and
showed superior properties compared to the unconjugated small
molecule. Covalent attachment of PEG molecules to small molecule
therapeutics has also been described (Li, W. et al., Progress in
Polymer Science, 2013 38:421-44).
[0560] In embodiments, compounds of the present invention are
effective in the treatment and prevention of IBD (e.g., Crohn's
disease and ulcerative colitis, both of which are chronic
idiopathic diseases that can affect any part of the
gastrointestinal tract, and are associated with many untoward
effects, and patients with prolonged ulcerative colitis are at an
increased risk of developing colon cancer). Current IBD treatments
are aimed at controlling inflammatory symptoms, and while certain
agents (e.g., corticosteroids, aminosalicylates and standard
immunosuppressive agents (e.g., cyclosporine, azathioprine, and
methotrexate)) have met with limited success, long-term therapy may
cause liver damage (e.g., fibrosis or cirrhosis) and bone marrow
suppression, and patients often become refractory to such
treatments.
[0561] The compounds of the present invention can be used to
increase or enhance an immune response; to improve immunization,
including increasing vaccine efficacy; and to increase
inflammation. Immune deficiencies associated with immune deficiency
diseases, immunosuppressive medical treatment, acute and/or chronic
infection, and aging can be treated using the compounds disclosed
herein. The compounds described herein can also be used to
stimulate the immune system of patients suffering from
iatrogenically-induced immune suppression, including those who have
undergone bone marrow transplants, chemotherapy, or
radiotherapy.
[0562] In accordance with the present invention, a compound or
pharmaceutical salt thereof can be used to treat or prevent a
proliferative condition or disorder, including a cancer, for
example, cancer of the uterus, cervix, breast, prostate, testes,
gastrointestinal tract (e.g., esophagus, oropharynx, stomach, small
or large intestines, colon, or rectum), kidney, renal cell,
bladder, bone, bone marrow, skin, head or neck, liver, gall
bladder, heart, lung, pancreas, salivary gland, adrenal gland,
thyroid, brain (e.g., gliomas), ganglia, central nervous system
(CNS) and peripheral nervous system (PNS), and cancers of the
hematopoietic system and the immune system (e.g., spleen or
thymus). The present invention also provides methods of treating or
preventing other cancer-related diseases, disorders or conditions,
including, for example, immunogenic tumors, non-immunogenic tumors,
dormant tumors, virus-induced cancers (e.g., epithelial cell
cancers, endothelial cell cancers, squamous cell carcinomas and
papillomavirus), adenocarcinomas, lymphomas, carcinomas, melanomas,
leukemias, myelomas, sarcomas, teratocarcinomas, chemically-induced
cancers, metastasis, and angiogenesis. The invention contemplates
reducing tolerance to a tumor cell or cancer cell antigen, e.g., by
modulating activity of a regulatory T-cell and/or a CD8+ T-cell
(see, e.g., Ramirez-Montagut, et al. (2003) Oncogene 22:3180-87;
and Sawaya, et al. (2003) New Engl. J. Med. 349:1501-09). In some
embodiments, the tumor or cancer is colon cancer, ovarian cancer,
breast cancer, melanoma, lung cancer, glioblastoma, or leukemia. In
particular embodiments, the cancer is gastric cancer. The use of
the term(s) cancer-related diseases, disorders and conditions is
meant to refer broadly to conditions that are associated, directly
or indirectly, with cancer, and includes, e.g., angiogenesis and
precancerous conditions such as dysplasia. In embodiments, the
cancer is thyroid carcinoma, cholangiocarcinoma, pancreatic cancer,
pancreatic adenocarcinoma, skin cutaneous melanoma, colon cancer,
colon adenocarcinoma, rectum adenocarcinoma, stomach
adenocarcinoma, esophageal carcinoma, head and neck squamous cell
carcinoma, breast invasive carcinoma, lung adenocarcinoma, lung
squamous cell carcinoma.
[0563] In embodiments, a cancer be metastatic or at risk of
becoming metastatic, or may occur in a diffuse tissue, including
cancers of the blood or bone marrow (e.g., leukemia). In some
further embodiments, the compounds of the invention can be used to
overcome T-cell tolerance.
[0564] In some embodiments, the present invention provides methods
for treating a proliferative condition, cancer, tumor, or
precancerous condition with a compound described herein and at
least one additional therapeutic or diagnostic agent, examples of
which are set forth elsewhere herein.
[0565] The present invention provides methods for treating and/or
preventing a proliferative condition, cancer, tumor, or
precancerous disease, disorder or condition with a compound
described herein.
[0566] In embodiments drawn to methods of treating cancer, the
administration of a therapeutically effective amount of a compound
described herein results in a cancer survival rate greater than the
cancer survival rate observed by administering either agent alone.
In further embodiments drawn to methods of treating cancer, the
administration of a therapeutically effective amount of a compound
described herein (e.g., CCR4 inhibitor) results in a reduction of
tumor size or a slowing of tumor growth greater than reduction of
tumor size or tumor growth observed following administration of
either agent alone. In embodiments, the methods of treating cancer
disclosed herein further include administering a chemotherapeutic
agent or anticancer agent in combination with a compound of
structural Formula (I), (II), (IIa), (IIb), (IIc), (IId), (III),
(IV), (V), (VI), or (VII), or a pharmaceutically acceptable salt
thereof. In embodiments, the chemotherapeutic agent or anticancer
agent is an antiproliferative/antineoplastic drug, an
antimetabolite, an antitumour antibiotic, an antimitotic agent, a
topoisomerase inhibitor, a cytostatic agent, an oestrogen receptor
down regulator, an antiandrogen, a LHRH antagonist or LHRH agonist,
a progestogen, an aromatase inhibitor, an inhibitor of
5.alpha.-reductase, an agent which inhibits cancer cell invasion,
an inhibitor of growth factor function, a farnesyl transferase
inhibitor, a tyrosine kinase inhibitor, a serine/threonine kinase
inhibitor, an inhibitor of the epidermal growth factor family, an
inhibitor of the platelet-derived growth factor family, an
inhibitor of the hepatocyte growth factor family; an antiangiogenic
agent, a vascular damaging agent, an agent used in antisense
therapy, an anti-ras antisense, an agent used in a gene therapy, an
immunotherapeutic agent, oran antibody. In embodiments, the methods
of treating cancer disclosed herein further include
co-administering a therapeutically effective amount of at least two
of: a CCR4 inhibitor, an inhibitor of the PD-L1/PD-1 pathway, an
inhibitor of CTLA-4 or an agonistic antibody of CD137 (4-1BB). In
embodiments, the methods of treating cancer disclosed herein
further include co-administering a therapeutically effective amount
of at least two of: a CCR4 inhibitor, an agent that may be an
immune modulator or an agent from Table 1.
[0567] Inhibition of CCR4 activity may also represent an important
strategy for the treatment or prevention of neurological,
neuropsychiatric, neurodegenerative or other diseases, disorders
and conditions having some association with the central nervous
system, including disorders associated with impairment of cognitive
function and/or motor function. Many of these diseases, disorders
and conditions comprise an immune and/or inflammatory component. In
embodiments, the disease or disorder is Parkinson's disease, extra
pyramidal syndrome (EPS), dystonia, akathisia, tardive dyskinesia,
restless leg syndrome, epilepsy, periodic limb movement in sleep,
attention deficit disorders, depression, anxiety, dementia,
Alzheimer's disease, Huntington's disease, multiple sclerosis,
cerebral ischemia, hemorrhagic stroke, subarachnoid hemorrhage, or
traumatic brain injury.
[0568] Embodiments of the present invention contemplate the
administration of the compounds described herein to a subject for
the treatment or prevention of any other disorder that may benefit
from at least some level of CCR4 modulation. Such diseases,
disorders and conditions may include, for example, asthma, chronic
obstructive pulmonary disease (COPD) including chronic bronchitis
and emphysema, idiopathic pulmonary fibrosis, atopic or contact
dermatitis, urticaria, allergic rhinitis, nasal polyps, allergic
conjunctivitis, thrombosis, reperfusion injury of the myocardium
and brain, chronic glomerulonephritis, sepsis, adult respiratory
distress syndrome, and pain. Additional diseases, disorders and
conditions include allergic bronchopulmonary aspergillosis,
allergic fungal sinusitis, severe asthma with fungal sensitization
and diseases involving a pathogenic role for fungi including
invasion or colonization (such as invasive aspergillosis,
aspergilloma or candidiasis).
[0569] In embodiments, the disease or disorder includes
cardiovascular (e.g., cardiac ischemia), metabolic (e.g.,
development of insulititis diabetes), hepatic (e.g., hepatic
fibrosis, NASH, and NAFLD), ophthalmologic (e.g., diabetic
retinopathy), and renal (e.g., renal failure) disorders.
[0570] The present invention contemplates the administration of the
compounds described herein, and compositions (e.g., pharmaceutical
salts, pharmaceutical composition) thereof, in any appropriate
manner. Suitable routes of administration include oral, parenteral
(e.g., intramuscular, intravenous, subcutaneous (e.g., injection or
implant), intraperitoneal, intracisternal, intraarticular,
intraperitoneal, intracerebral (intraparenchymal) and
intracerebroventricular), nasal, vaginal, sublingual, intraocular,
rectal, topical (e.g., transdermal), buccal and inhalation. Depot
injections, which are generally administered subcutaneously or
intramuscularly, may also be utilized to release the compounds
disclosed herein over a defined period of time. In embodiments, the
administration is oral administration.
[0571] The present invention provides methods for treating and/or
preventing certain cardiovascular- and/or metabolic-related
diseases, disorders and conditions, as well as disorders associated
therewith, with a compound described herein.
[0572] The compounds of the present invention may be administered
to a subject in an amount that is dependent upon, for example, the
goal of administration (e.g., the degree of resolution desired);
the age, weight, sex, and health and physical condition of the
subject to which the formulation is being administered; the route
of administration; and the nature of the disease, disorder,
condition or symptom thereof. The dosing regimen may also take into
consideration the existence, nature, and extent of any adverse
effects associated with the agent(s) being administered. Effective
dosage amounts and dosage regimens can readily be determined from,
for example, safety and dose-escalation trials, in vivo studies
(e.g., animal models), and other methods known to the skilled
artisan.
[0573] In general, dosing parameters dictate that the dosage amount
be less than an amount that could be irreversibly toxic to the
subject (the maximum tolerated dose (MTD)) and not less than an
amount required to produce a measurable effect on the subject. Such
amounts are determined by, for example, the pharmacokinetic and
pharmacodynamic parameters associated with ADME, taking into
consideration the route of administration and other factors.
[0574] An effective dose (ED) is the dose or amount of an agent
that produces a therapeutic response or desired effect in some
fraction of the subjects taking it. The "median effective dose" or
ED50 of an agent is the dose or amount of an agent that produces a
therapeutic response or desired effect in 50% of the population to
which it is administered. Although the ED50 is commonly used as a
measure of reasonable expectance of an agent's effect, it is not
necessarily the dose that a clinician might deem appropriate taking
into consideration all relevant factors. Thus, in some situations
the effective amount is more than the calculated ED50, in other
situations the effective amount is less than the calculated ED50,
and in still other situations the effective amount is the same as
the calculated ED50.
[0575] In addition, an effective dose of the compounds of the
present invention may be an amount that, when administered in one
or more doses to a subject, produces a desired result relative to a
healthy subject. For example, for a subject experiencing a
particular disorder, an effective dose may be one that improves a
diagnostic parameter, measure, marker and the like of that disorder
by at least about 5%, at least about 10%, at least about 20%, at
least about 25%, at least about 30%, at least about 40%, at least
about 50%, at least about 60%, at least about 70%, at least about
80%, at least about 90%, or more than 90%, where 100% is defined as
the diagnostic parameter, measure, marker and the like exhibited by
a normal subject.
[0576] In embodiments, the compounds contemplated by the present
invention may be administered (e.g., orally) at dosage levels of
about 0.01 mg/kg to about 50 mg/kg, or about 1 mg/kg to about 25
mg/kg, of subject body weight per day, one, two, three, four or
more times a day, to obtain the desired therapeutic effect. For
administration of an oral agent, the compositions can be provided
in the form of tablets, capsules and the like containing from 0.05
to 1000 milligrams of the active ingredient, particularly 0.05,
0.1, 0.25, 0.5, 0.75, 1.0, 1.25, 1.5, 1.75, 2.0, 2.5, 5.0, 7.5,
10.0, 15.0, 20.0, 25.0, 50.0, 75.0, 100.0, 125.0, 150.0, 175.0,
200.0, 250.0, 300.0, 400.0, 500.0, 600.0, 750.0, 800.0, 900.0, and
1000.0 milligrams of the active ingredient. A pharmaceutically
acceptable carrier(s), diluent(s) and/or excipient(s) may be
present in an amount of from about 0.1 g to about 2.0 g.
[0577] In embodiments, the dosage of the desired compound is
contained in a "unit dosage form". The phrase "unit dosage form"
refers to physically discrete units, each unit including a
predetermined amount of the compound (e.g., CCR4 inhibitor),
sufficient to produce the desired effect. It will be appreciated
that the parameters of a unit dosage form will depend on the
particular agent and the effect to be achieved.
V. Kits
[0578] In another aspect, provided herein is a kit including a
compound described herein (e.g., a CCR4 inhibitor) or
pharmaceutical compositions thereof. The kits are generally in the
form of a physical structure housing various components, as
described below, and may be utilized, for example, in practicing
the methods described above.
[0579] A kit may include one or more of the compounds disclosed
herein (e.g., provided in a sterile container), which may be in the
form of a pharmaceutical composition suitable for administration to
a subject. The compounds described herein (e.g., CCR4 inhibitors)
can be provided in a form that is ready for use (e.g., a tablet or
capsule) or in a form requiring, for example, reconstitution or
dilution (e.g., a powder) prior to administration. When the
compound (e.g., CCR4 inhibitor) is in a form that needs to be
reconstituted or diluted by a user, the kit may also include
diluents (e.g., sterile water), buffers, pharmaceutically
acceptable excipients, and the like, packaged with, or separately
from, the compound. Each component of the kit may be enclosed
within an individual container, and all of the various containers
may be within a single package. A kit of the present invention may
be designed for conditions necessary to properly maintain the
components housed therein (e.g., refrigeration or freezing).
[0580] A kit may contain a label or packaging insert including
identifying information for the components therein and instructions
for their use (e.g., dosing parameters, clinical pharmacology of
the active ingredient(s), including mechanism of action,
pharmacokinetics and pharmacodynamics, adverse effects,
contraindications, etc.). Labels or inserts can include
manufacturer information such as lot numbers and expiration dates.
The label or packaging insert may be, e.g., integrated into the
physical structure housing the components, contained separately
within the physical structure, or affixed to a component of the kit
(e.g., an ampule, tube or vial).
[0581] Labels or inserts can additionally include, or be
incorporated into, a computer readable medium, such as a disk
(e.g., hard disk, card, memory disk), optical disk such as CD- or
DVD-ROM/RAM, DVD, MP3, magnetic tape, or an electrical storage
media such as RAM and ROM or hybrids of these such as
magnetic/optical storage media, FLASH media or memory-type cards.
In some embodiments, the actual instructions are not present in the
kit, but means for obtaining the instructions from a remote source,
e.g., via the internet, are provided.
[0582] It is understood that the examples and embodiments described
herein are for illustrative purposes only and that various
modifications or changes in light thereof will be suggested to
persons skilled in the art and are to be included within the spirit
and purview of this application and scope of the appended claims.
All publications, patents, and patent applications cited herein are
hereby incorporated by reference in their entirety for all
purposes.
Additional Embodiments
[0583] Embodiments includes embodiment P1 to P41 following.
Embodiment P1
[0584] A compound having structural Formula (I):
##STR00065##
or a pharmaceutically acceptable salt thereof, wherein: X.sup.1 is
CR.sup.8 or N; X.sup.2 is CR.sup.9 or N; X.sup.3 is CR.sup.10 or N;
n1 and z3 are independently an integer from 0 to 4; m1 and v1 are
independently 1 or 2; z1 is an integer from 0 to 5; z2 is an
integer from 0 to 2; z4 is an integer from 0 to 2; L.sup.7 is a
bond, --O--, --S--, --NR.sup.7.2B--, --C(O)--, --C(O)O--, --S(O)--,
--S(O).sub.2--, substituted or unsubstituted alkylene, substituted
or unsubstituted heteroalkylene, substituted or unsubstituted
cycloalkylene, substituted or unsubstituted heterocycloalkylene,
substituted or unsubstituted arylene, or substituted or
unsubstituted heteroarylene; R.sup.1 is hydrogen, halogen,
--CX.sup.1.1.sub.3, --CHX.sup.1.1.sub.2, --CH.sub.2X.sup.1.1, --CN,
--SO.sub.n1R.sup.1A, --SO.sub.v1NR.sup.1BR.sup.1C,
--NHNR.sup.1BR.sup.1C, --ONR.sup.1BR.sup.1C,
--NHC(O)NHNR.sup.1BR.sup.1C, --NHC(O)NR.sup.1BR.sup.1C,
--N(O).sub.m1, --NR.sup.1BR.sup.1C, --C(O)R.sup.1D,
--C(O)OR.sup.1D, --C(O)NR.sup.1BR.sup.1C, --OR.sup.1A,
--NR.sup.1BSO.sub.2R.sup.1A, --NR.sup.1BC(O)R.sup.1D,
--NR.sup.1BC(O)OR.sup.1D, --NR.sup.1BOR.sup.1D,
--OCX.sup.1.1.sub.3, --OCHX.sup.1.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.2 is hydrogen,
halogen, --CX.sup.2.1.sub.3, --CHX.sup.2.1.sub.2,
--CH.sub.2X.sup.2.1, --CN, --SO.sub.n1R.sup.2A,
--SO.sub.v1NR.sup.2BR.sup.2C, --NHNR.sup.2BR.sup.2C,
--ONR.sup.2BR.sup.2C, --NHC(O)NHNR.sup.2BR.sup.2C,
--NHC(O)NR.sup.2BR.sup.2C, --N(O).sub.m1, --NR.sup.2BR.sup.2C,
--C(O)R.sup.2D, --C(O)OR.sup.2D, --C(O)NR.sup.2BR.sup.2C,
--OR.sup.2A, --NR.sup.2BSO.sub.2R.sup.2A, --NR.sup.2BC(O)R.sup.2D,
--NR.sup.2BC(O)OR.sup.2D, --NR.sup.2BOR.sup.2D,
--OCX.sup.2.1.sub.3, --OCHX.sup.2.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3 is hydrogen,
halogen, --CX.sup.3.1.sub.3, --CHX.sup.3.1.sub.2,
--CH.sub.2X.sup.3.1, --CN, --SO.sub.1R.sup.3A,
--SO.sub.v1NR.sup.3BR.sup.3C, --NHNR.sup.3BR.sup.3C,
--ONR.sup.3BR.sup.3C, --NHC(O)NHNR.sup.3BR.sup.3C,
--NHC(O)NR.sup.3BR.sup.3C, --N(O).sub.m1, --NR.sup.3BR.sup.3C,
--C(O)R.sup.3D, --C(O)OR.sup.3D, --C(O)NR.sup.3BR.sup.3C,
--OR.sup.3A, --NR.sup.3BSO.sub.2R.sup.3A, --NR.sup.3BC(O)R.sup.3D,
--NR.sup.3BC(O)OR.sup.3D, --NR.sup.3BOR.sup.3D,
--OCX.sup.3.1.sub.3, --OCHX.sup.3.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.4 is hydrogen,
halogen, --CX.sup.4.1.sub.3, --CHX.sup.4.1.sub.2,
--CH.sub.2X.sup.4.1, --CN, --SO.sub.n1R.sup.4A,
--SO.sub.v1NR.sup.4BR.sup.4C, --NHNR.sup.4BR.sup.4C,
--ONR.sup.4BR.sup.4C, --NHC(O)NHNR.sup.4BR.sup.4C,
--NHC(O)NR.sup.4BR.sup.4C, --N(O).sub.m1, --NR.sup.4BR.sup.4C,
--C(O)R.sup.4D, --C(O)OR.sup.4D, --C(O)NR.sup.4BR.sup.4C,
--OR.sup.4A, --NR.sup.4BSO.sub.2R.sup.4A, --NR.sup.4BC(O)R.sup.4D,
--NR.sup.4BC(O)OR.sup.4D, --NR.sup.4BOR.sup.4D,
--OCX.sup.4.1.sub.3, --OCHX.sup.4.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.5 is hydrogen,
halogen, oxo, --CX.sup.5.1.sub.3, --CHX.sup.5.1.sub.2,
--CH.sub.2X.sup.5.1, --CN, --SO.sub.n1R.sup.5A,
--SO.sub.v1NR.sup.5BR.sup.5C, --NHNR.sup.5BR.sup.5C,
--ONR.sup.5BR.sup.5C, --NHC(O)NHNR.sup.5BR.sup.5C,
--NHC(O)NR.sup.5BR.sup.5C, --N(O).sub.m1, --NR.sup.5BR.sup.5C,
--C(O)R.sup.5D, --C(O)OR.sup.5D, --C(O)NR.sup.5BR.sup.5C,
--OR.sup.5A, --NR.sup.5BSO.sub.2R.sup.5A, --NR.sup.5BC(O)R.sup.5D,
--NR.sup.5BC(O)OR.sup.5D, --NR.sup.5BOR.sup.5D,
--OCX.sup.5.1.sub.3, --OCHX.sup.5.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.6 is hydrogen,
halogen, oxo, --CX.sup.6.1.sub.3, --CHX.sup.6.1.sub.2,
--CH.sub.2X.sup.6.1, --CN, --SO.sub.n1R.sup.6A,
--SO.sub.v1NR.sup.6BR.sup.6C, --NHNR.sup.6BR.sup.6C,
--ONR.sup.6BR.sup.6C, --NHC(O)NHNR.sup.6BR.sup.6C,
--NHC(O)NR.sup.6BR.sup.6C, --N(O).sub.m1, --NR.sup.6BR.sup.6C,
--C(O)R.sup.6D, --C(O)OR.sup.6D, --C(O)NR.sup.6BR.sup.6C,
--OR.sup.6A, --NR.sup.6BSO.sub.2R.sup.6A, --NR.sup.6BC(O)R.sup.6D,
--NR.sup.6BC(O)OR.sup.6D, --NR.sup.6BOR.sup.6D,
--OCX.sup.6.1.sub.3, --OCHX.sup.6.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.7 is hydrogen,
halogen, --CX.sup.7.1.sub.3, --CHX.sup.7.1.sub.2,
--CH.sub.2X.sup.7.1, --CN, --SO.sub.n1R.sup.7A,
--SO.sub.v1NR.sup.7BR.sup.7C, --NHNR.sup.7BR.sup.7C,
--ONR.sup.7BR.sup.7C, --NHC(O)NHNR.sup.7BR.sup.7C,
--NHC(O)NR.sup.7BR.sup.7C, --N(O).sub.m1, --NR.sup.7BR.sup.7C,
--C(O)R.sup.7D, --C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C,
--OR.sup.7A, --NR.sup.7BSO.sub.2R.sup.7A, --NR.sup.7BC(O)R.sup.7D,
--NR.sup.7BC(O)OR.sup.7D, --NR.sup.7BOR.sup.7D,
--OCX.sup.7.1.sub.3, --OCHX.sup.7.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.8 is hydrogen,
halogen, --CX.sup.8.1.sub.3, --CHX.sup.8.1.sub.2,
--CH.sub.2X.sup.8.1, --CN, --SO.sub.n1R.sup.8A,
--SO.sub.v1NR.sup.8BR.sup.8C, --NHNR.sup.8BR.sup.8C,
--ONR.sup.8BR.sup.8C, --NHC(O)NHNR.sup.8BR.sup.8C,
--NHC(O)NR.sup.8BR.sup.8C, --N(O).sub.m1, --NR.sup.8BR.sup.8C,
--C(O)R.sup.8D, --C(O)OR.sup.8D, --C(O)NR.sup.8BR.sup.8C,
--OR.sup.8A, --NR.sup.8BSO.sub.2R.sup.8A, --NR.sup.8BC(O)R.sup.8D,
--NR.sup.8BC(O)OR.sup.8D, --NR.sup.8BOR.sup.8D,
--OCX.sup.8.1.sub.3, --OCHX.sup.8.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.9 is hydrogen,
halogen, --CX.sup.9.1.sub.3, --CHX.sup.9.1.sub.2,
--CH.sub.2X.sup.9.1, --CN, --SO.sub.n1R.sup.9A,
--SO.sub.v1NR.sup.9BR.sup.9C, --NHNR.sup.9BR.sup.9C,
--ONR.sup.9BR.sup.9C, --NHC(O)NHNR.sup.9BR.sup.9C,
--NHC(O)NR.sup.9BR.sup.9C, --N(O).sub.m1, --NR.sup.9BR.sup.9C,
--C(O)R.sup.9D, --C(O)OR.sup.9D, --C(O)NR.sup.9BR.sup.9C,
--OR.sup.9A, --NR.sup.9BSO.sub.2R.sup.9A, --NR.sup.9BC(O)R.sup.9D,
--NR.sup.9BC(O)OR.sup.9D, --NR.sup.9BOR.sup.9D,
--OCX.sup.9.1.sub.3, --OCHX.sup.9.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.10 is hydrogen,
halogen, --CX.sup.10.1.sub.3, --CHX.sup.10.1.sub.2,
--CH.sub.2X.sup.10.1, --CN, --SO.sub.n1R.sup.10A,
--SO.sub.v1NR.sup.10BR.sup.10C, --NHNR.sup.10BR.sup.10C,
--ONR.sup.10BR.sup.10C, --NHC(O)NHNR.sup.10BR.sup.10C,
--NHC(O)NR.sup.10BR.sup.10C, --N(O).sub.m1, --NR.sup.10BR.sup.10C,
--C(O)R.sup.10D, --C(O)OR.sup.10D, --C(O)NR.sup.10BR.sup.10C,
--OR.sup.10A, --NR.sup.10BSO.sub.2R.sup.10A,
--NR.sup.10BC(O)R.sup.10D, --NR.sup.10BC(O)OR.sup.10D,
--NR.sup.10BOR.sup.10D, --OCX.sup.10.1.sub.3,
--OCHX.sup.10.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl; R.sup.1A, R.sup.1B, R.sup.1C,
R.sup.1D, R.sup.2A, R.sup.2B, R.sup.2C, R.sup.2D, R.sup.3A,
R.sup.3B, R.sup.3C, R.sup.3D, R.sup.4A, R.sup.4B, R.sup.4C,
R.sup.4D, R.sup.5A, R.sup.5B, R.sup.5C, R.sup.5D, R.sup.6A,
R.sup.6B, R.sup.6C, R.sup.6D, R.sup.7A, R.sup.7B, R.sup.7C,
R.sup.7D, R.sup.7.2B, R.sup.8A, R.sup.8B, R.sup.8C, R.sup.8D,
R.sup.9A, R.sup.9B, R.sup.9C, R.sup.9D, R.sup.10A, R.sup.10B,
R.sup.10C and R.sup.10D are independently hydrogen, halogen,
--CF.sub.3, --CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH,
--CONH.sub.2, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, or substituted or unsubstituted heteroaryl;
R.sup.1B, R.sup.1C, R.sup.2B, R.sup.2C, R.sup.3B, R.sup.3C,
R.sup.4B, R.sup.4C, R.sup.5B, R.sup.5C, R.sup.6B, R.sup.6C,
R.sup.7B, R.sup.7C, R.sup.8B, R.sup.8C, R.sup.9B, R.sup.9C,
R.sup.10B and R.sup.10C substituents bonded to the same nitrogen
atom may optionally be joined to form a substituted or
unsubstituted heterocycloalkyl or substituted or unsubstituted
heteroaryl; and X.sup.1.1, X.sup.2.1, X.sup.3.1, X.sup.4.1,
X.sup.5.1, X.sup.6.1, X.sup.7.1, X.sup.8.1, X.sup.9.1 and
X.sup.10.1 are independently --Cl, --Br, --I or --F, wherein at
least one of X.sup.1, X.sup.2 and X.sup.3 is N.
Embodiment P2
[0585] The compound of embodiment P1, wherein: z1 is 2; z2 is 0; z4
is 1; and R.sup.7 is hydrogen, substituted or unsubstituted alkyl,
phenyl, --F, --OH, CH.sub.2OH, --(CH.sub.2).sub.2OH,
--(CH.sub.2).sub.3OH, --C(CH.sub.3).sub.2OH,
--CH.sub.2SO.sub.2NH.sub.2, --(CH.sub.2).sub.2SO.sub.2NH.sub.2,
--CH.sub.2C(O)NH.sub.2, --(CH.sub.2).sub.2C(O)NH.sub.2,
--(CH.sub.2).sub.3C(O)NH.sub.2, --CH.sub.2NHSO.sub.2CF.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2CF.sub.3,
--(CH.sub.2).sub.3NHSO.sub.2CF.sub.3, --CH.sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.3NHSO.sub.2CH.sub.3, --CH.sub.2SO.sub.2CH.sub.3,
--(CH.sub.2).sub.2SO.sub.2CH.sub.3, --CH.sub.2SO.sub.2NH.sub.2 or
--(CH.sub.2).sub.2SO.sub.2NH.sub.2.
Embodiment P3
[0586] The compound of embodiment P2, wherein R.sup.1 and R.sup.2
are independently hydrogen, substituted or unsubstituted alkyl or
substituted or unsubstituted heteroalkyl.
Embodiment P4
[0587] The compound of embodiment P1, wherein the compound has
structural Formula (II):
##STR00066##
or a pharmaceutically acceptable salt thereof, wherein: R.sup.4 is
hydrogen, --CX.sup.4.1.sub.3, --CN, --C(O)NR.sup.4BR.sup.4C,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, or substituted or unsubstituted heteroaryl; R.sup.3.2 is
hydrogen, halogen, --CX.sup.3.2.sub.3, --CHX.sup.3.2.sub.2,
--CH.sub.2X.sup.3.2, --CN, --SO.sub.n1R.sup.3.2A,
--SO.sub.v1NR.sup.3.2BR.sup.3.2C, --NHNR.sup.3.2BR.sup.3.2C,
--ONR.sup.3.2BR.sup.3.2C, --NHC(O)NHNR.sup.3.2BR.sup.3.2C,
--NHC(O)NR.sup.3.2BR.sup.3.2C, --N(O).sub.m1,
--NR.sup.3.2BR.sup.3.2C, --C(O)R.sup.3.2D, --C(O)OR.sup.3.2D,
--C(O)NR.sup.3.2BR.sup.3.2C, --OR.sup.3.2A,
--NR.sup.3.2BSO.sub.2R.sup.3.2A, --NR.sup.3.2BC(O)R.sup.3.2D,
--NR.sup.3.2BC(O)OR.sup.3.2D, --NR.sup.3.2BOR.sup.3.2D,
--OCX.sup.3.2.sub.3, --OCHX.sup.3.2.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3.3 is hydrogen,
halogen, --CX.sup.3.3.sub.3, --CHX.sup.3.3.sub.2,
--CH.sub.2X.sup.3.3, --CN, --SO.sub.n1R.sup.3.3A,
--SO.sub.v1NR.sup.3.3BR.sup.3.3C, --NHNR.sup.3.3BR.sup.3.3C,
--ONR.sup.3.3BR.sup.3.3C, --NHC(O)NHNR.sup.3.3BR.sup.3.3C,
--NHC(O)NR.sup.3.3BR.sup.3.3C, --N(O).sub.m1,
--NR.sup.3.3BR.sup.3.3C, --C(O)R.sup.3.3D, --C(O)OR.sup.3.3D,
--C(O)NR.sup.3.3BR.sup.3.3C, --OR.sup.3.3A,
--NR.sup.3.3BSO.sub.2R.sup.3.3A, --NR.sup.3.3BC(O)R.sup.3.3D,
--NR.sup.3.3BC(O)OR.sup.3.3D, --NR.sup.3.3BOR.sup.3.3D,
--OCX.sup.3.3.sub.3, --OCHX.sup.3.3.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3.2A, R.sup.3.2B,
R.sup.3.2C, R.sup.3.2D, R.sup.3.3A, R.sup.3.3B, R.sup.3.3C and
R.sup.3.3D are independently hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, or substituted or unsubstituted heteroaryl; R.sup.3.2B,
R.sup.3.2C, R.sup.3.2B and R.sup.3.2C substituents bonded to the
same nitrogen atom may optionally be joined to form a substituted
or unsubstituted heterocycloalkyl or substituted or unsubstituted
heteroaryl; and X.sup.3.2 and X.sup.3.3 are independently --Cl,
--Br, --I or --F.
Embodiment P5
[0588] The compound of embodiment P4, wherein the compound has
structural Formula (IIa):
##STR00067##
or a pharmaceutically acceptable salt thereof.
Embodiment P6
[0589] The compound of embodiment P4, wherein the compound has
structural Formula (IIb):
##STR00068##
or a pharmaceutically acceptable salt thereof.
Embodiment P7
[0590] The compound of embodiment P5, wherein the compound has
structural Formula (IIc):
##STR00069##
or a pharmaceutically acceptable salt thereof.
Embodiment P8
[0591] The compound of embodiment P6, wherein the compound has
structural Formula (IId):
##STR00070##
or a pharmaceutically acceptable salt thereof.
Embodiment P9
[0592] The compound of embodiment P7 or P8, wherein z4 is 1.
Embodiment P10
[0593] The compound of embodiment P7 or P8, wherein R.sup.1 and
R.sup.2 are independently hydrogen, substituted or unsubstituted
alkyl or substituted or unsubstituted heteroalkyl.
Embodiment P11
[0594] The compound of embodiment P10, wherein R.sup.1 is
hydrogen.
Embodiment P12
[0595] The compound of embodiment P10, wherein R.sup.2 is
substituted or unsubstituted alkyl.
Embodiment P13
[0596] The compound of embodiment P7 or P8, wherein R.sup.4 is
hydrogen, --CN, --C(O)NH.sub.2, --CX.sup.413 or substituted or
unsubstituted alkyl.
Embodiment P14
[0597] The compound of embodiment P13, wherein R.sup.4 is --CN,
--C(O)NH.sub.2, --CF.sub.3 or --CH.sub.3.
Embodiment P15
[0598] The compound of embodiment P7 or P8, wherein R.sup.3.2 and
R.sup.3.3 are independently halogen.
Embodiment P16
[0599] The compound of embodiment P15, wherein R.sup.3.2 and
R.sup.3.3 are independently chlorine.
Embodiment P17
[0600] The compound of embodiment P7 or P8, wherein R.sup.7 is
--OR.sup.7A, --C(O)R.sup.7D, --C(O)OR.sup.7D,
--C(O)NR.sup.7BR.sup.7C, --SO.sub.n1R.sup.7A,
--SO.sub.v1NR.sup.7BR.sup.7C, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl or substituted
or unsubstituted heteroaryl.
Embodiment P18
[0601] The compound of embodiment P17, wherein L.sup.7 is a bond or
substituted or unsubstituted alkylene.
Embodiment P19
[0602] The compound of embodiment P7 or P8, wherein: L.sup.7 is a
bond; and R.sup.7 is hydrogen, substituted or unsubstituted alkyl,
phenyl, --(CH.sub.2).sub.2OH, --CH.sub.2C(CH.sub.3).sub.2OH,
--(CH.sub.2).sub.3OH, --(CH.sub.2).sub.2CH(CH.sub.3).sub.2OH,
--(CH.sub.2).sub.2SO.sub.2NH.sub.2,
--(CH.sub.2).sub.3SO.sub.2NH.sub.2, --(CH.sub.2).sub.2CONH.sub.2,
--(CH.sub.2).sub.3CONH.sub.2--(CH.sub.2).sub.3CON(H)Me,
--(CH.sub.2).sub.3CON(Me).sub.2, --(CH.sub.2).sub.2SO.sub.2Me,
--(CH.sub.2).sub.3SO.sub.2Me, --CH.sub.2CH(OH)Me,
--CH.sub.2CO.sub.2H, --(CH.sub.2).sub.2CO.sub.2H,
--CH(CH.sub.3)CH.sub.2CO.sub.2H, --(CH.sub.2).sub.3CO.sub.2H,
--(CH.sub.2).sub.2SO.sub.2NHCH.sub.3,
--(CH.sub.2).sub.2SO.sub.2N(CH.sub.3).sub.2,
--(CH.sub.2).sub.2SO.sub.2--(N-morpholinyl),
--(CH.sub.2).sub.2NHCOCH.sub.3, --(CH.sub.2).sub.3NHCOCH.sub.3,
--(CH.sub.2).sub.2NHCOCH(CH.sub.3).sub.2,
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2CF.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2NHCH(CH.sub.3).sub.2,
--CH.sub.2CH(CH.sub.3)CH.sub.2OH (R and S),
--CH(CH.sub.3)(CH.sub.2).sub.2OH, --CH.sub.2-(2-imidazoyl),
--CH.sub.2-(4-imidazoyl), --CH.sub.2-(3-pyrazoyl),
4-tetrahydropyranyl, 3-oxetanyl, --(CH.sub.2).sub.2NHCO.sub.2Me,
--(CH.sub.2).sub.3NHCO.sub.2Me.
Embodiment P20
[0603] The compound of embodiment P1, wherein the compound has
structural Formula (III):
##STR00071##
or a pharmaceutically acceptable salt thereof.
Embodiment P21
[0604] The compound of embodiment P1, wherein the compound has
structural Formula (IV):
##STR00072##
or a pharmaceutically acceptable salt thereof.
Embodiment P22
[0605] The compound of embodiment P1, wherein the compound has
structural Formula (V):
##STR00073##
or a pharmaceutically acceptable salt thereof.
Embodiment P23
[0606] The compound of any one of embodiments P20 to P22, wherein
R.sup.2 is hydrogen.
Embodiment P24
[0607] The compound of any one of embodiments P20 to P22, wherein
R.sup.1 is hydrogen.
Embodiment P25
[0608] The compound of any one of embodiments P20 to P22, wherein
R.sup.1 is --CH.sub.3.
Embodiment P26
[0609] The compound of embodiment P1, wherein the compound has the
structure:
##STR00074## ##STR00075## ##STR00076## ##STR00077## ##STR00078##
##STR00079## ##STR00080## ##STR00081## ##STR00082## ##STR00083##
##STR00084## ##STR00085## ##STR00086## ##STR00087##
Embodiment P27
[0610] A pharmaceutical composition, comprising a compound of
structural Formula (I) of embodiment P1 and a pharmaceutically
acceptable excipient.
Embodiment P28
[0611] A method of inhibiting C--C chemokine receptor type 4
(CCR4), the method comprising contacting CCR4 with a compound of
structural Formula (I) of embodiment P1.
Embodiment P29
[0612] A method of treating or preventing a disease or disorder
mediated by CCR4, comprising administering to a subject in need
thereof a therapeutically effective amount of a compound of
structural Formula (I) of embodiment P1 or a pharmaceutically
acceptable salt thereof.
Embodiment P30
[0613] The method of embodiment P29, wherein the disease or
disorder is an immune or inflammatory disease or disorder.
Embodiment P31
[0614] The method of embodiment P30, further comprising
co-administering an anti-inflammatory agent in combination with a
compound of structural Formula (I).
Embodiment P32
[0615] The method of embodiment P31, wherein the anti-inflammatory
is thalidomide or a derivative thereof, a retinoid, dithranol or
calcipotriol, a non-steroidal anti-inflammatory agent (NSAID),
cyclo-oxygenase inhibiting nitric oxide donors (CINODs),
glucocorticosteroids, methotrexate, leflunomide,
hydroxychloroquine, d-penicillamine, auranofin, analgesics;
diacerein, hyaluronic acid derivatives or nutritional
supplements.
Embodiment P33
[0616] The method of embodiment P29, wherein the disease or
disorder is a cardiovascular or metabolic disease or disorder.
Embodiment P34
[0617] The method of embodiment P33, further comprising
co-administering a cardiovascular agent or a metabolic disorder
agent in combination with a compound of structural Formula (I).
Embodiment P35
[0618] The method of embodiment P31, wherein the cardiovascular
agent is a calcium channel blocker, a beta-adrenoceptor blocker, an
angiotensin-converting enzyme (ACE) inhibitor, an angiotensin-2
receptor antagonist, a lipid lowering agent, a modulator of blood
cell morphology, a thrombolytic or an anticoagulant.
Embodiment P36
[0619] The method of embodiment P29, wherein the disease or
disorder is cancer.
Embodiment P37
[0620] The method of embodiment P36, further comprising
co-administering a chemotherapeutic agent or anticancer agent in
combination with a compound of structural Formula (I).
Embodiment P38
[0621] The method of embodiment P37, wherein the chemotherapeutic
agent or anticancer agent is an antiproliferative/antineoplastic
drug, an antimetabolite, an antitumour antibiotic, an antimitotic
agent, a topoisomerase inhibitor, a cytostatic agent, an oestrogen
receptor down regulator, an antiandrogen, a LHRH antagonist or LHRH
agonist, a progestogen, an aromatase inhibitor, an inhibitor of
5.alpha.-reductase, an agent which inhibits cancer cell invasion,
an inhibitor of growth factor function, a farnesyl transferase
inhibitor, a tyrosine kinase inhibitor, a serine/threonine kinase
inhibitor, an inhibitor of the epidermal growth factor family, an
inhibitor of the platelet-derived growth factor family, an
inhibitor of the hepatocyte growth factor family; an antiangiogenic
agent, a vascular damaging agent, an agent used in antisense
therapy, an anti-ras antisense, an agent used in a gene therapy, an
immunotherapeutic agent, or an antibody.
Embodiment P39
[0622] The method of embodiment P36, further comprising
co-administering a therapeutically effective amount of at least two
of: a CCR4 inhibitor, an inhibitor of the PD-L1/PD-1 pathway, an
inhibitor of CTLA-4 or an agonistic antibody of CD137 (4-1BB).
Embodiment P40
[0623] The method of embodiment P36, further comprising
co-administering a therapeutically effective amount of at least two
of: a CCR4 inhibitor, an agent that may be an immune modulator or
an agent from Table 1.
Embodiment P41
[0624] The method of any one of embodiments P37 to P40, wherein the
cancer is colon cancer or pancreatic cancer.
[0625] Further embodiments include embodiments 1 to 68
following.
Embodiment 1
[0626] A compound having structural Formula (I):
##STR00088##
or a pharmaceutically acceptable salt thereof, wherein: X.sup.1 is
CR.sup.8 or N; X.sup.2 is CR.sup.9 or N; X.sup.3 is CR.sup.10 or N;
n1, n2, n3, n4, n5, n6, n7, n8, n9, and n10 are independently an
integer from 0 to 4; m1, m2, m3, m4, m5, m6, m7, m8, m9, m10, v1,
v2, v3, v4, v5, v6, v7, v8, v9 and v10 are independently 1 or 2; z1
is an integer from 0 to 5; z2 is an integer from 0 to 2; z3 is an
integer from 0 to 11; z4 is an integer from 0 to 2; L.sup.7 is a
bond, --O--, --S--, --NR.sup.7.2B, --C(O)--, --C(O)O--, --S(O)--,
--S(O).sub.2--, substituted or unsubstituted alkylene, substituted
or unsubstituted heteroalkylene, substituted or unsubstituted
cycloalkylene, substituted or unsubstituted heterocycloalkylene,
substituted or unsubstituted arylene, or substituted or
unsubstituted heteroarylene; R.sup.1 is hydrogen, halogen,
--CX.sup.1.1.sub.3, --CHX.sup.1.1.sub.2, --CH.sub.2X.sup.1.1, --CN,
--N.sub.3, --SO.sub.n1R.sup.1A, --SO.sub.v1NR.sup.1BR.sup.1C,
--NHNR.sup.1BR.sup.1C, --ONR.sup.1BR.sup.1C,
--NHC(O)NHNR.sup.1BR.sup.1C, --NHC(O)NR.sup.1BR.sup.1C,
--N(O).sub.m1, --NR.sup.1BR.sup.1C, --C(O)R.sup.1D,
--C(O)OR.sup.1D, --C(O)NR.sup.1BR.sup.1C, --OR.sup.1A,
--NR.sup.1BSO.sub.2R.sup.1A, --NR.sup.1BC(O)R.sup.1D,
--NR.sup.1BC(O)OR.sup.1D, --NR.sup.1BOR.sup.1D,
--OCX.sup.1.1.sub.3, --OCHX.sup.1.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.2 is hydrogen,
halogen, --CX.sup.2.1.sub.3, --CHX.sup.2.1.sub.2,
--CH.sub.2X.sup.2.1, --CN, --N.sub.3, --SO.sub.n2R.sup.2A,
--SO.sub.v2NR.sup.2BR.sup.2C, --NHNR.sup.2BR.sup.2C,
--ONR.sup.2BR.sup.2C, --NHC(O)NHNR.sup.2BR.sup.2C,
--NHC(O)NR.sup.2BR.sup.2C, --N(O).sub.m2, --NR.sup.2BR.sup.2C,
--C(O)R.sup.2D, --C(O)OR.sup.2D, --C(O)NR.sup.2BR.sup.2C,
--OR.sup.2A, --NR.sup.2BSO.sub.2R.sup.2A, --NR.sup.2BC(O)R.sup.2D,
--NR.sup.2BC(O)OR.sup.2D, --NR.sup.2BOR.sup.2D,
--OCX.sup.2.1.sub.3, --OCHX.sup.2.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3 is
independently hydrogen, halogen, --CX.sup.3.1.sub.3,
--CHX.sup.3.1.sub.2, --CH.sub.2X.sup.3.1, --CN,
--SO.sub.n3R.sup.3A, --SO.sub.v3NR.sup.3BR.sup.3C,
--NHNR.sup.3BR.sup.3C, --ONR.sup.3BR.sup.3C,
--NHC(O)NHNR.sup.3BR.sup.3C, --NHC(O)NR.sup.3BR.sup.3C,
--N(O).sub.m3, --NR.sup.3BR.sup.3C, --C(O)R.sup.3D,
--C(O)OR.sup.3D, --C(O)NR.sup.3BR.sup.3C, --OR.sup.3A,
--NR.sup.3BSO.sub.2R.sup.3A, --NR.sup.3BC(O)R.sup.3D,
--NR.sup.3BC(O)OR.sup.3D, --NR.sup.3BOR.sup.3D,
--OCX.sup.3.1.sub.3, --OCHX.sup.3.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.4 is hydrogen,
halogen, --CX.sup.4.1.sub.3, --CHX.sup.4.1.sub.2,
--CH.sub.2X.sup.4.1, --CN, --N.sub.3, --SO.sub.n4R.sup.4A,
--SO.sub.v4NR.sup.4BR.sup.4C, --NHNR.sup.4BR.sup.4C,
--ONR.sup.4BR.sup.4C, --NHC(O)NHNR.sup.4BR.sup.4C,
--NHC(O)NR.sup.4BR.sup.4C, --N(O).sub.m4, --NR.sup.4BR.sup.4C,
--C(O)R.sup.4D, --C(O)OR.sup.4D, --C(O)NR.sup.4BR.sup.4C,
--OR.sup.4A, --NR.sup.4BSO.sub.2R.sup.4A, --NR.sup.4BC(O)R.sup.4D,
--NR.sup.4BC(O)OR.sup.4D, --NR.sup.4BOR.sup.4D,
--OCX.sup.4.1.sub.3, --OCHX.sup.4.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.5 is
independently hydrogen, halogen, oxo, --CX.sup.5.1.sub.3,
--CHX.sup.5.1.sub.2, --CH.sub.2X.sup.5.1, --CN, --N.sub.3,
--SO.sub.n5R.sup.5A, --SO.sub.v5NR.sup.5BR.sup.5C,
--NHNR.sup.5BR.sup.5C, --ONR.sup.5BR.sup.5C,
--NHC(O)NHNR.sup.5BR.sup.5C, --NHC(O)NR.sup.5BR.sup.5C,
--N(O).sub.m5, --NR.sup.5BR.sup.5C, --C(O)R.sup.5D,
--C(O)OR.sup.5D, --C(O)NR.sup.5BR.sup.5C, --OR.sup.5A,
--NR.sup.5BSO.sub.2R.sup.5A, --NR.sup.5BC(O)R.sup.5D,
--NR.sup.5BC(O)OR.sup.5D, --NR.sup.5BOR.sup.5D,
--OCX.sup.5.1.sub.3, --OCHX.sup.5.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.6 is
independently hydrogen, halogen, oxo, --CX.sup.6.1.sub.3,
--CHX.sup.6.1.sub.2, --CH.sub.2X.sup.6.1, --CN, --N.sub.3,
--SO.sub.n6R.sup.6A, --SO.sub.v6NR.sup.6BR.sup.6C,
--NHNR.sup.6BR.sup.6C, --ONR.sup.6BR.sup.6C,
--NHC(O)NHNR.sup.6BR.sup.6C, --NHC(O)NR.sup.6BR.sup.6C,
--N(O).sub.m6, --NR.sup.6BR.sup.6C, --C(O)R.sup.6D,
--C(O)OR.sup.6D, --C(O)NR.sup.6BR.sup.6C, --OR.sup.6A,
--NR.sup.6BSO.sub.2R.sup.6A, --NR.sup.6BC(O)R.sup.6D,
--NR.sup.6BC(O)OR.sup.6D, --NR.sup.6BOR.sup.6D,
--OCX.sup.6.1.sub.3, --OCHX.sup.6.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.7 is hydrogen,
halogen, --CX.sup.7.1.sub.3, --CHX.sup.7.1.sub.2,
--CH.sub.2X.sup.7.1, --CN, --N.sub.3, --SO.sub.n7R.sup.7A,
--SO.sub.v7NR.sup.7BR.sup.7C, --NHNR.sup.7BR.sup.7C,
--ONR.sup.7BR.sup.7C, --NHC(O)NHNR.sup.7BR.sup.7C,
--NHC(O)NR.sup.7BR.sup.7C, --N(O).sub.m7, --NR.sup.7BR.sup.7C,
--C(O)R.sup.7D, --C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C,
--OR.sup.7A, --NR.sup.7BSO.sub.2R.sup.7A, --NR.sup.7BC(O)R.sup.7D,
--NR.sup.7BC(O)OR.sup.7D, --NR.sup.7BOR.sup.7D,
--OCX.sup.7.1.sub.3, --OCHX.sup.7.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.8 is hydrogen,
halogen, --CX.sup.8.1.sub.3, --CHX.sup.8.1.sub.2,
--CH.sub.2X.sup.8.1, --CN, --N.sub.3, --SO.sub.n8R.sup.8A,
--SO.sub.v8NR.sup.8BR.sup.8C, --NHNR.sup.8BR.sup.8C,
--ONR.sup.8BR.sup.8C, --NHC(O)NHNR.sup.8BR.sup.8C,
--NHC(O)NR.sup.8BR.sup.8C, --N(O).sub.m8, --NR.sup.8BR.sup.8C,
--C(O)R.sup.8D, --C(O)OR.sup.8D, --C(O)NR.sup.8BR.sup.8C,
--OR.sup.8A, --NR.sup.8BSO.sub.2R.sup.8A, --NR.sup.8BC(O)R.sup.8D,
--NR.sup.8BC(O)OR.sup.8D, --NR.sup.8BOR.sup.8D,
--OCX.sup.8.1.sub.3, --OCHX.sup.8.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.9 is hydrogen,
halogen, --CX.sup.9.1.sub.3, --CHX.sup.9.1.sub.2,
--CH.sub.2X.sup.9.1, --CN, --N.sub.3, --SO.sub.9R.sup.9A,
--SO.sub.v9NR.sup.9BR.sup.9C, --NHNR.sup.9BR.sup.9C,
--ONR.sup.9BR.sup.9C, --NHC(O)NHNR.sup.9BR.sup.9C,
--NHC(O)NR.sup.9BR.sup.9C, --N(O).sub.m9, --NR.sup.9BR.sup.9C,
--C(O)R.sup.9D, --C(O)OR.sup.9D, --C(O)NR.sup.9BR.sup.9C,
--OR.sup.9A, --NR.sup.9BSO.sub.2R.sup.9A, --NR.sup.9BC(O)R.sup.9D,
--NR.sup.9BC(O)OR.sup.9D, --NR.sup.9BOR.sup.9D,
--OCX.sup.9.1.sub.3, --OCHX.sup.9.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.10 is hydrogen,
halogen, --CX.sup.10.1.sub.3, --CHX.sup.10.1.sub.2,
--CH.sub.2X.sup.10.1, --CN, --N.sub.3, --SO.sub.n1OR.sup.10A,
--SO.sub.v10NR.sup.10BR.sup.10C, --NHNR.sup.10BR.sup.10C,
--ONR.sup.10BR.sup.10C, --NHC(O)NHR.sup.10BR.sup.10C,
--NHC(O)NR.sup.10BR.sup.10C, --N(O).sub.m10, --NR.sup.10BR.sup.10C,
--C(O)R.sup.10D, --C(O)OR.sup.10D, --C(O)NR.sup.10BR.sup.10C,
--OR.sup.10A, --NR.sup.10B SO.sub.2R.sup.10A,
--NR.sup.10BC(O)R.sup.10D, --NR.sup.10BC(O)OR.sup.10D,
--NR.sup.10BOR.sup.10D, --OCX.sup.10.1.sub.3,
--OCHX.sup.10.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl; R.sup.1A, R.sup.1B, R.sup.1C,
R.sup.1D, R.sup.2A, R.sup.2B, R.sup.2C, R.sup.2D, R.sup.3A,
R.sup.3B, R.sup.3C, R.sup.3D, R.sup.4A, R.sup.4B, R.sup.4C,
R.sup.4D, R.sup.5A, R.sup.5B, R.sup.5C, R.sup.5D, R.sup.6A,
R.sup.6B, R.sup.6C, R.sup.6D, R.sup.7A, R.sup.7B, R.sup.7C,
R.sup.7D, R.sup.7.2B, R.sup.8A, R.sup.8B, R.sup.8C, R.sup.8D,
R.sup.9A, R.sup.9B, R.sup.9C, R.sup.9D, R.sup.10A, R.sup.10B,
R.sup.10C and R.sup.10D are independently hydrogen, halogen,
--CF.sub.3, --CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH,
--CONH.sub.2, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, or substituted or unsubstituted heteroaryl;
R.sup.1B, R.sup.1C, R.sup.2B, R.sup.2C, R.sup.3B, R.sup.3C,
R.sup.4B, R.sup.4C, R.sup.5B, R.sup.5C, R.sup.6B, R.sup.6C,
R.sup.7B, R.sup.7C, R.sup.8B, R.sup.8C, R.sup.9B, R.sup.9C,
R.sup.10B and R.sup.10C substituents bonded to the same nitrogen
atom may optionally be joined to form a substituted or
unsubstituted heterocycloalkyl or substituted or unsubstituted
heteroaryl; and X.sup.1.1, X.sup.2.1, X.sup.3.1, X.sup.4.1,
X.sup.5.1, X.sup.6.1, X.sup.7.1, X.sup.8.1, X.sup.9.1 and
X.sup.10.1 are independently --Cl, --Br, --I or --F, wherein at
least one of X.sup.1, X.sup.2 and X.sup.3 is N.
Embodiment 2
[0627] The compound of embodiment 1, or a pharmaceutically
acceptable salt thereof, wherein: z1 is 2; z2 is 0; z4 is 1; and
R.sup.7 is hydrogen, substituted or unsubstituted alkyl, phenyl,
--F, --OH, CH.sub.2OH, --(CH.sub.2).sub.2OH, --(CH.sub.2).sub.3OH,
--C(CH.sub.3).sub.2OH, --CH.sub.2SO.sub.2NH.sub.2,
--(CH.sub.2).sub.2SO.sub.2NH.sub.2, --CH.sub.2C(O)NH.sub.2,
--(CH.sub.2).sub.2C(O)NH.sub.2, --(CH.sub.2).sub.3C(O)NH.sub.2,
--CH.sub.2NHSO.sub.2CF.sub.3, --(CH.sub.2).sub.2NHSO.sub.2CF.sub.3,
--(CH.sub.2).sub.3NHSO.sub.2CF.sub.3, --CH.sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.3NHSO.sub.2CH.sub.3, --CH.sub.2SO.sub.2CH.sub.3,
--(CH.sub.2).sub.2SO.sub.2CH.sub.3, --CH.sub.2SO.sub.2NH.sub.2 or
--(CH.sub.2).sub.2SO.sub.2NH.sub.2.
Embodiment 3
[0628] The compound of embodiment 2, or a pharmaceutically
acceptable salt thereof, wherein R.sup.1 and R.sup.2 are
independently hydrogen, substituted or unsubstituted alkyl or
substituted or unsubstituted heteroalkyl.
Embodiment 4
[0629] The compound of embodiment 1, or a pharmaceutically
acceptable salt thereof, wherein the compound has structural
Formula (II):
##STR00089##
wherein: n3.2, and n3.3 are independently an integer from 0 to 4;
m3.2, m3.3, v3.2 and v3.3 are independently 1 or 2; R.sup.4 is
hydrogen, --CX.sup.4.1.sub.3, --CN, --C(O)NR.sup.4BR.sup.4C,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, or substituted or unsubstituted heteroaryl; R.sup.3.2 is
hydrogen, halogen, --CX.sup.3.2.sub.3, --CHX.sup.3.2.sub.2,
--CH.sub.2X.sup.3.2, --CN, --N.sub.3, --SO.sub.n3.2R.sup.3.2A,
--SO.sub.v3.2NR.sup.3.2BR.sup.3.2C, --NHNR.sup.3.2BR.sup.3.2C,
--ONR.sup.3.2BR.sup.3.2C, --NHC(O)NHNR.sup.3.2BR.sup.3.2C,
--NHC(O)NR.sup.3.2BR.sup.3.2C, --N(O).sub.m3.2,
--NR.sup.3.2BR.sup.3.2C, --C(O)R.sup.3.2D, --C(O)OR.sup.3.2D,
--C(O)NR.sup.3.2BR.sup.3.2C, --OR.sup.3.2A,
--NR.sup.3.2BSO.sub.2R.sup.3.2A, --NR.sup.3.2BC(O)R.sup.3.2D,
--NR.sup.3.2BC(O)OR.sup.3.2D, --NR.sup.3.2BOR.sup.3.2D,
--OCX.sup.3.2.sub.3, --OCHX.sup.3.2.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3.3 is hydrogen,
halogen, --CX.sup.3.3.sub.3, --CHX.sup.3.3.sub.2,
--CH.sub.2X.sup.3.3, --CN, --N.sub.3, --SO.sub.n3.3R.sup.3.3A,
--SO.sub.v3.3NR.sup.3.3BR.sup.3.3C, --NHNR.sup.3.3BR.sup.3.3C,
--ONR.sup.3.3BR.sup.3.3C, --NHC(O)NHNR.sup.3.3BR.sup.3.3C,
--NHC(O)NR.sup.3.3BR.sup.3.3C, --N(O).sub.m3.3,
--NR.sup.3.3BR.sup.3.3C, --C(O)R.sup.3.3D, C(O)OR.sup.3.3D,
--C(O)NR.sup.3.3BR.sup.3.3C, --OR.sup.3.3A,
--NR.sup.3.3BSO.sub.2R.sup.3.3A, --NR.sup.3.3BC(O)R.sup.3.3D,
--NR.sup.3.3BC(O)OR.sup.3.3D, --NR.sup.3.3BOR.sup.3.3D,
--OCX.sup.3.3.sub.3, --OCHX.sup.3.3.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3.2A, R.sup.3.2B,
R.sup.3.2C, R.sup.3.2D, R.sup.3.3A, R.sup.3.3B, R.sup.3.3C and
R.sup.3.3D are independently hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, or substituted or unsubstituted heteroaryl; R.sup.3.2B,
R.sup.3.2C, R.sup.3.2B and R.sup.3.2C substituents bonded to the
same nitrogen atom may optionally be joined to form a substituted
or unsubstituted heterocycloalkyl or substituted or unsubstituted
heteroaryl; and X.sup.3.2 and X.sup.3.3 are independently --Cl,
--Br, --I or --F.
Embodiment 5
[0630] The compound of embodiment 4, or a pharmaceutically
acceptable salt thereof, wherein the compound has structural
Formula (IIa):
##STR00090##
Embodiment 6
[0631] The compound of embodiment 4, or a pharmaceutically
acceptable salt thereof, wherein the compound has structural
Formula (IIb):
##STR00091##
Embodiment 7
[0632] The compound of embodiment 5, or a pharmaceutically
acceptable salt thereof, wherein the compound has structural
Formula (IIc):
##STR00092##
Embodiment 8
[0633] The compound of embodiment 6, or a pharmaceutically
acceptable salt thereof, wherein the compound has structural
Formula (IId):
##STR00093##
Embodiment 9
[0634] The compound of embodiment 7 or 8, or a pharmaceutically
acceptable salt thereof, wherein z4 is 1.
Embodiment 10
[0635] The compound of embodiment 7 or 8, or a pharmaceutically
acceptable salt thereof, wherein R.sup.1 and R.sup.2 are
independently hydrogen, substituted or unsubstituted alkyl or
substituted or unsubstituted heteroalkyl.
Embodiment 11
[0636] The compound of embodiment 10, or a pharmaceutically
acceptable salt thereof, wherein R.sup.1 is hydrogen.
Embodiment 12
[0637] The compound of embodiment 10, or a pharmaceutically
acceptable salt thereof, wherein R.sup.2 is substituted or
unsubstituted alkyl.
Embodiment 13
[0638] The compound of embodiment 7 or 8, or a pharmaceutically
acceptable salt thereof, wherein R.sup.4 is hydrogen, --CN,
--C(O)NH.sub.2, --CX.sup.413 or substituted or unsubstituted
alkyl.
Embodiment 14
[0639] The compound of embodiment 13, or a pharmaceutically
acceptable salt thereof, wherein R.sup.4 is --CN, --C(O)NH.sub.2,
--CF.sub.3 or --CH.sub.3.
Embodiment 15
[0640] The compound of embodiment 7 or 8, or a pharmaceutically
acceptable salt thereof, wherein R.sup.3.2 and R.sup.3.3 are
independently halogen.
Embodiment 16
[0641] The compound of embodiment 15, or a pharmaceutically
acceptable salt thereof, wherein R.sup.3.2 and R.sup.3.3 are
independently chlorine.
Embodiment 17
[0642] The compound of embodiment 7 or 8, or a pharmaceutically
acceptable salt thereof, wherein R.sup.7 is --OR.sup.7A,
--C(O)R.sup.7D, --C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C,
--SO.sub.n7R.sup.7A, SO.sub.v7NR.sup.7BR.sup.7C, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl.
Embodiment 18
[0643] The compound of embodiment 17, or a pharmaceutically
acceptable salt thereof, wherein L.sup.7 is a bond or substituted
or unsubstituted alkylene.
Embodiment 19
[0644] The compound of embodiment 7 or 8, or a pharmaceutically
acceptable salt thereof, wherein: L.sup.7 is a bond; and R.sup.7 is
hydrogen, substituted or unsubstituted alkyl, phenyl,
--(CH.sub.2).sub.2OH, --CH.sub.2C(CH.sub.3).sub.2OH,
--(CH.sub.2).sub.3OH, --(CH.sub.2).sub.2CH(CH.sub.3).sub.2OH,
--(CH.sub.2).sub.2SO.sub.2NH.sub.2,
--(CH.sub.2).sub.3SO.sub.2NH.sub.2, --(CH.sub.2).sub.2CONH.sub.2,
--(CH.sub.2).sub.3CONH.sub.2--(CH.sub.2).sub.3CON(H)Me,
--(CH.sub.2).sub.3CON(Me).sub.2, --(CH.sub.2).sub.2SO.sub.2Me,
--(CH.sub.2).sub.3SO.sub.2Me, --CH.sub.2CH(OH)Me,
--CH.sub.2CO.sub.2H, --(CH.sub.2).sub.2CO.sub.2H,
--CH(CH.sub.3)CH.sub.2CO.sub.2H, --(CH.sub.2).sub.3CO.sub.2H,
--(CH.sub.2).sub.2SO.sub.2NHCH.sub.3,
--(CH.sub.2).sub.2SO.sub.2N(CH.sub.3).sub.2,
--(CH.sub.2).sub.2SO.sub.2--(N-morpholinyl),
--(CH.sub.2).sub.2NHCOCH.sub.3, --(CH.sub.2).sub.3NHCOCH.sub.3,
--(CH.sub.2).sub.2NHCOCH(CH.sub.3).sub.2,
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2CF.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2NHCH(CH.sub.3).sub.2,
--CH.sub.2CH(CH.sub.3)CH.sub.2OH (R and S),
--CH(CH.sub.3)(CH.sub.2).sub.2OH, --CH.sub.2-(2-imidazoyl),
--CH.sub.2-(4-imidazoyl), --CH.sub.2-(3-pyrazoyl),
4-tetrahydropyranyl, 3-oxetanyl, --(CH.sub.2).sub.2NHCO.sub.2Me,
--(CH.sub.2).sub.3NHCO.sub.2Me.
Embodiment 20
[0645] The compound of embodiment 1, or a pharmaceutically
acceptable salt thereof, wherein the compound has structural
Formula (III):
##STR00094##
Embodiment 21
[0646] The compound of embodiment 1, or a pharmaceutically
acceptable salt thereof, wherein the compound has structural
Formula (IV):
##STR00095##
Embodiment 22
[0647] The compound of embodiment 1, or a pharmaceutically
acceptable salt thereof, wherein the compound has structural
Formula (V):
##STR00096##
Embodiment 23
[0648] The compound of any one of embodiments 20 to 22, or a
pharmaceutically acceptable salt thereof, wherein R.sup.2 is
hydrogen.
Embodiment 24
[0649] The compound of any one of embodiments 20 to 22, or a
pharmaceutically acceptable salt thereof, wherein R.sup.1 is
hydrogen.
Embodiment 25
[0650] The compound of any one of embodiments 20 to 22, or a
pharmaceutically acceptable salt thereof, wherein R.sup.1 is
--CH.sub.3.
Embodiment 26
[0651] The compound of embodiment 1, or a pharmaceutically
acceptable salt thereof, wherein the compound has the
structure:
##STR00097## ##STR00098## ##STR00099## ##STR00100## ##STR00101##
##STR00102## ##STR00103## ##STR00104## ##STR00105## ##STR00106##
##STR00107## ##STR00108## ##STR00109## ##STR00110##
Embodiment 27
[0652] The compound of embodiment 1, or a pharmaceutically
acceptable salt thereof, wherein the compound has the
structure:
##STR00111## ##STR00112## ##STR00113## ##STR00114## ##STR00115##
##STR00116## ##STR00117## ##STR00118## ##STR00119## ##STR00120##
##STR00121## ##STR00122## ##STR00123## ##STR00124## ##STR00125##
##STR00126## ##STR00127## ##STR00128## ##STR00129## ##STR00130##
##STR00131## ##STR00132##
Embodiment 28
[0653] A pharmaceutical composition, comprising a compound having
structural Formula (I) and a pharmaceutically acceptable
excipient:
##STR00133##
or a pharmaceutically acceptable salt thereof, wherein: X.sup.1 is
CR.sup.8 or N; X.sup.2 is CR.sup.9 or N; X.sup.3 is CR.sup.10 or N;
n1, n2, n3, n4, n5, n6, n7, n8, n9 and n10 are independently an
integer from 0 to 4; m1, m2, m3, m4, m5, m6, m7, m8, m9, m10, v1,
v2, v3, v4, v5, v6, v7, v8, v9 and v10 are independently 1 or 2; z1
is an integer from 0 to 5; z2 is an integer from 0 to 2; z3 is an
integer from 0 to 11; z4 is an integer from 0 to 2; L.sup.7 is a
bond, --O--, --S--, --NR.sup.7.2B--, --C(O)--, --C(O)O--, --S(O)--,
--S(O).sub.2--, substituted or unsubstituted alkylene, substituted
or unsubstituted heteroalkylene, substituted or unsubstituted
cycloalkylene, substituted or unsubstituted heterocycloalkylene,
substituted or unsubstituted arylene, or substituted or
unsubstituted heteroarylene; R.sup.1 is hydrogen, halogen,
--CX.sup.1.1.sub.3, --CHX.sup.1.1.sub.2, --CH.sub.2X.sup.1.1, --CN,
--N.sub.3, --SO.sub.n1R.sup.1A, --SO.sub.v1NR.sup.1BR.sup.1C,
--NHNR.sup.1BR.sup.1C, --ONR.sup.1BR.sup.1C,
--NHC(O)NHNR.sup.1BR.sup.1C, --NHC(O)NR.sup.1BR.sup.1C,
--N(O).sub.m1, --NR.sup.1BR.sup.1C, --C(O)R.sup.1D,
--C(O)OR.sup.1D, --C(O)NR.sup.1BR.sup.1C, --OR.sup.1A,
--NR.sup.1BSO.sub.2R.sup.1A, --NR.sup.1BC(O)R.sup.1D,
--NR.sup.1BC(O)OR.sup.1D, --NR.sup.1BOR.sup.1D,
--OCX.sup.1.1.sub.3, --OCHX.sup.1.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.2 is hydrogen,
halogen, --CX.sup.2.1.sub.3, --CHX.sup.2.1.sub.2,
--CH.sub.2X.sup.2.1, --CN, --N.sub.3, --SO.sub.n2R.sup.2A,
--SO.sub.v2NR.sup.2BR.sup.2C, --NHNR.sup.2BR.sup.2C,
--ONR.sup.2BR.sup.2C, --OR.sup.2BR.sup.2C,
--NHC(O)NHNR.sup.2BR.sup.2C, --NHC(O)NR.sup.2BR.sup.2C,
--N(O).sub.m2, --NR.sup.2BR.sup.2C, --C(O)R.sup.2D,
--C(O)OR.sup.2D, --C(O)NR.sup.2BR.sup.2C, --OR.sup.2A,
--NR.sup.2BSO.sub.2R.sup.2A, --NR.sup.2BC(O)R.sup.2D,
--NR.sup.2BC(O)OR.sup.2D, --NR.sup.2BOR.sup.2D,
--OCX.sup.2.1.sub.3, --OCHX.sup.2.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3 is
independently hydrogen, halogen, --CX.sup.3.1.sub.3,
--CHX.sup.3.1.sub.2, --CH.sub.2X.sup.3.1, --CN, --N.sub.3,
--SO.sub.n3R.sup.3A, --SO.sub.v3NR.sup.3BR.sup.3C,
--NHNR.sup.3BR.sup.3C, --ONR.sup.3BR.sup.3C,
--NHC(O)NHNR.sup.3BR.sup.3C, --NHC(O)NR.sup.3BR.sup.3C,
--N(O).sub.m3, --NR.sup.3BR.sup.3C, --C(O)R.sup.3D,
--C(O)OR.sup.3D, --C(O)NR.sup.3BR.sup.3C, --OR.sup.3A,
--NR.sup.3BSO.sub.2R.sup.3A, --NR.sup.3BC(O)R.sup.3D,
--NR.sup.3BC(O)OR.sup.3D, --NR.sup.3BOR.sup.3D,
--OCX.sup.3.1.sub.3, --OCHX.sup.3.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.4 is hydrogen,
halogen, --CX.sup.4.1.sub.3, --CHX.sup.4.1.sub.2,
--CH.sub.2X.sup.4.1, --CN, --N.sub.3, --SO.sub.n4R.sup.4A,
--SO.sub.v4NR.sup.4BR.sup.4C, --NHNR.sup.4BR.sup.4C,
--ONR.sup.4BR.sup.4C, --ONR.sup.4BR.sup.4C,
--NHC(O)NHNR.sup.4BR.sup.4C, --NHC(O)NR.sup.4BR.sup.4C,
--N(O).sub.m4, --NR.sup.4BR.sup.4C, --C(O)R.sup.4D,
--C(O)OR.sup.4D, --C(O)NR.sup.4BR.sup.4C, --OR.sup.4A,
--NR.sup.4BSO.sub.2R.sup.4A, --NR.sup.4BC(O)R.sup.4D,
--NR.sup.4BC(O)OR.sup.4D, --NR.sup.4BOR.sup.4D,
--OCX.sup.4.1.sub.3, --OCHX.sup.4.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.5 is
independently hydrogen, halogen, oxo, --CX.sup.5.1.sub.3,
--CHX.sup.5.1.sub.2, --CH.sub.2X.sup.5.1, --CN, --N.sub.3,
--SO.sub.n5R.sup.5A, --SO.sub.v5NR.sup.5BR.sup.5C,
--NHNR.sup.5BR.sup.5C, --ONR.sup.5BR.sup.5C,
--NHC(O)NHNR.sup.5BR.sup.5C, --NHC(O)NR.sup.5BR.sup.5C,
--N(O).sub.m5, --NR.sup.5BR.sup.5C, --C(O)R.sup.5D,
--C(O)OR.sup.5D, --C(O)NR.sup.5BR.sup.5C, --OR.sup.5A,
--NR.sup.5BSO.sub.2R.sup.5A, --NR.sup.5BC(O)R.sup.5D,
--NR.sup.5BC(O)OR.sup.5D, --NR.sup.5BOR.sup.5D,
--OCX.sup.5.1.sub.3, --OCHX.sup.5.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.6 is
independently hydrogen, halogen, oxo, --CX.sup.6.1.sub.3,
--CHX.sup.6.1.sub.2, --CH.sub.2X.sup.6.1, --CN, --N.sub.3,
--SO.sub.n6R.sup.6A, --SO.sub.v6NR.sup.6BR.sup.6C,
--NHNR.sup.6BR.sup.6C, --ONR.sup.6BR.sup.6C,
--NHC(O)NHNR.sup.6BR.sup.6C, --NHC(O)NR.sup.6BR.sup.6C,
--N(O).sub.m6, --NR.sup.6BR.sup.6C, --C(O)R.sup.6D,
--C(O)OR.sup.6D, --C(O)NR.sup.6BR.sup.6C, --OR.sup.6A,
--NR.sup.6BSO.sub.2R.sup.6A, --NR.sup.6BC(O)R.sup.6D,
--NR.sup.6BC(O)OR.sup.6D, --NR.sup.6BOR.sup.6D,
--OCX.sup.6.1.sub.3, --OCHX.sup.6.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.7 is hydrogen,
halogen, --CX.sup.7.1.sub.3, --CHX.sup.7.1.sub.2,
--CH.sub.2X.sup.7.1, --CN, --N.sub.3, --SO.sub.n7R.sup.7A,
--SO.sub.v7NR.sup.7BR.sup.7C, --NHNR.sup.7BR.sup.7C,
--ONR.sup.7BR.sup.7C, --NHC(O)NHNR.sup.7BR.sup.7C,
--NHC(O)NR.sup.7BR.sup.7C, --N(O).sub.m7, --NR.sup.7BR.sup.7C,
--C(O)R.sup.7D, --C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C,
--OR.sup.7A, --NR.sup.7BSO.sub.2R.sup.7A, --NR.sup.7BC(O)R.sup.7D,
--NR.sup.7BC(O)OR.sup.7D, --NR.sup.7BOR.sup.7D, --OCX.sup.7B,
--OCHX.sup.7.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl or substituted
or unsubstituted heteroaryl; R.sup.8 is hydrogen, halogen,
--CX.sup.8.1.sub.3, --CHX.sup.8.1.sub.2, --CH.sub.2X.sup.8.1, --CN,
--N.sub.3, --SO.sub.n8R.sup.8A, --SO.sub.v8NR.sup.8BR.sup.8C,
--NHNR.sup.8BR.sup.8C, --ONR.sup.8BR.sup.8C,
--NHC(O)NHNR.sup.8BR.sup.8C, --NHC(O)NR.sup.8BR.sup.8C,
--N(O).sub.m8, --NR.sup.8BR.sup.8C, --C(O)R.sup.8D,
--C(O)OR.sup.8D, --C(O)NR.sup.8BR.sup.8C, --OR.sup.8A,
--NR.sup.8BSO.sub.2R.sup.8A, --NR.sup.8BC(O)R.sup.8D,
--NR.sup.8BC(O)OR.sup.8D, --NR.sup.8BOR.sup.8D,
--OCX.sup.8.1.sub.3, --OCHX.sup.8.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.9 is hydrogen,
halogen, --CX.sup.9.1.sub.3, --CHX.sup.9.1.sub.2,
--CH.sub.2X.sup.9.1, --CN, --N.sub.3, --SO.sub.n9R.sup.9A,
--SO.sub.v9NR.sup.9BR.sup.9C, --NHNR.sup.9BR.sup.9C,
--ONR.sup.9BR.sup.9C, --NHC(O)NHNR.sup.9BR.sup.9C,
--NHC(O)NR.sup.9BR.sup.9C, --N(O).sub.m9, --NR.sup.9BR.sup.9C,
C(O)R.sup.9D, --C(O)OR.sup.9D, --C(O)NR.sup.9BR.sup.9C,
--OR.sup.9A, --NR.sup.9BSO.sub.2R.sup.9A, --NR.sup.9BC(O)R.sup.9D,
--NR.sup.9BC(O)OR.sup.9D, --NR.sup.9BOR.sup.9D,
--OCX.sup.9.1.sub.3, --OCHX.sup.9.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.10 is hydrogen,
halogen, --CX.sup.10.1.sub.3, --CHX.sup.10.1.sub.2,
--CH.sub.2X.sup.10.1, --CN, --N.sub.3, --SO.sub.n10R.sup.10A,
--SO.sub.v10NR.sup.10BR.sup.10C, --NHNR.sup.10BR.sup.10C,
--ONR.sup.10BR.sup.10C, --NHC(O)NHNR.sup.10BR.sup.10C,
--NHC(O)NR.sup.10BR.sup.10C, --N(O).sub.m10, --NR.sup.10BR.sup.10C,
--C(O)R.sup.10D, --C(O)OR.sup.10D, --C(O)NR.sup.10BR.sup.10C,
--OR.sup.10A, --NR.sup.10BSO.sub.2R.sup.10A,
--NR.sup.10BC(O)R.sup.10D, --NR.sup.10BC(O)OR.sup.10D,
--NR.sup.10BOR.sup.10D, --OCX.sup.10.1.sub.3,
--OCHX.sup.10.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl; R.sup.1A, R.sup.1B, R.sup.1C,
R.sup.1D, R.sup.2A, R.sup.2B, R.sup.2C, R.sup.2D, R.sup.3A,
R.sup.3B, R.sup.3C, R.sup.3D, R.sup.4A, R.sup.4B, R.sup.4C,
R.sup.4D, R.sup.5A, R.sup.5B, R.sup.5C, R.sup.5D, R.sup.6A,
R.sup.6B, R.sup.6C, R.sup.6D, R.sup.7A, R.sup.7B, R.sup.7C,
R.sup.7D, R.sup.7.2B, R.sup.8A, R.sup.8B, R.sup.8C, R.sup.8D,
R.sup.9A, R.sup.9B, R.sup.9C, R.sup.9D, R.sup.10A, R.sup.10B,
R.sup.10C and R.sup.10D are independently hydrogen, halogen,
--CF.sub.3, --CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH,
--CONH.sub.2, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, or substituted or unsubstituted heteroaryl;
R.sup.1B, R.sup.1C, R.sup.2B, R.sup.2C, R.sup.3B, R.sup.3C,
R.sup.4B, R.sup.4C, R.sup.5B, R.sup.5C, R.sup.6B, R.sup.6C,
R.sup.7B, R.sup.7C, R.sup.8B, R.sup.8C, R.sup.9B, R.sup.9C,
R.sup.10B and R.sup.10C substituents bonded to the same nitrogen
atom may optionally be joined to form a substituted or
unsubstituted heterocycloalkyl or substituted or unsubstituted
heteroaryl; and X.sup.1.1, X.sup.2.1, X.sup.3.1, X.sup.4.1,
X.sup.5.1, X.sup.6.1, X.sup.7.1, X.sup.8.1, X.sup.9.1 and
X.sup.10.1 are independently --Cl, --Br, --I or --F, wherein at
least one of X.sup.1, X.sup.2 and X.sup.3 is N.
Embodiment 29
[0654] A method of treating or preventing a disease or disorder
mediated by CCR4, comprising administering to a subject in need
thereof a therapeutically effective amount of the pharmaceutical
composition of embodiment 28.
Embodiment 30
[0655] A method of inhibiting C--C chemokine receptor type 4
(CCR4), comprising contacting CCR4 with a compound having
structural Formula (I):
##STR00134##
or a pharmaceutically acceptable salt thereof, wherein: X.sup.1 is
CR.sup.8 or N; X.sup.2 is CR.sup.9 or N; X.sup.3 is CR.sup.10 or N;
n1, n2, n3, n4, n5, n6, n7, n8, n9 and n10 are independently an
integer from 0 to 4; m1, m2, m3, m4, m5, m6, m7, m8, m9, m10, v1,
v2, v3, v4, v5, v6, v7, v8, v9 and v10 are independently 1 or 2; z1
is an integer from 0 to 5; z2 is an integer from 0 to 2; z3 is an
integer from 0 to 11; z4 is an integer from 0 to 2; L.sup.7 is a
bond, --O--, --S--, --NR.sup.7.2B--, --C(O)--, --C(O)O--, --S(O)--,
--S(O).sub.2--, substituted or unsubstituted alkylene, substituted
or unsubstituted heteroalkylene, substituted or unsubstituted
cycloalkylene, substituted or unsubstituted heterocycloalkylene,
substituted or unsubstituted arylene, or substituted or
unsubstituted heteroarylene; R.sup.1 is hydrogen, halogen,
--CX.sup.1.1.sub.3, --CHX.sup.1.1.sub.2, --CH.sub.2X.sup.1.1, --CN,
--N.sub.3, --SO.sub.n1R.sup.1A, --SO.sub.v1NR.sup.1BR.sup.1C,
--NHNR.sup.1BR.sup.1C, --ONR.sup.1BR.sup.1C,
--NHC(O)NHNR.sup.1BR.sup.1C, --NHC(O)NR.sup.1BR.sup.1C,
--N(O).sub.m1, --NR.sup.1BR.sup.1C, --C(O)R.sup.1D,
--C(O)OR.sup.1D, --C(O)NR.sup.1BR.sup.1C, --OR.sup.1A,
--NR.sup.1BSO.sub.2R.sup.1A, --NR.sup.1BC(O)R.sup.1D,
--NR.sup.1BC(O)OR.sup.1D, --NR.sup.1BOR.sup.1D,
--OCX.sup.1.1.sub.3, --OCHX.sup.1.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.2 is hydrogen,
halogen, --CX.sup.2.1.sub.3, --CHX.sup.2.1.sub.2,
--CH.sub.2X.sup.2.1, --CN, --N.sub.3, --SO.sub.n2R.sup.2A,
--SO.sub.v2NR.sup.2BR.sup.2C, --NHNR.sup.2BR.sup.2C,
--ONR.sup.2BR.sup.2C, --NHC(O)NHNR.sup.2BR.sup.2C,
--NHC(O)NR.sup.2BR.sup.2C, --N(O).sub.m2, --NR.sup.2BR.sup.2C,
--C(O)R.sup.2D, --C(O)OR.sup.2D, --C(O)NR.sup.2BR.sup.2C,
--OR.sup.2A, --NR.sup.2BSO.sub.2R.sup.2A, --NR.sup.2BC(O)R.sup.2D,
--NR.sup.2BC(O)OR.sup.2D, --NR.sup.2BOR.sup.2D,
--OCX.sup.2.1.sub.3, --OCHX.sup.2.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3 is
independently hydrogen, halogen, --CX.sup.3.1.sub.3,
--CHX.sup.3.1.sub.2, --CH.sub.2X.sup.3.1, --CN, --N.sub.3,
--SO.sub.n3R.sup.3A, --SO.sub.3NR.sup.3BR.sup.3C,
--NHNR.sup.3BR.sup.3C, --ONR.sup.3BR.sup.3C,
--NHC(O)NHNR.sup.3BR.sup.3C, --NHC(O)NR.sup.3BR.sup.3C,
--N(O).sub.m3, --NR.sup.3BR.sup.3C, --C(O)R.sup.3D,
--C(O)OR.sup.3D, --C(O)NR.sup.3BR.sup.3C, --OR.sup.3A,
--NR.sup.3BSO.sub.2R.sup.3A, --NR.sup.3BC(O)R.sup.3D,
--NR.sup.3BC(O)OR.sup.3D, --NR.sup.3BOR.sup.3D,
--OCX.sup.3.1.sub.3, --OCHX.sup.3.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.4 is hydrogen,
halogen, --CX.sup.4.1.sub.3, --CHX.sup.4.1.sub.2,
--CH.sub.2X.sup.4.1, --CN, --N.sub.3, --SO.sub.n4R.sup.4A,
--SO.sub.v4NR.sup.4BR.sup.4C, --NHNR.sup.4BR.sup.4C,
--ONR.sup.4BR.sup.4C, --NHC(O)NHNR.sup.4BR.sup.4C,
--NHC(O)NR.sup.4BR.sup.4C, --N(O).sub.m4, --NR.sup.4BR.sup.4C,
--C(O)R.sup.4D, --C(O)OR.sup.4D, --C(O)NR.sup.4BR.sup.4C,
--OR.sup.4A, --NR.sup.4BSO.sub.2R.sup.4A, --NR.sup.4BC(O)R.sup.4D,
--NR.sup.4BC(O)OR.sup.4D, --NR.sup.4BOR.sup.4D,
--OCX.sup.4.1.sub.3, OCHX.sup.4.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.5 is
independently hydrogen, halogen, oxo, --CX.sup.5.1.sub.3,
--CHX.sup.5.1.sub.2, --CH.sub.2X.sup.5.1, --CN, --N.sub.3,
--SO.sub.n5R.sup.5A, --SO.sub.v5NR.sup.5BR.sup.5C,
--NHNR.sup.5BR.sup.5C, --ONR.sup.5BR.sup.5C,
--NHC(O)NHNR.sup.5BR.sup.5C, --NHC(O)NR.sup.5BR.sup.5C,
--N(O).sub.m5, --NR.sup.5BR.sup.5C, --C(O)R.sup.5D,
--C(O)OR.sup.5D, --C(O)NR.sup.5BR.sup.5C, --OR.sup.5A,
--NR.sup.5BSO.sub.2R.sup.5A, --NR.sup.5BC(O)R.sup.5D,
--NR.sup.5BC(O)OR.sup.5D, --NR.sup.5BOR.sup.5D,
--OCX.sup.5.1.sub.3, --OCHX.sup.5.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.6 is
independently hydrogen, halogen, oxo, --CX.sup.6.1.sub.3,
--CHX.sup.6.1.sub.2, --CH.sub.2X.sup.6.1, --CN, --N.sub.3,
--SO.sub.n6R.sup.6A, --SO.sub.v6NR.sup.6BR.sup.6C,
--NHNR.sup.6BR.sup.6C, --ONR.sup.6BR.sup.6C,
--NHC(O)NHNR.sup.6BR.sup.6C, --NHC(O)NR.sup.6BR.sup.6C,
--N(O).sub.m6, --NR.sup.6BR.sup.6C, --C(O)R.sup.6D,
--C(O)OR.sup.6D, --C(O)NR.sup.6BR.sup.6C, --OR.sup.6A,
--NR.sup.6BSO.sub.2R.sup.6A, --NR.sup.6BC(O)R.sup.6D,
--NR.sup.6BC(O)OR.sup.6D, --NR.sup.6BOR.sup.6D,
--OCX.sup.6.1.sub.3, --OCHX.sup.6.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.7 is hydrogen,
halogen, --CX.sup.7.1.sub.3, --CHX.sup.7.1.sub.2,
--CH.sub.2X.sup.7.1, --CN, --N.sub.3, --SO.sub.n7R.sup.7A,
--SO.sub.v7NR.sup.7BR.sup.7C, --NHNR.sup.7BR.sup.7C,
--ONR.sup.7BR.sup.7C, --NHC(O)NHNR.sup.7BR.sup.7C,
--NHC(O)NR.sup.7BR.sup.7C, --N(O).sub.m7, --NR.sup.7BR.sup.7C,
--C(O)R.sup.7D, --C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C,
--OR.sup.7A, --NR.sup.7BSO.sub.2R.sup.7A, --NR.sup.7BC(O)R.sup.7D,
--NR.sup.7BC(O)OR.sup.7D, --NR.sup.7BOR.sup.7D, --OCX.sup.7B,
--OCHX.sup.7.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl or substituted
or unsubstituted heteroaryl; R.sup.8 is hydrogen, halogen,
--CX.sup.8.1.sub.3, --CHX.sup.8.1.sub.2, --CH.sub.2X.sup.8.1, --CN,
--N.sub.3, --SO.sub.n8R.sup.8A, --SO.sub.v8NR.sup.8BR.sup.8C,
--NHNR.sup.8BR.sup.8C, --ONR.sup.8BR.sup.8C,
--NHC(O)NHNR.sup.8BR.sup.8C, --NHC(O)NR.sup.8BR.sup.8C,
--N(O).sub.m8, --NR.sup.8BR.sup.8C, --C(O)R.sup.8D,
--C(O)OR.sup.8D, --C(O)NR.sup.8BR.sup.8C, --OR.sup.8A,
--NR.sup.8BSO.sub.2R.sup.8A, --NR.sup.8BC(O)R.sup.8D,
--NR.sup.8BC(O)OR.sup.8D, --NR.sup.8BOR.sup.8D,
--OCX.sup.8.1.sub.3, --OCHX.sup.8.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.9 is hydrogen,
halogen, --CX.sup.9.1.sub.3, --CHX.sup.9.1.sub.2,
--CH.sub.2X.sup.9.1, --CN, --N.sub.3, --SO.sub.n9R.sup.9A,
--SO.sub.v9NR.sup.9BR.sup.9C, --NHNR.sup.9BR.sup.9C,
--ONR.sup.9BR.sup.9C, --NHC(O)NHNR.sup.9BR.sup.9C,
--NHC(O)NR.sup.9BR.sup.9C, --N(O).sub.m9, --NR.sup.9BR.sup.9C,
--C(O)R.sup.9D, --C(O)OR.sup.9D, --C(O)NR.sup.9BR.sup.9C,
--OR.sup.9A, --NR.sup.9BSO.sub.2R.sup.9A, --NR.sup.9BC(O)R.sup.9D,
--NR.sup.9BC(O)OR.sup.9D, NR.sup.9BOR.sup.9D, --OCX.sup.9.1.sub.3,
--OCHX.sup.9.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl; R.sup.10 is hydrogen, halogen,
--CX.sup.10.1.sub.3, --CHX.sup.10.1.sub.2, --CH.sub.2X.sup.10.1,
--CN, --N.sub.3, --SO.sub.n10R.sup.10A,
--SO.sub.v10NR.sup.10BR.sup.10C, --NHNR.sup.10BR.sup.10C,
--ONR.sup.10BR.sup.10C, --NHC(O)NHNR.sup.10BR.sup.10C,
--NHC(O)NR.sup.10BR.sup.10C, --N(O).sub.m10, --NR.sup.10BR.sup.10C,
--C(O)R.sup.10D, --C(O)OR.sup.10D, --C(O)NR.sup.10BR.sup.10C,
--OR.sup.10A, --NR.sup.10BSO.sub.2R.sup.10A,
--NR.sup.10BC(O)R.sup.10D, --NR.sup.10BC(O)OR.sup.10D,
--NR.sup.10BOR.sup.10D, --OCX.sup.10.1.sub.3,
--OCHX.sup.10.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl; R.sup.1A, R.sup.1B, R.sup.1C,
R.sup.1D, R.sup.2A, R.sup.2B, R.sup.2C, R.sup.2D, R.sup.3A,
R.sup.3B, R.sup.3C, R.sup.3D, R.sup.4A, R.sup.4B, R.sup.4C,
R.sup.4D, R.sup.5A, R.sup.5B, R.sup.5C, R.sup.5D, R.sup.6A,
R.sup.6B, R.sup.6C, R.sup.6D, R.sup.7A, R.sup.7B, R.sup.7C,
R.sup.7D, R.sup.7.2B, R.sup.8A, R.sup.8B, R.sup.8C, R.sup.8D,
R.sup.9A, R.sup.9B, R.sup.9C, R.sup.9D, R.sup.10A, R.sup.10B,
R.sup.10C and R.sup.10D are independently hydrogen, halogen,
--CF.sub.3, --CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH,
--CONH.sub.2, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, or substituted or unsubstituted heteroaryl;
R.sup.1B, R.sup.1C, R.sup.2B, R.sup.2C, R.sup.3B, R.sup.3C,
R.sup.4B, R.sup.4C, R.sup.5B, R.sup.5C, R.sup.6B, R.sup.6C,
R.sup.7B, R.sup.7C, R.sup.8B, R.sup.8C, R.sup.9B, R.sup.9C,
R.sup.10B and R.sup.10C substituents bonded to the same nitrogen
atom may optionally be joined to form a substituted or
unsubstituted heterocycloalkyl or substituted or unsubstituted
heteroaryl; and X.sup.1.1, X.sup.2.1, X.sup.3.1, X.sup.4.1,
X.sup.5.1, X.sup.6.1, X.sup.7.1, X.sup.8.1, X.sup.9.1 and
X.sup.10.1 are independently --Cl, --Br, --I or --F, wherein at
least one of X.sup.1, X.sup.2 and X.sup.3 is N.
Embodiment 31
[0656] A method of treating or preventing a disease or disorder
mediated by CCR4, comprising administering to a subject in need
thereof a therapeutically effective amount of a compound having
structural Formula (I):
##STR00135##
or a pharmaceutically acceptable salt thereof, wherein: X.sup.1 is
CR.sup.8 or N; X.sup.2 is CR.sup.9 or N; X.sup.3 is CR.sup.10 or N;
n1, n2, n3, n4, n5, n6, n7, n8, n9 and n10 are independently an
integer from 0 to 4; m1, m2, m3, m4, m5, m6, m7, m8, m9, m10, v1,
v2, v3, v4, v5, v6, v7, v8, v9 and v10 are independently 1 or 2; z1
is an integer from 0 to 5; z2 is an integer from 0 to 2; z3 is an
integer from 0 to 11; z4 is an integer from 0 to 2; L.sup.7 is a
bond, --O--, --S--, --NR.sup.7.2B--, --C(O)--, --C(O)O--, --S(O)--,
--S(O).sub.2--, substituted or unsubstituted alkylene, substituted
or unsubstituted heteroalkylene, substituted or unsubstituted
cycloalkylene, substituted or unsubstituted heterocycloalkylene,
substituted or unsubstituted arylene, or substituted or
unsubstituted heteroarylene; R.sup.1 is hydrogen, halogen,
--CX.sup.1.1.sub.3, --CHX.sup.1.1.sub.2, --CH.sub.2X.sup.1.1, --CN,
--N.sub.3, --SO.sub.n1R.sup.1A, --SO.sub.v1NR.sup.1BR.sup.1C,
--NHNR.sup.1BR.sup.1C, --ONR.sup.1BR.sup.1C,
--NHC(O)NHNR.sup.1BR.sup.1C, --NHC(O)NR.sup.1BR.sup.1C,
--N(O).sub.m1, --NR.sup.1BR.sup.1C, --C(O)R.sup.1D,
--C(O)OR.sup.1D, --C(O)NR.sup.1BR.sup.1C, --OR.sup.1A,
--NR.sup.1BSO.sub.2R.sup.1A, --NR.sup.1BC(O)R.sup.1D,
--NR.sup.1BC(O)OR.sup.1D, --NR.sup.1BOR.sup.1D,
--OCX.sup.1.1.sub.3, --OCHX.sup.1.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.2 is hydrogen,
halogen, --CX.sup.2.1.sub.3, --CHX.sup.2.1.sub.2,
--CH.sub.2X.sup.2.1, --CN, --N.sub.3, --SO.sub.n2R.sup.2A,
--SO.sub.v2NR.sup.2BR.sup.2C, --NHNR.sup.2BR.sup.2C,
--ONR.sup.2BR.sup.2C, --NHC(O)NHNR.sup.2BR.sup.2C,
--NHC(O)NR.sup.2BR.sup.2C, --N(O).sub.m2, --NR.sup.2BR.sup.2C,
--C(O)R.sup.2D, --C(O)OR.sup.2D, --C(O)NR.sup.2BR.sup.2C,
--OR.sup.2A, --NR.sup.2BSO.sub.2R.sup.2A, --NR.sup.2BC(O)R.sup.2D,
--NR.sup.2BC(O)OR.sup.2D, --NR.sup.2BOR.sup.2D,
--OCX.sup.2.1.sub.3, --OCHX.sup.2.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3 is
independently hydrogen, halogen, --CX.sup.3.1.sub.3,
--CHX.sup.3.1.sub.2, --CH.sub.2X.sup.3.1, --CN, --N.sub.3,
--SO.sub.n3R.sup.3A, --SO.sub.v3NR.sup.3BR.sup.3C,
--NHNR.sup.3BR.sup.3C, --ONR.sup.3BR.sup.3C,
--NHC(O)NHNR.sup.3BR.sup.3C, --NHC(O)NR.sup.3BR.sup.3C,
--N(O).sub.m3, --NR.sup.3BR.sup.3C, --C(O)R.sup.3D,
--C(O)OR.sup.3D, --C(O)NR.sup.3BR.sup.3C, --OR.sup.3A,
--NR.sup.3BSO.sub.2R.sup.3A, --NR.sup.3BC(O)R.sup.3D,
--NR.sup.3BC(O)OR.sup.3D, --NR.sup.3BOR.sup.3D,
--OCX.sup.3.1.sub.3, --OCHX.sup.3.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.4 is hydrogen,
halogen, --CX.sup.4.1.sub.3, --CHX.sup.4.1.sub.2,
--CH.sub.2X.sup.4.1, --CN, --N.sub.3, --SO.sub.n4R.sup.4A,
--SO.sub.v4NR.sup.4BR.sup.4C, --NHR.sup.4BR.sup.4C,
--ONR.sup.4BR.sup.4C, --ONR.sup.4BR.sup.4C,
--NHC(O)NHNR.sup.4BR.sup.4C, --NHC(O)NR.sup.4BR.sup.4C,
--N(O).sub.m4, --NR.sup.4BR.sup.4C, --C(O)R.sup.4D,
--C(O)OR.sup.4D, --C(O)NR.sup.4BR.sup.4C, --OR.sup.4A,
--NR.sup.4BSO.sub.2R.sup.4A, --NR.sup.4BC(O)R.sup.4D,
--NR.sup.4BC(O)OR.sup.4D, --NR.sup.4BOR.sup.4D,
--OCX.sup.4.1.sub.3, --OCHX.sup.4.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.5 is
independently hydrogen, halogen, oxo, --CX.sup.5.1.sub.3,
--CHX.sup.5.1.sub.2, --CH.sub.2X.sup.5.1, --CN, --N.sub.3,
--SO.sub.n5R.sup.5A, --SO.sub.v5NR.sup.5BR.sup.5C,
--NHNR.sup.5BR.sup.5C, --ONR.sup.5BR.sup.5C,
--NHC(O)NHNR.sup.5BR.sup.5C, --NHC(O)NR.sup.5BR.sup.5C,
--N(O).sub.m5, --NR.sup.5BR.sup.5C, --C(O)R.sup.5D,
--C(O)OR.sup.5D, --C(O)NR.sup.5BR.sup.5C, --OR.sup.5A,
--NR.sup.5BSO.sub.2R.sup.5A, --NR.sup.5BC(O)R.sup.5D,
--NR.sup.5BC(O)OR.sup.5D, --NR.sup.5BOR.sup.5D,
--OCX.sup.5.1.sub.3, --OCHX.sup.5.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.6 is
independently hydrogen, halogen, oxo, --CX.sup.6.1.sub.3,
--CHX.sup.6.1.sub.2, --CH.sub.2X.sup.6.1, --CN, --N.sub.3,
--SO.sub.n6R.sup.6A, --SO.sub.v6NR.sup.6BR.sup.6C,
--NHNR.sup.6BR.sup.6C, --ONR.sup.6BR.sup.6BR.sup.6C,
--NHC(O)NHNR.sup.6BR.sup.6C, --NHC(O)NR.sup.6BR.sup.6C,
--N(O).sub.m6, --NR.sup.6BR.sup.6C, --C(O)R.sup.6D,
--C(O)OR.sup.6D, --C(O)NR.sup.6BR.sup.6C, --OR.sup.6A,
--NR.sup.6BSO.sub.2R.sup.6A, --NR.sup.6BC(O)R.sup.6D,
--NR.sup.6BC(O)OR.sup.6D, --NR.sup.6BOR.sup.6D,
--OCX.sup.6.1.sub.3, --OCHX.sup.6.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.7 is hydrogen,
halogen, --CX.sup.7.1.sub.3, --CHX.sup.7.1.sub.2,
--CH.sub.2X.sup.7.1, --CN, --N.sub.3, --SO.sub.n7R.sup.7A--,
--SO.sub.v7NR.sup.7BR.sup.7C, --NHNR.sup.7BR.sup.7C,
--ONR.sup.7BR.sup.7C, --NHC(O)NHNR.sup.7BR.sup.7C,
--NHC(O)NR.sup.7BR.sup.7C, --N(O).sub.m7, --NR.sup.7BR.sup.7C,
--C(O)R.sup.7D, --C(O)OR.sup.7D, --C(O)NR.sup.7BR.sup.7C,
--OR.sup.7A, --NR.sup.7BSO.sub.2R.sup.7A, --NR.sup.7BC(O)R.sup.7D,
--NR.sup.7BC(O)OR.sup.7D, --NR.sup.7BOR.sup.7D,
--OCX.sup.7.1.sub.3, --OCHX.sup.7.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl
or substituted or unsubstituted heteroaryl; R.sup.8 is hydrogen,
halogen, --CX.sup.8.1.sub.3, --CHX.sup.8.1.sub.2,
--CH.sub.2X.sup.8.1, --CN, --N.sub.3, --SO.sub.n8R.sup.8A,
--SO.sub.v8NR.sup.8BR.sup.8C, --NHNR.sup.8BR.sup.8C,
--ONR.sup.8BR.sup.8C, --NHC(O)NHNR.sup.8BR.sup.8C,
--NHC(O)NR.sup.8BR.sup.8C, --N(O).sub.m8, --NR.sup.8BR.sup.8C,
--C(O)R.sup.8D, --C(O)OR.sup.8D, --C(O)NR.sup.8BR.sup.8C,
--OR.sup.8A, --NR.sup.8BSO.sub.2R.sup.8A, --NR.sup.8BC(O)R.sup.8D,
--NR.sup.8BC(O)OR.sup.8D, --NR.sup.8BOR.sup.8D,
--OCX.sup.8.1.sub.3, --OCHX.sup.8.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.9 is hydrogen,
halogen, --CX.sup.9.1.sub.3, --CHX.sup.9.1.sub.2,
--CH.sub.2X.sup.9.1, --CN, --N.sub.3, --SO.sub.n9R.sup.9A,
--SO.sub.v9NR.sup.9BR.sup.9C, --NHNR.sup.9BR.sup.9C,
--ONR.sup.9BR.sup.9C, --NHC(O)NHNR.sup.9BR.sup.9C,
--NHC(O)NR.sup.9BR.sup.9C, --N(O).sub.m9, --NR.sup.9BR.sup.9C,
--C(O)R.sup.9D, --C(O)OR.sup.9D, --C(O)NR.sup.9BR.sup.9C,
--OR.sup.9A, --NR.sup.9BSO.sub.2R.sup.9A, --NR.sup.9BC(O)R.sup.9D,
--NR.sup.9BC(O)OR.sup.9D, --NR.sup.9BOR.sup.9D,
--OCX.sup.9.1.sub.3, --OCHX.sup.9.1.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.10 is hydrogen,
halogen, --CX.sup.10.1.sub.3, --CHX.sup.10.1.sub.2,
--CH.sub.2X.sup.10.1, --CN, --N.sub.3, --SO.sub.n10R.sup.10A,
--SO.sub.v10NR.sup.10BR.sup.10C, --NHNR.sup.10BR.sup.10C,
--ONR.sup.10BR.sup.10C, --NHC(O)NHNR.sup.10BR.sup.10C,
--NHC(O)NR.sup.10BR.sup.10C, --N(O).sub.m10, --NR.sup.10BR.sup.10C,
--C(O)R.sup.10D, C(O)OR.sup.10D, --C(O)NR.sup.10BR.sup.10C,
--OR.sup.10A, --NR.sup.10BSO.sub.2R.sup.10A,
--NR.sup.10BC(O)R.sup.10D, --NR.sup.10BC(O)OR.sup.10D,
--NR.sup.10BOR.sup.10D, --OCX.sup.10.1.sub.3,
--OCHX.sup.10.1.sub.2, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, or substituted
or unsubstituted heteroaryl; R.sup.1A, R.sup.1B, R.sup.1C,
R.sup.1D, R.sup.2A, R.sup.2B, R.sup.2C, R.sup.2D, R.sup.3A,
R.sup.3B, R.sup.3C, R.sup.3D, R.sup.4A, R.sup.4B, R.sup.4C,
R.sup.4D, R.sup.5A, R.sup.5B, R.sup.5C, R.sup.5D, R.sup.6A,
R.sup.6B, R.sup.6C, R.sup.6D, R.sup.7A, R.sup.7B, R.sup.7C,
R.sup.7D, R.sup.7.2B, R.sup.8A, R.sup.8B, R.sup.8C, R.sup.8D,
R.sup.9A, R.sup.9B, R.sup.9C, R.sup.9D, R.sup.10A, R.sup.10B,
R.sup.10C and R.sup.10D are independently hydrogen, halogen,
--CF.sub.3, --CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH,
--CONH.sub.2, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, or substituted or unsubstituted heteroaryl;
R.sup.1B, R.sup.1C, R.sup.2B, R.sup.2C, R.sup.3B, R.sup.3C,
R.sup.4B, R.sup.4C, R.sup.5B, R.sup.5C, R.sup.6B, R.sup.6C,
R.sup.7B, R.sup.7C, R.sup.8B, R.sup.8C, R.sup.9B, R.sup.9C,
R.sup.10B and R.sup.10C substituents bonded to the same nitrogen
atom may optionally be joined to form a substituted or
unsubstituted heterocycloalkyl or substituted or unsubstituted
heteroaryl; and X.sup.1.1, X.sup.2.1, X.sup.3.1, X.sup.4.1,
X.sup.5.1, X.sup.6.1, X.sup.7.1, X.sup.8.1, X.sup.9.1 and
X.sup.10.1 are independently --Cl, --Br, --I or --F, wherein at
least one of X.sup.1, X.sup.2 and X.sup.3 is N.
Embodiment 32
[0657] The method of embodiment 31, wherein: z1 is 2; z4 is 1; and
R.sup.7 is hydrogen, substituted or unsubstituted alkyl, phenyl,
--F, --OH, CH.sub.2OH, --(CH.sub.2).sub.2OH, --(CH.sub.2).sub.3OH,
--C(CH.sub.3).sub.2OH, --CH.sub.2SO.sub.2NH.sub.2,
--(CH.sub.2).sub.2SO.sub.2NH.sub.2, --CH.sub.2C(O)NH.sub.2,
--(CH.sub.2).sub.2C(O)NH.sub.2, --(CH.sub.2).sub.3C(O)NH.sub.2,
--CH.sub.2NHSO.sub.2CF.sub.3, --(CH.sub.2).sub.2NHSO.sub.2CF.sub.3,
--(CH.sub.2).sub.3NHSO.sub.2CF.sub.3, --CH.sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.3NHSO.sub.2CH.sub.3, --CH.sub.2SO.sub.2CH.sub.3,
--(CH.sub.2).sub.2SO.sub.2CH.sub.3, --CH.sub.2SO.sub.2NH.sub.2 or
--(CH.sub.2).sub.2SO.sub.2NH.sub.2.
Embodiment 33
[0658] The method of embodiment 32, wherein R.sup.1 and R.sup.2 are
independently hydrogen, substituted or unsubstituted alkyl or
substituted or unsubstituted heteroalkyl.
Embodiment 34
[0659] The method of embodiment 31, wherein the compound has
structural Formula (II):
##STR00136##
or a pharmaceutically acceptable salt thereof, wherein: n3.2, and
n3.3 are independently an integer from 0 to 4; m3.2, m3.3, v3.2 and
v3.3 are independently 1 or 2; R.sup.4 is hydrogen,
--CX.sup.4.1.sub.3, --CN, --C(O)NR.sup.4BR.sup.4C, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3.2 is hydrogen,
halogen, --CX.sup.3.2.sub.3, --CHX.sup.3.2.sub.2,
--CH.sub.2X.sup.3.2, --CN, --N.sub.3, --SO.sub.n3.2R.sup.3.2A,
--SO.sub.v3.2NR.sup.3.2BR.sup.3.2C, --NHNR.sup.3.2BR.sup.3.2C,
--ONR.sup.3.2BR.sup.3.2C, --NHC(O)NHNR.sup.3.2BR.sup.3.2C,
--NHC(O)NR.sup.3.2BR.sup.3.2C, --N(O).sub.m3.2,
--NR.sup.3.2BR.sup.3.2C, --C(O)R.sup.3.2D, --C(O)OR.sup.3.2D,
--C(O)NR.sup.3.2BR.sup.3.2C, --OR.sup.3.2A,
--NR.sup.3.2BSO.sub.2R.sup.3.2A, --NR.sup.3.2BC(O)R.sup.3.2D,
--NR.sup.3.2BC(O)OR.sup.3.2D, --NR.sup.3.2BOR.sup.3.2D,
--OCX.sup.3.2.sub.3, --OCHX.sup.3.2.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3.3 is hydrogen,
halogen, --CX.sup.3.3, --CHX.sup.3.3.sub.2, --CH.sub.2X.sup.3.3,
--CN, --N.sub.3, --SO.sub.n3.3R.sup.3.3A,
--SO.sub.v3.3NR.sup.3BR.sup.3BR.sup.3.3C,
--NHNR.sup.3.3BR.sup.3.3C, --ONR.sup.3.3BR.sup.3.3C,
--NHC(O)NHNR.sup.3.3BR.sup.3.3C, --NHC(O)NR.sup.3.3BR.sup.3.3C,
--N(O).sub.m3.3, --NR.sup.3.3BR.sup.3.3C, --C(O)R.sup.3.3D,
--C(O)OR.sup.3.3D, --C(O)NR.sup.3.3BR.sup.3.3C, --OR.sup.3.3A,
--NR.sup.3.3BSO.sub.2R.sup.3.3A, --NR.sup.3.3BC(O)R.sup.3.3D,
--NR.sup.3.3BC(O)OR.sup.3.3D, --NR.sup.3.3BOR.sup.3.3D,
--OCX.sup.3.3.sub.3, --OCHX.sup.3.3.sub.2, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
or substituted or unsubstituted heteroaryl; R.sup.3.2A, R.sup.3.2B,
R.sup.3.2C, R.sup.3.2D, R.sup.3.3A, R.sup.3.3B, R.sup.3.3C and
R.sup.3.3D are independently hydrogen, halogen, --CF.sub.3,
--CCl.sub.3, --CBr.sub.3, --CI.sub.3, --COOH, --CONH.sub.2,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, or substituted or unsubstituted heteroaryl; R.sup.3.2B,
R.sup.3.2C, R.sup.3.2B and R.sup.3.2C substituents bonded to the
same nitrogen atom may optionally be joined to form a substituted
or unsubstituted heterocycloalkyl or substituted or unsubstituted
heteroaryl; and X.sup.3.2 and X.sup.3.3 are independently --Cl,
--Br, --I or --F.
Embodiment 35
[0660] The method of embodiment 34, wherein the compound has
structural Formula (IIa):
##STR00137##
or a pharmaceutically acceptable salt thereof.
Embodiment 36
[0661] The method of embodiment 34, wherein the compound has
structural Formula (IIb):
##STR00138##
or a pharmaceutically acceptable salt thereof.
Embodiment 37
[0662] The method of embodiment 35, wherein the compound has
structural Formula (IIc):
##STR00139##
or a pharmaceutically acceptable salt thereof.
Embodiment 38
[0663] The method of embodiment 36, wherein the compound has
structural Formula (IId):
##STR00140##
or a pharmaceutically acceptable salt thereof.
Embodiment 39
[0664] The method of embodiment 37 or 38, wherein z4 is 1.
Embodiment 40
[0665] The method of embodiment 37 or 38, wherein R.sup.1 and
R.sup.2 are independently hydrogen, substituted or unsubstituted
alkyl or substituted or unsubstituted heteroalkyl.
Embodiment 41
[0666] The method of embodiment 40, wherein R.sup.1 is
hydrogen.
Embodiment 42
[0667] The method of embodiment 40, wherein R.sup.2 is substituted
or unsubstituted alkyl.
Embodiment 43
[0668] The method of embodiment 37 or 38, wherein R.sup.4 is
hydrogen, --CN, --C(O)NH.sub.2, --CX.sup.4.1.sub.3 or substituted
or unsubstituted alkyl.
Embodiment 44
[0669] The method of embodiment 43, wherein R.sup.4 is --CN,
--C(O)NH.sub.2, --CF.sub.3 or --CH.sub.3.
Embodiment 45
[0670] The method of embodiment 37 or 38, wherein R.sup.3.2 and
R.sup.3.3 are independently halogen.
Embodiment 46
[0671] The method of embodiment 45, wherein R.sup.3.2 and R.sup.3.3
are independently chlorine.
Embodiment 47
[0672] The method of embodiment 37 or 38, wherein R.sup.7 is
--OR.sup.7A, --C(O)R.sup.7D, C(O)OR.sup.7D,
--C(O)NR.sup.7BR.sup.7C, --SO.sub.n7R.sup.7A,
--SO.sub.v7NR.sup.7BR.sup.7C, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl or substituted
or unsubstituted heteroaryl.
Embodiment 48
[0673] The method of embodiment 47, wherein L.sup.7 is a bond or
substituted or unsubstituted alkylene.
Embodiment 49
[0674] The method of embodiment 37 or 38, wherein: L.sup.7 is a
bond; and R.sup.7 is hydrogen, substituted or unsubstituted alkyl,
phenyl, --(CH.sub.2).sub.2OH, --CH.sub.2C(CH.sub.3).sub.2OH,
--(CH.sub.2).sub.3OH, --(CH.sub.2).sub.2CH(CH.sub.3).sub.2OH,
--(CH.sub.2).sub.2SO.sub.2NH.sub.2,
--(CH.sub.2).sub.3SO.sub.2NH.sub.2, --(CH.sub.2).sub.2CONH.sub.2,
--(CH.sub.2).sub.3CONH.sub.2--(CH.sub.2).sub.3CON(H)Me,
--(CH.sub.2).sub.3CON(Me).sub.2, --(CH.sub.2).sub.2SO.sub.2Me,
--(CH.sub.2).sub.3SO.sub.2Me, --CH.sub.2CH(OH)Me,
--CH.sub.2CO.sub.2H, --(CH.sub.2).sub.2CO.sub.2H,
--CH(CH.sub.3)CH.sub.2CO.sub.2H, --(CH.sub.2).sub.3CO.sub.2H,
--(CH.sub.2).sub.2SO.sub.2NHCH.sub.3,
--(CH.sub.2).sub.2SO.sub.2N(CH.sub.3).sub.2,
--(CH.sub.2).sub.2SO.sub.2--(N-morpholinyl),
--(CH.sub.2).sub.2NHCOCH.sub.3, --(CH.sub.2).sub.3NHCOCH.sub.3,
--(CH.sub.2).sub.2NHCOCH(CH.sub.3).sub.2,
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2CF.sub.3,
--(CH.sub.2).sub.2NHSO.sub.2NHCH(CH.sub.3).sub.2,
--CH.sub.2CH(CH.sub.3)CH.sub.2OH (R and S),
--CH(CH.sub.3)(CH.sub.2).sub.2OH, --CH.sub.2-(2-imidazoyl),
--CH.sub.2-(4-imidazoyl), --CH.sub.2-(3-pyrazoyl),
4-tetrahydropyranyl, 3-oxetanyl, --(CH.sub.2).sub.2NHCO.sub.2Me,
--(CH.sub.2).sub.3NHCO.sub.2Me.
Embodiment 50
[0675] The method of embodiment 31, wherein the compound has
structural Formula (III):
##STR00141##
or a pharmaceutically acceptable salt thereof.
Embodiment 51
[0676] The method of embodiment 31, wherein the compound has
structural Formula (IV):
##STR00142##
or a pharmaceutically acceptable salt thereof.
Embodiment 52
[0677] The method of embodiment 31, wherein the compound has
structural Formula (V):
##STR00143##
or a pharmaceutically acceptable salt thereof.
Embodiment 53
[0678] The method of any one of embodiments 50 to 52, wherein
R.sup.2 is hydrogen.
Embodiment 54
[0679] The method of any one of embodiments 50 to 52, wherein
R.sup.1 is hydrogen.
Embodiment 55
[0680] The method of any one of embodiments 50 to 52, wherein
R.sup.1 is --CH.sub.3.
Embodiment 56
[0681] The method of embodiment 31, wherein the compound has the
structure:
##STR00144## ##STR00145## ##STR00146## ##STR00147## ##STR00148##
##STR00149## ##STR00150## ##STR00151## ##STR00152## ##STR00153##
##STR00154## ##STR00155## ##STR00156## ##STR00157## ##STR00158##
##STR00159## ##STR00160##
or a pharmaceutically acceptable salt thereof.
Embodiment 57
[0682] The method of embodiment 31, wherein the disease or disorder
is an immune or inflammatory disease or disorder.
Embodiment 58
[0683] The method of embodiment 57, further comprising
co-administering an anti-inflammatory agent in combination with a
compound of structural Formula (I) or a pharmaceutically acceptable
salt thereof.
Embodiment 59
[0684] The method of embodiment 58, wherein the anti-inflammatory
is thalidomide or a derivative thereof, a retinoid, dithranol,
calcipotriol, a non-steroidal anti-inflammatory agent (NSAID), a
cyclo-oxygenase inhibiting nitric oxide donor (CINOD), a
glucocorticosteroid, methotrexate, leflunomide, hydroxychloroquine,
d-penicillamine, auranofin, ananalgesic, a diacerein, hyaluronic
acid derivative, or a nutritional supplement.
Embodiment 60
[0685] The method of embodiment 31, wherein the disease or disorder
is a cardiovascular or metabolic disease or disorder.
Embodiment 61
[0686] The method of embodiment 60, further comprising
co-administering a cardiovascular agent or a metabolic disorder
agent in combination with a compound of structural Formula (I).
Embodiment 62
[0687] The method of embodiment 61, wherein the cardiovascular
agent is a calcium channel blocker, a beta-adrenoceptor blocker, an
angiotensin-converting enzyme (ACE) inhibitor, an angiotensin-2
receptor antagonist, a lipid lowering agent, a modulator of blood
cell morphology, a thrombolytic or an anticoagulant.
Embodiment 63
[0688] The method of embodiment 31, wherein the disease or disorder
is cancer.
Embodiment 64
[0689] The method of embodiment 63, further comprising
co-administering a chemotherapeutic agent or anticancer agent in
combination with a compound of structural Formula (I).
Embodiment 65
[0690] The method of embodiment 64, wherein the chemotherapeutic
agent or anticancer agent is an antiproliferative/antineoplastic
drug, an antimetabolite, an antitumour antibiotic, an antimitotic
agent, a topoisomerase inhibitor, a cytostatic agent, an oestrogen
receptor down regulator, an antiandrogen, a LHRH antagonist or LHRH
agonist, a progestogen, an aromatase inhibitor, an inhibitor of
5.alpha.-reductase, an agent which inhibits cancer cell invasion,
an inhibitor of growth factor function, a farnesyl transferase
inhibitor, a tyrosine kinase inhibitor, a serine/threonine kinase
inhibitor, an inhibitor of the epidermal growth factor family, an
inhibitor of the platelet-derived growth factor family, an
inhibitor of the hepatocyte growth factor family; an antiangiogenic
agent, a vascular damaging agent, an agent used in antisense
therapy, an anti-ras antisense, an agent used in a gene therapy, an
immunotherapeutic agent, or an antibody.
Embodiment 66
[0691] The method of embodiment 65, further comprising
co-administering a therapeutically effective amount of at least two
of: a CCR4 inhibitor, an inhibitor of the PD-L1/PD-1 pathway, an
inhibitor of CTLA-4 or an agonistic antibody of CD137 (4-1BB).
Embodiment 67
[0692] The method of embodiment 65, further comprising
co-administering a therapeutically effective amount of at least two
of: a CCR4 inhibitor, an immune modulator agent or an agent from
Table 1, or any combination thereof.
Embodiment 68
[0693] The method of any one of embodiments 63 to 67, wherein the
cancer is colon cancer or pancreatic cancer.
EXAMPLES
[0694] It is understood that the examples and embodiments described
herein are for illustrative purposes only and that various
modifications or changes in light thereof will be suggested to
persons skilled in the art and are to be included within the spirit
and purview of this application and scope of the appended claims.
All publications, patents, and patent applications cited herein are
hereby incorporated by reference in their entirety for all
purposes.
[0695] The successful operation of the host defense system is the
result of several processes that work together to eliminate foreign
pathogens. Coordinated innate and acquired immune responses are
required, and many secreted and cell-associated factors have been
identified as important mediators coordinating and regulating these
two arms of host defense (see, e.g., Ness, T. et al. (2006) J
Immunol 177:7531-39).
[0696] Chemokines are a family of cytokines that act as
chemoattractants to guide leukocyte migration. They are secreted by
a wide variety of cells and can be functionally divided into two
groups, hemostatic chemokines and inflammatory chemokines.
Hemostatic chemokines are constituently produced in certain tissues
and control cells of the immune system during processes of immune
surveillance, such as directing lymphocytes to the lymph nodes to
allow them to screen for invasion of pathogens. Inflammatory
chemokines are released from cells in response to a pathological
event (e.g., pro-inflammatory stimuli such as IL-1 or viruses).
They function primarily as chemoattractants as part of the
inflammatory response and serve to guide cells of both the innate
and adaptive immune systems to the site of inflammation. [See,
e.g., Le, Y. et al. (2004) Cellular & Molec Immuno
1(2):95-104.]
[0697] Structurally, there are four subgroups of chemokines,
classified according to the spacing of the first two cysteine
residues: i) CC chemokines (.beta.-chemokines) have adjacent
cysteines; ii) CXC chemokines (.alpha.-chemokines) having a single
amino acid residue between the first two cysteines; iii) C
chemokines (.gamma.-chemokines) have only a single N-terminal
cysteine residue; and iv) CX.sub.3C chemokines (.delta.-chemokines)
having three amino acid residues between the first two cysteines.
CC chemokines, examples of which include monocyte chemoattractant
protein-1 (MCP-1 or CCL2) and CCL5 (RANTES), induce the migration
of monocytes and other cell types; at least 27 members have been
identified. CXC chemokines (some 17 in number) can be subdivided
into two groups, both of which have unique structural and
functional features; the CXC chemokines bind to CXC chemokine
receptors, of which 7 are known (designated CXCR1-7). Only two
members of the C chemokine subgroup have been identified, XCL1 and
XCL2 (lymphotactin-.alpha. and -.beta., respectively). Finally, the
CX.sub.3C chemokine subgroup has only one member, CX.sub.3CL1,
which is both secreted and associated with the surface of the cells
that express it, resulting in both chemoattractant and adhesion
properties. [See Sokol, C. and Luster, A. (2015) Cold Spring Harb
Prospect Biol doi: 10.1101/cshperspect.a016303.]
[0698] Chemokines bind to specific G protein-coupled receptors
("chemokine receptors"), which are characterized by containing
seven transmembrane domains, found on the surface of leukocytes
(see Horuk (1994) Trends Pharm. Sci. 15:159-165). Approximately 20
human chemokine receptors have been identified, which are divided
into four subgroups depending on the type of chemokine they bind:
CXCR bind CXC chemokines; CCR bind CC chemokines; CX3CR1 binds
CX3CL1, the sole CXC3 chemokine; and XCR1 binds XCL1 and XCL2, the
two XC chemokines. Binding of a chemokine ligand to its cognate
receptor triggers the receptor, resulting in dissociation of an
intracellular heterotrimeric G-protein complex into G.alpha. and
G.beta..gamma. subunits. These second messengers play an integral
role in the activation of several signaling cascades (e.g., the MAP
kinase pathway), resulting in responses that include chemotaxis,
inflammatory mediator release, degranulation, and changes in cell
shape. Chemokine receptors have been implicated as being important
mediators of inflammatory and immunoregulatory disorders and
diseases, including asthma and allergic diseases, as well as
autoimmune pathologies such as rheumatoid arthritis and
atherosclerosis. [See, e.g., Comerford, I. and McColl, S. (2011)
Immunol Cell Biol 89:183-84.]
[0699] The C--C chemokine receptor type 4 (CCR4), first identified
by Power et al. (J. Biol. Chem. 270:19495-500 (1995)), plays a
vital role in the progression of a number of inflammation-related
and other disorders (Gadhe, C G (February 2015) Mol Biosyst
11(2):618-34). CCR4 is a high affinity receptor for the C--C-type
chemokines CCL2 (MCP-1), CCL4 (MIP-1), CCL5 (RANTES), CCL17 (TARC),
and CCL22 (MDC). Increased expression of CCR4 and its ligands is
associated with the pathogenesis of a diverse array of diseases,
including pulmonary fibrosis, hepatic inflammation, granuloma
development, certain cancers and diabetes, each of which is
characterized by the infiltration of CCR4.sup.+ T cells into
affected sites. The identification of compounds that modulate CCR4
function provides an opportunity for the development of therapeutic
agents for the treatment of a diverse array of diseases and
disorders associated with CCR4 activation.
[0700] The present invention relates to compounds that inhibit C--C
chemokine receptor type 4 (CCR4) activity, and compositions (e.g.,
pharmaceutical compositions) comprising the compounds. Such
compounds, including methods of their synthesis, and compositions
are described in detail herein. The present invention also relates
to the use of such compounds and compositions for the treatment
and/or prevention of diseases, disorders and conditions mediated,
in whole or in part, by CCR4.
[0701] Many subjects suffer from the debilitating effects of
inflammatory- and/or immune-related disorders such as asthma and
rheumatoid arthritis. Recently generated data support the role of
inhibitors of CCR4 function to modulate such inflammatory- and/or
immune-related activity in a therapeutically beneficial manner. In
addition, subjects diagnosed with cancer and the number of deaths
attributable to cancer continue to rise, both in the US and abroad.
Traditional treatment approaches comprising chemotherapy and
radiotherapy are generally difficult for the patient to tolerate
and become less effective as cancers (e.g., tumors) evolve to
circumvent such treatments.
[0702] Identification of CCR4 Inhibitors
[0703] In embodiments, compounds described herein possess at least
one property or characteristic that is of therapeutic relevance.
Candidate inhibitors may be identified by using, for example, an
art-accepted assay or model. The Example section described assay(s)
that were used to determine the CCR4 inhibitory activity of the
compounds described herein, as well as assays that could be used to
evaluate one or more characteristics of the compounds; the skilled
artisan is aware of other procedures, assay formats, and the like
that can be employed to generate data and information useful to
assess the CCR4 inhibitors described herein.
[0704] After identification, candidate inhibitors can be further
evaluated by using techniques that provide data regarding
characteristics of the inhibitors (e.g., pharmacokinetic
parameters). Comparisons of the candidate inhibitors to a reference
standard (which may the "best-of-class" of current inhibitors) are
indicative of the potential viability of such candidates. CCR4
inhibitors that can serve as reference or benchmark compounds
include those shown to demonstrate desired activity and
characteristics as described in, for example, US Patent Publn
2012/0015932 and PCT Publn 2013/082490. Other means of analyzing
candidate inhibitors will be apparent to the skilled artisan.
[0705] Synthesis Details
[0706] The following general schemes represent synthetic methods
that may be used in the preparation of the compounds of the present
invention, as well as common chemical intermediates generated in
the preparation thereof. The skilled artisan will recognize that
these schemes are representative only, and that in many instances
alternative synthetic means may be employed.
[0707] The following examples are put forth so as to provide those
of ordinary skill in the art with a complete disclosure and
description of how to make and use the present invention, and are
not intended to limit the scope of what the inventors regard as
their invention, nor are they intended to represent that the
experiments below were performed or that they are all of the
experiments that may be performed. It is to be understood that
exemplary descriptions written in the present tense were not
necessarily performed, but rather that the descriptions can be
performed to generate data and the like of a nature described
therein. Efforts have been made to ensure accuracy with respect to
numbers used (e.g., amounts, temperature, etc.), but some
experimental errors and deviations should be accounted for.
[0708] Unless indicated otherwise, parts are parts by weight,
molecular weight is weight average molecular weight, temperature is
in degrees Celsius (.degree. C.), and pressure is at or near
atmospheric. Standard abbreviations are used, including the
following: wt=wildtype; bp=base pair(s); kb=kilobase(s);
nt=nucleotides(s); aa=amino acid(s); s or sec=second(s);
min=minute(s); h or hr=hour(s); ng=nanogram; Lg=microgram;
mg=milligram; g=gram; kg=kilogram; dl or dL=deciliter; .mu.l or
.mu.L=microliter; ml or mL=milliliter; l or L=liter; M=micromolar;
mM=millimolar; M=molar; kDa=kilodalton; i.m.=intramuscular(ly);
i.p.=intraperitoneal(ly); SC or SQ=subcutaneous(ly); QD=daily;
BID=twice daily; QW=weekly; QM=monthly; psi=pounds per square inch;
HPLC=high performance liquid chromatography; BW=body weight;
U=unit; ns=not statistically significant;
HATU=(1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium
3-oxid hexafluorophosphate); TFA=trifluoroacetic acid; MBTE=methyl
t-butyl ether; DCM=dichloromethane; PBS=phosphate-buffered saline;
IHC=immunohistochemistry; DMSO=dimethylsulfoxide; EtOAc=ethyl
acetate; EtOH=ethanol; DMEM=Dulbeco's Modification of Eagle's
Medium; EDTA=ethylenediaminetetraacetic acid; Me=methyl; Et=ethyl;
S--singlet; D--doublet; dd--doublet of doublet; m--multiplet.
[0709] General preparation of the hydrazine starting material:
##STR00161##
[0710] A substituted aminomethyl benzene of general structure 1 can
be reacted with an alkaline metal cyanate such as potassium cyanate
in an acidified solvent such as concentrated HCl. The resulting
urea of general structure 2 can be isolated by standard methods
such as filtration. After suitable purification, the urea of
general structure 2 can be dissolved in a mixture of organic
solvents such as toluene and tert-butanol and treated with t-butyl
hypochlorite under a nitrogen atmosphere and the mixture is cooled
to a temperature between -40 and 0.degree. C. preferably around
-20.degree. C. The mixture is then warmed to 0.degree. C. and the
resulting solution is transferred to a flask containing a solution
of an alkoxide base such a potassium t-butoxide in a mixture of
organic solvents such as toluene and t-butanol which was being
maintained at temperature between -40 and 0.degree. C. preferably
at -20.degree. C. After the addition the reaction is stirred for 15
min at a temperature of 0.degree. C. and then poured onto ice
water. The mixture is allowed to warm to room temperature over 20
min and is then extracted with an organic solvent such as ethyl
acetate. The organic extract is washed with water, an aqueous
solution of sodium thiosulfate, and brine. The mixture is then
concentrated to give the desired tert-butyl hydrazine carboxylate
intermediate which can be immediate hydrolyzed in an acidic organic
mixture such as HCl in dioxane for 8-24 h. Concentration of the
solution followed by trituration of the resulting residue with an
organic solvent such as ethyl acetate to give the desired hydrazine
hydrochloride 3.
[0711] General synthesis of pyrazolopyrazine and pyridines:
##STR00162##
[0712] A solution of hydrazine hydrochloride of general structure 3
in a protic organic solvent such as ethanol is treated with the
ketone of general structure 4. The mixture was stirred for 8 h at
room temperature. The reaction is concentrated under reduced
pressure to give a residue. The residue was suspended in the
mixture of organic solvents such as ethyl acetate and hexanes and
then filtered through a silica gel plug and eluted with a similar
solvent mixture. The filtrate is concentrated to give the crude
hydrazone of the general structure 5 as a mixture of E and Z
isomers.
[0713] The mixture of E and Z hydrazine isomers of general
structure 5 is dissolved in a polar aprotic solvent such as
N-methyl-2-pyrrolidinone and treated with excess of a Lewis base,
for example 2,6-lutidine. The mixture is degassed with nitrogen and
stirred under a nitrogen atmosphere at an elevated temperature for
example 100.degree. C., for eight h. The reaction mixture is cooled
to room temperature and then poured into an acidic aqueous solution
such as 1M HCl and the resulting mixture is extracted with an
organic solvent such as ethyl acetate. The layers were separated
and the organic layer was washed with an acidic aqueous solution
such as 1M HCl, dried over a drying agent such as magnesium
sulfate, and concentrated under reduced pressure. The resulting
residue could be optionally be purified by recrystallization or
silica gel chromatography using a mixture of organic solvents for
example a mixture of MBTE and DCM to give compounds of the general
formula 6.
[0714] In certain instances, where ketone 4 is not commercially
available, it can be prepared in the following way:
##STR00163##
[0715] A solution of halide of general structure 4a and a source of
acetate in polar aprotic solvent such as THF is treated with a
strong alkali complex base such as LiTMP at low temperature
-78.degree. C. to afford 4 which is used right away in the next
step described in the previous procedure to afford compounds of the
general formula 6.
##STR00164##
[0716] A solution of halide of general structure 6 in an organic
solvent such as dioxane is treated with ammonia source such as
ammonium hydroxide (29% in water). The mixture is stirred at room
temperature for 3 d. The reaction is diluted with a solvent such as
ethyl acetate and washed with a weak aqueous base such as aqueous
sodium carbonate. The organic layer is separated and dried over a
drying agent such as magnesium sulfate. The organic layer is
concentrated under reduced pressure to give compounds of general
formula 7. A solution of primary amide of general structure 7 in a
polar aprotic organic solvent such as DCM at room temperature under
innert atmosphere is added dehydration agent such as Burgess'
reagent. The mixture was stirred at room temperature for about 2d.
The resulting mixture can be purified by silica gel chromatography
using a mixture of organic solvents for example a mixture of EtOAc
and Hexanes to give compounds of the general formula 8.
[0717] General synthesis of azetidine derivatives:
##STR00165##
[0718] To a solution of the protected ketone of general structure
10 in an organic solvent such as dichloroethane is added amine 9
and an imine reducing agent such as sodium triacetoxyborohydride
and the mixture is stirred for between 4 and 18 h. The reaction is
treated with a weak aqueous base such as aqueous sodium carbonate
and the mixture is extracted with an organic solvent such as ethyl
acetate. The organic solvent is separated, treated with a drying
agent such as sodium sulfate and the dried solution is evaporated
to give amine of general structure 11. The protective group on
compound of general structure 11 can be exposed to an acidic
organic solution, for example HCl in dioxane or trifluoroacetic
acid in DCM or can be removed using catalytic Pd. The mixture is
stirred at room temperature for a time between one and 16 h. The
reaction mixture can be concentrated or filtered through a celite
pad and then concentrated under reduced pressure to give an amine
salt of the general structure 12 that can be used in subsequent
reactions without further purification.
[0719] Alternatively the piperidine 9 can be be reacted with an
alkyl halide optionally in the presence sodium iodide, in the
presence of a base such as sodium carbonate in a solvent such as
DMF. After stirring between 4 and 18 h, the reaction is diluted
with water, and the mixture is extracted with an organic solvent
such as ethyl acetate. The organic solvent is separated, treated
with a drying agent such as sodium sulfate and the dried solution
is evaporated to give amine of general structure 11. The protective
group on compound of general structure 11 can be exposed to an
acidic organic solution, for example HCl in dioxane or
trifluoroacetic acid in DCM or can be removed using catalytic Pd.
The mixture is stirred at room temperature for a time between one
and 16 h. The reaction mixture can be concentrated or filtered
through a celite pad and then concentrated under reduced pressure
to give an amine salt of the general structure 12 that can be used
in subsequent reactions without further purification.
##STR00166##
[0720] For instances where R.sup.8 contains electron withdrawing
groups (EWG):
##STR00167##
[0721] To a solution of amine of general structure 9 in dry organic
solvent such as DCM is added Michael acceptor 13. Reaction mixture
was stirred either at room temperature or at 50.degree. C. until
complete conversion which can be monitored using TLC or LCMS. Upon
completion solvent is removed. The resulting residue can be
purified by silica gel chromatography using a mixture of organic
solvents for example a mixture of MeOH and DCM to give compounds of
the general formula 14. The protective group on compound of general
structure 14 can be exposed to an acidic organic solution, for
example HCl in dioxane or trifluoroacetic acid in DCM or can be
removed using catalytic Pd. The mixture is stirred at room
temperature for a time between one and 16 h. The reaction mixture
can be concentrated or filtered through a celite pad and then
concentrated under reduced pressure to give an amine salt of the
general structure 12 that can be used in subsequent reactions
without further purification.
##STR00168##
[0722] Compounds of general formulas 12 and 6 in an organic solvent
such as DMF are heated in the presence of a base such as
di-isopropyl ethyl amine to a temperature ranging between 70 and
100.degree. C. for 1 hour. The reaction mixture can be partitioned
between ethyl acetate and water containing TFA. The aqueous layer
is evaporated and the resulting residue can be purified by reversed
phase preparative HPLC using a stationary phase such as C-18 and a
solvent system such as varying amounts of water and acetonitrile
containing 0.1% TFA. The resulting mixture of stereoisomers could
be converted to the free base by passing through amyberlyst resin
and the basified amines purified using a chiral HPLC column such as
Chiracel OZ-H and the like using a mixture of organic solvents such
as ethanol and heptanes containing 0.1% diethyl amine as the
solvent. The purified stereoisomers could be dissolved in ethanol
and treated with HCl in ether and the solvents were removed under
reduced pressure to give the desired compound 15 as HCl salt.
##STR00169##
[0723] In certain instances where
R.sup.8.dbd.--(CH.sub.2).sub.nCO.sub.2Et in compound 15 is
dissolved in an organic solvent such as MeOH and then treated with
an alkali metal hydroxide such as LiOH and the resulting mixture is
stirred for 3 h. An aqueous acid such as 3M HCl is then added to
the reaction. The mixture is concentrated under reduced pressure
and the resulting residue is purified by reversed phase preparative
HPLC using a stationary phase such as C-18 and a solvent system
such as varying amounts of water and acetonitrile containing 0.1%
TFA to give a compound of general structure 16.
Precursor I. Preparation of
(R)-6-chloro-1-(1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,4-d]p-
yrimidine
Step 1. Preparation of (R)-1-(2,4-dichlorophenyl)ethan-1-ol
##STR00170##
[0725] To a solution of 2',4'-dichloroacetophenone (10.9 g, 77.0
mmol) in anhydrous THF (80 mL) at -78.degree. C. under nitrogen was
slowly added a solution of (+)-B-chlorodiisopinocampheylborane
((+)--Ipc2BC1, 27.2, 85.0 mmol) in THF (15 mL). After the addition
is complete, the reaction mixture was slowly warmed to -25.degree.
C. and stirred at this temperature for 2 h (monitored by TLC and
LCMS). The reaction mixture was then quenched with diethanolamine
(17.9 g, 170 mmol), and stirred for 10 min. During this time, a
solid formed and it was filtered off. The filtrate was dried with
Na.sub.2SO.sub.4, filtered, and concentrated in vacuo. The residue
was purified flash chromatography (SiO.sub.2, 0-20% ethyl acetate
in hexanes) to give (R)-1-(2,4-dichlorophenyl)ethanol. Yield 12.0
g, 63.3 mmol, 82%. Enantiomeric purity was determined on CHIRALPAK
ID column, using 5% isopropanol in heptanes (98% ee, retention time
5.3 min). .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. ppm 7.55 (d,
J=8.4 Hz, 1H), 7.35 (t, J=2.2 Hz, 1H), 7.29 (ddd, J=8.4, 2.1, 0.5
Hz, 1H), 5.26 (q, J=6.4 Hz, 1H), 1.47 (d, J=6.4 Hz, 3H).
Step 2. Preparation of
(S)-2,4-dichloro-1-(1-chloroethyl)benzene
##STR00171##
[0727] To a stirred solution of N-chlorosuccinimide (11.0 g, 82.4
mmol) in THF at 0.degree. C. (240 mL) was added triphenylphosphine
(21.6 g, 82.4 mmol). The reaction mixture was stirred at 0.degree.
C. for 10 min and then stirred at room temperature for 30 min. The
mixture was cooled to 0.degree. C. and then the
(R)-1-(2,4-dichlorophenyl)ethanol (12.0 g, 63.4 mmol) was added
(dissolved in 25 mL of THF). After the addition was completed, the
mixture was allowed to warm up to room temperature and stirred for
an additional 3 h. The reaction mixture was concentrated in vacuo
and suspended in hexanes. The solid was filtered off and discarded.
The filtrate was then concentrated in vacuo and the resulting
residue was re-suspended in hexanes. The solid was filtered off and
discarded. The filtrate was then concentrated in vacuo and the
crude material was used without further purification. Yield 12.1 g,
58 mmol, 91%. Enantiomeric purity was determined on CHIRALPAK IC-3
column, using 100% heptanes (96% ee, retention time 4.5 min).
.sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 7.59 (d, J=8.5 Hz, 1H),
7.39 (d, J=2.2 Hz, 1H), 7.30 (dd, J=8.5, 2.2 Hz, 1H), 5.51 (q,
J=6.8 Hz, 1H), 1.81 (d, J=6.8 Hz, 1H).
Step 3. Alkylation of
6-chloro-3-methyl-1H-pyrazolo[3,4-d]pyrimidine with
(S)-2,4-dichioro-1-(1-chloroethyl)benzene
##STR00172##
[0729] 6-Chloro-3-methyl-1H-pyrazolo[3,4-d]pyrimidine (500 mg, 2.97
mmol) was dissolved in 10 mL of anhydrous DMF. Anhydrous
Cs.sub.2CO.sub.3 (2.42 g, 7.43 mmol) was added to the solution
immediately followed by 1.74 g (8.91 mmol) of
(S)-2,4-dichloro-1-(1-chloroethyl)benzene (96% ee). Reaction
mixture was allowed to stir at room temperature for 24 h and
progress was monitored by LCMS. Upon completion the reaction
mixture was diluted with 20 mL of water and extracted 3 times with
20 mL of ethyl acetate. Combined organic fraction was dried with
MgSO.sub.4, filtered and purified by silica gel chromatography
using ethyl acetate and hexanes (0 to 100% gradient). Yield 500 mg,
49%. Enantiomeric purity determined by chiral HPLC using CHIRACEL
OZ-H column 5% isopropanol in heptanes (retention time 6.9 min, 94%
ee). .sup.1H NMR (400 MHz, DMSO-d6): .delta. ppm 9.27 (s, 1H),
7.63-7.65 (m, 1H), 7.41-7.49 (m, 2H), 6.31 (q, J=7.0 Hz, 1H), 2.56
(s, 3H), 1.83 (d, J=7.0 Hz, 3H). [M+H] 341.0.
Precursor II. Preparation of
(R)-6-chloro-1-(1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,4-b]p-
yrazine
Step 1. Preparation of (R)-1-(1-(2,4-dichlorophenyl)ethyl)urea
##STR00173##
[0731] To a 6 L flask equipped with overhead stirrer was added
(R)-1-(2,4-dichlorophenyl)ethan-1-amine (211 g, 1.11 mol)[reference
WO 2013082490], water (3.4 L) and concentrated HCl (92.5 mL, 1.11
mol). The mixture was a slurry. Then solid KOCN (90 g, 1.11 mol)
was added in one portion at rt. All solids went into solution and a
white precipitate began to form after 1 h. The white precipitate
was isolated by filtration. The filtrate was allowed to stand at
room temperature and more precipitate formed. The precipitate was
isolated by filtration. This was repeated several times until no
more precipitate formed in the filtrate upon standing at room
temperature for 1 d. All the solids were combined and dried under
high vacuum.
Step 2. Preparation of (R)-(1-(2,4-dichlorophenyl)ethyl)hydrazine
hydrochloride
##STR00174##
[0733] (R)-1-(1-(2,4-dichlorophenyl)ethyl)urea (Example 5, Step 1,
50 g, 214.6 mmol) was milled into a fine powder and placed into a 2
L flask. The 2 L flask was purged with nitrogen gas and a degassed
mixture of 1000 mL of toluene and 375 mL of tBuOH added via cannula
under nitrogen gas. KOtBu (240.3 g, 2146 mmol) was milled into fine
powder and added to a separate 5 L, 3 neck flask. The 5 L flask was
purged with nitrogen, and a degassed mixture of 1000 mL of toluene
and 650 mL of tBuOH was added via cannula under nitrogen gas. The 2
L and the 5 L mixtures were slurries and were cooled to -20.degree.
C. The lights inside the hood were turned off. tBuOCl (23.18 g, 24
mL, 214.6 mmol) was added to the 2 L flask at -20.degree. C. Then
the -20.degree. C. bath was removed and the mixture was placed in a
0.degree. C. bath. As soon as the slurry went all into solution,
the mixture was transferred to the 5 L flask via cannula under
nitrogen at -20.degree. C. The lights in the hood were turned on.
The -20.degree. C. bath was removed, and the mixture was placed
into 0.degree. C. bath. The mixture was stirred at 0.degree. C. for
10 min and then warmed to rt. The mixture was poured onto ice. The
mixture was extracted with EtOAc (2.times.). The combined organic
layers were washed with 1 L water, 500 mL sat. sodium thiosulfate,
and 1 L brine. The mixture was concentrated under reduced pressure
to give tert-butyl
(R)-2-(1-(2,4-dichlorophenyl)ethyl)hydrazine-1-carboxylate with
98.9% enantiomeric excess. Enantiomeric excess was determined by
HPLC using a Chiralpak.RTM. IF-3 column and eluting with 5%
isopropanol in heptanes (retention time 5.3 min).
[0734] The residue was dissolved in 250 mL of 1.4-dioxane and HCl
in 1.4-dioxane (4 M, 161 mL, 643.8 mmol) was added at room
temperature. The mixture was stirred at room temperature overnight
and then concentrated under reduced pressure. The residue was
triturated from 25% EtOAc in hexanes (1 mL of solvent per 1 g of
residue) to give (R)-(1-(2,4-dichlorophenyl)ethyl)hydrazine
hydrochloride with 99.2% enantiomeric excess. Enantiomeric excess
was determined by HPLC using a Chiralpak.RTM. IF-3 column and
eluting with 20% isopropanol in heptanes (retention time 4.7 min).
.sup.1H NMR (400 MHz, CDCl.sub.3, HCl salt) .delta. 7.75 (d, J=8.4
Hz, 1H), 7.43 (d, J=2.1 Hz, 1H), 7.35 (dd, J=8.4, 2.2 Hz, 1H), 5.76
(bs, 4H), 4.91 (q, J=6.7 Hz, 1H), 1.64 (d, J=6.8 Hz, 3H). [M+H]
205.2.
Step 3. Preparation of 3,5-dichloropyrazine-2-carboxamide
##STR00175##
[0736] 2,6-Dichloropyrazine (55 g, 0.37 mol) and formamide (300 mL)
were combined and heated to 90.degree. C. Sodium persulfate (86.7
g, 0.36 mol) was added to the mixture at 90.degree. C. in portions
(.about.1 g) 20-30 second intervals. An exotherm was observed and
the color of the mixture turned from yellow to dark red/brown. The
mixture was stirred at 90.degree. C. for 2 h and then cooled to
room temperature. The mixture was diluted with water (500 mL) and
filtered. The filtrate layers were separated. The aqueous layer was
extracted with IPA/chloroform (1/3, 3.times.750 mL). The combined
organic layers were dried over sodium sulfate and concentrated
under vacuum to afford a viscous oil. The oil was purified by
silica gel chromatography (0 to 100% EtOAc in hexanes) to provide
the title product as a colorless solid (25 g, 36% yield). .sup.1H
NMR (400 MHz, DMSO-d6): .delta. ppm 8.87 (s, 1H), 8.18 (br.s., 1H),
8.01 (br.s., 1H).
Step 4. Preparation of 3,5-dichloropyrazine-2-carbonitrile
##STR00176##
[0738] To a solution of 3,5-dichloropyrazine-2-carboxamide (Example
12, Step 2, 52 g, 0.27 mol) in acetonitrile (1 L) was added
POCl.sub.3 (146 g, 89 mL, 0.95 mol) at room temperature. The
mixture was heated to 90-100.degree. C. for 4 h. The mixture was
cooled to room temperature and poured slowly into a vigorously
stirring solution of saturated aq. NaHCO.sub.3. Evolution of gas
was observed. The mixture was extracted with EtOAc (3.times.). The
combined organic layers were dried over sodium sulfate then
concentrated under reduced pressure to give a residue. The residue
was purified by silica gel chromatography (0-30% EtOAc in hexanes)
to give the title compound as a pale yellow solid. .sup.1H NMR (400
MHz, CDCl3): .delta. ppm 8.64 (s, 1H): .sup.13C NMR (101 MHz,
CDCl.sub.3) .delta. ppm 150.8, 150.43, 143.24, 128.06, 113.06.
Step 5. Preparation of 1-(3,5-dichloropyrazin-2-yl)ethan-1-one
##STR00177##
[0740] 3,5-Dichloropyrazine-2-carbonitrile (Example 12, Step 2,
31.0 g, 178.18 mmol) was dissolved in anhydrous diethyl ether (890
mL, 0.2 M) and cooled to -78.degree. C. Then MeMgBr in diethyl
ether (3.0 M, 65.3 mL, 190 mmol) was added slowly to maintain low
temperature. After the addition was complete, the mixture was
slowly warmed room temperature and stirred at room temperature for
1 h. The mixture was poured into a beaker containing a mixture of
HCl in water (1.0 M, 1 L) and ice (1 kg). The mixture was stirred
vigorously for 10 min. The mixture was extracted with diethyl ether
(3.times.1 L). The combined organic layers were dried over
Na.sub.2SO.sub.4 and concentrated under reduced pressure to afford
the title compound as an orange oil (34 g, 99% yield). The mixture
was used for the next reaction without further purification.
.sup.1H NMR (400 MHz, CDCl.sub.3): .delta. ppm 8.56 (s, 1H), 2.71
(s, 3H).
Step 6. Preparation of
(R,Z)-3,5-dichloro-2-(1-(2-(1-(2,4-dichlorophenyl)ethyl)hydrazono)ethyl)p-
yrazine and
(R,E)-3,5-dichloro-2-(1-(2-(1-(2,4-dichlorophenyl)ethyl)hydrazono)ethyl)p-
yrazine
##STR00178##
[0742] (R)-(1-(2,4-dichlorophenyl)ethyl)hydrazine hydrochloride
(Example 5, Step 2, 47.3 g, 196 mmol) was dissolved in ethanol (356
mL, 0.5 M) at room temperature, and then
1-(3,5-dichloropyrazin-2-yl)ethan-1-one (34.0 g, 178 mmol) was
added. The mixture was stirred at room temperature for 8 h. The
mixture was concentrated under reduced pressure to give a residue.
The residue was suspended in 20% EtOAc in hexanes (200 mL) and then
filtered through a silica gel plug and eluted using a 20% EtOAc in
hexanes. The filtrate was concentrated under reduced pressure to
give the title products as a viscous orange oil.
Step 7. Cyclization of
(R,Z)-3,5-dichloro-2-(1-(2-(1-(2,4-dichlorophenyl)ethyl)hydrazono)ethyl)p-
yrazine and
(R,E)-3,5-dichloro-2-(1-(2-(1-(2,4-dichlorophenyl)ethyl)hydrazono)ethyl)p-
yrazine
##STR00179##
[0744] A mixture of
(R,Z)-3,5-dichloro-2-(1-(2-(1-(2,4-dichlorophenyl)ethyl)hydrazono)ethyl)p-
yrazine and
(R,E)-3,5-dichloro-2-(1-(2-(1-(2,4-dichlorophenyl)ethyl)hydrazono)ethyl)p-
yrazine (9:1) (33 g, 87 mmol) was dissolved in
N-methyl-2-pyrrolidone (218 mL) at room temperature. 2,6-Lutidine
(30.3 mL, 262 mmol) was added. The mixture was degassed with
nitrogen and then heated to 100.degree. C. under nitrogen for 8 h.
The reaction mixture was cooled to room temperature and then poured
into a separatory funnel containing 500 mL of HCl in water (1 M)
and 500 mL of ethyl acetate. The layers were separated and the
organic layer was washed with 500 mL of HCl in water (1 M), dried
over MgSO.sub.4, and concentrated under reduced pressure. The
residue was purified by silica gel chromatography (0 to 20% (1:1
MTBE:CH.sub.2Cl.sub.2) in hexanes) to provide the title compounds
as off-white solid (67% yield). Enantiomeric purity was determined
by HPLC using CHIRALPAK IA-3 and eluting with 5% isopropanol in
heptanes. .sup.1H NMR (400 MHz, CDCl.sub.3): .delta. ppm 8.46 (s,
1H), 7.43 (d, J=8.5 Hz, 1H), 7.39 (d, J=2.2 Hz, 1H), 7.20 (dd,
J=8.5, 2.2 Hz, 1H), 6.49 (q, J=7.1 Hz, 1H), 2.67 (s, 3H), 1.94 (d,
J=7.1 Hz, 3H); [M+H] 341.0.
Precursor III. Preparation of
(R)-6-chloro-1-(1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-
-carboxamide
Step 1. Preparation of Ethyl
2-(3,5-dichloropyrazin-2-yl)-2-oxoacetate
##STR00180##
[0746] To a solution of 2,4,6-trimethylpyridine (67 mL, 0.40 moles)
in THF (600 mL) at -78.degree. C. was added nBuLi (2.5 M in
hexanes, 208 mL, 0.52 moles). The mixture was stirred at
-78.degree. C. for 20 min and then warmed to 0.degree. C. In a
separate flask, diethyloxalate (65 mL, 0.48 moles) and
2,6-dichloropyrazine (60 g, 0.40 moles) were dissolved in THF (600
mL) and cooled to -78.degree. C. The lithium
2,4,6-trimethylpyridine solution was added to the
2,6-dichloropyrazine solution via cannula over 1 h at -78.degree.
C. The mixture was stirred at -78.degree. C. for 20 min and then
the mixture was poured into a mixture of sat. NH.sub.4Cl (300 mL)
and water (300 mL). The mixture was diluted with EtOAc (300 mL) and
the layers were separated. The aqueous layer was extracted with
EtOAc (300 mL) and the combined organic layers were dried over
MgSO.sub.4. The mixture was concentrated under reduced pressure.
The residue was purified by silica gel chromatography (5 to 20%
EtOAc in hexanes) to provide the title compound (32 g, 32% yield).
.sup.1H NMR (400 MHz, DMSO-d6): .delta. ppm 8.87 (s, 1H), 8.18 (br.
s., 1H), 8.01 (br. s., 1H).
Step 2. Preparation of Ethyl
(R)-6-chloro-l-(1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-
-carboxylate
##STR00181##
[0748] To a solution of ethyl
2-(3,5-dichloropyrazin-2-yl)-2-oxoacetate (14.5 g, 58.4 mmol) in
THF (97 mL) was added (R)-(1-(2,4-dichlorophenyl)ethyl)hydrazine
hydrochloride (Example 5, Step 2, 11.7 g, 48.7 mmol). The mixture
was warmed to 80.degree. C. for 2 h and then cooled to room
temperature. The mixture was allowed to stand at room temperature
under argon for 12 h. The mixture was diluted with brine and the
layers were separated. The aqueous layer was extracted with EtOAc
2.times.. The combined organic layers were dried over MgSO.sub.4
and concentrated under reduced pressure to give a red oil.
[0749] The red oil was dissolved in THF (240 mL) and cooled to
0.degree. C. Sodium hydride (60% dispersion in mineral oil, 3.9 g,
97 mmol) was added and the mixture was stirred at room temperature
for 15 h. The mixture was diluted with sat. NH.sub.4Cl (200 mL),
water (200 mL), and EtOAc (200 mL). The layers were separated and
the aqueous layer was extracted with EtOAc (100 mL). The combined
organic layers were dried over MgSO.sub.4 and concentrated under
reduced pressure. The residue was purified by silica gel
chromatography (10 to 20% EtOAc in hexanes) to provide the title
compound (9.0 g, 46% yield) with >99% enantiomeric excess.
Enantiomeric excess was determined by HPLC using a CHIRALPAK IF-3
column and eluting with 5% isopropanol in heptanes (retention time
7.2 min).
Step 3. Reaction of ammonia with ethyl
(R)-6-chloro-1-(1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-
-carboxylate
##STR00182##
[0751] To a solution of ethyl
(R)-6-chloro-l-(1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-
-carboxylate (4.0 g, 10 mmol) in dioxane (40 mL) at room
temperature was added ammonium hydroxide (29% in water, 40 mL). The
mixture was stirred in a sealed tube at room temperature for 3 d.
The mixture was diluted with sat. NaHCO.sub.3. The mixture was
extracted with EtOAc (2.times.). The combined organic layers were
dried over MgSO.sub.4 and concentrated under reduced pressure to
give the title compound (3.4 g, 92% yield) as a light yellow solid.
.sup.1H NMR (400 MHz, DMSO-d6): .delta. ppm 8.87 (s, 1H), 7.93 (bs,
1H), 7.84 (bs, 1H), 7.65-7.68 (m, 1H), 7.46-7.50 (m, 1H), 7.51-7.45
(m, 1H), 6.49 (q, J=6.9 Hz, 1H), 1.91 (d, J=7.0 Hz, 3H); [M+H]
370.0.
Precursor IV.
(R)-6-Chloro-1-(1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-
-carbonitrile
##STR00183##
[0753] To a solution of
(R)-6-chloro-l-(1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-
-carboxamide (4.5 g, 12.2 mmol) in dichloromethane (30 mL) at room
temperature under argon was added methyl
N-(triethylammoniumsulfonyl)carbamate (Burgess's reagent, 4.3 g,
18.1 mmol). The mixture was stirred at room temperature for 2 d.
The mixture was preabsorbed onto silica gel and purified by
chromatography (5% to 20% EtOAc in hexanes) to give the title
compound (3.68 g, 88% yield) as a sticky colorless solid. .sup.1H
NMR (400 MHz, CDCl.sub.3): .delta. ppm 8.69 (s, 1H), 7.40-7.45 (m,
2H), 7.25-7.29 (m, 1H), 6.68 (q, J=7.0 Hz, 1H), 1.98 (d, J=7.1 Hz,
3H); [M+H] 351.9.
Precursor V.
(R)-6-Chloro-1-(1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromethyl)-1H-pyraz-
olo[3,4-b]pyrazine
Step 1.
(E)-3,5-Dichloro-2-(1-(2-(1-(2,4-dichlorophenyl)ethyl)hydrazono)-2-
,2,2-trifluoroethyl)pyrazine and
(Z)-3,5-dichloro-2-(1-(2-(1-(2,4-dichlorophenyl)ethyl)
hydrazono)-2,2,2-trifluoroethyl)pyrazine
##STR00184##
[0755] To a solution of 2,2,6,6-tetramethylpiperidine (13.71 mL,
80.55 mmol) in THF (200 mL) at -40.degree. C. was added n-BuLi (2.5
M in hexanes, 34.91 mL, 87.26 mmol). The mixture was stirred at
-40.degree. C. for 30 min. In a separate flask, ethyl
2,2,2-trifluoroacetate (10.38 mL, 87.26 mmol) and
2,6-dichloropyrazine (10.00 g, 67.13 mmol) were dissolved in THF
(200 mL) and cooled to -90.degree. C. The lithium
2,2,6,6-tetramethylpiperidine solution was added to the
2,6-dichloropyrazine solution via cannula over 30 min at
-90.degree. C. The mixture was stirred at -90.degree. C. for 30 min
and (R)-(1-(2,4-dichlorophenyl)ethyl)hydrazine hydrochloride
(Example 5, Step 2, 11.7 g, 9.73 g, 40.28 mmol) was added, and then
the mixture was allowed to warm up to room temperature. The mixture
was concentrated under reduced pressure, then ethanol (200 mL) was
added and the mixture was stirred at room temperature for 24 h. The
mixture was concentrated under reduced pressure and then the
residue was purified by silica gel chromatography (0 to 100% EtOAc
in hexanes) to provide the title compounds as a viscous orange
oil.
Step 2.
(R)-6-Chloro-1-(1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromethyl)-1-
H-pyrazolo[3,4-b]pyrazine
##STR00185##
[0757] (Mixture of E/Z of
(R))-3,5-Dichloro-2-(1-(2-(1-(2,4-dichlorophenyl)ethyl)hydrazono)-2,2,2-t-
rifluoroethyl)pyrazine (2.5 g, 5.8 mmol) was dissolved in THF (58
mL) and then the solution was cooled to 0.degree. C. Then,
1,8-diazabicyclo[5.4.0]undec-7-ene (1.73 mL, 11.8 mmol) was then
added dropwise. After the addition was completed, the mixture was
allowed to warm up to room temperature and stirred for 10 h. The
mixture was concentrated under reduced pressure and then the
residue was purified by silica gel chromatography (0 to 20% EtOAc
in hexanes) to provide the title compound as a light orange
oil.
[0758] General procedure A: Alkylation of tert-butyl
3-(piperidin-3-yl)azetidine-1-carboxylate by reductive
amination.
##STR00186##
[0759] Commercially available tert-butyl
3-(piperidin-3-yl)azetidine-1-carboxylate (240 mg, 1 mmol) was
dissolved in 6 mL of dry 1,2-dichloromethane and carbonyl compound
(1 mmol) was added all at once. Mixture was allowed to stir at room
temperature for 5 min and then NaBH(OAc).sub.3 (2 mmol) was added
and reaction mixture was stirred for 1-18 hrs at room temperature.
Conversion was monitored by LCMS. Upon completion, saturated sodium
bicarbonate solution was added and the reaction mixture was allowed
to stir for additional 30 min. The mixture was extracted 3 times
with dichloromethane, combined organic phase was dried over
MgSO.sub.4, filtered, and the residue was purified on silica using
methanol dichloromethane as eluent.
[0760] General procedure B: Alkylation of tert-butyl
3-(piperidin-3-yl)azetidine-1-carboxylate.
##STR00187##
[0761] tert-Butyl 3-(piperidin-3-yl)azetidine-1-carboxylate (240
mg, 1 mmol) was dissolved in 5 mL of dry solvent and either (a)
Michael acceptor (1 mmol) was added to the solution all at once and
reaction mixture was stirred either at room temperature or at
50.degree. C. until complete conversion was achieved (followed by
LCMS); upon completion solvent was removed in vacuo and product
purified by silica gel chromatography using methanol and
dichloromethane as eluent, or (b) 1 mmol of alkyl halide, 10 mol %
of sodium iodide, and sodium carbonate (2 mmol) were added to the
solution all at once and the reaction mixture was heated to
75.degree. C. under nitrogen atmosphere and monitored by LCMS; upon
completion the reaction mixture was diluted with 20 mL of water,
extracted 3 times with ethyl acetate, combined organic phase was
dried over sodium sulfate, filtered, and concentrated under reduced
pressure; the residue was purified on silica using methanol and
dichloromethane as the eluent.
[0762] General procedure C: Deprotection of 1-alkyl tert-butyl
3-(piperidin-3-yl)azetidine-1-carboxylate.
##STR00188##
[0763] 1-Alkyl tert-butyl 3-(piperidin-3-yl)azetidine-1-carboxylate
(0.7 mmol) was dissolved in 3 mL of dichloromethane and 2 mL of 4M
solution of HCl in 1,4-dioxane was added to it. The resulting
mixture was stirred at room temperature until complete conversion
was reached (1-3 h). After that solvents were removed in vacuo and
residue was dried on high vacuum for 12 h. Product was used in the
next step without purification.
[0764] General procedure D: Nucleophilic aromatic substitution with
1-alkyl 3-(azetidin-3-yl)piperidine.
##STR00189##
[0765] 1-Alkyl 3-(azetidin-3-yl)piperidine (0.55 mmol) and
appropriate heteroaryl precursor I, II, III, IV or V (0.5 mmol)
were dissolved in 2 mL of dry DMF or DMSO. Diisopropylethylamine
(2.5 mmol) was added and mixture was stirred at room temperature
(Y=CH, X=N, R.sup.2=CN) or at 80.degree. C. (Y=N, X=CH, R.sup.2=Me
and Y=CH, X=N, R.sup.2=Me). Reaction progress was monitored by
LCMS. Upon completion, reaction mixture was either (a) diluted with
2 mL of acetonitrile and injected directly on reverse phase HPLC
for purification or (b) concentrated in vacuo, and purified by
normal phase silica gel chromatography using dichloromethane and
methanol as eluent.
[0766] Precursors VI and VII. Chiral resolution of tert-butyl
3-(piperidin-3-yl)azetidine-1-carboxylate.
[0767] tert-Butyl 3-(3-piperidyl)azetidine-1-carboxylate (77.02 g,
320 mmol) was dissolved in tert-butylmethyl ether (1,700 mL) in a
5-L three-necked flask equipped with a mechanical stirring and a
water condenser. When the mixture was stirred at reflux,
L-(+)-mandelic acid (24.38 g, 160 mmol) was added. The resulting
mixture was allowed to stir at reflux for 15 min and then cooled to
rt overnight. The white solid was collected by filtration, rinsing
with tert-butylmethyl ether (500 mL). The white solid was stirred
at reflux in tert-butylmethyl ether (1700 mL) for 30 min. The salt
was collected by filtration and washed with tert-butylmethyl ether
(500 mL). The process was repeated once more to afford a white
solid (95% ee).
[0768] The white salt (.about.62.8 g) was further purified by
re-crystallization from chloroform/tert-butylmethyl ether (900
mL/900 mL). The salt was dissolved in chloroform (900 mL) on a hot
plate making it slightly boiling, then tert-butylmethyl ether (900
mL) was slowly added. It was a clear solution when it was hot. The
solution was cooled to ambient temperature overnight, and crystals
appeared. The crystals were isolated by filtration and further
dried under high vacuum for 4h to afford 64.85 g of the mandelate
salt with 1 equiv of chloroform by .sup.1H nuclear magnetic
resonance ("NMR") in methanol (>99% ee).
[0769] Method for % ee determination: Chiral high performance
liquid chromatography ("HPLC"), 210 nm, IC-3 column (4.6.times.250
mm, 3 .mu.M), 50% heptane, 50% isopropanol, 1 mL/min, 210 nM,
tert-butyl (R)-3-(piperidin-3-yl)azetidine-1-carboxylate (precursor
VI) Rt=8.8-9 min, tert-butyl
(S)-3-(piperidin-3-yl)azetidine-1-carboxylate (precursor VII)
Rt=8.5 min.
[0770] Precursor VIII.
1-((R)-1-(4-chloro-2-fluorophenyl)ethyl)-6-(3-((R)-1-(2-hydroxyethyl)pipe-
ridin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile.
Step 1: (R)-1-(4-Chloro-2-fluorophenyl)ethan-1-ol
##STR00190##
[0772] To a solution of 1-(4-chloro-2-fluorophenyl)ethan-1-one (10
g, 58 mmol) in tetrahydrofuran (100 mL) at -78.degree. C. under a
nitrogen atmosphere was added (+)-B-Chlorodiisopinocampheylborane
(50 to 60% wt in hexanes, 9.2 mL, 64 mmol), slowly. The resulting
mixture was slowly warmed to -25.degree. C. and stirred at this
temperature for 2 h. 1-(4-Chloro-2-fluorophenyl)ethan-1-one was
detected by LCMS ("liquid chromatography mass spectrometry") and
HPLC, and the mixture was cooled back to -78.degree. C. Additional
(+)-B-Chlorodiisopinocampheylborane (50 to 65% wt in hexanes, 5.4
mL, 38 mmol) was added to the mixture at -78.degree. C. The
resulting mixture was slowly warmed to -25.degree. C. and stirred
at this temperature for 5 h. Diethanolamine (18 mL, 191 mmol) was
added to the reaction mixture, which was then stirred at room
temperature for 3 d. The reaction was filtered, and the filtrate
was concentrated and purified by silica gel chromatography (0 to
30% ethyl acetate in hexanes) to afford 18.8 g impure
(R)-1-(chloro-2-fluorophenyl)ethan-1-ol.
Step 2: 4-Chloro-1-(1-chloroethyl)-2-fluorobenzene
##STR00191##
[0774] To a flask containing
(R)-1-(4-chloro-2-fluorophenyl)ethan-1-ol (18.8 g, 108 mmol) in
dichloromethane ("DCM") (1 L) was added triphenylphosphine (113 g,
432 mmol) and carbon tetrachloride (41.7 mL, 432 mmol). The mixture
was stirred at ambient temperature for 3 d, then silica gel
(.about.400 g) was added to the mixture. The mixture was then
concentrated under reduced pressure, and the residue was purified
by silica gel column chromatography (100% hexanes) to afford
4-chloro-1-(1-chloroethyl)-2-fluorobenzene (8 g) as a colorless
oil.
Step 3: (1-(4-Chloro-2-fluorophenyl)ethyl)hydrazine
hydrochloride
##STR00192##
[0776] To a solution of 4-chloro-1-(1-chloroethyl)-2-fluorobenzene
(4.0 g, 41 mmol) in ethanol (120 mL) was added hydrazine hydrate
(excess). The mixture was stirred at 35.degree. C. for 3 d. The
reaction was concentrated, and diethyl was added to the mixture.
The bottom hydrazine layer was removed, and about 5 mL of 4 M HCl
in 1,4-dioxane was added to the mixture at 0.degree. C. The mixture
was kept at 0.degree. C. until all of the hydrazine HCl salt
precipitated. The mixture was filtered, washed with cold diethyl
ether, and concentrated in vacuo to afford the title compound as
the hydrochloride salt (3.95 g), which was used without further
purification.
Step 4.
(R)-6-chloro-l-(1-(4-chloro-2-fluorophenyl)ethyl)-3-methyl-1H-pyra-
zolo[3,4-b]pyrazine
##STR00193##
[0778] The title compound was synthesized according to the
procedures outlined in Precursor III, Steps 1-3 and Precursor VI.
The crude product was purified using an alumina column (eluting
with 25% to 50% DCM in hexanes) to afford impure
6-chloro-1-(1-(4-chloro-2-fluorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,4-b]-
pyrazine (2.2 g). This material was repurified by alumina column to
afford the title compound (1.94 g) as a light yellow oil which was
purified by SFC (Lux-amylose 4 (two 2.times.15 cm columns), eluting
with 10% methanol with 0.1% DEA and CO2 at 100 bar, 60 mL/min) to
afford the pure product as a mixture of enantiomers. The
enantiomers were separated by preparative chiral SFC (OJ-H
(2.times.25 cm), eluting with 10% isopropanol with 0.1% DEA and CO2
at 100 bar, 70 mL/min) to afford the desired enantiomer as the
first eluting enantiomer (485 mg) at 2.67 min.
EXEMPLARY COMPOUNDS
Example 1
##STR00194##
[0780] Ethyl
2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,4-
-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)acetate
2,2,2-trifluoroacetate and 2,2,2-trifluoroacetate ethyl
2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,4-
-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)acetate. Prepared as a
mixture of the above two diastereomers using general procedure A
with 50% toluene solution of ethyl 2-oxoacetate, followed by
procedure C. The resulting diasteromeric mixture product was
condensed with Precursor II using procedure D (a). .sup.1H NMR (400
MHz, CDCl.sub.3, trifluoroacetic acid salt): .delta. ppm 10.43 (bs,
1H), 7.66 (s, 1H), 7.37-7.39 (m, 2H), 7.12-7.17 (m, 1H), 6.26-6.35
(m, 1H), 4.16-4.29 (m, 4H), 3.88-3.96 (m, 4H), 3.54-3.68 (m, 2H),
3.07-3.20 (m, 1H), 2.80-2.94 (m, 1H), 2.54-2.68 (m, 4H), 2.30-2.43
(m, 1H), 1.92-2.10 (m, 3H), 1.88 (d, J=7.1 Hz, 3H), 1.29 (t, J=7.1
Hz, 3H), 1.08-1.23 (m, 1H). [M+H] 531.3.
Example 2
##STR00195##
[0782]
2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)acetic acid. The
diastereomers of Example 1 were separated using 5% isopropanol in
heptanes (0.1% diethylamine) on CHIRALPAK IF SFC 20.times.250 mm (5
.mu.M), followed by treatment of the first eluting diastereomer
with 5 equiv of LiOH in MeOH at room temperature for 12 hrs, and
repurifying by reverse phase HPLC using water (0.1% TFA) and
acetonitrile (0.1% TFA) as eluent. .sup.1H NMR (400 MHz,
CDCl.sub.3, trifluoroacetic acid salt): .delta. ppm 7.68 (m, 1H),
7.35-7.40 (m, 1H), 7.31-7.33 (m, 1H), 7.12-7.16 (m, 1H), 6.29 (q,
J=7.0 Hz, 1H), 4.16-4.26 (m, 2H), 3.86-3.98 (m, 4H), 3.64-3.78 (m,
2H), 2.75-2.88 (m, 1H), 2.48-2.65 (m, 5H), 2.28-2.41 (m, 1H),
1.84-2.10 (m, 6H), 1.00-1.18 (m, 1H); [M+H] 503.3.
Example 3
##STR00196##
[0784]
2-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)acetic acid. The
diastereomers of Example 1 were separated at the ester stage using
5% isopropanol in heptanes (0.1% diethylamine) on CHIRALPAK IF SFC
20.times.250 mm (5 .mu.M), followed by treatment of the second
eluting diastereomer with 5 equiv of LiOH in MeOH at room
temperature for 12 h, and repurifying by reverse phase HPLC using
water (0.1% TFA) and acetonitrile (0.1% TFA) as eluent. .sup.1H NMR
(400 MHz, CDCl.sub.3, trifluoroacetic acid salt): .delta. ppm 11.42
(bs, 2H), 7.68 (s, 1H), 7.36-7.40 (m, 1H), 7.32-7.34 (m, 1H),
7.12-716 (m, 1H), 6.31 (q, J=7.0 Hz, 1H), 4.18-4.26 (m, 2H),
3.85-3.98 (m, 4H), 3.65-3.78 (m, 2H), 2.74-2.88 (m, 1H), 2.48-2.60
(m, 5H), 2.28-2.40 (m, 1H), 1.85-2.08 (m, 6H), 1.00-1.15 (m, 1H).
[M+H] 503.3.
Example 4
##STR00197##
[0786]
2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethane-1-sulfonamide
and
2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-H-pyrazolo[-
3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethane-1-sulfonamide.
Prepared as a mixture of the above two diastereomers using general
procedure B (a) with ethenesulfonyl fluoride and treating resulting
mixture with aqueous ammonia at 70.degree. C. for 30 min followed
by procedure C and the resulting diasteromeric mixture product was
condensed with Precursor II using procedure D (a). [M+H] 552.2.
Example 5
##STR00198##
[0788]
2-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethane-1-sulfonamide.
The diastereomers of example 4 were separated using 45% isopropanol
in heptanes (0.1% diethylamine) on CHIRALPAK IF SFC 20.times.250 mm
(5 .mu.M). The first eluting diastereomer had the structure
indicated above. .sup.1H NMR (400 MHz, CD.sub.3OD, trifluoroacetic
acid salt): .delta. ppm 7.71 (s, 1H), 7.29-7.44 (m, 1H), 7.35-7.39
(m, 1H), 7.23-7.27 (m, 1H), 6.28 (q, J=7.1 Hz, 1H), 4.21 (dt, J=2.6
Hz, J=8.5 Hz, 2H), 3.89-3.95 (m, 2H), 3.28-3.33 (m, 1H), 2.83-2.94
(m, 4H), 2.52-2.64 (m, 1H), 2.49 (s, 3H), 2.03-2.13 (m, 1H),
1.72-1.89 (m, 7H), 1.52-1.65 (m, 1H), 1.15 (d, J=6.2 Hz, 3H),
0.88-1.02 (m, 1H). [M+H] 552.2.
Example 6
##STR00199##
[0790]
2-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethane-1-sulfonamide.
The diastereomers of example 4 were separated using 45% isopropanol
in heptanes (0.1% diethylamine) on CHIRALPAK IF SFC 20.times.250 mm
(5 .mu.M). The second eluting diastereomer had the structure
indicated above. .sup.1H NMR (400 MHz, CD.sub.3OD, trifluoroacetic
acid salt): .delta. ppm 7.71 (s, 1H), 7.42-7.45 (m, 1H), 7.35-7.39
(m, 1H), 7.23-7.27 (m, 1H), 6.28 (q, J=7.0 Hz, 1H), 4.21 (dt, J=5.6
Hz, J=8.4 Hz, 2H) ppm 3.91 (dt, J=5.9 Hz, J=9.4 Hz, 2H), 3.27-3.33
(m, 1H), 2.83-2.94 (m, 4H), 2.53-2.63 (m, 1H), 2.49 (s, 3H),
2.02-2.12 (m, 1H), 1.70-1.90 (m, 7H), 1.52-1.64 (m, 1H), 1.15 (d,
J=6.2 Hz, 1H), 0.87-1.00 (m, 1H). [M+H] 552.3.
Example 7
##STR00200##
[0792]
3-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propanoic acid
and
3-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,4-
-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propanoic acid.
Prepared as a mixture of the above two diastereomers using general
procedure B (a) with methyl acrylate, followed by procedure C and
the resulting diasteromeric mixture product was condensed with
Precursor II using procedure D (a), followed by treatment of the
diastereomeric mixture with 5 equiv of LiOH in MeOH at room
temperature for 12 h, and repurifying by reverse phase HPLC using
water (0.1% TFA) and acetonitrile (0.1% TFA) as eluent. [M+H]
517.3.
Example 8
##STR00201##
[0794]
3-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propanoic acid.
The example was prepared using general procedure B (a) with methyl
acrylate, followed by procedure C and the resulting product was
condensed with Precursor II using procedure D (a), followed by
treatment of the diastereomeric mixture with 5 equiv of LiOH in
MeOH at room temperature for 12 h, and purifying by reverse phase
HPLC using water (0.1% TFA) and acetonitrile (0.1% TFA) as the
eluent. Diastereomers were separated using 40% isopropanol (0.1%
diethylamine) and 100 bar CO.sub.2 on AD-H SFC 20.times.250 mm (5
.mu.M). The first eluting diastereomer had the structure indicated
above. .sup.1H NMR (400 MHz, CD.sub.3OD, trifluoroacetic acid
salt): .delta. ppm 7.74 (s, 1H), 7.44-7.46 (m, 1H), 7.34-7.38 (m,
1H), 7.24-7.28 (m, 1H), 6.29 (q, J=7.1 Hz, 1H), 4.21-4.31 (m, 2H),
3.98-4.01 (m, 2H), 3.33-3.43 (m, 2H), 3.11-3.19 (m, 2H), 2.62-2.75
(m, 2H), 2.54 (t, J=6.9 Hz, 2H), 2.42-2.52 (m, 4H), 1.68-2.12 (m,
7H), 1.10-1.23 (m, 1H). [M+H] 517.3.
Example 9
##STR00202##
[0796]
3-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propanoic acid.
The example was prepared using general procedure B (a) with methyl
acrylate, followed by procedure C and the resulting product was
condensed with Precursor II using procedure D (a), followed by
treatment of the diastereomeric mixture with 5 equiv of LiOH in
MeOH at room temperature for 12 h, and purifying by reverse phase
HPLC using water (0.1% TFA) and acetonitrile (0.1% TFA) as eluent.
Diastereomers were separated using 40% isopropanol (0.1%
diethylamine) and 100 bar CO.sub.2 on AD-H SFC 20.times.250 mm (5
.mu.M). The second eluting diastereomer had the structure indicated
above. .sup.1H NMR (400 MHz, CD.sub.3OD, trifluoroacetic acid
salt): .delta. ppm 7.73 (s, 1H), 7.43-7.45 (m, 1H), 7.34-7.38 (m,
1H), 7.23-7.28 (m, 1H), 6.28 (q, J=7.1 Hz, 1H), 4.22-4.29 (m, 2H),
3.93-4.01 (m, 2H), 3.30-3.40 (m, 2H), 3.10-3.17 (m, 2H), 2.62-2.72
(m, 2H), 2.50-2.56 (m, 2H), 2.50 (s, 3H), 2.36-2.50 (m, 1H),
1.99-2.10 (m, 1H), 1.84-1.99 (m, 5H), 1.68-1.80 (m, 1H), 1.09-1.22
(m, 1H). [M+H] 517.3.
Example 10
##STR00203##
[0798]
4-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic acid.
The example was prepared using general procedure A with methyl
4-oxobutanoate, followed by procedure C and the resulting product
was condensed with Precursor II using procedure D (a).
Diastereomers were separated at the ester stage using 25% ethanol
in heptanes (0.1% diethylamine) on CHIRACEL OZ-H 20.times.250 mm (5
.mu.M), followed by treatment of the first eluting diastereomer
with 5 equiv of LiOH in MeOH at room temperature for 12 h, and
purifying by reverse phase HPLC using water (0.1% TFA) and
acetonitrile (0.1% TFA) as eluent. .sup.1H NMR (400 MHz, ACN-d3,
trifluoroacetic acid salt): .delta. ppm 8.03 (bs, 1H), 7.73 (s,
1H), 7.46-7.48 (m, 1H), 7.39-7.43 (m, 1H), 7.24-7.28 (m, 1H), 6.25
(q, J=7.1 Hz, 1H), 4.14-4.24 (m, 2H), 3.86-3.94 (m, 2H), 3.44-3.58
(m, 2H), 3.04-3.12 (m, 2H), 2.73-2.85 (m, 1H), 2.48-2.65 (m, 2H),
2.41-2.47 (m, 5H), 1.68-2.16 (m, 8H), 1.06-1.20 (m, 1H). [M+H]
531.2.
Example 11
##STR00204##
[0800]
4-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic acid.
Prepared using general procedure A with methyl 4-oxobutanoate,
followed by procedure C and the resulting product was condensed
with Precursor II using procedure D (a). Diastereomers were
separated at the ester stage using 25% ethanol in heptanes (0.1%
diethylamine) on CHIRACEL OZ-H 20.times.250 mm (5.mu.), followed by
treatment of the second eluting diastereomer with 5 eq of LiOH in
MeOH at room temperature for 12 hrs, and repurifying by reverse
phase HPLC using water (0.1% TFA) and acetonitrile (0.1% TFA) as
eluent. .sup.1H NMR (400 MHz, ACN-d3, trifluoroacetic acid salt):
.delta. ppm 8.27 (bs, 1H), 7.73 (s, 1H), 7.46-7.48 (m, 1H),
7.40-7.44 (m, 1H), 7.24-7.28 (m, 1H), 6.24 (q, J=7.1 Hz, 1H),
4.15-4.23 (m, 2H), 3.85-3.95 (m, 2H), 3.43-3.58 (m, 2H), 3.03-3.13
(m, 2H), 2.72-2.84 (m, 1H), 2.47-2.65 (m, 2H), 2.41-2.46 (m, 5H),
2.05-2.18 (m, 1H), 1.92-2.02 (m, 3H), 1.69-1.92 (m, 5H), 1.06-1.19
(m, 1H). [M+H] 531.2.
Example 12
##STR00205##
[0802]
3-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propanamide.
Prepared using general procedure B (a) using acrylamide, followed
by procedure C and the resulting product was condensed with
Precursor II using procedure D (a). Diastereomers were separated
using 20% ethanol in heptanes (0.1% diethylamine) on CHIRALPAK ID
20.times.250 mm (5 .mu.M). The first eluting diastereomer had the
structure indicated above. .sup.1H NMR (400 MHz, CDCl.sub.3, free
base): .delta. ppm 8.08 (bs, 1H), 7.64 (s, 1H), 7.35-7.38 (m, 1H),
7.32-7.35 (m, 1H), 7.10-7.15 (m, 1H), 6.30 (q, J=7.1 Hz, 1H), 5.80
(bs, 1H), 4.14-4.22 (m, 2H), 3.83-3.90 (m, 2H), 2.85-2.98 (m, 2H),
2.63-2.72 (m, 2H), 2.52-2.62 (m, 4H), 2.40-2.48 (m, 2H), 2.00-2.10
(m, 1H), 1.73-1.91 (m, 7H), 1.52-1.64 (m, 1H), 0.90-1.14 (m, 1H).
[M+H] 516.3.
Example 13
##STR00206##
[0804]
3-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propanamide. The
example was prepared using general procedure B (a) using
acrylamide, followed by procedure C and the resulting product was
condensed with Precursor II using procedure D (a). Diastereomers
were separated using 20% ethanol in heptanes (0.1% diethylamine) on
CHIRALPAK ID 20.times.250 mm (5 .mu.M). The second eluting
diastereomer had the structure indicated above. .sup.1H NMR (400
MHz, CDCl.sub.3, free base): .delta. ppm 8.09 (bs, 1H), 7.64 (s,
1H), 7.35-7.39 (m, 1H), 7.33-7.35 (m, 1H), 7.11-7.15 (m, 1H), 6.31
(q, J=7.1 Hz, 1H), 5.54 (bs, 1H), 4.15-4.24 (m, 2H), 3.82-3.90 (m,
2H), 2.83-2.96 (m, 2H), 2.60-2.66 (m, 2H), 2.55-2.60 (m, 4H),
2.40-2.46 (m, 2H), 1.97-2.07 (m, 1H), 1.70-1.90 (m, 7H), 1.50-1.63
(m, 1H), 0.90-1.03 (m, 1H). [M+H] 516.3.
Example 14
##STR00207##
[0806]
3-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propan-1-ol. The
example was prepared using general procedure A with methyl
4-oxobutanoate, followed by reduction of ester with 5 equiv of
LiBH.sub.4 in THF/MeOH at room temperature, and then applying
general procedure C and the resulting product was coupled with
Precursor II using procedure D (a). Diastereomers were separated
using 20% ethanol in heptanes (0.1% diethylamine) on CHIRACEL OZ-H
20.times.250 mm (5 .mu.M). The first eluting diastereomer had the
structure indicated above. .sup.1H NMR (400 MHz, CDCl.sub.3, free
base): .delta. ppm 7.64 (s, 1H), 7.36-7.40 (m, 1H), 7.33-7.36 (m,
1H), 7.12-7.16 (m, 1H), 6.31 (q, J=7.1 Hz, 1H), 4.15-4.23 (m, 2H),
3.88-3.94 (m, 1H), 3.83-3.88 (m, 1H), 3.77-3.82 (m, 2H), 2.92-3.06
(m, 2H), 2.53-2.65 (m, 6H), 1.50-2.06 (m, 11H), 0.88-1.02 (m, 1H).
[M+H] 503.0.
Example 15
##STR00208##
[0808]
3-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propan-1-ol. The
example was prepared using general procedure A with methyl
4-oxobutanoate, followed by reduction of ester with 5 equiv of
LiBH.sub.4 in THF/MeOH at room temperature, and then applying
general procedures C and the resulting product was coupled with
Precursor II using procedure D (a). Diastereomers were separated
using 20% ethanol in heptanes (0.1% diethylamine) on CHIRACEL OZ-H
20.times.250 mm (5 .mu.M). The second eluting diastereomer had the
structure indicated above. .sup.1H NMR (400 MHz, CDCl.sub.3, free
base): .delta. ppm 7.63 (s, 1H), 7.34-7.39 (m, 2H), 7.11-7.15 (m,
1H), 6.30 (q, J=7.1 Hz, 1H), 4.14-4.22 (m, 2H), 3.84-3.94 (m, 2H),
3.77-3.82 (m, 2H), 2.89-3.03 (m, 2H), 2.52-2.64 (m, 6H), 1.65-2.05
(m, 10H), 1.49-1.63 (m, 1H), 0.88-1.02 (m, 1H). [M+H] 503.0.
Example 16
##STR00209##
[0810]
Cis-3-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-H-pyr-
azolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)cyclobutane-1-carbox-
ylic acid;
trans-3-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-
-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)cyclobutane-1-
-carboxylic acid;
Cis-3-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo-
[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)cyclobutane-1-carboxylic
acid; and
trans-3-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-
-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)cyclobutane-1-
-carboxylic acid. Prepared as a mixture of the above four
diastereomers using general procedure A using
3-oxocyclobutane-1-carboxylic acid, followed by procedure C and the
resulting diasteromeric mixture product was coupled with Precursor
II using procedure D(a). [M+H] 543.2.
Example 17
##STR00210##
[0812]
4-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic acid
and 4-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-i
H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic
acid. Prepared as a mixture of the above two diastereomers using
general procedure A with methyl 4-oxobutanoate, followed by
procedure C and the resulting diasteromeric mixture product was
coupled with Precursor II using procedure D (a), followed by
treating diastereomeric mixture with 5 equiv of LiOH in MeOH at
room temperature for 12 h, and purifying by reverse phase HPLC
using water (0.1% TFA) and acetonitrile (0.1% TFA) as the eluent.
[M+H] 542.2.
Example 18
##STR00211##
[0814]
4-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic acid.
The diastereomers from example 17 were separated on AD-H
20.times.250 mm column using 40% isopropanol (0.1% diethylamine)
and 100 bar CO.sub.2. The first eluting diastereomer had the
structure indicated above. .sup.1H NMR (400 MHz, CDCl.sub.3, free
base): .delta. ppm 7.82 (s, 1H), 6.34-7.38 (m, 2H), 7.17-7.21 (m,
1H), 6.45 (q, J=7.1 Hz, 1H), 4.20-4.30 (m, 2H), 3.88-4.00 (m, 2H),
3.02-3.14 (m, 2H), 2.57-2.70 (m, 3H), 2.45-2.55 (m, 2H), 2.18-2.30
(m, 1H), 1.68-2.10 (m, 10H), 0.93-1.07 (m, 1H). [M+H] 542.2.
Example 19
##STR00212##
[0816]
4-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic acid
and 4-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-i
H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic
acid. The example was prepared using general procedure A with
methyl 4-oxobutanoate, C and D (a), followed by treating
diastereomeric mixture with 5 equiv of LiOH in MeOH at room
temperature for 12 h, and purifying by reverse phase HPLC using
water (0.1% TFA) and acetonitrile (0.1% TFA) as eluent.
Disatereomers were separated on AD-H 20.times.250 mm column using
40% isopropanol (0.1% diethylamine) and 100 bar CO.sub.2. The
second eluting diastereomer had the structure indicated above.
.sup.1H NMR (400 MHz, CDCl.sub.3, free base): .delta. ppm 7.82 (s,
1H), 7.34-7.38 (m, 2H), 7.17-7.21 (m, 1H), 6.44 (q, J=7.1 Hz, 1H),
4.19-4.29 (m, 2H), 3.90-4.02 (m, 2H), 3.04-3.16 (m, 2H), 2.48-2.74
(m, 5H), 2.23-2.33 (m, 1H), 1.95-2.20 (m, 2H), 1.70-1.91 (m, 8H),
0.96-1.09 (m, 1H). [M+H] 542.2.
Example 20
##STR00213##
[0818]
4-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-d]pyrimidin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic acid
and
4-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,4-
-d]pyrimidin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic acid.
Prepared as a mixture of the above two diastereomers using general
procedure A with methyl 4-oxobutanoate, followed by procedure C and
the resulting diasteromeric mixture product was condensed with
Precursor I using procedure D (a), followed by treating the
diastereomeric mixture with 5 equiv of LiOH in MeOH at room
temperature for 12 h, and purified by reverse phase HPLC using
water (0.1% TFA) and acetonitrile (0.1% TFA) as eluent. [M+H]
531.3.
Example 21
##STR00214##
[0820]
4-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-d]pyrimidin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic acid.
The example was prepared using general procedure A with methyl
4-oxobutanoate, followed by procedure C and condensing the product
with Precursor I using procedure D (a), followed by treating
diastereomeric mixture with 5 equiv of LiOH in MeOH at room
temperature for 12 h, and purifying by reverse phase HPLC using
water (0.1% TFA) and acetonitrile (0.1% TFA) as eluent.
Diastereomers were separated on AD-H 20.times.250 mm column using
30% ethanol (0.1% diethylamine) and 100 bar CO.sub.2. The first
eluting diastereomer had the structure indicated above. .sup.1H NMR
(400 MHz, CDCl.sub.3, free base): .delta. ppm 8.61 (s, 1H),
7.39-7.43 (m, 1H), 7.33-7.36 (m, 1H), 7.13-7.17 (m, 1H), 6.29 (q,
J=7.1 Hz, 1H), 4.12-4.23 (m, 2H), 3.82-3.94 (m, 2H), 3.06-3.21 (m,
2H), 2.66-2.76 (m, 2H), 2.53-2.63 (m, 2H), 2.42-2.52 (m, 4H),
2.22-2.35 (m, 1H), 1.95-22.10 (m, 2H), 1.75-1.94 (m, 7H), 1.22-1.32
(m, 1H), 0.94-1.06 (m, 1H). [M+H] 531.3.
Example 22
##STR00215##
[0822]
4-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-d]pyrimidin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic acid
The example was prepared using general procedure A with methyl
4-oxobutanoate, followed by procedure C and condensing the product
with Precursor I using procedure D (a), followed by treating the
diastereomeric mixture with 5 equiv of LiOH in MeOH at room
temperature for 12 h, and purifying by reverse phase HPLC using
water (0.1% TFA) and acetonitrile (0.1% TFA) as the eluent.
Diastereomers were separated on AD-H 20.times.250 mm column using
30% ethanol (0.1% diethylamine) and 100 bar CO.sub.2. The structure
was assigned to the second eluting diastereomer. .sup.1H NMR (400
MHz, CDCl.sub.3, free base): .delta. ppm 8.61 (s, 1H), 7.40-7.44
(m, 1H), 7.34-7.36 (m, 1H), 7.13-7.17 (m, 1H), 6.28 (q, J=7.1 Hz,
1H), 4.13-4.23 (m, 2H), 3.85-3.93 (m, 2H), 3.03-3.17 (m, 2H),
2.65-2.76 (m, 2H), 2.57-2.62 (m, 2H), 2.45-2.55 (m, 4H), 2.21-2.32
(m, 1H), 1.94-2.10 (m, 2H), 1.73-1.92 (m, 8H), 0.95-1.18 (m, 1H).
[M+H] 531.3.
Example 23
##STR00216##
[0824]
1-((R)-1-(2,4-Dichlorophenyl)ethyl)-6-(3-((S)-1-(2-(methylsulfonyl)-
ethyl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitr-
ile and 1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-(2-(methyl
sulfonyl)ethyl)piperidin-3-yl)azetidin-1-yl)-l
H-pyrazolo[3,4-b]pyrazine-3-carbonitrile. Prepared as a mixture of
the above two diastereomers using general procedure B (a) with
methylvinyl sulfone, procedure C and condensation of the resulting
diasteromeric mixture product with Precursor IV using procedure D
(a). .sup.1H NMR (400 MHz, CDCl.sub.3; trifluoroacetic acid salt):
.delta. ppm 9.76 (bs, 1H), 7.85 (s, 1H), 7.39-7.34 (m, 2H), 7.20
(dd, J=8.5, 2.1 Hz, 1H), 6.45 (qd, J=7.0, 3.2 Hz, 1H), 4.35-4.23
(m, 2H), 4.06-3.94 (m, 2H), 3.78-3.52 (m, 5H), 3.04 (s, 3H),
2.92-2.78 (m, 1H), 2.74-2.59 (m, 1H), 2.60-2.47 (m, 1H), 2.36-2.21
(m, 1H), 2.14-1.93 (m, 4H), 1.90 (d, J=7.1 Hz, 3H), 1.28-1.11 (m,
1H). [M+H] 562.0.
Example 24
##STR00217##
[0826]
3-((S)-3-(1-(3-Cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazol-
o[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propanamide and
3-((R)-3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4--
b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propanamide. Prepared
as a mixture of the above two diastereomers using general procedure
B (a) using acrylamide, followed by procedure C and condensation of
the resulting diasteromeric mixture product with Precursor IV using
procedure D (a). [M+H] 527.2.
Example 25
##STR00218##
[0828]
3-((S)-3-(1-(3-Cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazol-
o[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propanamide. The
diastereomers prepared in Example 24 were separated on an AD-H
20.times.250 mm column using 30% ethanol (0.1% diethylamine) and
100 bar CO.sub.2. The first eluting isomer was assigned the
structure. .sup.1H NMR (400 MHz, DMSO-d6, free base): .delta. ppm
8.04 (s, 1H), 7.64-7.66 (m, 1H), 7.41-7.49 (m, 2H), 7.36 (bs, 1H),
7.76 (bs, 1H), 6.32 (q, J=7.0 Hz, 1H), 4.08-4.36 (bm, 2H),
3.30-4.08 (bm, 2H), 2.67-2.75 (m, 2H), 2.54-2.64 (m, 1H), 2.43-2.53
(m, 2H), 2.17-2.24 (m, 2H), 1.80.1-96 (m, 4H), 1.56-1.80 (m, 4H),
1.34-1.48 (m, 1H), 0.78-0.92 (m, 1H). [M+H] 527.2.
Example 26
##STR00219##
[0830]
3-((R)-3-(1-(3-Cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazol-
o[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propanamide. The
diastereomers prepared in Example 24 were separated on an AD-H
20.times.250 mm column using 30% ethanol (0.1% diethylamine) and
100 bar CO.sub.2. The second eluting isomer was assigned the
structure indicated above. .sup.1H NMR (400 MHz, DMSO-d6, free
base): .delta. ppm 8.05 (s, 1H), 7.65-7.67 (m, 1H), 7.41-7.48 (m,
2H), 7.36 (bs, 1H), 6.76 (bs, 1H), 6.32 (q, J=7.1 Hz, 1H),
4.06-4.36 (bm, 2H), 3.80-4.06 (bm, 2H), 2.67-2.77 (m, 2H),
2.52-2.63 (m, 1H), 2.46-2.53 (m, 2H), 2.17-2.23 (m, 2H), 1.82-1.95
(m, 4H), 1.57-1.79 (m, 4H), 1.35-1.49 (m, 1H), 0.78-0.92 (m, 1H).
[M+H] 527.2.
Example 27
##STR00220##
[0832]
1-((R)-1-(2,4-Dichlorophenyl)ethyl)-6-(3-((S)-1-((S)-2-hydroxypropy-
l)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile;
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-((R)-2-hydroxypropyl)pipe-
ridin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile;
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-((S)-2-hydroxypropyl)pipe-
ridin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile;
and
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-((R)-2-hydroxypropyl)pipe-
ridin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile.
Prepared as a mixture of the above four diastereomers using general
procedure A hydroxyacetone, followed by procedure C, and
condensation of the resulting diasteromeric mixture product with
Precursor IV using procedure D (a). LCMS: [M+H] 514.3. The
diastereomers separated on AD-H 20.times.250 mm column using 40%
isopropanol (0.2% n-propylamine) and 100 bar CO.sub.2.
Example 28
##STR00221##
[0834] First eluting isomer of Example 27 mixture. .sup.1H NMR (400
MHz, CDCl.sub.3, free base): .delta. ppm 7.82 (s, 1H), 7.33-7.43
(bm, 2H), 7.16-7.23 (m, 1H), 6.40-6.50 (bq, 1H), 4.18-4.30 (m, 2H),
3.87-3.97 (m, 2H), 3.24-3.45 (m, 2H), 2.46-2.90 (m, 5H), 1.50-1.96
(m, 10H), 0.85-1.04 (2H). [M+H] 514.3.
Example 29
##STR00222##
[0836] Second eluting isomer of Example 27 mixture. .sup.1H NMR
(400 MHz, CD.sub.3OD, trifluoroacetic acid salt): .delta. ppm 7.96
(s, 1H), 7.47-7.49 (m, 1H), 7.29-7.38 (m, 2H), 6.45 (q, J=7.1 Hz,
1H), 4.28-4.38 (m, 2H), 3.96-4.10 (m, 2H), 3.84-3.90 (m, 1H),
3.66-3.74 (m, 1H), 3.38-3.59 (m, 3H), 3.95-4.05 (m, 1H), 2.82-2.92
(m, 1H), 2.64-2.76 (m, 1H), 2.15-2.29 (m, 1H), 2.74-2.10 (m, 6H),
1.33 (d, J=6.8 Hz, 3H), 1.15-1.28 (m, 1H). [M+H] 514.3.
Example 30
##STR00223##
[0838] Third eluting isomer of Example 27 mixture. .sup.1H NMR (400
MHz, CD.sub.3OD, trifluoroacetic acid salt): .delta. ppm 7.97 (s,
1H), 7.48-7.50 (m, 1H), 7.35-7.39 (m, 1H), 7.30-7.34 (m, 1H), 6.46
(q, J=7.1 Hz, 1H), 4.27-4.39 (m, 2H), 3.98-4.08 (m, 2H), 3.85-3.92
(m, 1H), 3.69-3.76 (m, 1H), 3.43-3.51 (m, 3H), 3.07-3.18 (m, 1H),
2.74-2.84 (m, 1H), 2.65-2.74 (m, 1H), 1.82-2.20 (m, 7H), 1.35 (d,
J=6.8 Hz, 3H), 1.15-1.28 (m, 1H). [M+H] 514.3.
Example 31
##STR00224##
[0840] Fourth eluting isomer of Example 27 mixture. .sup.1H NMR
(400 MHz, CD.sub.3OD, trifluoroacetic acid salt): .delta. ppm 7.96
(s, 1H), 7.46-7.48 (m, 1H), 7.34-7.39 (m, 1H), 7.29-7.33 (m, 1H),
6.45 (q, J=7.0 Hz, 1H), 4.26-4.38 (m, 2H), 4.00-4.08 (m, 2H),
3.84-3.90 (m, 1H), 3.66-3.73 (m, 1H), 3.39-3.59 (m, 3H), 2.95-3.05
(m, 1H), 2.82-2.92 (m, 1H), 2.65-2.75 (m, 1H), 2.16-2.28 (m, 1H),
1.75-2.10 (m, 6H), 1.34 (d, J=6.8 Hz, 3H), 1.14-1.27 (m, 1H). [M+H]
514.3.
Example 32
##STR00225##
[0842]
4-((S)-3-(1-(3-Carbamoyl-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyr-
azolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic
acid. The example was prepared using general procedure A with
methyl 4-oxobutanoate, then applying procedure C and condensing the
product with precursor III using procedure D (a). Diastereomers
were separated at the ester stage on OJ-H 20.times.250 mm column
using 25% ethanol (0.1% diethylamine) and 100 bar CO.sub.2,
followed by treating the first eluting peak with 5 equiv of LiOH in
MeOH at room temperature for 12 h, and repurifying by reverse phase
HPLC using water (0.1% TFA) and acetonitrile (0.1% TFA) as the
eluent. .sup.1H NMR (400 MHz, CD.sub.3OD, trifluoroacetic acid
salt): .delta. ppm 7.74 (s, 1H), 7.43-7.45 (m, 1H), 7.38-7.42 (m,
1H), 7.23-7.28 (m, 1H), 6.41 (q, J=7.1 Hz, 1H), 4.19-4.29 (m, 2H),
3.90-4.00 (m, 2H), 3.54-3.68 (m, 2H), 3.17-3.24 (m, 2H), 2.86-2.96
(m, 1H), 2.60-2.73 (m, 2H), 2.44-2.50 (m, 2H), 1.76-2.22 (m, 9H),
1.14-1.27 (m, 1H). [M+H] 560.2.
Example 33
##STR00226##
[0844]
4-((R)-3-(1-(3-Carbamoyl-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyr-
azolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)butanoic
acid. The example was prepared using general procedure A with
methyl 4-oxobutanoate, C and D (a). Diastereomers were separated at
the ester stage on OJ-H 20.times.250 mm column using 25% ethanol
(0.1% diethylamine) and 100 bar CO.sub.2, followed by treating the
second eluting peak with 5 equiv of LiOH in MeOH at room
temperature for 12 h and repurifying by reverse phase HPLC using
water (0.1% TFA) and acetonitrile (0.1% TFA) as the eluent. .sup.1H
NMR (400 MHz, CD.sub.3OD, trifluoroacetic acid salt): .delta. ppm
7.80 (s, 1H), 7.44-7.46 (m, 1H), 7.39-7.43 (m, 1H), 7.24-7.28 (m,
1H), 6.43 (q, J=7.0 Hz, 1H), 4.21-4.32 (m, 2H), 3.94-4.02 (m, 2H),
3.54-3.68 (m, 2H), 3.16-3.25 (m, 2H), 2.86-2.96 (m, 1H), 2.61-2.73
(m, 2H), 2.44-2.50 (m, 2H), 1.77-2.20 (m, 9H), 1.14-1.28 (m, 1H).
[M+H] 560.2.
Example 34
##STR00227##
[0846]
1-((R)-1-(2,4-Dichlorophenyl)ethyl)-6-(3-((S)-1-(2-hydroxyethyl)pip-
eridin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile
and
1-((S)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-(2-hydroxyethyl)piperidin-
-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile.
Prepared as a mixture of the above two diastereomers using general
procedure A with 2-((tert-butyldimethylsilyl)oxy)acetaldehyde,
followed by procedure C and condensing the resulting diasteromeric
mixture product with Precursor IV using procedure D (b). [M+H]
500.3.
Example 35
##STR00228##
[0848]
1-((R)-1-(2,4-Dichlorophenyl)ethyl)-6-(3-((S)-1-(2-hydroxyethyl)pip-
eridin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile
The diastereomers prepared in Example 34 were separated on
CHIRALPAK IF SFC 210.times.50 mm column using 40% ethanol (0.1%
diethylamine) in heptanes. The first eluting isomer had the
structure indicated above. .sup.1H NMR (400 MHz, CD.sub.3OD, HCl
salt): .delta. ppm 7.93 (s, 1H), 7.51-7.53 (m, 1H), 7.41-7.45 (m,
1H), 7.31-7.35 (m, 1H), 6.42 (q, J=7.1 Hz, 1H), 4.19-4.33 (m, 2H),
3.97-4.07 (m, 2H), 3.86-3.91 (m, 2H), 3.51-3.64 (m, 2H), 3.11-3.17
(m, 2H), 2.90-3.00 (m, 2H), 2.72-2.84 (m, 1H), 2.58-2.68 (m, 1H),
2.48-2.56 (m, 2H), 2.05-2.40 (m, 2H), 1.88-1.93 (m, 3H), 1.08-1.20
(m, 1H). [M+H] 500.3.
Example 36
##STR00229##
[0850]
1-((S)-1-(2,4-Dichlorophenyl)ethyl)-6-(3-((S)-1-(2-hydroxyethyl)pip-
eridin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile
The diastereomers prepared in example 34 were separated on
CHIRALPAK IF SFC 210.times.50 mm column using 40% ethanol (0.1%
diethylamine) in heptanes. The second eluting isomer had the
structure indicated above. .sup.1H NMR (400 MHz, CD.sub.3OD, free
base): .delta. ppm 7.92 (s, 1H), 7.43-7.46 (m, 1H), 7.33-7.38 (m,
1H), 7.26-.732 (m, 1H), 6.43 (q, J=6.9 Hz, 1H), 4.27-4.37 (m, 2H),
3.98-4.09 (m, 2H), 3.88-3.94 (m, 2H), 3.57-3.70 (m, 2H), 3.24-3.30
(m, 2H), 2.90-3.00 (m, 1H), 2.65-2.78 (m, 2H), 2.13-2.26 (m, 1H),
1.80-2.08 (m, 6H), 1.15-1.28 (m, 1H). [M+H] 500.3.
Example 37
##STR00230##
[0852]
2-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-d]pyrimidin-6-yl)azetidin-3-yl)piperidin-1-yl)ethan-1-ol and
2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,4-
-d]pyrimidin-6-yl)azetidin-3-yl)piperidin-1-yl)ethan-1-ol. Prepared
as a mixture of the above two diastereomers using general procedure
A with 2-((tert-butyldimethylsilyl)oxy)acetaldehyde, followed by
procedure C and condensation of the resulting diasteromeric mixture
product with Precursor I using procedure D (b). [M+H] 489.1.
Example 38
##STR00231##
[0854]
2-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-d]pyrimidin-6-yl)azetidin-3-yl)piperidin-1-yl)ethan-1-ol.
The diastereomers prepared in Example 37 were separated on AD-H
20.times.250 mm column using 25% ethanol (0.1% diethylamine) and
100 bar CO.sub.2. The first eluting diastereomer had the structure
indicated above. .sup.1H NMR (400 MHz, CDCl.sub.3, free base):
.delta. ppm 8.61 (s, 1H), 7.40-7.44 (m, 1H), 7.34-7.36 (m, 1H),
7.13-7.17 (m, 1H), 6.30 (q, J=7.1 Hz, 1H), 4.13-4.23 (m, 1H),
3.82-3.92 (m, 2H), 3.61-3.66 (m, 2H), 2.85-2.95 (m, 2H), 2.54-2.60
(m, 2H), 2.42-2.52 (m, 4H), 2.04-2.14 (m, 1H), 1.55-1.94 (m, 9H),
0.87-1.00 (m, 1H). [M+H]489.1.
Example 39
##STR00232##
[0856]
2-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-d]pyrimidin-6-yl)azetidin-3-yl)piperidin-1-yl)ethan-1-ol.
The diastereomers prepared in Example 37 were separated on AD-H
20.times.250 mm column using 25% ethanol (0.1% diethylamine) and
100 bar CO.sub.2. The second eluting diastereomer had the structure
indicated above. .sup.1H NMR (400 MHz, CDCl.sub.3, free base):
.delta. ppm 8.61 (s, 1H), 7.41-7.45 (m, 1H), 7.35-7.37 (m, 1H),
7.13-7.17 (m, 1H), 6.29 (q, J=7.1 Hz, 1H), 4.14-4.22 (m, 2H),
3.84-3.92 (m, 2H), 3.58-3.63 (m, 2H), 2.79-2.89 (m, 2H), 2.43-2.56
(m, 6H), 2.00-2.10 (m, 2H), 1.68-1.88 (m, 8H), 1.50-1.63 (m, 1H),
0.86-1.00 (m, 1H). [M+H]489.1.
Example 40
##STR00233##
[0858]
2-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-methyl-1H-pyrazo-
lo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethan-1-ol and
2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,4-
-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethan-1-ol. Prepared
as a mixture of the above two diastereomers using general procedure
A with 2-((tert-butyldimethylsilyl)oxy)acetaldehyde, followed by
procedure C and condensation of the resulting diasteromeric mixture
product with Precursor II using procedure D (b). [M+H] 489.3.
Example 41
##STR00234##
[0860]
1-((R)-1-(2,4-Dichlorophenyl)ethyl)-6-(3-((S)-1-(2-hydroxyethyl)pip-
eridin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carboxamide
and
1-((S)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-(2-hydroxyethyl)piperidin-
-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carboxamide.
Prepared as a mixture of the above two diastereomers using general
procedure A with 2-((tert-butyldimethylsilyl)oxy)acetaldehyde,
followed by procedure C and condensation of the resulting
diasteromeric mixture product with Precursor III using procedure D
(b). [M+H] 518.3.
Example 42
##STR00235##
[0862]
2-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-(trifluoromethyl-
)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethan-1-ol
and
2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromethyl)--
1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethan-1-ol.
Prepared as a mixture of the above two diastereomers using general
procedure A with 2-((tert-butyldimethylsilyl)oxy)acetaldehyde,
followed by procedure C and condensation of the resulting
diasteromeric mixture product with Precursor V using procedure D
(b). LCMS [M+H]: 543.0.
Example 43
##STR00236##
[0864]
2-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-(trifluoromethyl-
)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethan-1-ol.
The diastereomers prepared in Example 42 were separated on CHIRACEL
IF column using 5% ethanol and heptanes (0.1% diethylamine). The
first eluting diastereomer had the structure indicated above.
.sup.1H NMR (400 MHz, CDCl.sub.3, free base): .delta. ppm 7.83 (s,
1H), 7.38 (d, J=2.3 Hz, 1H), 7.37 (d, J=8.7 Hz, 1H), 7.19 (dd,
J=8.5, 2.1 Hz, 1H), 6.46 (q, J=7.0 Hz, 1H), 4.24 (q, J=8.8 Hz, 2H),
3.97-3.86 (m, 2H), 3.62 (t, J=5.4 Hz, 2H), 2.84 (t, J=9.9 Hz, 2H),
2.68-2.59 (m, 1H), 2.56-2.52 (m, 2H), 2.08 (t, J=10.3 Hz, 1H), 1.93
(d, J=7.1 Hz, 3H), 1.88-1.70 (m, 4H), 1.63-1.53 (m, 1H), 1.01-0.92
(m, 1H). LCMS [M+H]: 543.0.
Example 44
##STR00237##
[0866]
2-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-(trifluoromethyl-
)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethan-1-ol.
The diastereomers prepared in Example 42 were separated on CHIRACEL
IF column using 5% ethanol and heptanes (0.1% diethylamine). The
second eluting diastereomer had the structure indicated above.
.sup.1H NMR (400 MHz, CDCl.sub.3; free base) .delta. 7.83 (s, 1H),
7.39 (d, J=2.1 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 7.19 (dd, J=8.5,
2.1 Hz, 1H), 6.45 (q, J=7.1 Hz, 1H), 4.24 (t, J=8.5 Hz, 2H),
3.97-3.92 (m, 2H), 3.73 (t, J=4.6 Hz, 2H), 3.08-2.97 (m, 2H),
2.72-2.62 (m, 3H), 2.29-2.19 (m, 1H), 2.12-1.96 (m, 2H), 1.93 (d,
J=7.1 Hz, 3H), 1.89-1.73 (m, 3H), 1.06-0.97 (m, 1H). LCMS [M+H]:
543.0.
Example 45
##STR00238##
[0868]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)ace-
tamide and
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluor-
omethyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl-
)acetamide. Prepared as a mixture of the above two diastereomers
according to general procedure A using
2-(1,3-dioxoisoindolin-2-yl)acetaldehyde, deprotection with 5 equiv
of hydrazine hydrate in methanol over 5 h, and acylation with 1.2
equiv of acetic anhydride in dichloromethane with 2 equiv of
trimethylamine, followed by procedure C and condensation of the
resulting diasteromeric mixture product with Precursor V using
procedure D (a). [M+H] 584.0.
Example 46
##STR00239##
[0870]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)met-
hanesulfonamide and
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromethyl)-1-
H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)methanesu-
lfonamide. Prepared as a mixture of the above two diastereomers
using general procedure A using
2-(1,3-dioxoisoindolin-2-yl)acetaldehyde, deprotection with 5 equiv
of hydrazine hydrate in methanol over 5 h, and reaction with 1.2
equiv mesyl chloride in dichloromethane with 2 equiv of
trimethylamine, followed by procedure C and the resulting
diasteromeric mixture product was condensed with Precursor V using
procedure D (a). [M+H]620.1.
Example 47
##STR00240##
[0872]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)pro-
pane-2-sulfonamide and
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromethyl)-1-
H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)propane-2-
-sulfonamide Prepared as a mixture of the above two diastereomers
employing general procedure A using
2-(1,3-dioxoisoindolin-2-yl)acetaldehyde, deprotection with 5 equiv
of hydrazine hydrate in methanol over 5 h, and reaction with 1.2
equiv isopropylsulfonyl chloride in dichloromethane with 2 equiv of
trimethylamine, followed by procedure C. The resulting
diasteromeric mixture product was condensed with Precursor V using
procedure D (a). [M+H]648.1.
Example 48
##STR00241##
[0874]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)iso-
butyramide and
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromethyl)-1-
H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)isobutyra-
mide. Prepared as a mixture of the above two diastereomers using
general procedure A using 2-(1,3-dioxoisoindolin-2-yl)acetaldehyde,
deprotection with 5 equiv of hydrazine hydrate in methanol over 5
h, and reaction with 1.2 equiv 2-methylpropionyl chloride in
dichloromethane with 2 equiv of trimethylamine, followed by
procedure C. The resulting diasteromeric mixture product was
condensed with Precursor V using procedure D (a). [M+H] 612.2.
Example 49
##STR00242##
[0876] Methyl
(2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromethyl)-1H--
pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)carbamate
and methyl
(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromethyl)-1H--
pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)carbamate.
Prepared as a mixture of the above two diastereomers using general
procedure A using 2-(1,3-dioxoisoindolin-2-yl)acetaldehyde,
deprotection with 5 equiv of hydrazine hydrate in methanol over 5
h, and reaction with 1.2 equiv methyl chloroformate in
dichloromethane with 2 equiv of trimethylamine, followed by
procedure C. The resulting diasteromeric mixture product was
condensed with Precursor V using procedure D (a). [M+H]600.1.
Example 50
##STR00243##
[0878]
1-((R)-1-(2,4-Dichlorophenyl)ethyl)-6-(3-((R)-1-(3-(methylsulfonyl)-
propyl)piperidin-3-yl)azetidin-1-yl)-3-(trifluoromethyl)-1H-pyrazolo[3,4-b-
]pyrazine and
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-(3-(methyl
sulfonyl)propyl)piperidin-3-yl)azetidin-1-yl)-3-(trifluoromethyl)-1H-pyra-
zolo[3,4-b]pyrazine. Prepared as a mixture of the above two
diastereomers employing general procedure B (b) using
1-bromo-3-(methylsulfonyl)propane, followed by procedure C and the
resulting diasteromeric mixture product was condensed with
Precursor V using procedure D (a). [M+H] 619.0.
Example 51
##STR00244##
[0880]
N-(2-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)iso-
butyramide. The diastereomers prepared in Example 48 were separated
on AD-H 20.times.250 mm column using 25% ethanol (0.1%
diethylamine) and 100 bar CO.sub.2. The first eluting diastereomer
had the structure indicated above. .sup.1H NMR (400 MHz,
CD.sub.3OD, HCl salt): .delta. ppm 7.93 (s, 1H), 7.47 (d, J=2.0 Hz,
1H), 7.33 (d, J=8.5 Hz, 1H), 7.29 (dd, J=8.5, 2.0 Hz, 1H), 6.43 (q,
J=7.1 Hz, 1H), 4.31 (t, J=8.7 Hz, 2H), 4.09-3.98 (m, 2H), 3.57 (d,
J=5.8 Hz, 3H), 3.21 (d, J=2.8 Hz, 2H), 2.92 (s, 1H), 2.69 (s, 2H),
2.48 (dt, J=13.8, 6.9 Hz, 1H), 2.21-2.07 (m, 1H), 2.07-1.92 (m,
2H), 1.90 (d, J=7.1 Hz, 3H), 1.87-1.75 (m, 1H), 1.34-1.18 (m, 2H),
1.16-1.09 (m, 6H). [M+H] 612.2.
Example 52
##STR00245##
[0882]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)iso-
butyramide. The diastereomers prepared in Example 48 were separated
on AD-H 20.times.250 mm column using 25% ethanol (0.1%
diethylamine) and 100 bar CO.sub.2. The second eluting diastereomer
had the structure indicated above. .sup.1H NMR (400 MHz,
CD.sub.3OD, HCl salt) .delta. ppm 7.93 (d, J=0.6 Hz, 1H), 7.48 (d,
J=2.1 Hz, 1H), 7.35 (d, J=8.5 Hz, 1H), 7.30 (dd, J=8.5, 2.1 Hz,
1H), 6.44 (q, J=6.9 Hz, 1H), 4.39-4.22 (m, 2H), 4.07-3.97 (m, 2H),
3.60-3.38 (m, 3H), 3.09 (br s, 2H), 2.87-2.41 (m, 4H), 2.47 (dt,
J=13.7, 6.8 Hz, 1H), 2.16-2.02 (m, 1H), 2.02-1.93 (m, 2H), 1.90 (d,
J=7.1 Hz, 3H), 1.85-1.71 (m, 1H), 1.37-1.15 (m, 1H), 1.13 (d, J=6.9
Hz, 6H). [M+H] 612.2.
Example 53
##STR00246##
[0884]
N-(2-((S)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)ace-
tamide. The diastereomers prepared in Example 45 were separated on
AD-H 20.times.250 mm column using 20% methanol (0.1% diethylamine)
and 100 bar CO.sub.2. The first eluting diastereomer had the
structure indicated above. .sup.1H NMR (400 MHz, CD.sub.3OD, HCl
salt): .delta. ppm 7.93 (s, 1H), 7.47 (d, J=2.0 Hz, 1H), 7.34 (d,
J=8.5 Hz, 1H), 7.29 (dd, J=8.5, 1.9 Hz, 1H), 6.43 (q, J=7.0 Hz,
1H), 4.31 (t, J=8.7 Hz, 2H), 4.10-3.99 (m, 2H), 3.77-3.49 (m, 4H),
3.25 (t, J=5.8 Hz, 2H), 2.92 (t, J=11.3 Hz, 1H), 2.67 (t, J=12.0
Hz, 2H), 2.14 (d, J=9.8 Hz, 1H), 2.08-1.92 (m, 2H), 1.99 (s, 3H),
1.90 (d, J=7.1 Hz, 3H), 1.88-1.77 (m, 1H), 1.27-1.16 (m, 1H). [M+H]
584.0.
Example 54
##STR00247##
[0886]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-Dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)ace-
tamide The diastereomers prepared in Example 45 were separated on
AD-H 20.times.250 mm column using 20% methanol (0.1% diethylamine)
and 100 bar CO.sub.2. The second eluting diastereomer had the
structure indicated above. .sup.1H NMR (400 MHz, CD.sub.3OD, HCl
salt): .delta. ppm 7.93 (s, 1H), 7.48 (s, 1H), 7.35 (d, J=8.5 Hz,
1H), 7.30 (dd, J=8.5, 2.0 Hz, 1H), 6.44 (q, J=7.1 Hz, 1H),
4.36-4.25 (m, 2H), 4.08-3.96 (m, 2H), 3.65-3.42 (m, 4H), 3.15-3.06
(m, 2H), 2.84-2.62 (m, 2H), 2.60-2.44 (m, 1H), 2.05 (s, 1H), 1.98
(s, 3H), 2.02-1.93 (m, 2H), 1.90 (d, J=7.1 Hz, 3H), 1.86-1.71 (m,
1H), 1.25-1.10 (m, 1H). [M+H] 584.0.
Example 55
##STR00248##
[0888]
1-((R)-1-(4-chloro-2-fluorophenyl)ethyl)-6-(3-((R)-1-(2-hydroxyethy-
l)piperidin-3-yl)azetidin-1-yl)-l
H-pyrazolo[3,4-b]pyrazine-3-carbonitrile. The title compound was
prepared using general procedure B with Precursor VI and
2-bromoethan-1-ol, followed by procedure C. The resulting product
was condensed with Precursor VIII using procedure D and converted
to the corresponding HCl salt by dissolution in EtOH, cooling to
0.degree. C., and addition of 1 equiv. of 0.01M HCl in EtOH.
.sup.1H NMR (300 MHz, Methanol-d.sub.4; HCl Salt) .delta. 7.92 (s,
1H), 7.37 (t, J=8.1 Hz, 1H), 7.22-7.17 (m, 2H), 6.34 (q, J=6.9 Hz,
1H), 4.32 (q, J=9.0 Hz, 2H), 4.03 (t, J=7.2 Hz, 2H), 3.87 (t, J=5.1
Hz, 2H), 3.55-3.41 (m, 2H), 3.17-3.08 (m, 2H), 2.78-2.52 (m, 2H),
2.18-2.06 (m, 1H), 1.98-1.75 (m, 4H), 1.92 (d, J=7.2 Hz, 3H),
1.24-1.12 (m, 1H). LCMS [M+H] 484.1.
Example 56
##STR00249##
[0890]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-(4-hydroxy-4-methyl-
pentyl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonit-
rile and
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-(4-hydroxy-4-meth-
ylpentyl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbon-
itrile. tert-Butyl
3-(1-(4-methoxy-4-oxobutyl)piperidin-3-yl)azetidine-1-carboxylate
was prepared using general procedure A with methyl 4-oxobutanoate.
The tert-butyl
3-(1-(4-methoxy-4-oxobutyl)piperidin-3-yl)azetidine-1-carboxylate
(251 mg, 0.737 mmol) was dissolved in tetrahydrofurane ("THF") (7
mL) and treated with a 3M solution of methyl magnesium bromide in
diethyl ether (0.61 mL, 1.84 mmol, 2.5 eq) at -78.degree. C. The
solution was stirred for 1 h, then warmed to room temperature and
quenched with saturated aq. ammonium chloride (25 mL) and extracted
with ethyl acetate (3.times.25 mL). The organic layers were dried
over sodium sulfate, filtered, and concentrated in vacuo.
tert-butyl
3-(1-(4-hydroxy-4-methylpentyl)piperidin-3-yl)azetidine-1-carboxylate
was isolated by flash column chromatography (silica gel, 0-10% 7N
NH.sub.3 in methanol in DCM) (176 mg, 70% yield). The title
compound as a mixture of the two diastereomers was prepared from
tert-butyl
3-(1-(4-hydroxy-4-methylpentyl)piperidin-3-yl)azetidine-1-carboxylate
using general procedures C and D using Precursor IV. .sup.1H NMR
(400 MHz, Methanol-d.sub.4, trifluoroacetic acid salt): .delta.
7.96 (s, 1H), 7.51-7.45 (m, 1H), 7.38-7.33 (m, 1H), 7.31 (dd,
J=8.5, 2.1 Hz, 1H), 6.45 (q, J=7.0 Hz, 1H), 4.40-4.23 (m, 2H),
4.12-3.94 (m, 2H), 3.57 (dd, J=23.3, 12.2 Hz, 2H), 3.16-3.07 (m,
2H), 2.95-2.80 (m, 1H), 2.77-2.57 (m, 2H), 2.15-1.70 (m, 9H),
1.59-1.47 (m, 2H), 1.34-1.08 (m, 7H). LCMS [M+H] 557.1.
Example 57
##STR00250##
[0892]
2-((S)-3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazol-
o[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)-N-methylethane-1-sulfon-
amide and
2-((R)-3-(1-(3-cyano-l-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyra-
zolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)-N-methylethane-1-sul-
fonamide. tert-Butyl
3-[1-(2-fluorosulfonylethyl)-3-piperidyl]azetidine-1-carboxylate
was prepared from vinyl sulfonyl fluoride according to general
procedure B. To tert-butyl
3-[1-(2-fluorosulfonylethyl)-3-piperidyl]azetidine-1-carboxylate
(231 mg, 0.66 mmol) in THF (3 mL) was added a 33% solution of
methylamine in ethanol (0.6 mL, 6.6 mmol, 10 equiv.). The mixture
was heated in a sealed tube at 70.degree. C. for 2.5 h. The mixture
was concentrated in vacuo, and the residue was purified by flash
column chromatography (silica gel, 0-10% 7N NH.sub.3 in methanol in
DCM) (133 mg, 56% yield). The title compound as a mixture of the
two diastereomers was prepared from tert-butyl
3-[1-[2-(methylsulfamoyl)ethyl]-3-piperidyl]azetidine-1-carboxylate
according to general procedures C and D using Precursor IV. .sup.1H
NMR (400 MHz, Methanol-d.sub.4, free base): .delta. 7.95 (s, 1H),
7.48 (d, J=2.1 Hz, 1H), 7.38 (dd, J=8.6, 1.2 Hz, 1H), 7.31 (dd,
J=8.5, 2.2 Hz, 1H), 6.45 (q, J=7.1 Hz, 1H), 4.33-4.19 (m, 2H),
4.04-3.88 (m, 2H), 3.29-3.21 (m, 2H), 2.94-2.86 (m, 2H), 2.86-2.75
(m, 2H), 2.71 (s, 3H), 2.68-2.55 (m, 1H), 2.08 (s, 1H), 1.90 (d,
J=7.1 Hz, 3H), 1.87-1.69 (m, 4H), 1.66-1.52 (m, 1H), 1.03-0.87 (m,
1H). LCMS [M+H] 577.0.
Example 58
##STR00251##
[0894]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-(2-(morpholinosulfo-
nyl)ethyl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbo-
nitrile and
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-(2-(morpholinosulfonyl)et-
hyl)piperidin-3-yl)azetidin-1-yl)-l
H-pyrazolo[3,4-b]pyrazine-3-carbonitrile. tert-Butyl
3-[1-(2-fluorosulfonylethyl)-3-piperidyl]azetidine-1-carboxylate
was prepared from vinyl sulfonyl fluoride according to general
procedure B. To tert-butyl
3-[1-(2-fluorosulfonylethyl)-3-piperidyl]azetidine-1-carboxylate
(230 mg, 0.53 mmol) and N,N-diisopropyl-N-ethylamine (85 mg, 0.66
mmol, 1.0 equiv.) in THF (3 mL) is added morpholine (69 mg, 0.79
mmol, 1.2 equiv.). The mixture was heated in a sealed tube at
70.degree. C. for 2.5 h and concentrated in vacuo. The residue was
purified by flash column chromatography (silica gel, 0-10% 7N
NH.sub.3 in methanol in DCM) to afford tert-butyl
3-[1-(2-morpholinosulfonylethyl)-3-piperidyl]azetidine-1-carboxylate
(230 mg, 83% yield). The title compound as a mixture of the two
diastereomers was prepared from tert-butyl
3-[1-(2-morpholinosulfonylethyl)-3-piperidyl]azetidine-1-carboxylate
according to general procedures C and D using Precursor IV. .sup.1H
NMR (400 MHz, Methanol-d.sub.4, trifluoroacetic acid salt): .delta.
7.97 (s, 1H), 7.48 (dd, J=2.1, 0.4 Hz, 1H), 7.35 (dd, J=8.5, 2.8
Hz, 1H), 7.31 (dd, J=8.5, 2.1 Hz, 1H), 6.45 (q, J=7.1 Hz, 1H),
4.88-4.87 (m, 4H), 4.40-4.25 (m, 2H), 4.13-3.95 (m, 2H), 3.79-3.50
(m, 8H), 3.33-3.29 (m, 2H), 3.05-2.88 (m, 1H), 2.85-2.62 (m, 2H),
2.17-1.94 (m, 3H), 1.90 (d, J=7.1 Hz, 3H), 1.88-1.71 (m, 1H),
1.34-1.12 (m, 1H). LCMS [M+H] 633.1.
Example 59
##STR00252##
[0896]
6-(3-((S)-1-((1H-pyrazol-3-yl)methyl)piperidin-3-yl)azetidin-1-yl)--
1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitr-
ile and
6-(3-((R)-1-((1H-pyrazol-3-yl)methyl)piperidin-3-yl)azetidin-1-yl)-
-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonit-
rile. The title compound as a mixture of the two diastereomers was
prepared using general procedure A using 1H-pyrazole-3-carbaldehyde
and 4:2:1 1,2-dichloroethane/dimethylformamide
("DMF")/trifluoroethanol as the solvent, followed by procedure C.
The resulting product was condensed with Precursor IV using
procedure D. .sup.1H NMR (400 MHz, Methanol-d.sub.4, free base):
.delta. 7.93 (s, 1H), 7.63 (s, 1H), 7.48 (dd, J=2.1, 1.3 Hz, 1H),
7.38 (dd, J=8.5, 1.1 Hz, 1H), 7.31 (dd, J=8.5, 2.1 Hz, 1H), 6.45
(q, J=7.1 Hz, 1H), 6.32 (s, 1H), 4.32-4.14 (m, 2H), 4.04-3.81 (m,
2H), 3.70-3.53 (m, 2H), 3.02-2.72 (m, 2H), 2.71-2.47 (m, 1H),
2.12-1.98 (m, 1H), 1.90 (d, J=7.1 Hz, 3H), 1.86-1.68 (m, 4H),
1.68-1.43 (m, 1H), 1.07-0.76 (m, 1H). LCMS [M+H] 536.0.
Example 60
##STR00253##
[0898]
6-(3-((S)-1-((1H-imidazol-4-yl)methyl)piperidin-3-yl)azetidin-1-yl)-
-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonit-
rile and
6-(3-((R)-1-((1H-imidazol-4-yl)methyl)piperidin-3-yl)azetidin-1-y-
l)-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-carbon-
itrile. The title compound as a mixture of the two diastereomers
was prepared using general procedure A from
1H-imidazole-5-carbaldehyde using 2:1 1,2-dichloroethane/DMF as the
solvent, followed by procedure C. The resulting product was
condensed with Precursor IV using procedure D. .sup.1H NMR (400
MHz, Methanol-d.sub.4, free base): .delta. 7.94 (s, 1H), 7.71 (dd,
J=2.0, 1.2 Hz, 1H), 7.48 (dd, J=2.1, 1.6 Hz, 1H), 7.37 (dd, J=8.5,
1.4 Hz, 1H), 7.31 (dd, J=8.5, 2.1 Hz, 1H), 7.13 (s, 1H), 6.45 (q,
J=7.0 Hz, 1H), 4.34-4.16 (m, 2H), 4.06-3.84 (m, 2H), 3.80 (s, 2H),
3.16-3.01 (m, 2H), 2.69-2.55 (m, 1H), 2.42-2.25 (m, 1H), 2.12-1.97
(m, 1H), 1.99-1.76 (m, 6H), 1.73-1.57 (m, 1H), 1.06-0.92 (m, 1H).
LCMS [M+H] 536.0.
Example 61
##STR00254##
[0900]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-(1,1-dioxidotetrahy-
dro-2H-thiopyran-4-yl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyra-
zine-3-carbonitrile and
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-(1,1-dioxidotetrahydro-2H-
-thiopyran-4-yl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-
-carbonitrile. The title compound as a mixture of the two
diastereomers was prepared from tetrahydro-4H-thiopyran-4-one
1,1-dioxide by general procedure A using 2:1 1,2-dichloroethane/DMF
as the solvent, followed by procedure C. The resulting product was
treated with Precursor IV using general procedure D. .sup.1H NMR
(400 MHz, Methanol-d.sub.4, free base): .delta. 7.94 (s, 1H), 7.48
(d, J=2.1 Hz, 1H), 7.38 (dd, J=8.6, 1.2 Hz, 1H), 7.31 (dd, J=8.5,
2.1 Hz, 1H), 6.45 (q, J=7.1 Hz, 1H), 4.36-4.18 (m, 2H), 4.03-3.86
(m, 2H), 3.19-3.02 (m, 4H), 2.87-2.79 (m, 2H), 2.75-2.58 (m, 2H),
2.27 (t, J=10.9 Hz, 1H), 2.22-2.04 (m, 5H), 2.03-1.94 (m, 1H), 1.90
(d, J=7.0 Hz, 3H), 1.87-1.70 (m, 2H), 1.66-1.45 (m, 1H), 1.03-0.87
(m, 1H). LCMS [M+H] 588.0.
Example 62
##STR00255##
[0902]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-(tetrahydro-2H-pyra-
n-4-yl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonit-
rile and
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-(tetrahydro-2H-py-
ran-4-yl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbon-
itrile. The title compound as a mixture of the two diastereomers
was prepared from tetrahydro-4H-pyran-4-one by general procedure A,
followed by procedure C. The resulting product was treated with
Precursor IV using general procedure D. .sup.1H NMR (400 MHz,
Methanol-d4, free base): .delta. 7.95 (s, 1H), 7.48 (dd, J=2.2, 1.0
Hz, 1H), 7.41-7.34 (m, 1H), 7.31 (dd, J=8.5, 2.1 Hz, 1H), 6.45 (q,
J=7.1 Hz, 1H), 4.34-4.20 (m, 2H), 4.04-3.90 (m, 4H), 3.40 (t,
J=11.8 Hz, 2H), 3.05-2.90 (m, 2H), 2.68-2.46 (m, 2H), 2.25-2.12 (m,
1H), 1.90 (d, J=7.1 Hz, 3H), 1.88-1.71 (m, 5H), 1.68-1.48 (m, 4H),
1.02-0.86 (m, 1H). LCMS [M+H] 540.0.
Example 63
##STR00256##
[0904]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyr-
azolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)acetamide
and
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[-
3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)acetamide.
The title compound as a mixture of the two diastereomers was
prepared using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, and the organic layer
was dried over sodium sulfate, filtered and concentrated in vacuum.
Crude tert-Butyl
3-[1-(2-aminoethyl)-3-piperidyl]azetidine-1-carboxylate (120 mg,
0.423 mmol) in DCM (2 mL) was treated with triethylamine (129 mg,
1.27 mmol, 3.0 equiv.) and acetyl chloride (40.0 mg, 0.51 mmol, 1.2
equiv). After 30 min, the mixture was quenched with 1M aq. sodium
carbonate (10 mL) and extracted with ethyl acetate (3.times.10 mL).
The combined organic layers were dried over sodium sulfate,
filtered, and concentrated in vacuo to afford tert-butyl
3-(1-(2-acetamidoethyl)piperidin-3-yl)azetidine-1-carboxylate. The
title compound as a mixture of the two diastereomers was prepared
from tert-butyl
3-(1-(2-acetamidoethyl)piperidin-3-yl)azetidine-1-carboxylate
according to general procedures C and D using Precursor II. .sup.1H
NMR (400 MHz, Methanol-d.sub.4, trifluoroacetic acid salt): .delta.
7.75 (s, 1H), 7.44 (dd, J=2.2, 1.3 Hz, 1H), 7.35 (dd, J=8.5, 2.4
Hz, 2H), 7.27-7.21 (m, 1H), 6.31-6.25 (m, 1H), 4.34-4.19 (m, 2H),
4.04-3.93 (m, 2H), 3.81-3.42 (m, 4H), 3.23 (t, J=5.9 Hz, 2H),
2.98-2.83 (m, 1H), 2.71-2.59 (m, 2H), 2.50 (s, 3H), 2.12-1.93 (m,
5H), 1.88-1.74 (m, 4H), 1.30-1.16 (m, 1H). LCMS [M+H] 530.0.
Example 64
##STR00257##
[0906]
N-[2-[(R)-3-[1-[1-[(1R)-1-(2,4-dichlorophenyl)ethyl]-3-methyl-pyraz-
olo[3,4-b]pyrazin-6-yl]azetidin-3-yl]-1-piperidyl]ethyl]methanesulfonamide
and
N-[2-[(S)-3-[1-[1-[(1R)-1-(2,4-dichlorophenyl)ethyl]-3-methyl-pyrazol-
o[3,4-b]pyrazin-6-yl]azetidin-3-yl]-1-piperidyl]ethyl]methanesulfonamide.
The title compound as a mixture of the two diastereomers was
prepared using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. Crude
tert-butyl 3-[1-(2-aminoethyl)-3-piperidyl]azetidine-1-carboxylate
(120 mg, 0.423 mmol) in DCM (2 mL) was treated with triethylamine
(129 mg, 1.27 mmol, 3.0 equiv.) and methanesulfonyl chloride (58
mg, 0.51 mmol, 1.2 equiv). After 30 min, the mixture was quenched
with 1M aq. sodium carbonate (10 mL) and extracted with ethyl
acetate (3.times.10 mL). The combined organic layers were dried
over sodium sulfate, filtered, and concentrated in vacuo to afford
tert-butyl
3-(1-(2-(methylsulfonamido)ethyl)piperidin-3-yl)azetidine-1-carboxylate.
The title compound as a mixture of the two diastereomers was
prepared from tert-butyl 3-(1-(2-(methyl
sulfonamido)ethyl)piperidin-3-yl)azetidine-1-carboxylate according
to general procedures C and D using Precursor II. .sup.1H NMR (400
MHz, Methanol-d.sub.4, trifluoroacetic acid salt): .delta. 7.73 (s,
1H), 7.44 (d, J=2.1 Hz, 1H), 7.37 (dd, J=8.5, 2.2 Hz, 1H),
7.30-7.21 (m, 1H), 6.33-6.23 (m, 1H), 4.33-4.20 (m, 2H), 4.03-3.91
(m, 2H), 3.77-3.59 (m, 2H), 3.59-3.40 (m, 2H), 3.30-3.25 (m, 2H),
3.02 (s, 3H), 3.00-2.87 (m, 1H), 2.75-2.57 (m, 2H), 2.50 (s, 3H),
2.21-1.93 (m, 3H), 1.93-1.74 (m, 4H), 1.30-1.09 (m, 1H). [M+H]
566.0.
Example 65
##STR00258##
[0908]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyr-
azolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)propane-2-sulf-
onamide and
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[-
3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)propane-2-sulfonamid-
e. The title compound as a mixture of the two diastereomers was
prepared using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. Crude
tert-butyl 3-[1-(2-aminoethyl)-3-piperidyl]azetidine-1-carboxylate
(120 mg, 0.423 mmol) in DCM (2 mL) was treated with triethylamine
(129 mg, 1.27 mmol, 3.0 equiv.) and 2-propanesulfonyl chloride (73
mg, 0.51 mmol, 1.2 equiv). After 30 min, the mixture was quenched
with 1M aq. sodium carbonate (10 mL) and extracted with ethyl
acetate (3.times.10 mL). The combined organic layers were dried
over sodium sulfate, filtered, and concentrated in vacuo to afford
tert-butyl
3-(1-(2-((1-methylethyl)sulfonamido)ethyl)piperidin-3-yl)azetidine-1-carb-
oxylate. The title compound as a mixture of the two diastereomers
was prepared from tert-butyl
3-(1-(2-((1-methylethyl)sulfonamido)ethyl)piperidin-3-yl)azetidine-1-carb-
oxylate according to general procedures C and D using Precursor II.
.sup.1H NMR (400 MHz, Methanol-d.sub.4, trifluoroacetic acid salt):
.delta. 7.74 (s, 1H), 7.46-7.42 (m, 1H), 7.37 (d, J=8.5 Hz, 1H),
7.26 (dd, J=8.5, 2.1 Hz, 1H), 6.34-6.21 (m, 1H), 4.33-4.18 (m, 2H),
4.05-3.94 (m, 2H), 3.78-3.59 (m, 2H), 3.59-3.41 (m, 2H), 3.36-3.19
(m, 4H), 3.03-2.92 (m, 1H), 2.75-2.57 (m, 2H), 2.50 (s, 3H),
2.21-1.93 (m, 2H), 1.93-1.76 (m, 4H), 1.41-1.32 (m, 6H), 1.28-1.12
(m, 1H). LCMS [M+H] 594.0.
Example 66
##STR00259##
[0910]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)pro-
pane-2-sulfonamide and
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromethyl)-1-
H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)propane-2-
-sulfonamide. The title compound as a mixture of the two
diastereomers was prepared from tert-butyl
3-(1-(2-((1-methylethyl)sulfonamido)ethyl)piperidin-3-yl)azetidine-1-carb-
oxylate (see preparation in the previous example) according to
general procedures C and D using Precursor V. .sup.1H NMR (400 MHz,
Methanol-d.sub.4, trifluoroacetic acid salt): .delta. 7.75 (s, 1H),
7.45-7.40 (m, 1H), 7.35 (dd, J=8.5, 4.3 Hz, 1H), 7.26 (dd, J=8.5,
2.2 Hz, 1H), 6.33-6.24 (m, 1H), 4.34-4.20 (m, 2H), 4.06-3.92 (m,
2H), 3.73-3.49 (m, 4H), 3.24 (t, J=6.2 Hz, 2H), 2.93 (t, J=12.7 Hz,
1H), 2.75-2.58 (m, 2H), 2.54-2.40 (m, 4H), 2.17-1.90 (m, 3H),
1.90-1.84 (m, 3H), 1.84-1.72 (m, 1H), 1.30-1.17 (m, 1H), 1.17-1.09
(m, 6H). LCMS [M+H]558.1.
Example 67
##STR00260##
[0912] Methyl
(2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,-
4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)carbamate and
methyl
(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,-
4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)carbamate. The
title compound as a mixture of the two diastereomers was prepared
using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. Crude
tert-butyl 3-[1-(2-aminoethyl)-3-piperidyl]azetidine-1-carboxylate
(120 mg, 0.423 mmol) in DCM (2 mL) was treated with triethylamine
(129 mg, 1.27 mmol, 3.0 equiv.) and methyl chloroformate (48 mg,
0.51 mmol, 1.2 equiv). After 30 min, the mixture was quenched with
1M aq. sodium carbonate (10 mL) and extracted with ethyl acetate
(3.times.10 mL). The combined organic layers were dried over sodium
sulfate, filtered, and concentrated in vacuo to afford tert-butyl
3-(1-(2-((methoxycarbonyl)amino)ethyl)piperidin-3-yl)azetidine-1-carboxyl-
ate. The title compound as a mixture of the two diastereomers was
prepared from tert-butyl
3-(1-(2-((methoxycarbonyl)amino)ethyl)piperidin-3-yl)azetidine-1-carboxyl-
ate using general procedures C and D using Precursor II. .sup.1H
NMR (400 MHz, Methanol-d.sub.4, trifluoroacetic acid salt): .delta.
7.74 (s, 1H), 7.48-7.40 (m, 1H), 7.35 (dd, J=8.5, 2.2 Hz, 1H), 7.26
(dd, J=8.5, 2.2 Hz, 1H), 6.34-6.23 (m, 1H), 4.35-4.22 (m, 2H),
4.05-3.91 (m, 2H), 3.76-3.61 (m, 5H), 3.60-3.42 (m, 2H), 3.24 (t,
J=5.9 Hz, 2H), 2.98-2.84 (m, 1H), 2.71-2.59 (m, 2H), 2.50 (s, 3H),
2.16-1.93 (m, 3H), 1.93-1.72 (m, 4H), 1.30-1.12 (m, 1H). LCMS [M+H]
546.0.
Example 68
##STR00261##
[0914]
4-((S)-3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazol-
o[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)-N-methylbutanamide.
tert-Butyl
3-[1-(4-methoxy-4-oxo-butyl)-3-piperidyl]azetidine-1-carboxylate
was prepared from methyl 4-oxobutanoate according to general
procedure A. tert-Butyl
3-(1-(4-methoxy-4-oxobutyl)piperidin-3-yl)azetidine-1-carboxylate
was hydrolyzed with 4 equiv. of lithium hydroxide in methanol/water
(3:1 by volume) mixture at ambient temperature for 18 hours,
followed by removing methanol in vacuum, acidifying reaction
mixture with conc. HCl until pH 7 and extracting with DCM. Drying
with sodium sulfate, filtering, and removing solvent in vacuum
afforded the corresponding acid as a white solid.
4-(3-(1-(tert-butoxycarbonyl)azetidin-3-yl)piperidin-1-yl)butanoic
acid (288 mg, 0.88 mmol) in DMF (5 mL) was treated with HATU (402
mg, 1.06 mmol, 1.2 equiv.). The mixture was stirred for 5 min, then
N,N-diisopropyl-N-ethylamine (0.46 mL, 2.65 mmol, 3.0 equiv.) was
added. After 10 min, a 33% solution of methylamine in ethanol (0.15
mL, 4.4 mmol, 5.0 equiv.) was added and the reaction was allowed to
stir overnight. The reaction was quenched with 1M aq. sodium
carbonate (5 mL), diluted with ethyl acetate (10 mL), and the
organic layer was washed with water (3.times.5 mL). The organic
layer was dried over sodium sulfate, filtered, and concentrated in
vacuo to afford tert-butyl
3-[1-[4-(methylamino)-4-oxo-butyl]-3-piperidyl]
azetidine-1-carboxylate.
4-(3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]py-
razin-6-yl)azetidin-3-yl)piperidin-1-yl)-N-methylbutanamide was
prepared from tert-butyl
3-[1-[4-(methylamino)-4-oxo-butyl]-3-piperidyl]azetidine-1-carboxylate
using general procedures C and D using Precursor IV. The title
compound was isolated by chiral supercritical fluid chromatography
("SFC") (OD-H, 30% methanol (0.1% diethylamine)/CO.sub.2 100 bars)
as the first eluting peak. .sup.1H NMR (400 MHz, Methanol-d.sub.4,
free base): .delta. 7.92 (s, 1H), 7.46 (d, J=2.1 Hz, 1H), 7.37 (d,
J=8.5 Hz, 1H), 7.30 (dd, J=8.5, 2.1 Hz, 1H), 6.44 (q, J=7.0 Hz,
1H), 4.25 (t, J=8.1 Hz, 2H), 4.02-3.86 (m, 2H), 2.99-2.83 (m, 2H),
2.83-2.51 (m, 2H), 2.71 (s, 3H), 2.40-2.30 (m, 2H), 2.19 (t, J=7.4
Hz, 2H), 2.04-1.92 (m, 1H), 1.90 (d, J=7.1 Hz, 3H), 1.87-1.50 (m,
5H), 1.23-1.12 (m, 1H), 1.01-0.81 (m, 1H). LCMS [M+H] 555.1.
Example 69
##STR00262##
[0916]
4-((R)-3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazol-
o[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)-N-methylbutanamide.
tert-Butyl
3-[1-(4-methoxy-4-oxo-butyl)-3-piperidyl]azetidine-1-carboxylate
was prepared from methyl 4-oxobutanoate according to general
procedure A. tert-Butyl
3-(1-(4-methoxy-4-oxobutyl)piperidin-3-yl)azetidine-1-carboxylate
was hydrolyzed with 4 equiv. of lithium hydroxide in methanol/water
(3:1 by volume) mixture at ambient temperature for 18 hours,
followed by removing methanol in vacuum, acidifying reaction
mixture with conc. HCl until pH 7 and extracting with DCM. Drying
with sodium sulfate, filtering, and removing solvent in vacuum
afforded the corresponding acid as a white solid.
4-(3-(1-(tert-butoxycarbonyl)azetidin-3-yl)piperidin-1-yl)butanoic
acid (288 mg, 0.88 mmol) in DMF (5 mL) was treated with HATU (402
mg, 1.06 mmol, 1.2 equiv.). The mixture was stirred for 5 min, then
N,N-diisopropyl-N-ethylamine (0.46 mL, 2.65 mmol, 3.0 equiv.) was
added. After 10 min, a 33% solution of methylamine in ethanol (0.15
mL, 4.4 mmol, 5.0 equiv.) was added and the reaction was allowed to
stir overnight. The reaction was quenched with 1M aq. sodium
carbonate (5 mL), diluted with ethyl acetate (10 mL), and the
organic layer was washed with water (3.times.5 mL). The organic
layer was dried over sodium sulfate, filtered, and concentrated in
vacuo to afford tert-butyl
3-[1-[4-(methylamino)-4-oxo-butyl]-3-piperidyl]azetidine-1-carboxylate.
4-(3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]py-
razin-6-yl)azetidin-3-yl)piperidin-1-yl)-N-methylbutanamide was
prepared from tert-butyl
3-[1-[4-(methylamino)-4-oxo-butyl]-3-piperidyl]azetidine-1-carboxylate
using general procedures C and D using Precursor IV. The title
compound was isolated by chiral SFC chromatography (OD-H, 30%
methanol (0.1% diethylamine)/CO.sub.2 100 bars) as the second
eluting peak. .sup.1H NMR (400 MHz, Methanol-d.sub.4, free base):
.delta. 7.92 (s, 1H), 7.46 (d, J=2.1 Hz, 1H), 7.37 (d, J=8.5 Hz,
1H), 7.30 (dd, J=8.5, 2.1 Hz, 1H), 6.44 (q, J=7.0 Hz, 1H),
4.31-4.18 (m, 2H), 4.02-3.86 (m, 2H), 2.96-2.83 (m, 2H), 2.70 (s,
3H), 2.75-2.52 (m, 2H), 2.41-2.30 (m, 2H), 2.19 (t, J=7.4 Hz, 2H),
2.01-1.92 (m, 1H), 1.90 (d, J=7.0 Hz, 3H), 1.86-1.50 (m, 5H), 1.15
(t, J=7.2 Hz, 1H), 1.00-0.84 (m, 1H). LCMS [M+H]555.1.
Example 70
##STR00263##
[0918]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-(2-hydroxy-2-methyl-
propyl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonit-
rile. tert-butyl
3-[1-(2-ethoxy-2-oxo-ethyl)-3-piperidyl]azetidine-1-carboxylate was
prepared from ethyl glyoxylate according to general procedure A.
tert-Butyl
3-[1-(2-ethoxy-2-oxo-ethyl)-3-piperidyl]azetidine-1-carboxylate
(240 mg, 0.74 mmol) in anhydrous THF (7 mL) was cooled to
-78.degree. C. and MeMgBr was added as a 3M solution in diethyl
ether (0.52 mL, 1.54 mmol, 2.1 equiv.). The mixture was warmed to
0.degree. C. and let stir for 1 h before being quenched with sat.
aq. ammonium chloride (5 mL) and extracted with DCM (10 mL). The
organic layer was dried over magnesium sulfate, filtered, and
concentrated in vacuo. The residue was purified by flash column
chromatography (silica gel, 0-10% methanol in DCM) to afford
tert-butyl
3-(1-(2-hydroxy-2-methylpropyl)piperidin-3-yl)azetidine-1-carboxylate
(100 mg, 43% yield).
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-(1-(2-hydroxy-2-methylpropyl)pip-
eridin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile
was prepared from tert-butyl
3-(1-(2-hydroxy-2-methylpropyl)piperidin-3-yl)azetidine-1-carboxylate
using general procedures C and D using Precursor IV. The title
compound was isolated by chiral SFC (AD-H, 40% isopropanol (0.1%
diethylamine)/CO.sub.2 100 bars) as the first eluting peak. .sup.1H
NMR (400 MHz, Methanol-d.sub.4, free base): .delta. 7.94 (s, 1H),
7.48 (d, J=2.1 Hz, 1H), 7.38 (d, J=8.5 Hz, 1H), 7.31 (dd, J=8.5,
2.2 Hz, 1H), 6.50-6.40 (m, 1H), 4.30-4.20 (m, 2H), 3.98-3.85 (m,
2H), 3.40-3.21 (m, 2H), 2.95-2.75 (m, 2H), 2.75-2.62 (m, 1H),
2.34-2.11 (m, 2H), 2.06-1.80 (m, 4H), 1.80-1.47 (m, 3H), 1.18 (d,
J=3.9 Hz, 3H), 1.15 (d, J=6.1 Hz, 3H), 1.06-0.81 (m, 1H). LCMS
[M+H] 528.1.
Example 71
##STR00264##
[0920]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-(2-hydroxy-2-methyl-
propyl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonit-
rile. tert-butyl
3-[1-(2-ethoxy-2-oxo-ethyl)-3-piperidyl]azetidine-1-carboxylate was
prepared from ethyl glyoxylate according to general procedure A.
tert-butyl
3-[1-(2-ethoxy-2-oxo-ethyl)-3-piperidyl]azetidine-1-carboxylate
(240 mg, 0.74 mmol) in THF (7 mL) was cooled to -78.degree. C. and
MeMgBr was added as a 3M solution in diethyl ether (0.52 mL, 1.54
mmol, 2.1 equiv.). The mixture was warmed to 0.degree. C. and let
stir for 1 h before being quenched with sat. aq. ammonium chloride
(5 mL) and extracted with DCM (10 mL). The organic layer was dried
over magnesium sulfate, filtered, and concentrated in vacuo. The
residue was purified by flash column chromatography (silica gel,
0-10% methanol in DCM) to afford tert-butyl
3-(1-(2-hydroxy-2-methylpropyl)piperidin-3-yl)azetidine-1-carboxylate
(100 mg, 43% yield).
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-(1-(2-hydroxy-2-methylpropyl)pip-
eridin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile
was prepared from tert-butyl
3-(1-(2-hydroxy-2-methylpropyl)piperidin-3-yl)azetidine-1-carboxylate
using general procedures C and D using Precursor IV. The title
compound was isolated from its diastereomer by chiral SFC (AD-H,
40% isopropanol (0.1% diethylamine)/CO.sub.2 100 bars) as the
second eluting peak. .sup.1H NMR (400 MHz, Methanol-d.sub.4, free
base): .delta. 7.94 (s, 1H), 7.48 (d, J=2.1 Hz, 1H), 7.38 (d, J=8.5
Hz, 1H), 7.31 (dd, J=8.5, 2.1 Hz, 1H), 6.44 (q, J=7.1 Hz, 1H),
4.33-4.19 (m, 2H), 4.00-3.85 (m, 2H), 3.33-3.28 (m, 2H), 2.98-2.78
(m, 2H), 2.73-2.61 (m, 1H), 2.36-2.11 (m, 2H), 2.04-1.81 (m, 4H),
1.79-1.55 (m, 3H), 1.18 (d, J=3.9 Hz, 3H), 1.15 (d, J=6.2 Hz, 3H),
1.04-0.84 (m, 1H). LCMS [M+H] 528.1.
Example 72
##STR00265##
[0922]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-propylpiperidin-3-y-
l)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile.
tert-Butyl 3-(1-propylpiperidin-3-yl)azetidine-1-carboxylate was
prepared according to general procedure B (b) using 1-iodopropane.
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-(1-propylpiperidin-3-yl)azetidin-
-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile was prepared from
tert-butyl 3-(1-propylpiperidin-3-yl)azetidine-1-carboxylate using
general procedures C and D using Precursor IV. The title compound
was isolated from its diastereomer by chiral SFC (AD-H, 40%
isopropanol (0.1% diethylamine)/CO.sub.2 100 bars) as the first
eluting peak. .sup.1H NMR (400 MHz, Methanol-d.sub.4) .delta. 7.95
(s, 1H), 7.51-7.46 (m, 1H), 7.38 (d, J=8.5 Hz, 1H), 7.35-7.28 (m,
1H), 6.45 (q, J=7.1 Hz, 1H), 4.32-4.22 (m, 2H), 4.02-3.86 (m, 2H),
3.30-3.23 (m, 2H), 3.03-2.87 (m, 2H), 2.67-2.55 (m, 1H), 2.42-2.28
(m, 2H), 2.06-1.94 (m, 1H), 1.90 (d, J=7.1 Hz, 3H), 1.88-1.65 (m,
3H), 1.65-1.49 (m, 2H), 1.03-0.88 (m, 4H). LCMS [M+H] 498.0.
Example 73
##STR00266##
[0924]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-propylpiperidin-3-y-
l)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile.
tert-butyl 3-(1-propylpiperidin-3-yl)azetidine-1-carboxylate was
prepared according to general procedure B (b) using 1-iodopropane.
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-(1-propylpiperidin-3-yl)azetidin-
-1-yl)-l H-pyrazolo[3,4-b]pyrazine-3-carbonitrile was prepared from
tert-butyl 3-(1-propylpiperidin-3-yl)azetidine-1-carboxylate using
general procedures C and D using Precursor IV. The title compound
was isolated from its diastereomer by chiral SFC (AD-H, 40%
isopropanol (0.1% diethylamine)/CO.sub.2 100 bars) as the second
eluting peak. .sup.1H NMR (400 MHz, Methanol-d.sub.4, free base):
.delta. 7.95 (s, 1H), 7.49 (d, J=2.1 Hz, 1H), 7.38 (d, J=8.5 Hz,
1H), 7.35-7.24 (m, 1H), 6.45 (q, J=7.0 Hz, 1H), 4.33-4.20 (m, 2H),
4.02-3.84 (m, 2H), 3.39-3.19 (m, 2H), 3.02-2.89 (m, 2H), 2.67-2.55
(m, 1H), 2.48-2.26 (m, 2H), 2.07-1.95 (m, 1H), 1.90 (d, J=7.1 Hz,
3H), 1.88-1.65 (m, 2H), 1.65-1.45 (m, 3H), 0.98-0.87 (m, 4H). [LCMS
M+H] 498.0.
Example 74
##STR00267##
[0926]
4-((S)-3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazol-
o[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)-N,N-dimethylbutanamide.
The diastereomeric mixture was prepared starting with general
procedure A and methyl 4-oxobutanoate. tert-Butyl
3-(1-(4-methoxy-4-oxobutyl)piperidin-3-yl)azetidine-1-carboxylate
was hydrolyzed with 4 equiv. of lithium hydroxide in methanol/water
(3:1 by volume) mixture at ambient temperature for 18 hours,
followed by removing methanol in vacuum, acidifying reaction
mixture with conc. HCl until pH 7 and extracting with DCM. Drying
with sodium sulfate, filtering, and removing solvent in vacuum
afforded the corresponding acid as white solid.
4-(3-(1-(tert-butoxycarbonyl)azetidin-3-yl)piperidin-1-yl)butanoic
acid was mixed with HATU (1.2 equiv.) in anhydrous DMF (0.2M) and
stirred for 5 minutes, followed by the addition of
diisopropylethylamine (3 equiv.) and additional 10 minutes of
stirring at ambient temperature. 2M solution of dimethylamine in
THF was then added to the reaction mixture (5 equiv.), reaction was
stirred at ambient temperature for 18 hours, quenched with 1M
sodium carbonate, and extracted with ethyl acetate. Combined
organic layer was dried over sodium sulfate, filtered, and
concentrated in vacuum. Crude material was deprotected using
general procedure C, and final coupling with precursor IV using
general procedure D. The title compound was separated from its
diastereomer on an AD-H column using 35% isopropanol (0.1%
diethylamine)/CO.sub.2, 100 bars as the first peak. .sup.1H NMR
(400 MHz, CD.sub.3OD; free base): .delta. ppm 7.93 (s, 1H), 7.47
(d, J=2.1 Hz, 1H), 7.38 (d, J=8.51 Hz, 1H), 7.31 (dd, J=2.1 Hz,
J=8.5 Hz, 1H), 6.45 (q, J=7.0 Hz, 1H), 4.21-4.31 (m, 2H), 3.92-4.02
(m, 2H), 3.07 (m, 3H), 2.88-2.96 (m, 5H), 2.55-2.66 (m, 1H),
2.37-2.46 (m, 4H), 1.94-2.04 (m, 1H), 1.90 (d, J=7.1 Hz, 3H),
152-1.88 (m, 7H), 0.87-1.01 (m, 1H). LCMS [M+H]: 569.1.
Example 75
##STR00268##
[0928]
4-((R)-3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazol-
o[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)-N,N-dimethylbutanamide.
A mixture of the title compound and its diastereomer was prepared
as described in the previous example. The title compound was
separated from its diastereomer on an AD-H column using 35%
isopropanol (0.1% diethylamine)/CO.sub.2, 100 bar as the second
eluting peak. .sup.1H NMR (400 MHz, CD.sub.3OD; free base): .delta.
ppm 7.92 (s, 1H), 7.47 (d, J=2.1 Hz, 1H), 7.38 (d, J=8.5 Hz, 1H),
7.31 (dd, J=2.1 Hz, J=8.5 Hz, 1H), 6.45 (q, J=7.1 Hz, 1H),
4.21-4.31 (m, 2H), 3.92-4.02 (m, 2H), 3.06 (s, 3H), 2.88-2.96 (m,
5H), 2.55-2.66 (m, 1H), 2.37-2.45 (m, 4H), 1.94-2.04 (m, 1H), 1.91
(d, J=7.1 Hz, 3H), 1.53-1.88 (m, 7H), 0.87-1.00 (m, 1H). LCMS
[M+H]: 569.1.
Example 76
##STR00269##
[0930]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-isopropylpiperidin--
3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile. A
mixture of the title compound and its diastereomer was prepared
according to general procedure A with acetone, general procedure C,
and general procedure D with precursor IV. The title compound was
separated from its diastereomer on an AD-H column using 30%
isopropanol (0.1% diethylamine)/100 bars CO.sub.2 as the first
eluting peak. .sup.1H NMR (400 MHz, CD.sub.3OD; free base): .delta.
ppm 7.94 (s, 1H), 7.47 (d, J=2.1 Hz, 1H), 7.38 (d, J=8.5 Hz, 1H),
7.31 (dd, J=2.1 Hz, J=8.5 Hz, 1H), 6.45 (q, J=7.0 Hz, 1H),
4.23-4.33 (m, 2H), 3.92-4.02 (m, 2H), 2.84-2.94 (m, 2H), 2.74-2.84
(m, 1H), 2.55-2.65 (m, 1H), 2.13-2.23 (m, 1H), 1.72-1.94 (m, 7H),
1.52-1.66 (m, 1H), 1.07-1.20 (m, 7H), 0.85-0.98 (m, 1H). LCMS
[M+H]: 498.2.
Example 77
##STR00270##
[0932]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-isopropylpiperidin--
3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile. A
mixture of the title compound and its diastereomer was prepared
according to general procedure A with acetone, general procedure C,
and general procedure D with precursor IV. The title compound was
separated from its diastereomer on an AD-H column using 30%
isopropanol (0.1% diethylamine)/100 bars CO.sub.2 as the second
eluting peak. .sup.1H NMR (400 MHz, CD.sub.3OD; free base): .delta.
ppm 7.94 (s, 1H), 7.48 (d, J=2.1 Hz, 1H), 7.39 (d, J=8.5 Hz, 1H),
7.31 (dd, J=2.1 Hz, J=8.5 Hz, 1H), 6.45 (q, J=7.1 Hz, 1H),
4.22-4.32 (m, 2H), 3.92-4.02 (m, 2H), 2.84-2.94 (m, 2H), 2.73-2.83
(m, 1H), 2.55-2.66 (m, 1H), 2.12-2.22 (m, 1H), 1.72-1.94 (m, 7H),
1.52-1.66 (m, 1H), 1.07-1.21 (m, 7H), 0.85-0.98 (m, 1H). LCMS
[M+H]: 498.2.
Example 78
##STR00271##
[0934]
4-((R)-3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazol-
o[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)butanamide. A
mixture of the title compound and its diastereomer was prepared
starting with general procedure A and methyl 4-oxobutanoate.
tert-Butyl
3-(1-(4-methoxy-4-oxobutyl)piperidin-3-yl)azetidine-1-carboxylate
was hydrolyzed with 4 equiv. of lithium hydroxide in methanol/water
(3:1 by volume) mixture at ambient temperature for 18 hours,
followed by removing methnol in vacuum, acidifying reaction mixture
with conc. HCl until pH 7 and extracting with DCM. Drying with
sodium sulfate, filtering, and removing solvent in vacuum afforded
the corresponding acid as white solid.
4-(3-(1-(tert-butoxycarbonyl)azetidin-3-yl)piperidin-1-yl)butanoic
acid was mixed with HATU (1.2 equiv.) in anhydrous DMF (0.2M) and
stirred for 5 minutes, followed by the addition of
diisopropylethylamine (3 equiv.) and additional 10 minutes of
stirring at ambient temperature. 2M solution of dimethylamine in
THF was then added to the reaction mixture (5 equiv.), reaction was
stirred at ambient temperature for 18 hours, quenched with 1M
sodium carbonate, and extracted with ethyl acetate. Combined
organic layer was dried over sodium sulfate, filtered, and
concentrated in vacuum. Crude material was deprotected using
procedure C, and final coupling with precursor IV using general
procedure D. The title compound was separated from its diastereomer
on an AD-H column using 30% ethanol (0.1% diethylamine)/CO.sub.2,
100 bars as the second eluting peak. .sup.1H NMR (400 MHz,
CD.sub.3OD; free base): .delta. ppm 7.92 (s, 1H), 7.47 (d, J=2.1
Hz, 1H), 7.38 (d, J=8.5 Hz, 1H), 7.30 (dd, J=2.1 Hz, J=8.5 Hz, 1H),
6.44 (q, J=7.1 Hz, 1H), 4.21-4.31 (m, 2H), 3.92-4.02 (m, 2H),
2.87-2.96 (m, 2H), 2.55-2.68 (m, 1H), 2.37-2.44 (m, 2H), 2.23 (t,
J=7.4 Hz, 2H), 1.94-2.06 (m, 1H), 1.90 (d, J=7.1 Hz, 3H), 1.53-1.89
(m, 7H), 0.87-1.00 (m, 1H). LCMS [M+H]: 541.2.
Example 79
##STR00272##
[0936]
4-((S)-3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazol-
o[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)butanamide. A
mixture of the title compound and its diastereomer was prepared as
shown in previous example. The title compound was separated from
its diastereomer on an AD-H column using 30% ethanol (0.1%
diethylamine)/CO.sub.2, 100 bars as the first eluting peak. .sup.1H
NMR (400 MHz, CD.sub.3OD; free base): .delta. ppm 7.93 (s, 1H),
7.47 (d, J=2.1 Hz, 1H), 7.38 (d, J=8.5 Hz, 1H), 7.31 (dd, J=2.1 Hz,
J=8.5 Hz, 1H), 6.45 (q, J=7.1 Hz, 1H), 4.22-4.32 (m, 2H), 3.92-4.02
(m, 2H), 2.88-2.98 (m, 2H), 2.55-2.68 (m, 1H), 2.37-2.45 (m, 2H),
2.23 (t, J=7.4 Hz, 2H), 1.95-2.06 (m, 1H), 1.90 (d, J=7.1 Hz, 3H),
1.53-1.99 (m, 7H), 0.84-1.01 (m, 1H). LCMS [M+H]: 541.2.
Example 80
##STR00273##
[0938]
6-(3-((R)-1-((1H-imidazol-2-yl)methyl)piperidin-3-yl)azetidin-1-yl)-
-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonit-
rile. A mixture of the title compound and its diastereomer was
prepared starting with general procedure A and
1H-imidazole-2-carbaldehyde, followed by general procedure C, and
final coupling with precursor IV using general procedure D. The
title compound was separated from its diastereomer on an AD-H
column using 20% ethanol (0.1% diethylamine)/CO.sub.2, 100 bars as
the second eluting peak. .sup.1H NMR (400 MHz, CD.sub.3OD; free
base): .delta. ppm 7.89 (s, 1H), 7.46 (d, J=2.1 Hz, 1H), 7.37 (d,
J=8.5 Hz, 1H), 7.29 (dd, J=2.1 Hz, J=8.5 Hz, 1H), 7.00 (bs, 2H),
6.43 (q, J=7.0 Hz, 1H), 4.16-4.30 (m, 2H), 3.85-3.98 (m, 2H), 3.62
(bs, 2H), 2.76-2.88 (m, 2H), 2.58-2.70 (m, 1H), 2.06-2.16 (m, 1H),
1.52-1.94 (m, 8H), 0.85-1.00 (m, 1H). LCMS [M+H]: 536.0.
Example 81
##STR00274##
[0940]
6-(3-((S)-1-((1H-imidazol-2-yl)methyl)piperidin-3-yl)azetidin-1-yl)-
-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonit-
rile. A mixture of the title compound and its diastereomer was
prepared starting with general procedure A and
1H-imidazole-2-carbaldehyde, followed by general procedure C, and
final coupling with precursor IV using general procedure D. The
title compound was separated from its diastereomer on an AD-H
column using 20% ethanol (0.1% diethylamine)/CO.sub.2, 100 bars as
the first eluting peak. .sup.1H NMR (400 MHz, CD.sub.3OD; free
base): .delta. ppm 7.92 (s, 1H), 7.47 (d, J=2.1 Hz, 1H), 7.37 (d,
J=8.5 Hz, 1H), 7.30 (dd, J=2.1 Hz, J=8.5 Hz, 1H), 7.00 (bs, 2H),
6.44 (q, J=7.1 Hz, 1H), 4.18-4.32 (m, 2H), 3.82-4.00 (m, 2H), 3.63
(bs, 2H), 2.77-2.89 (m, 2H), 2.58-2.70 (m, 1H), 2.04-2.14 (m, 1H),
1.53-1.94 (m, 8H), 0.86-1.00 (m, 1H). LCMS [M+H]: 536.0.
Example 82
##STR00275##
[0942]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-((R)-4-hydroxybutan-
-2-yl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitr-
ile and
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-((S)-4-hydroxybuta-
n-2-yl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonit-
rile. A mixture of the two titled compounds and their respective
diastereomers (four diastereomers) was prepared using general
procedure A with 4-hydroxybutan-2-one, followed by general
procedure C, and coupling using general procedure D and precursor
IV. Single diastereomers were separated on an AD-H column using 35%
isopropanol (0.1% diethylamine)/CO.sub.2, 100 bars and the
compounds corresponding to peaks 1 and 2 were then additionally
purified on an OJ-H column using 20% isopropanol (0.1%
diethylamine)/CO.sub.2, 100 bars. The first eluting isomer had the
following .sup.1H NMR (400 MHz, CDCl.sub.3; free base): .delta. ppm
7.61 (s, 1H), 7.37 (s, 1H), 7.36 (d, J=5.9 Hz, 1H), 7.20 (dd, J=2.1
Hz, J=8.5 Hz, 1H), 6.46 (q, J=7.1 Hz, 1H), 4.20-4.30 (m, 2H),
3.76-4.03 (m, 4H), 2.86-3.02 (m, 2H), 2.70-2.80 (m, 1H), 2.47-2.68
(m, 2H), 1.87-1.98 (m, 4H), 1.70-1.84 (m, 4H), 1.54-1.70 (m, 1H),
1.29-1.38 (m, 1H), 0.87-1.04 (m, 4H). LCMS [M+H]: 528.2. The second
eluting isomer had the following .sup.1H NMR (400 MHz, CD.sub.3OD;
free base): .delta. ppm 7.82 (s, 1H), 7.37 (s, 1H), 7.36 (d,
J=6.Hz, 1H), 7.20 (dd, J=2.2 Hz, J=8.5 Hz, 1H), 6.46 (q, J=7.0 Hz,
1H), 4.19-4.29 (m, 2H), 3.72-4.00 (m, 4H), 2.87-3.00 (m, 2H),
2.70-2.80 (m, 1H), 2.52-2.64 (m, 1H), 2.14-2.24 (m, 1H), 1.98-2.10
(m, 1H), 1.72-1.97 (m, 8H), 1.41-1.54 (m, 1H), 1.27-1.37 (m, 1H),
0.84-1.02 (m, 4H). LCMS [M+H]: 528.2.
Example 83
##STR00276##
[0944]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-((R)-4-hydroxybutan-
-2-yl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitr-
ile and
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-((S)-4-hydroxybuta-
n-2-yl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonit-
rile. A mixture of the two titled compounds and their respective
diastereomers (four diastereomers) was prepared using general
procedure A with 4-hydroxybutan-2-one, followed by general
procedure C, and coupling using general procedure D and precursor
IV. Single diastereomers were separated on an AD-H column using 35%
isopropanol (0.1% diethylamine)/CO.sub.2, 100 bars. The third
eluting isomer had the following .sup.1H NMR (400 MHz, CDCl.sub.3;
free base): .delta. ppm 7.82 (s, 1H), 7.34-7.37 (m, 2H), 7.19 (dd,
J=2.2 Hz, J=8.5 Hz, 1H), 6.45 (q, J=7.0 Hz, 1H), 4.19-4.27 (m, 2H),
3.73-4.06 (m, 4H), 2.88-3.00 (m, 2H), 2.70-2.78 (m, 1H), 2.53-2.66
(m, 1H), 2.15-2.25 (m, 1H), 2.00-2.10 (m, 1H), 1.72-1.98 (m, 8H),
1.40-1.54 (m, 1H), 1.28-1.37 (m, 1H), 0.84-1.01 (m, 4H). LCMS
[M+H]: 528.2. The fourth eluting isomer had the following .sup.1H
NMR (400 MHz, CDCl.sub.3; free base): .delta. ppm 7.81 (s, 1H),
7.38 (d, J=2.1 Hz, 1H), 7.35 (d, J=8.4 Hz, 1H), 7.19 (dd, J=2.2 Hz,
J=8.4 Hz, 1H), 6.44 (q, J=7.2 Hz, 1H), 4.18-4.29 (m, 2H), 3.68-4.08
(m, 4H), 2.86-3.00 (m, 2H), 2.46-2.78 (m, 3H), 1.54-1.98 (m, 10H),
1.28-1.41 (m, 1H), 0.87-1.04 (m, 4H). LCMS [M+H]: 528.2.
Example 84
##STR00277##
[0946] Methyl
(2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,-
4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)carbamate. A
mixture of the title compound and its diastereomer was prepared
using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. The crude
material was dissolved in DCM (0.26M) and 3 equiv. of triethylamine
was added, followed by methylchloroformate (1.2 equiv.) dropwise at
ambient temperature. Reaction mixture was stirred for 70 minutes,
quenched with 1M sodium carbonate, and extracted with ethyl
acetate. Organic phase was dried over sodium sulfate, filtered, and
solvent was removed in vacuum. Crude material was deprotected using
general procedure C, and coupled with precursor II using general
procedure D. The title compound was separated from its diastereomer
on an AD-H column using 35% isopropanol (0.1%
diethylamine)/CO.sub.2, 100 bars as the first eluting peak. .sup.1H
NMR (400 MHz, CD.sub.3OD; free base): .delta. ppm 7.75 (s, 1H),
7.45 (d, J=2.1 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 7.26 (dd, J=2.1 Hz,
J=8.5 Hz, 1H), 6.29 (q, J=7.2 Hz, 1H), 4.22-4.32 (m, 2H), 3.94-4.04
(m, 2H), 3.43-3.69 (m, 7H), 3.12-3.22 (m, 2H), 2.80-2.92 (m, 1H),
2.56-2.72 (m, 2H), 2.50 (s, 3H), 1.75-2.16 (m, 7H), 1.12-1.30 (m,
1H). LCMS [M+H]: 546.1.
Example 85
##STR00278##
[0948] Methyl
(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyrazolo[3,-
4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)carbamate. A
mixture of the title compound and its diastereomer was prepared as
shown in the previous example. The title compound was separated
from its diastereomer on an AD-H column using 35% isopropanol (0.1%
diethylamine)/CO.sub.2, 100 bars as the second eluting peak.
.sup.1H NMR (400 MHz, CD.sub.3OD; free base): .delta. ppm 7.75 (s,
1H), 7.44 (d, J=2.1 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 7.26 (dd,
J=2.2 Hz, J=8.5 Hz, 1H), 6.29 (q, J=7.0 Hz, 1H), 4.24-4.32 (m, 2H),
3.95-4.05 (m, 2H), 3.61-3.77 (m, 5H), 3.44-3.60 (m, 2H), 3.21-3.29
(m, 2H), 2.88-2.98 (m, 1H), 2.62-2.73 (m, 2H), 2.50 (s, 3H),
1.92-2.18 (m, 3H), 1.76-1.92 (m, 4H), 1.14-1.30 (m, 1H). LCMS
[M+H]: 546.1.
Example 86
##STR00279##
[0950]
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)ace-
tamide. A mixture of the title compound and its diastereomer was
prepared using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. The crude
material was dissolved in DCM (0.23M) and 3 equiv. of triethylamine
was added, followed by acetic anhydride (1.1 equiv.) dropwise at
ambient temperature. Reaction mixture was stirred for 12 hours,
quenched with water, and extracted with DCM, dried over sodium
sulfate, filtered, and concentrated in vacuum. Crude material was
deprotected using general procedure C, and coupled with precursor V
using general procedure D. The title compound was separated from
its diastereomer on an OD-H column using 20% methanol (0.1%
diethylamine)/CO.sub.2, 100 bars as the first eluting isomer.
.sup.1H NMR (400 MHz, CD.sub.3OD; free base): .delta. ppm 7.94 (s,
1H), 7.47 (d, J=2.0 Hz, 1H), 7.27-7.37 (m, 2H), 6.44 (q, J=7.0 Hz,
1H), 4.27-4.37 (m, 2H), 4.00-4.10 (m, 2H), 3.50-3.78 (m, 5H),
3.23-3.29 (m, 2H), 2.87-2.98 (m, 1H), 2.63-2.73 (m, 1H), 1.78-2.20
(m, 10H), 1.14-1.30 (m, 1H). LCMS [M+H]: 584.0.
Example 87
##STR00280##
[0952]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)ace-
tamide. A mixture of the title compound and its diastereomer was
prepared as shown in previous example. The title compound was
separated from its diastereomer on an OD-H column using 20%
methanol (0.1% diethylamine)/CO.sub.2, 100 bars as the second
eluting isomer. .sup.1H NMR (400 MHz, CD.sub.3OD; free base):
.delta. ppm 7.93 (s, 1H), 7.48 (d, J=2.1 Hz, 1H), 7.28-7.38 (m,
2H), 6.44 (q, J=7.1 Hz, 1H), 4.26-4.37 (m, 2H), 3.98-4.08 (m, 2H),
3.44-3.64 (m, 4H), 3.06-3.16 (m, 2H), 2.63-2.88 (m, 2H), 2.46-2.60
(m, 1H), 1.72-2.16 (m, 9H), 1.12-1.26 (m, 1H). LCMS [M+H]:
584.0.
Example 88
##STR00281##
[0954]
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)iso-
butyramide. A mixture of the title compound and its diastereomer
was prepared using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanol, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM (3.times.10 mL), and the
organic layer was dried over sodium sulfate, filtered and
concentrated in vacuum. The crude material was dissolved in DMF
(0.5M) and 3 equiv. of triethylamine and 1.2 equiv. of HATU was
added and stirred for 15 minutes. Solution of isobutyric acid in
DCM was added and the reaction mixture was stirred at ambient
temperature. As soon as reaction was complete it was quenched by 1M
sodium carbonate, extracted 3 times with ethylacetate, dried with
sodium sulfate, filtered, and concentrated in vacuum. Crude
material was deprotected using general procedure C, and coupled
with precursor V using general procedure D. The title compound was
separated from its diastereomer on an AS-H column using 25%
isopropanol (0.1% diethylamine)/CO.sub.2, 100 bars as the second
eluting isomer. .sup.1H NMR (400 MHz, CD.sub.3OD; free base):
.delta. ppm 7.93 (s, 1H), 7.48 (d, J=2.0 Hz, 1H), 7.28-7.36 (m,
2H), 6.44 (q, J=7.1 Hz, 1H), 4.28-4.38 (m, 2H), 3.99-4.10 (m, 2H),
3.50-3.68 (m, 4H), 3.17-3.27 (m, 2H), 2.84-3.00 (bm, 1H), 2.62-2.78
(bm, 2H), 2.43-2.55 (m, 1H), 1.76-2.22 (m, 7H), 1.11-1.34 (m, 7H).
LCMS [M+H]: 612.2.
Example 89
##STR00282##
[0956]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)iso-
butyramide. A mixture of the title compound and its diastereomer
was prepared as shown in previous example. The title compound was
separated from its diastereomer on an AS-H column using 25%
isopropanol (0.1% diethylamine)/CO.sub.2, 100 bars as the first
eluting isomer. .sup.1H NMR (400 MHz, CD.sub.3OD; free base):
.delta. ppm 7.93 (s, 1H) ppm 7.48 (d, J=2.1 Hz, 1H), 7.28-7.37 (m,
2H), 6.44 (q, J=7.1 Hz, 1H), 4.24-4.37 (m, 2H), 3.98-4.08 (m, 2H),
3.40-3.60 (m, 4H), 3.03-3.16 (m, 2H), 2.63-2.87 (bm, 2H), 2.41-2.60
(m, 2H), 1.72-2.15 (m, 7H), 1.11-1.25 (m, 7H). LCMS [M+H]:
612.2.
Example 90
##STR00283##
[0958]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyr-
azolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)isobutyramide.
A mixture of the title compound and its diastereomer was prepared
using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanol, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM (3.times.10 mL), organic
layer was dried over sodium sulfate, filtered and concentrated in
vacuum. The crude material was dissolved in DMF (0.5M) and 3 equiv.
of triethylamine and 1.2 equiv. of HATU was added and stirred for
15 minutes. Solution of isobutyric acid in DCM was added and the
reaction mixture was stirred at ambient temperature. As soon as
reaction was complete it was quenched by 1M sodium carbonate,
extracted 3 times with ethylacetate, dried with sodium sulfate,
filtered, and concentrated in vacuum. Crude material was
deprotected using general procedure C, and coupled with precursor
II using general procedure D. The title compound was separated from
its diastereomer on an AD-H column using 25% ethanol (0.1%
diethylamine)/CO.sub.2, 100 bars as the first eluting isomer.
.sup.1H NMR (400 MHz, CD.sub.3OD; free base): .delta. ppm 7.75 (s,
1H), 7.45 (d, J=2.1 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 7.26 (dd,
J=2.2 Hz, J=8.5 Hz, 1H), 6.29 (q, J=7.1 Hz, 1H), 4.22-4.33 (m, 2H),
3.95-4.05 (m, 2H), 3.53-3.73 (m, 4H), 3.21-3.31 (m, 2H), 2.89-3.00
(m, 1H), 2.62-2.78 (m, 2H), 2.45-2.52 (m, 4H), 1.80-2.20 (m, 7H),
1.09-1.16 (m, 7H). LCMS [M+H]: 558.1.
Example 91
##STR00284##
[0960]
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyr-
azolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)isobutyramide.
A mixture of the title compound and its diastereomer was prepared
as shown in previous example. The title compound was separated from
its diastereomer on an AD-H column using 25% ethanol (0.1%
diethylamine)/CO.sub.2, 100 bars as the second eluting isomer.
.sup.1H NMR (400 MHz, CD.sub.3OD; free base): .delta. ppm 7.76 (s,
1H), 7.44 (d, J=2.1 Hz, 1H), 7.35 (d, J=8.5 Hz, 1H), 7.26 (dd,
J=2.1 Hz, J=8.5 Hz, 1H), 6.29 (q, J=7.1 Hz, 1H), 4.23-4.33 (m, 2H),
3.96-4.05 (m, 2H), 3.50-3.70 (m, 5H), 3.22-3.28 (m, 2H), 2.90-3.00
(m, 1H), 2.62-2.72 (m, 1H), 2.43-2.53 (m, 4H), 1.77-2.20 (m, 7H),
1.08-1.30 (m, 7H). LCMS [M+H]: 558.1.
Example 92
##STR00285##
[0962]
N-(2-((R)-3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyra-
zolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)acetamide.
A mixture of the title compound and its diastereomer was prepared
using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanol, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. The crude
material was dissolved in DCM (0.23M) and 3 equiv. of triethylamine
was added, followed by acetic anhydride (1.1 equiv.) dropwise at
ambient temperature. Reaction mixture was stirred for 12 hours,
quenched with water, and extracted with DCM, dried over sodium
sulfate, filtered, and concentrated in vacuum. Crude material was
deprotected using general procedure C, and coupled with precursor
IV using general procedure D. The title compound was separated from
its diastereomer on an AD-H column using 40% ethanol (0.1%
diethylamine)/CO.sub.2, 100 bars as the first eluting isomer.
.sup.1H NMR (400 MHz, CD.sub.3OD; free base): .delta. ppm 7.91 (s,
1H), 7.46 (d, J=2.1 Hz, 1H), 7.37 (d, J=8.5 Hz, 1H), 7.30 (dd,
J=2.1 Hz, J=8.4 Hz, 1H), 6.44 (q, J=7.1 Hz, 1H), 4.20-4.30 (m, 2H),
3.92-4.02 (m, 2H), 3.34 (t, J=7.0 Hz, 2H), 2.88-2.98 (m, 2H),
2.55-2.67 (m, 1H), 2.45-2.53 (m, 2H), 1.53-2.08 (m, 12H), 0.87-1.01
(m, 1H). LCMS [M+H] 541.1.
Example 93
##STR00286##
[0964]
N-(2-((S)-3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyra-
zolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)acetamide.
A mixture of the title compound and its diastereomer was prepared
using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. The crude
material was dissolved in DCM (0.23M) and 3 equiv. of triethylamine
was added, followed by acetic anhydride (1.1 equiv.) dropwise at
ambient temperature. Reaction mixture was stirred for 12 hours,
quenched with water, and extracted with DCM, dried over sodium
sulfate, filtered, and concentrated in vacuum. Crude material was
deprotected using general procedure C, and coupled with precursor
IV using general procedure D. The title compound was separated from
its diastereomer on an AD-H column using 40% ethanol (0.1%
diethylamine)/CO.sub.2, 100 bars as the second eluting isomer.
.sup.1H NMR (400 MHz, CD.sub.3OD; free base): .delta. ppm 7.92 (s,
1H), 7.46 (d, J=2.1 Hz, 1H), 7.37 (d, J=8.5 Hz, 1H), 7.30 (dd,
J=2.1 Hz, J=8.5 Hz, 1H), 6.44 (q, J=7.1 Hz, 1H), 4.20-4.30 (m, 2H),
3.91-4.02 (m, 2H), 3.30-3.38 (m, 2H), 2.87-3.87 (m, 2H), 2.55-2.67
(m, 1H), 2.45-2.53 (m, 2H), 1.52-2.10 (m, 12H), 0.86-1.00 (m, 1H).
LCMS [M+H] 541.1.
Example 94
##STR00287##
[0966]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-(3-hydroxypropyl)py-
rrolidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonitrile.
A mixture of the title compound and its diastereomer was prepared
using commercially available tert-butyl
3-(1-(2-hydroxyethyl)pyrrolidin-3-yl)azetidine-1-carboxylate
instead of tert-butyl 3-(piperidin-3-yl)azetidine-1-carboxylate in
general procedure A. Followed by deprotection using general
procedure C and coupling with precursor IV according to the general
procedure D. In all of these general procedures the corresponding
pyrrolidine analog was used. The title compound was separated from
its diastereomer on an OJ-H column with 20% methanol (0.1%
diethylamine)/CO.sub.2, 100 bars as the first eluting isomer.
.sup.1H NMR (400 MHz, CDCl.sub.3; free base): .delta. ppm 7.81 (s,
1H), 7.34-7.38 (m, 2H), 7.19 (dd, J=2.2 Hz, J=8.5 Hz, 1H), 6.45 (q,
J=7.1 Hz, 1H), 4.22-4.30 (m, 2H), 3.77-3.87 (m, 4H), 2.72-2.88 (m,
5H), 2.60-2.70 (m, 1H), 2.49-2.60 (m, 1H), 2.42-2.49 (m, 1H),
2.03-2.13 (m, 1H), 1.89 (d, J=7.1 Hz, 3H), 1.70-1.79 (m, 2H),
1.42-1.53 (m, 1H). LCMS [M+H] 500.0.
Example 95
##STR00288##
[0968]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-(3-hydroxypropyl)py-
rrolidin-3-yl)azetidin-1-yl)-l
H-pyrazolo[3,4-b]pyrazine-3-carbonitrile. A mixture of the title
compound and its diastereomer was prepared using commercially
available tert-butyl
3-(1-(2-hydroxyethyl)pyrrolidin-3-yl)azetidine-1-carboxylate
instead of tert-butyl 3-(piperidin-3-yl)azetidine-1-carboxylate in
general procedure A. Followed by deprotection using general
procedure C and coupling with precursor IV according to the general
procedure D. In all of these general procedures the corresponding
pyrrolidine analog was used. The title compound was separated from
its diastereomer on an OJ-H column with 20% methanol (0.1%
diethylamine)/CO.sub.2, 100 bars as the second eluting isomer.
.sup.1H NMR (400 MHz, CDCl.sub.3; free base): .delta. ppm 7.81 (s,
1H), 7.34-7.38 (m, 2H), 7.19 (dd, J=2.1 Hz, J=8.5 Hz, 1H), 6.45 (q,
J=7.1 Hz, 1H), 4.20-4.30 (m, 2H), 3.77-3.88 (m, 4H), 2.72-2.88 (m,
5H), 2.60-2.70 (m, 1H), 2.48-2.60 (m, 1H), 2.41-2.48 (m, 1H),
2.02-2.13 (m, 1H), 1.89 (d, J=7.1 Hz, 3H), 1.70-1.78 (m, 2H),
1.42-1.53 (m, 1H). LCMS [M+H] 500.0.
Example 96
##STR00289##
[0970]
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyr-
azzol[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)propane-2-sulf-
onamide. A mixture of the title compound and its diastereomer was
prepared using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. The crude
tert-butyl 3-[1-(2-aminoethyl)-3-piperidyl]azetidine-1-carboxylate
(120 mg, 0.423 mmol) in DCM (2 mL) was treated with triethylamine
(129 mg, 1.27 mmol, 3.0 equiv.) and 2-propanesulfonyl chloride (73
mg, 0.51 mmol, 1.2 equiv). After 30 min, the mixture was quenched
with 1M aq. sodium carbonate (10 mL) and extracted with ethyl
acetate (3.times.10 mL). The combined organic layers were dried
over sodium sulfate, filtered, and concentrated in vacuo to afford
tert-butyl 3-(1-(2-((1-methyl
ethyl)sulfonamido)ethyl)piperidin-3-yl)azetidine-1-carboxylate.
tert-Butyl
3-(1-(2-((1-methylethyl)sulfonamido)ethyl)piperidin-3-yl)azetidine-1-carb-
oxylate was then condensed with Precursor II according to general
procedures C and D to afford a mixture of diastereomers. The title
compound was separated from its diastereomer by SFC using a AS-H
20.times.250 mm column and eluting with 25% isopropanol (0.1%
diethylamine) in CO.sub.2 to give the free base of the title
compound as the first eluting isomer and converted to the
corresponding HCl salt by dissolution in EtOH, cooling to 0.degree.
C., and addition of 1 equiv. of 0.01M HCl in EtOH. .sup.1H NMR (400
MHz, Methanol-d.sub.4; HCl Salt) .delta. 7.74 (s, 1H), 7.43 (d,
J=2.1 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 7.26 (dd, J=8.5, 2.2 Hz,
1H), 6.28 (q, J=7.1 Hz, 1H), 4.26 (q, J=8.6 Hz, 2H), 4.04-3.94 (m,
2H), 3.77-3.69 (m, 1H), 3.68-3.61 (m, 1H), 3.57-3.46 (m, 2H),
3.37-3.32 (m, 1H), 3.29-3.21 (m, 2H), 3.02-2.92 (m, 1H), 2.75-2.61
(m, 2H), 2.50 (s, 3H), 2.20-2.09 (m, 1H), 2.07-1.88 (m, 3H), 1.86
(d, J=7.1 Hz, 3H), 1.37 (d, J=6.8, Hz, 3H), 1.36 (d, J=6.8, Hz,
3H), 1.27-1.20 (m, 1H). LCMS [M+H] 594.1.
Example 97
##STR00290##
[0972]
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyr-
azolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)propane-2-sulf-
onamide. A mixture of the title compound and its diastereomer was
prepared using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. The crude
tert-butyl 3-[1-(2-aminoethyl)-3-piperidyl]azetidine-1-carboxylate
(120 mg, 0.423 mmol) in DCM (2 mL) was treated with triethylamine
(129 mg, 1.27 mmol, 3.0 equiv.) and 2-propanesulfonyl chloride (73
mg, 0.51 mmol, 1.2 equiv). After 30 min, the mixture was quenched
with 1M aq. sodium carbonate (10 mL) and extracted with ethyl
acetate (3.times.10 mL). The combined organic layers were dried
over sodium sulfate, filtered, and concentrated in vacuo to afford
tert-butyl 3-(1-(2-((1-methyl
ethyl)sulfonamido)ethyl)piperidin-3-yl)azetidine-1-carboxylate.
tert-Butyl
3-(1-(2-((1-methylethyl)sulfonamido)ethyl)piperidin-3-yl)azetidine-1-carb-
oxylate was then condensed with Precursor II according to general
procedures C and D to afford a mixture of diastereomers. The title
compound was separated from its diastereomer by SFC using a AS-H
20.times.250 mm column and eluting with 25% isopropanol (0.1%
diethylamine) in CO.sub.2 to give the free base of the title
compound as the second eluting isomer and converted to the
corresponding HCl salt by dissolution in EtOH, cooling to 0.degree.
C., and addition of 1 equiv. of 0.01M HCl in EtOH. .sup.1H NMR (400
MHz, Methanol-d.sub.4; HCl Salt) .delta. 7.74 (s, 1H), 7.44 (d,
J=2.1 Hz, 1H), 7.37 (d, J=8.5 Hz, 1H), 7.26 (dd, J=8.5, 2.1 Hz,
1H), 6.29 (q, J=7.1 Hz, 1H), 4.33-4.22 (m, 2H), 4.04-3.96 (m, 2H),
3.77-3.70 (m, 1H), 3.68-3.59 (m, 1H), 3.56-3.45 (m, 2H), 3.37-3.32
(m, 1H), 3.27-3.23 (m, 2H), 3.01-2.91 (m, 2H), 2.74-2.62 (m, 2H),
2.50 (s, 3H), 2.19-2.10 (m, 1H), 2.08-1.88 (m, 2H), 1.86 (d, J=7.1
Hz, 3H), 1.37 (d, J=6.8 Hz, 3H), 1.35 (d, J=6.8 Hz, 3H), 1.24-1.18
(m, 1H). LCMS [M+H] 594.0.
Example 98
##STR00291##
[0974]
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyr-
azolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)methanesulfona-
mide. A mixture of the title compound and its diastereomer was
prepared using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. The crude
tert-butyl 3-[1-(2-aminoethyl)-3-piperidyl]azetidine-1-carboxylate
(120 mg, 0.423 mmol) in DCM (2 mL) was treated with triethylamine
(129 mg, 1.27 mmol, 3.0 equiv.) and methanesulfonyl chloride (58
mg, 0.51 mmol, 1.2 equiv). After 30 min, the mixture was quenched
with 1M aq. sodium carbonate (10 mL) and extracted with ethyl
acetate (3.times.10 mL). The combined organic layers were dried
over sodium sulfate, filtered, and concentrated in vacuo to afford
tert-butyl
3-(1-(2-(methylsulfonamido)ethyl)piperidin-3-yl)azetidine-1-carboxylate.
tert-Butyl
3-(1-(2-(methylsulfonamido)ethyl)piperidin-3-yl)azetidine-1-carboxylate
was then condensed with Precursor II according to general
procedures C and D to afford a mixture of diastereomers. The title
compound was separated from its diastereomer by SFC using a AS-H
column and eluting with 30% ethanol (0.1% diethylamine) in CO.sub.2
to give the free base of the title compound as the first eluting
isomer and converted to the corresponding HCl salt by dissolution
in EtOH, cooling to 0.degree. C., and addition of 1 equiv. of 0.01M
HCl in EtOH. .sup.1H NMR (400 MHz, Methanol-d.sub.4, HCl Salt)
.delta. 7.73 (s, 1H), 7.44 (d, J=2.1 Hz, 1H), 7.37 (d, J=8.5 Hz,
1H), 7.26 (dd, J=8.5, 2.1 Hz, 1H), 6.29 (q, J=7.1 Hz, 1H),
4.32-4.19 (m, 2H), 4.03-3.93 (m, 2H), 3.57-3.40 (m, 4H), 3.22-3.11
(m, 2H), 3.02 (s, 3H), 2.88-2.75 (m, 1H), 2.72-2.47 (m, 2H), 2.50
(s, 3H), 2.17-2.03 (m, 1H), 2.02-1.89 (m, 2H), 1.87 (d, J=7.1 Hz,
3H), 1.85-1.76 (m, 1H), 1.25-1.08 (m, 1H). LCMS [M+H] 566.0
(M+H.sup.+).
Example 99
##STR00292##
[0976]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyr-
azolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)methanesulfona-
mide. A mixture of the title compound and its diastereomer was
prepared using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. The crude
tert-butyl 3-[1-(2-aminoethyl)-3-piperidyl]azetidine-1-carboxylate
(120 mg, 0.423 mmol) in DCM (2 mL) was treated with triethylamine
(129 mg, 1.27 mmol, 3.0 equiv.) and methanesulfonyl chloride (58
mg, 0.51 mmol, 1.2 equiv). After 30 min, the mixture was quenched
with 1M aq. sodium carbonate (10 mL) and extracted with ethyl
acetate (3.times.10 mL). The combined organic layers were dried
over sodium sulfate, filtered, and concentrated in vacuo to afford
tert-butyl
3-(1-(2-(methylsulfonamido)ethyl)piperidin-3-yl)azetidine-1-carboxylate.
tert-Butyl
3-(1-(2-(methylsulfonamido)ethyl)piperidin-3-yl)azetidine-1-carboxylate
was then condensed with Precursor II according to general
procedures C and D to afford a mixture of diastereomers. The title
compound was separated from its diastereomer by SFC using a AS-H
column and eluting with 30% ethanol (0.1% diethylamine) in CO.sub.2
to give the free base of the title compound as the second eluting
isomer and converted to the corresponding HCl salt by dissolution
in EtOH, cooling to 0.degree. C., and addition of 1 equiv. of 0.01M
HCl in EtOH. .sup.1H NMR (400 MHz, Methanol-d.sub.4; HCl Salt)
.delta. 7.76 (s, 1H), 7.45 (d, J=2.1 Hz, 1H), 7.37 (d, J=8.5 Hz,
1H), 7.27 (dd, J=8.5, 2.1 Hz, 1H), 6.29 (q, J=7.1 Hz, 1H),
4.34-4.21 (m, 2H), 4.04-3.96 (m, 2H), 3.82-3.41 (m, 4H), 3.29-3.26
(m, 1H), 3.03 (s, 3H), 3.02-2.92 (m, 2H), 2.76-2.60 (m, 2H), 2.50
(s, 3H), 2.23-2.10 (m, 1H), 2.08-1.89 (m, 3H), 1.87 (d, J=7.1 Hz,
3H), 1.25-1.18 (m, 1H). LCMS [M+H] 566.0.
Example 100
##STR00293##
[0978]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyr-
azolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)acetamide.
A mixture of the title compound and its diastereomer was prepared
using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. The crude
tert-butyl 3-[1-(2-aminoethyl)-3-piperidyl]azetidine-1-carboxylate
(120 mg, 0.423 mmol) in DCM (2 mL) was treated with triethylamine
(129 mg, 1.27 mmol, 3.0 equiv.) and acetyl chloride (40.0 mg, 0.51
mmol, 1.2 equiv). After 30 min, the mixture was quenched with 1M
aq. sodium carbonate (10 mL) and extracted with ethyl acetate
(3.times.10 mL). The combined organic layers were dried over sodium
sulfate, filtered, and concentrated in vacuo to afford tert-butyl
3-(1-(2-acetamidoethyl)piperidin-3-yl)azetidine-1-carboxylate.
tert-butyl
3-(1-(2-acetamidoethyl)piperidin-3-yl)azetidine-1-carboxylate was
then condensed with Precursor II according to general procedures C
and D to afford a mixture of diastereomers. The title compound was
separated from its diastereomer by SFC using an AD-H column and
eluting with 25% ethanol (0.1% diethylamine) in CO.sub.2 to give
the free base of the title compound as the first eluting isomer and
converted to the corresponding HCl salt by dissolution in EtOH,
cooling to 0.degree. C., and addition of 1 equiv. of 0.01M HCl in
EtOH. .sup.1H NMR (400 MHz, Methanol-d.sub.4; HCl Salt) .delta.
7.75 (s, 1H), 7.44 (d, J=2.1 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 7.26
(dd, J=8.5, 2.1 Hz, 1H), 6.29 (q, J=7.1 Hz, 1H), 4.27 (q, J=8.9 Hz,
2H), 4.00 (ddd, J=11.6, 8.9, 5.6 Hz, 2H), 3.78-3.63 (m, 2H),
3.58-3.46 (m, 1H), 3.25 (t, J=5.8 Hz, 2H), 2.98-2.86 (m, 1H),
2.73-2.62 (m, 2H), 2.50 (s, 3H), 2.14-1.94 (m, 4H), 1.99 (s, 3H),
1.86 (d, J=7.1 Hz, 3H), 1.86-1.77 (m, 1H), 1.21 (d, J=17.3 Hz, 1H).
LCMS [M+H] 530.1.
Example 101
##STR00294##
[0980]
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-1H-pyr-
azolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)acetamide.
A mixture of the title compound and its diastereomer was prepared
using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. The crude
tert-butyl 3-[1-(2-aminoethyl)-3-piperidyl]azetidine-1-carboxylate
(120 mg, 0.423 mmol) in DCM (2 mL) was treated with triethylamine
(129 mg, 1.27 mmol, 3.0 equiv.) and acetyl chloride (40.0 mg, 0.51
mmol, 1.2 equiv). After 30 min, the mixture was quenched with 1M
aq. sodium carbonate (10 mL) and extracted with ethyl acetate
(3.times.10 mL). The combined organic layers were dried over sodium
sulfate, filtered, and concentrated in vacuo to afford tert-butyl
3-(1-(2-acetamidoethyl)piperidin-3-yl)azetidine-1-carboxylate.
tert-butyl
3-(1-(2-acetamidoethyl)piperidin-3-yl)azetidine-1-carboxylate was
then condensed with Precursor II according to general procedures C
and D to afford a mixture of diastereomers. The title compound was
separated from its diastereomer by SFC using an AD-H column and
eluting with 25% ethanol (0.1% diethylamine) in CO.sub.2 to give
the free base of the title compound as the second eluting isomer
and converted to the corresponding HCl salt by dissolution in EtOH,
cooling to 0.degree. C., and addition of 1 equiv. of 0.01M HCl in
EtOH. .sup.1H NMR (400 MHz, Methanol-d.sub.4; HCl Salt) .delta.
7.75 (s, 1H), 7.44 (d, J=2.1 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 7.26
(dd, J=8.5, 2.2 Hz, 1H), 6.29 (q, J=7.1 Hz, 1H), 4.27 (t, J=8.3 Hz,
2H), 3.99 (ddd, J=8.5, 5.6, 2.2 Hz, 2H), 3.75-3.44 (m, 3H), 3.21
(t, J=5.8 Hz, 2H), 2.99-2.81 (m, 1H), 2.77-2.57 (m, 2H), 2.50 (s,
3H), 2.18-2.00 (m, 3H), 2.00 (s, 3H), 1.99-1.92 (m, 1H), 1.87 (d,
J=7.1 Hz, 3H), 1.81 (s, 1H), 1.27-1.18 (m, 1H). LCMS [M+H]
530.1.
Example 102
##STR00295##
[0982]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-isopropylpiperidin--
3-yl)azetidin-1-yl)-3-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyrazine.
The title compound was prepared using general procedure A with
Precursor VI and acetone, followed by procedure C. The resulting
product was condensed with Precursor V using procedure D. .sup.1H
NMR (400 MHz, Methanol-d.sub.4; HCl Salt) .delta. 7.94 (s, 1H),
7.49 (d, J=2.0 Hz, 1H), 7.35 (d, J=8.5 Hz, 1H), 7.31 (dd, J=8.5,
2.0 Hz, 1H), 6.44 (q, J=7.0 Hz, 1H), 4.38-4.26 (m, 2H), 4.08-3.98
(m, 2H), 3.49-3.34 (m, 2H), 3.03-2.90 (m, 1H), 2.82-2.63 (m, 2H),
2.21-2.13 (m, 2H), 2.11-2.03 (m, 1H), 2.02-1.95 (m, 1H), 1.91 (d,
J=7.1 Hz, 3H), 1.88-1.80 (m, 1H), 1.38 (d, J=4.5 Hz, 6H), 1.26-1.20
(m, 1H). LCMS [M+H] 541.0.
Example 103
##STR00296##
[0984]
(R)-1-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluorome-
thyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propan-2-
-ol. Precursor VI (270 mg, 1.30 mmol) was condensed with
(2R)-2-hydroxypropanoic acid (152 mg, 1.69 mmol) in DMF (5 mL)
using 1H-benzo[d][1,2,3]triazol-1-ol (258 mg, 1.69 mmol) and
3-(((ethylimino)methylene)amino)-N,N-dimethylpropan-1-amine
hydrochloride (324 mg, 1.69 mmol) for 30 min and then poured into
ethyl acetate (50 mL), washed with brine (50 mL), dried over sodium
sulfate, filtered and concentrated under reduced pressure, the
residue was purified by flash chromatography using silica gel and a
gradient of methanol (0 to 20%) in DCM to afford tert-butyl
3-[(3R)-1-[(2R)-2-hydroxypropanoyl]-3-piperidyl]azetidine-1-carboxylate
(350 mg, 1.12 mmol).
3-[(3R)-1-[(2R)-2-hydroxypropanoyl]-3-piperidyl]azetidine-1-carboxylate
(350 mg, 1.12 mmol) was dissolved in tetrahydrofuran (6 mL) and
treated with borane-tetrahydrofuran complex (3.36 mL, 3.36 mmol, 1M
in tetrahydrofuran) and stirred for 12 hours, quenched with
methanol and concentrated under reduced pressure, the residue was
purified by flash chromatography using silica gel and a gradient of
methanol (0 to 20%) in DCM to afford tert-butyl
3-[(3R)-1-[(2R)-2-hydroxypropyl]-3-piperidyl]azetidine-1-carboxylate
(193 mg, 0.6500 mmol). tert-butyl
3-[(3R)-1-[(2R)-2-hydroxypropyl]-3-piperidyl]azetidine-1-carboxylate
was then condensed with Precursor V using general procedures C and
D to afford the title compound. .sup.1H NMR (400 MHz,
Methanol-d.sub.4; HCl Salt) .delta. 7.93 (s, 1H), 7.49 (d, J=2.0
Hz, 1H), 7.35 (d, J=8.5 Hz, 1H), 7.30 (dd, J=8.5, 2.0 Hz, 1H), 6.44
(q, J=7.1 Hz, 1H), 4.38-4.26 (m, 2H), 4.26-4.17 (m, 1H), 4.07-3.96
(m, 2H), 3.76-3.70 (m, 1H), 3.70-3.65 (m, 1H), 3.58-3.54 (m, 1H),
3.15-3.00 (m, 2H), 2.93-2.81 (m, 1H), 2.79-2.58 (m, 2H), 2.28-2.12
(m, 1H), 2.11-1.92 (m, 2H), 1.91 (d, J=7.1 Hz, 3H), 1.89-1.75 (m,
1H), 1.24 (d, J=6.2 Hz, 3H), 1.22-1.18 (m, 1H). LCMS [M+H]
557.0.
Example 104
##STR00297##
[0986]
(S)-1-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluorome-
thyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propan-2-
-ol. Precursor VI (270 mg, 1.30 mmol) was condensed with
(2S)-2-hydroxypropanoic acid (152 mg, 1.69 mmol) in DMF (5 mL)
using 1H-benzo[d][1,2,3]triazol-1-ol (258 mg, 1.69 mmol) and
3-(((ethylimino)methylene)amino)-N,N-dimethylpropan-1-amine
hydrochloride (324 mg, 1.69 mmol) for 30 min and then poured into
ethyl acetate (50 mL), washed with brine (50 mL), dried over sodium
sulfate, filtered and concentrated under reduced pressure, the
residue was purified by flash chromatography using silica gel and a
gradient of methanol (0 to 20%) in DCM to afford tert-butyl
3-[(3R)-1-[(2S)-2-hydroxypropanoyl]-3-piperidyl]azetidine-1-carboxylate
(350 mg, 1.12 mmol).
3-[(3R)-1-[(2S)-2-hydroxypropanoyl]-3-piperidyl]azetidine-1-carboxylate
(350 mg, 1.12 mmol) was dissolved in tetrahydrofuran (6 mL) and
treated with borane-tetrahydrofuran complex (3.36 mL, 3.36 mmol, 1M
in tetrahydrofuran) and stirred for 12 hours, quenched with
methanol and concentrated under reduced pressure, the residue was
purified by flash chromatography using silica gel and a gradient of
methanol (0 to 20%) in DCM to afford tert-butyl
3-[(3R)-1-[(2S)-2-hydroxypropyl]-3-piperidyl]azetidine-1-carboxylate
(90 mg, 0.3016 mmol). tert-butyl
3-[(3R)-1-[(2S)-2-hydroxypropyl]-3-piperidyl]
azetidine-1-carboxylate was then condensed with Precursor V using
general procedures C and D to afford the title compound. .sup.1H
NMR (400 MHz, Methanol-d.sub.4; HCl Salt) .delta. 7.93 (s, 1H),
7.48 (d, J=2.0 Hz, 1H), 7.35 (d, J=8.5 Hz, 1H), 7.30 (dd, J=8.5,
2.1 Hz, 1H), 6.44 (q, J=7.1 Hz, 1H), 4.37-4.25 (m, 2H), 4.23-4.10
(m, 1H), 4.07-3.97 (m, 2H), 3.77-3.56 (m, 2H), 3.55-3.39 (m, 1H),
3.07-2.76 (m, 3H), 2.19-2.03 (m, 1H), 1.98-1.92 (m, 2H), 1.91 (d,
J=7.1 Hz, 3H), 1.90-1.80 (m, 2H), 1.22 (d, J=6.2 Hz, 3H), 1.20-1.17
(m, 1H). LCMS [M+H] 557.0.
Example 105
##STR00298##
[0988]
N--((R)-1-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluo-
romethyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)prop-
an-2-yl)acetamide. Precursor VI (270 mg, 1.13 mmol) was condensed
with (2R)-2-(benzyloxycarbonylamino)propanoic acid (376.7 mg, 1.69
mmol) in DMF (3 mL) using
2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium
hexafluorophosphate(V) (642 mg, 1.69 mmol) and
N,N-Diisopropylethylamine (0.587 mL, 3.38 mmol) for 12 hours and
then poured into ethyl acetate (50 mL), washed with brine (50 mL),
dried over sodium sulfate, filtered and concentrated under reduced
pressure, the residue was purified by flash chromatography using
silica gel and a gradient of ethyl acetate (10 to 100%) in hexanes
to afford tert-butyl
3-[(3R)-1-[(2R)-2-(benzyloxycarbonylamino)propanoyl]-3-piperidyl]azetidin-
e-1-carboxylate (306 mg, 0.687 mmol). tert-butyl
3-[(3R)-1-[(2R)-2-(b enzyloxycarbonylamino)propanoyl]-3-piperidyl]
azetidine-1-carboxylate (306 mg, 0.687 mmol) was dissolved in
tetrahydrofuran (6 mL) and treated with borane-tetrahydrofuran
complex (2.06 mL, 2.06 mmol, 1M in tetrahydrofuran) and stirred for
12 hours, quenched with methanol and concentrated under reduced
pressure, the residue was purified by flash chromatography using
silica gel and a gradient of methanol (0 to 20%) in DCM to afford
tert-butyl
3-[(3R)-1-[(2R)-2-(benzyloxycarbonylamino)propyl]-3-piperidyl]azetidine-1-
-carboxylate (296 mg, 0.687 mmol). tert-butyl
3-[(3R)-1-[(2R)-2-(benzyloxycarbonylamino)propyl]-3-piperidyl]azetidine-1-
-carboxylate (296 mg, 0.687 mmol) was dissolved in methanol (5 mL)
and palladium on carbon 10 wt. % (89.4 mg) was added, the mixture
was then placed under a hydrogen atmosphere (balloon) and stirred
for 15 minutes, filtered through celite, concentrated under reduced
pressure, diluted with DCM (5 mL), treated with triethylamine (0.29
mL, 2.07 mmol) and acetyl chloride (0.15 mL, 2.07 mmol), stirred
for 30 minutes, quenched with 1M sodium carbonate, extracted with
ethyl acetate (2.times.5 mL), dried over sodium sulfate,
concentrated in vacuo to afford tert-butyl
3-[(3R)-1-[(2R)-2-acetamidopropyl]-3-piperidyl]azetidine-1-carboxylate
(220 mg, 0.648 mmol). tert-butyl
3-[(3R)-1-[(2R)-2-acetamidopropyl]-3-piperidyl]azetidine-1-carboxylate
was then condensed with Precursor V using general procedures C and
D to afford the title compound. .sup.1H NMR (400 MHz,
Methanol-d.sub.4; HCl Salt) .delta. 7.93 (s, 1H), 7.49 (d, J=2.1
Hz, 1H), 7.35 (d, J=8.5 Hz, 1H), 7.31 (dd, J=8.5, 2.0 Hz, 1H), 6.44
(q, J=7.2 Hz, 1H), 4.39-4.24 (m, 3H), 4.08-3.93 (m, 2H), 3.58-3.47
(m, 1H), 3.44-3.34 (m, 1H), 3.17-2.94 (m, 2H), 2.86-2.49 (m, 2H),
2.19-2.00 (m, 1H), 2.00 (s, 3H), 1.98-1.94 (m, 3H), 1.91 (d, J=7.1
Hz, 3H), 1.83-1.68 (m, 1H), 1.24 (d, J=6.8 Hz, 3H), 1.20-1.17 (m,
1H). LCMS [M+H] 598.1.
Example 106
##STR00299##
[0990]
N--((S)-1-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluo-
romethyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)prop-
an-2-yl)acetamide. Precursor VI (270 mg, 1.13 mmol) was condensed
with (2S)-2-(benzyloxycarbonylamino)propanoic acid (376.7 mg, 1.69
mmol) in DMF (3 mL) using
2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium
hexafluorophosphate(V) (642 mg, 1.69 mmol) and
N,N-Diisopropylethylamine (0.587 mL, 3.38 mmol) for 12 hours and
then poured into ethyl acetate (50 mL), washed with brine (50 mL),
dried over sodium sulfate, filtered and concentrated under reduced
pressure, the residue was purified by flash chromatography using
silica gel and a gradient of ethyl acetate (10 to 100%) in hexanes
to afford tert-butyl
3-[(3R)-1-[(2S)-2-(benzyloxycarbonylamino)propanoyl]-3-piperidyl]azetidin-
e-1-carboxylate (501 mg, 1.13 mmol). tert-butyl
3-[(3R)-1-[(2S)-2-(benzyloxycarbonylamino)propanoyl]-3-piperidyl]azetidin-
e-1-carboxylate (501 mg, 1.13 mmol) was dissolved in
tetrahydrofuran (6 mL) and treated with borane-tetrahydrofuran
complex (3.37 mL, 3.37 mmol, 1M in tetrahydrofuran) and stirred for
12 hours, quenched with methanol and concentrated under reduced
pressure, the residue was purified by flash chromatography using
silica gel and a gradient of methanol (0 to 20%) in DCM to afford
tert-butyl
3-[(3R)-1-[(2S)-2-(benzyloxycarbonylamino)propyl]-3-piperidyl]azetidine-1-
-carboxylate (485 mg, 1.13 mmol). tert-butyl
3-[(3R)-1-[(2S)-2-(benzyloxycarbonylamino)propyl]-3-piperidyl]azetidine-1-
-carboxylate (485 mg, 1.13 mmol) was dissolved in methanol (5 mL)
and palladium on carbon 10 wt. % (89.4 mg) was added, the mixture
was then placed under a hydrogen atmosphere (balloon) and stirred
for 15 minutes, filtered through celite, concentrated under reduced
pressure, diluted with DCM (5 mL), treated with triethylamine
(0.468 mL, 3.38 mmol) and acetyl chloride (0.245 mL, 3.38 mmol),
stirred for 30 minutes, quenched with 1M sodium carbonate,
extracted with ethyl acetate (2.times.5 mL), dried over sodium
sulfate, concentrated in vacuo to afford tert-butyl
3-[(3R)-1-[(2S)-2-acetamidopropyl]-3-piperidyl]azetidine-1-carboxylate
(230 mg, 0.678 mmol). tert-butyl
3-[(3R)-1-[(2S)-2-acetamidopropyl]-3-piperidyl]azetidine-1-carboxylate
was then condensed with Precursor V using general procedures C and
D to afford the title compound. .sup.1H NMR (400 MHz,
Methanol-d.sub.4; HCl Salt) .delta. 7.95 (s, 1H), 7.48 (d, J=2.1
Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 7.31 (dd, J=8.5, 2.1 Hz, 1H), 6.45
(q, J=7.0 Hz, 1H), 4.50-4.39 (m, 1H), 4.37-4.26 (m, 2H), 4.18-3.97
(m, 4H), 3.52-3.42 (m, 1H), 3.23-3.06 (m, 2H), 3.06-2.90 (m, 1H),
2.76-2.62 (m, 1H), 2.61-2.48 (m, 1H), 2.06-2.00 (m, 1H), 2.00 (s,
3H), 2.00-1.93 (m, 1H), 1.91 (d, J=7.1 Hz, 3H), 1.89-1.82 (m, 1H),
1.25 (d, J=6.8 Hz, 3H), 1.23-1.14 (m, 1H). LCMS [M+H] 598.2.
Example 107
##STR00300##
[0992]
3-((R)-3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazol-
o[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propane-1-sulfonamide.
A mixture of the title compound and its diastereomer was prepared
using general procedure B (b) and 3-chloropropane-1-sulfonamide,
followed by general procedure C and D with precursor IV. The title
compound was separated from its diastereomer by SFC using a AD-H
column and eluting with 30% isopropanol (0.1% diethylamine) in
CO.sub.2 to give the title compound as the first eluting isomer.
.sup.1H NMR (400 MHz, CDCl.sub.3, HCl Salt) .delta. 7.83 (s, 1H),
7.38 (d, J=2.1 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 7.20 (dd, J=8.5,
2.1 Hz, 1H), 6.46 (q, J=7.0 Hz, 1H), 4.29-4.17 (m, 2H), 4.02-3.96
(m, 1H), 3.95-3.87 (m, 1H), 3.26-3.15 (m, 2H), 3.04-2.85 (m, 2H),
2.65-2.49 (m, 3H), 2.23-1.94 (m, 3H), 1.90 (d, J=7.1 Hz, 3H),
1.84-1.50 (m, 5H), 1.02-0.88 (m, 1H). LCMS [M+H] 577.1.
Example 108
##STR00301##
[0994]
3-((S)-3-(1-(3-cyano-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazol-
o[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)propane-1-sulfonamide.
A mixture of the title compound and its diastereomer was prepared
as described in the previous example. The title compound was
separated from its diastereomer by SFC using a AD-H column and
eluting with 30% isopropanol (0.1% diethylamine) in CO.sub.2 to
give the title compound as the second eluting isomer. .sup.1H NMR
(400 MHz, CDCl.sub.3, HCl Salt) .delta. 7.83 (s, 1H), 7.38 (d,
J=2.1 Hz, 1H), 7.37 (d, J=8.5 Hz, 1H), 7.20 (dd, J=8.5, 2.1 Hz,
1H), 6.45 (q, J=7.0 Hz, 1H), 4.29-4.17 (m, 2H), 4.04-3.89 (m, 2H),
3.26-3.16 (m, 2H), 3.00-2.85 (m, 2H), 2.68-2.48 (m, 3H), 2.25-1.92
(m, 4H), 1.90 (d, J=7.1 Hz, 3H), 1.85-1.67 (m, 3H), 1.64-1.49 (m,
1H), 1.03-0.89 (m, 1H). LCMS [M+H] 577.0.
Example 109
##STR00302##
[0996]
N-(2-((R)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)pro-
pane-2-sulfonamide. A mixture of the title compound and its
diastereomer was prepared using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. The crude
material was dissolved in DCM and 3 equviv. of triethylamine was
added to the reaction mixture followed by 1.2 equviv. of
2-propanesulfonyl chloride. The reaction mixture was stirred at
ambient temperature until complete conversion (by LCMS) was
achieved. The reaction was quenched with 1M sodium carbonate,
extracted with ethylacetate, organic phase was dried over sodium
sulfate, filtered, and concentrated in vacuum. The crude product
was then used in general procedure C and coupled with precursor V
using general procedure D. The title compound was separated from
its diastereomer by SFC using an AD-H column and eluting with 20%
isopropanol (0.1% diethylamine) in CO.sub.2 to give the free base
of as the first eluting isomer. .sup.1H NMR (400 MHz,
Methanol-d.sub.4, HCl Salt) .delta. 7.93 (s, 1H), 7.50-7.46 (m,
1H), 7.36 (d, J=8.5 Hz, 1H), 7.31 (dd, J=8.5, 2.1 Hz, 1H), 6.45 (q,
J=7.1 Hz, 1H), 4.40-4.25 (m, 2H), 4.14-3.93 (m, 2H), 3.81-3.70 (m,
1H), 3.69-3.61 (m, 1H), 3.61-3.43 (m, 2H), 3.39-3.32 (m, 1H),
3.30-3.22 (m, 1H), 3.06-2.88 (m, 1H), 2.78-2.57 (m, 2H), 2.23-2.11
(m, 1H), 2.10-1.93 (m, 4H), 1.91 (d, J=7.0 Hz, 3H), 1.38 (d, J=6.8
Hz, 3H), 1.36 (d, J=6.8 Hz, 3H), 1.28-1.17 (m, 1H). LCMS [M+H]
648.1.
Example 110
##STR00303##
[0998]
N-(2-((S)-3-(1-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-(trifluoromet-
hyl)-1H-pyrazolo[3,4-b]pyrazin-6-yl)azetidin-3-yl)piperidin-1-yl)ethyl)pro-
pane-2-sulfonamide. A mixture of the title compound and its
diastereomer was prepared using general procedure A with
3-(1,3-dioxoisoindolin-2-yl)propanal, followed by removal of
phthaloyl group with hydrazine hydrate (4 equiv.) in methanol
(0.4M) at ambient temperature for 18 hours. The reaction mixture
was diluted with water, extracted with DCM, organic layer was dried
over sodium sulfate, filtered and concentrated in vacuum. The crude
material was dissolved in DCM and 3 equviv. of triethylamine was
added to the reaction mixture followed by 1.2 equviv. of
2-propanesulfonyl chloride. The reaction mixture was stirred at
ambient temperature until complete conversion (by LCMS) was
achived. The reaction was quenched with 1M sodium carbonate,
extracted with ethylacetate, organic phase was dried over sodium
sulfate, filtered, and concentrated in vacuum. The crude product
was then used in general procedure C and coupled with precursor V
using general procedure D. The title compound was separated from
its diastereomer by SFC using an AD-H column and eluting with 20%
isopropanol (0.1% diethylamine) in CO.sub.2 to give the free base
of as the second eluting isomer. .sup.1H NMR (400 MHz,
Methanol-d.sub.4, HCl Salt).sup.1H NMR (400 MHz, Methanol-d.sub.4)
.delta. 7.93 (s, 1H), 7.48 (d, J=2.1 Hz, 1H), 7.36 (d, J=8.5 Hz,
1H), 7.31 (dd, J=8.5, 2.1 Hz, 1H), 6.44 (q, J=7.1 Hz, 1H),
4.38-4.25 (m, 2H), 4.11-3.97 (m, 2H), 3.80-3.71 (m, 1H), 3.69-3.60
(m, 1H), 3.61-3.45 (m, 2H), 3.40-3.33 (m, 1H), 3.29-3.21 (m, 1H),
3.03-2.93 (m, 1H), 2.77-2.63 (m, 2H), 2.23-2.10 (m, 1H), 2.09-1.92
(m, 3H), 1.91 (d, J=7.1 Hz, 3H), 1.89-1.81 (m, 1H), 1.38 (d, J=6.8
Hz, 3H), 1.37 (d, J=6.8 Hz, 3H), 1.28-1.14 (m, 1H). LCMS [M+H]
648.1.
Example 111
##STR00304##
[1000]
6-(3-((S)-1-((1H-imidazol-5-yl)methyl)piperidin-3-yl)azetidin-1-yl)-
-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonit-
rile. A mixture of the title compound and its diastereomer was
prepared using general procedure A from 1H-imidazole-5-carbaldehyde
using 2:1 1,2-dichloroethane/DMF as the solvent, followed by
procedure C. The resulting product was condensed with Precursor IV
using procedure D. The title compound was separated from its
diastereomer by SFC using an AD-H 20.times.250 mm column and
eluting with 30% isopropanol (0.1% diethylamine) in CO.sub.2 to
give the free base of the title compound as the first eluting
isomer and converted to the HCl salt by dissolution in EtOH,
cooling to 0.degree. C., and addition of 1 equiv. of 0.01M HCl in
EtOH. .sup.1H NMR (400 MHz, Methanol-d.sub.4, HCl Salt) .delta.
7.94 (s, 1H), 7.64 (d, J=1.1 Hz, 1H), 7.48 (d, J=2.1 Hz, 1H), 7.38
(d, J=8.5 Hz, 1H), 7.31 (dd, J=8.5, 2.1 Hz, 1H), 7.01 (s, 1H), 6.45
(q, J=7.0 Hz, 1H), 4.33-4.18 (m, 2H), 4.03-3.93 (m, 1H), 3.93-3.84
(m, 1H), 3.58 (s, 2H), 3.34-3.32 (m, 1H), 2.98-2.85 (m, 2H),
2.68-2.54 (m, 1H), 2.12-2.01 (m, 1H), 1.90 (d, J=7.0 Hz, 3H),
1.87-1.70 (m, 4H), 0.98-0.84 (m, 1H). LCMS [M+H] 536.0.
Example 112
##STR00305##
[1002]
6-(3-((R)-1-((1H-imidazol-5-yl)methyl)piperidin-3-yl)azetidin-1-yl)-
-1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-pyrazolo[3,4-b]pyrazine-3-carbonit-
rile. A mixture of the title compound and its diastereomer was
prepared using general procedure A from 1H-imidazole-5-carbaldehyde
using 2:1 1,2-dichloroethane/DMF as the solvent, followed by
procedure C. The resulting product was condensed with Precursor IV
using procedure D. The title compound was separated from its
diastereomer by SFC using an AD-H 20.times.250 mm column and
eluting with 30% isopropanol (0.1% diethylamine) in CO.sub.2 to
give the free base of the title compound as the second eluting
isomer and converted to the HCl salt by dissolution in EtOH,
cooling to 0.degree. C., and addition of 1 equiv. of 0.01M HCl in
EtOH. .sup.1H NMR (400 MHz, Methanol-d.sub.4, HCl Salt) .delta.
7.94 (s, 1H), 7.64 (d, J=1.2 Hz, 1H), 7.49 (d, J=2.1 Hz, 1H), 7.38
(d, J=8.5 Hz, 1H), 7.31 (dd, J=8.5, 2.1 Hz, 1H), 7.01 (s, 1H), 6.45
(q, J=7.0 Hz, 1H), 4.34-4.16 (m, 2H), 4.03-3.86 (m, 2H), 3.58 (s,
2H), 3.34-3.32 (m, 1H), 2.97-2.84 (m, 2H), 2.67-2.56 (m, 1H),
2.13-2.01 (m, 1H), 1.90 (d, J=7.0 Hz, 3H), 1.88-1.70 (m, 3H),
1.72-1.53 (m, 1H), 0.97-0.83 (m, 1H). LCMS [M+H] 536.0.
Example 113
##STR00306##
[1004]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-6-(3-((S)-1-(3-(methyl-
sulfonyl)propyl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine.
A mixture of the title compound and its diastereomer was prepared
using procedure B(b) using 1-bromo-3-(methylsulfonyl)propane,
followed by general procedure C and coupling with precursor II
using general procedure D. The title compound was separated from
its diastereomer by SFC using an IC 20.times.250 mm column and
eluting with 40% ethanol (0.1% diethylamine) in CO.sub.2 to give
the free base of the title compound as the first eluting isomer.
.sup.1H NMR (400 MHz, Methanol-d.sub.4, HCl Salt) .delta. 7.74 (s,
1H), 7.45 (d, J=2.1 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 7.26 (dd,
J=8.5, 2.1 Hz, 1H), 6.29 (q, J=7.0 Hz, 1H), 4.32-4.22 (m, 2H),
4.01-3.94 (m, 2H), 3.51-3.45 (m, 1H), 3.35 (s, 2H), 3.34-3.32 (m,
1H), 3.28-3.23 (m, 3H), 3.17-3.10 (m, 1H), 3.03 (s, 3H), 2.75-2.63
(m, 1H), 2.50 (s, 3H), 2.28-2.20 (m, 2H), 2.10-1.91 (m, 3H), 1.87
(d, J=7.1 Hz, 3H), 1.82-1.70 (m, 1H), 1.23-1.14 (m, 1H). LCMS [M+H]
565.0.
Example 114
##STR00307##
[1006]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-3-methyl-6-(3-((R)-1-(3-(methyl-
sulfonyl)propyl)piperidin-3-yl)azetidin-1-yl)-1H-pyrazolo[3,4-b]pyrazine.
A mixture of the title compound and its diastereomer was prepared
using procedure B(b) using 1-bromo-3-(methylsulfonyl)propane,
followed by general procedure C and coupling with precursor II
using general procedure D. The title compound was separated from
its diastereomer by SFC using an IC 20.times.250 mm column and
eluting with 40% ethanol (0.1% diethylamine) in CO.sub.2 to give
the free base of the title compound as the second eluting isomer.
.sup.1H NMR (400 MHz, Methanol-d.sub.4, HCl Salt) .delta. 7.74 (s,
1H), 7.45 (d, J=2.1 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 7.26 (dd,
J=8.5, 2.1 Hz, 1H), 6.29 (q, J=7.0 Hz, 1H), 4.32-4.22 (m, 2H),
4.02-3.94 (m, 2H), 3.51-3.38 (m, 1H), 3.35 (s, 2H), 3.26 (t, J=7.3
Hz, 2H), 3.21-3.11 (m, 2H), 3.03 (s, 3H), 2.84-2.73 (m, 1H),
2.73-2.59 (m, 1H), 2.50 (s, 3H), 2.31-2.20 (m, 2H), 2.13-1.91 (m,
3H), 1.87 (d, J=7.1 Hz, 3H), 1.84-1.69 (m, 1H), 1.25-1.11 (m, 1H).
LCMS [M+H] 565.0.
Example 115
##STR00308##
[1008]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((S)-1-(3-(methylsulfonyl)-
propyl)piperidin-3-yl)azetidin-1-yl)-3-(trifluoromethyl)-1H-pyrazolo[3,4-b-
]pyrazine. A mixture of the title compound and its diastereomer was
prepared using procedure B(b) using
1-bromo-3-(methylsulfonyl)propane, followed by general procedure C
and coupling with precursor V using general procedure D. The title
compound was separated from its diastereomer by SFC using an IC
20.times.250 mm column and eluting with 35% ethanol (0.1%
diethylamine) in CO.sub.2 to give the free base of the title
compound as the first eluting isomer. .sup.1H NMR (400 MHz,
Methanol-d.sub.4, HCl Salt) .delta. 7.93 (s, 1H), 7.49 (d, J=2.0
Hz, 1H), 7.35 (d, J=8.5 Hz, 1H), 7.30 (dd, J=8.5, 2.0 Hz, 1H), 6.44
(q, J=7.1 Hz, 1H), 4.35-4.28 (m, 2H), 4.06-3.97 (m, 2H), 3.50-3.47
(m, 1H), 3.42-3.34 (m, 3H), 3.28-3.20 (m, 2H), 3.15-3.10 (m, 1H),
3.03 (s, 3H), 2.76-2.64 (m, 2H), 2.30-2.16 (m, 2H), 2.10-1.93 (m,
3H), 1.91 (d, J=7.1 Hz, 3H), 1.82-1.67 (m, 1H), 1.25-1.12 (m, 1H).
LCMS [M+H] 619.1.
Example 116
##STR00309##
[1010]
1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-(3-((R)-1-(3-(methylsulfonyl)-
propyl)piperidin-3-yl)azetidin-1-yl)-3-(trifluoromethyl)-1H-pyrazolo[3,4-b-
]pyrazine. A mixture of the title compound and its diastereomer was
prepared using procedure B(b) using
1-bromo-3-(methylsulfonyl)propane, followed by general procedure C
and coupling with precursor V using general procedure D. The title
compound was separated from its diastereomer by SFC using an IC
20.times.250 mm column and eluting with 35% ethanol (0.1%
diethylamine) in CO.sub.2 to give the free base of the title
compound as the second eluting isomer. .sup.1H NMR (400 MHz,
Methanol-d.sub.4, HCl Salt) .delta. 7.93 (s, 1H), 7.49 (d, J=2.0
Hz, 1H), 7.35 (d, J=8.5 Hz, 1H), 7.31 (dd, J=8.5, 2.0 Hz, 1H), 6.44
(q, J=7.1 Hz, 1H), 4.37-4.26 (m, 2H), 4.08-3.96 (m, 2H), 3.54-3.44
(m, 1H), 3.26 (t, J=7.4 Hz, 2H), 3.22-3.15 (m, 3H), 3.14-3.12 (m,
1H), 3.03 (s, 3H), 2.75-2.64 (m, 2H), 2.31-2.20 (m, 2H), 2.13-1.91
(m, 3H), 1.91 (d, J=7.1 Hz, 3H), 1.82-1.69 (m, 1H), 1.25-1.12 (m,
1H). LCMS [M+H] 619.1.
[1011] Biological Samples and Assays
[1012] The following general materials and methods were used, where
indicated, or may be used in the Examples. Standard methods in
molecular biology are described in the scientific literature (see,
e.g., Sambrook and Russell (2001) Molecular Cloning, 3.sup.rd ed.,
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.; and
Ausubel, et al. (2001) Current Protocols in Molecular Biology,
Vols. 1-4, John Wiley and Sons, Inc. New York, N.Y., which
describes cloning in bacterial cells and DNA mutagenesis (Vol. 1),
cloning in mammalian cells and yeast (Vol. 2), glycoconjugates and
protein expression (Vol. 3), and bioinformatics (Vol. 4)).
[1013] The scientific literature describes methods for protein
purification, including immunoprecipitation, chromatography,
electrophoresis, centrifugation, and crystallization, as well as
chemical analysis, chemical modification, post-translational
modification, production of fusion proteins, and glycosylation of
proteins (see, e.g., Coligan, et al. (2000) Current Protocols in
Protein Science, Vols. 1-2, John Wiley and Sons, Inc., NY).
[1014] Software packages and databases for determining, e.g.,
antigenic fragments, leader sequences, protein folding, functional
domains, glycosylation sites, and sequence alignments, are
available (see, e.g., GCG Wisconsin Package (Accelrys, Inc., San
Diego, Calif.); and DeCypher.TM. (TimeLogic Corp., Crystal Bay,
Nev.).
[1015] Multiple assays that can be used to evaluate the compounds
of the present invention are known to the skilled artisan and/or
are described in the patent and scientific literature (see, e.g.,
US 2006/0004010; US 2002/0173524; Imai et al. (1997) J. Biol. Chem.
272:15036-15042; Imai et al. (1998) J. Biol. Chem. 273:1764-1768,
each of which is hereby incorporated by reference). The following
procedures are representative of the types of experiments that can
be used to demonstrate, for example, the CCR4 compounds'
antagonistic activity, inhibitory activity for effector cell
functions, TNF.alpha.-regulating activity, and efficacy in animal
disease models.
[1016] Calcium Flux Assay. Compounds were evaluated in a calcium
flux assay substantially performed as follows. Chem5-hCCR4 cells
(EMD Millipore, Hayward, Calif.; HTS009C) were cultured under
standard conditions and frozen in aliquots of 10.times.10.sup.6
cells/mL. The day prior to compound testing, a vial was rapidly
thawed and pipetted into 20 mL media (DMEM+10% FBS+1% Pen-Strep+1%
L-glutamine). Cells were harvested by centrifugation and
re-suspended in fresh culture medium. 25 .mu.L of cell suspension
was seeded into 384-well plates (Corning, Tewksbury, Mass.;
CellBind with black wall/clear bottom). The plates were centrifuged
at 300 g for 10 seconds and incubated overnight at 37.degree. C.
and 5% CO.sub.2. The day of compound testing, media was removed
from the plates and 25 .mu.L serum free media was added to each
well. Plates were returned to the incubator for 2 h. 25 .mu.L assay
buffer (Hank's balanced salt solution+20 mM HEPES pH 7.4)
containing FLIPR Calcium 6 dye (Molecular Devices, Sunnyvale,
Calif.; # R8191) and probenecid (2.5 mM) was added to each well and
incubated at 37.degree. C. and 5% CO.sub.2 for 2 h. Compounds in
DMSO were added to the plates using an HP D300e digital dispenser,
and all wells were normalized to contain 0.25 .mu.L (0.5%) DMSO.
Plates were incubated for 1 hour at 37.degree. C. and 5% CO.sub.2.
CCL22 (Peprotech; Rockyhill, N.J.) was diluted in assay buffer
containing 0.1% BSA to 7.5 nM (corresponding to 5.times.EC.sub.50
of 1.5 nM).
[1017] Assay plates and working solution of CCL22 were transferred
to the FlexStation plate reader (Molecular Devices) at 37.degree.
C. for 5 min of equilibration. Fluorescence recordings at 485
excitation/525 emission were performed at 2.5 second intervals. At
t=16 seconds, 12.5 .mu.L of CCL22 solution was added to each well
and reads continued for 30 seconds at 2.5 second intervals. The
minimum fluorescence (F.sub.min) was calculated by averaging the
reads prior to ligand addition and the change in fluorescence
(.DELTA.F) was calculated by subtracting the F.sub.min from the
average of the reads following ligand addition. The response
.DELTA.F/F.sub.min was plotted as a function of the compound
concentration and the IC.sub.50 values were determined by
non-linear regression analysis using a 4-parameter fit in either
PRISM software (GraphPad; La Jolla, Calif.) or Dotmatics
Browser.
[1018] Using the calcium flex assay described herein, the activity
for several compounds described herein was determined.
[1019] The potency levels are set forth in Table 2, wherein
IC.sub.50: A<0.1 .mu.M; B=0.1-0.5 .mu.M; and C>0.5 .mu.M.
TABLE-US-00002 TABLE 2 Example Number Potency 1 C 2 C 3 C 4 B 5 C 6
A 7 B 8 A 9 C 10 A 11 B 12 B 13 A 14 A 15 B 16 C 17 A 18 A 19 A 20
B 21 A 22 C 23 A 24 A 25 A 26 A 27 A 28 A 29 A 30 A 31 A 32 B 33 A
34 A 35 A 36 A 37 A 38 A 39 C 40 A 41 A 42 B 43 A 44 B 45 B 46 B 47
A 48 A 49 A 50 A 51 B 52 A 53 B 54 A 55 A 56 A 57 A 58 B 59 A 60 A
61 A 62 A 63 A 64 A 65 A 66 A 67 A 68 B 69 A 70 A 71 A 72 B 73 A 74
B 75 A 76 B 77 A 78 A 79 B 80 A 81 B 82 A 83 B 84 A 85 A 86 B 87 A
88 B 89 A 90 A 91 A 92 A 93 A 94 B 95 A 96 B 97 A 98 B 99 A 100 A
101 A 102 B 103 A 104 A 105 A 106 A 107 A 108 B 109 A 110 B 111 B
112 A 113 B 114 A 115 B 116 A
[1020] Potent and Selective C--C Motif Chemokine Receptor (CCR4)
Antagonists Potentiate Anti-Tumor Immune Responses by Inhibiting
Regulatory T Cells (T.sub.reg)
[1021] Naturally occurring suppressive
CD4.sup.+Foxp3.sup.+T.sub.reg are essential for immune tolerance.
Although T.sub.reg-mediated suppression of effector cells is
important to control inflammatory responses and prevent autoimmune
diseases, the presence of T.sub.reg in the tumor microenvironment
(TME) has been shown to dampen anti-tumor immune responses. Human
T.sub.reg express CCR4, the receptor for the chemokines CCL17 and
CCL22. These chemokines are produced by tumor cells or
tumor-associated macrophages and dendritic cells, as well as by
effector T cells (T.sub.eff). Preclinical and clinical data in
various cancer types supports a role for CCR4-mediated recruitment
and accumulation of T.sub.reg in the TME which can be associated
with poor prognosis. Further, recent longitudinal studies in
patients receiving IO agents demonstrate an influx of T.sub.reg in
responding patients which may dampen optimal anti-tumor responses.
Therefore, CCR4 is an ideal target to selectively block T.sub.reg
recruitment into the TME.
[1022] Multiple structurally unique series of selective small
molecule antagonists of CCR4 have been developed. These antagonists
have cellular potencies in multiple assays (including in a
functional chemotaxis assay with primary human T.sub.reg in 100%
serum) in the low double-digit nM range. Representative compounds
are selective against other chemokine receptors, GPCRs and ion
channels, including the hERG channel, and lack inhibition of common
human CYP450 enzymes. Moreover, compounds have excellent in vitro
and in vivo ADME properties, consistent with convenient oral
dosing. In preclinical syngeneic tumor models, our CCR4 antagonists
block T.sub.reg migration and support expansion of activated
T.sub.eff. In contrast to the non-selective approach of depleting
anti-CCR4 antibodies, our compounds reduce T.sub.reg in the tumor,
but not in peripheral tissues such as blood, spleen or skin. In
preclinical efficacy studies, CCR4 antagonists potentiate the
anti-tumor effects of various checkpoint inhibitors and immune
stimulators such as anti-PD-L1 and anti-CD 137 antibodies. Enhanced
tumor growth inhibition and increases in the percentage of tumor
free mice when these agents are combined with CCR4 antagonists,
without any gross toxicity, was observed.
[1023] Chemotaxis Assays. Generally speaking, chemotaxis assays may
be performed using 5 .mu.m filterplates (Neuroprobe) with the
chemoattractant (MDC, TARC, or SDF) placed in the lower chamber,
and a cell suspension of 100,000 CEM cells in the upper chamber.
The assays may be incubated 1-2 h at 37.degree. C., and the number
of cells in the lower chamber quantified by the CyQUANT assay
(Molecular Probes).
[1024] The following serum chemotaxis assay was used to determine
the extent to which the compounds of the present invention block
cellular migration mediated through CCR4. The assay was performed
using the ChemoTX (Gaithersburg, Md.) migration system with a 5
.mu.m pore size polycarbonate trach-etch (PCTE) membrane. CCRF-CEM
cells which express CCR4 were collected by centrifugation at
400.times.g at room temperature, then suspended at 2 million
cells/mL in human serum. Compounds (or an equivalent volume of
solvent (DMSO)) were then added to the cell/serum mixture at a
final DMSO concentration of 0.25% (v/v), followed by a 30-minute
compound pre-incubation period. Separately, recombinant human MDC
was diluted to 0.9 nM in 1.times. HBSS with 0.1% BSA, and 29 .mu.L
of diluted MDC was placed in the lower wells of the ChemoTX plate.
The polycarbonate (or PCTE) membrane (5 .mu.am pore size) was
placed onto the plate, and 50 .mu.L of the cell/compound mixture
was transferred into each well of the membrane. The plates were
incubated at 37.degree. C. for 60 minutes, after which the
polycarbonate membranes were removed, and 10 .mu.L of the
DNA-intercalating agent CyQUANT was added to the lower wells. The
amount of fluorescence, corresponding to the number of migrated
cells, was measured using an Envision plate reader (PerkinElmer;
Waltham, Mass.)
[1025] Detection of radiolabeled TARC and/or MDC binding to
CCR4-Protocol A. Source plates of chemical libraries may be
obtained from commercial vendors and may contain individual
compounds at 5 mg/mL in DMSO. From these, multiple compound plates
containing 10 compounds in each well may be prepared and then
diluted in 20% DMSO to a concentration of 50 .mu.g/mL. An aliquot
of 20 .mu.L of each mixture may be put into the test plates and
stored frozen until use.
[1026] A CCR4-expressing stable transfectant cell line may be
prepared using current standard molecular biological methods. The
CCR4 transfectants may be cultured in IMDM-5% FBS, and harvested
when the concentration is between 0.5-1.0.times.10.sup.6 cells/mL.
The cells may be centrifuged and resuspended in assay buffer (20 mM
HEPES, pH 7.1, 140 mM NaCl, 1 mM CaCl.sub.2, 5 mM MgCl.sub.2, and
with 0.2% BSA) to a concentration of 5.6.times.10.sup.6 cells/mL.
To establish the screening assays, 0.09 mL of cells may be added to
the assay plates containing the compounds (yielding a final
compound concentration of 1-5 .mu.g/mL each (.about.2-10 .mu.M)),
and then 0.09 mL of .sup.125I-TARC or .sup.125I-MDC diluted in
assay buffer (final concentration .about.50 .mu.M, with
.about.30,000 cpm per well) may be added. The plates may then be
sealed and incubated for approximately 3 hrs at 4.degree. C. on a
shaker platform. The assay plates may be harvested using Packard
filter plates, pre-soaked in 0.3% PEI (polyethyleneimine) solution,
on a Packard vacuum cell harvester. Scintillation fluid (50 .mu.L)
was added to all wells and the plates may be sealed and counted in
a Top Count scintillation counter. Control wells containing either
diluent only (for total counts) or excess MDC or TARC (1 .mu.g/mL,
for non-specific binding) may be used to calculate the percent of
total inhibition for each set of compounds. IC.sub.50 values are
those concentrations required to reduce the binding of labeled MDC
or TARC to the receptor by 50%.
[1027] Detection of radiolabeled TARC and/or MDC binding to
CCR4--Protocol B. .sup.125I-labelled TARC and MDC are available
from commercial sources (e.g., Perkin Elmer Life Sciences). All
buffers and materials are available from commercial sources (e.g.,
Sigma).
[1028] To measure binding of .sup.125I-TARC or .sup.125I-MDC to
cells expressing CCR4 (e.g., CEM cells (e.g., ATCC HB-12624)), the
.sup.125I-TARC or .sup.125I-MDC is diluted to a concentration of
approximately 200 .mu.M in a buffered saline solution (e.g., RPMI
supplemented with 0.5% BSA), and added to an equal volume of a
suspension of cells (e.g., CEM cells at 5.times.10.sup.6 cells/mL).
The resulting mixture is incubated for a period of time (e.g., 2
hrs), and the unbound .sup.125I-TARC or .sup.125I-MDC is separated
from the cells by filtration, e.g., by passage through GF/B filter
plate (Packard Biosciences) pre-treated with 0.3% polyethyleneimine
(Sigma), using a Packard Filtermate 96 (Packard Biosciences). The
amount of .sup.125I-TARC or .sup.125I-MDC retained with the cells
on the filterplate is measured by adding a small amount of
scintillation fluid (e.g., 50 .mu.L of Microscint-20 Packard
Biosciences)), and reading scintillation on appropriate detection
equipment, e.g., a Packard TopCount 383 (Packard Biosciences).
[1029] Non-specific binding of .sup.125I-TARC or .sup.125I-MDC can
be estimated by measuring the amount of .sup.125I-TARC or
.sup.125I-MDC retained with the cells on the filterplate when the
assay is performed in the presence of a large excess of unlabeled
TARC or MDC. Inhibition of .sup.125I-TARC or .sup.125I-MDC binding
to CCR4 is defined as a decrease in the retention of .sup.125I-TARC
or .sup.125I-MDC to the cells on the filterplate.
[1030] Calcium Mobilization Assay.
[1031] Calcium mobilization experiments may be performed by
labeling the human T-cell line CEM with NDO-1 dye (45 min at room
temperature), washing with PBS, and re-suspending into flux buffer
(HBSS with 1% FBS). For each experiment, 1.times.10.sup.6 cells may
be incubated at 37.degree. C. in the cuvette of a PTI spectrometer,
and the ratio of 410/490 nm emission plotted over time (typically
2-3 minutes), with compounds added at 5 seconds, followed by MDC,
TARC or other chemokines.
[1032] Production of TNF.alpha..
[1033] The present invention contemplates the use of a murine model
of TNF.alpha. production by LPS stimulation. A CCR4 antagonistic
compound(s) may be suspended in a medium, orally administered to a
mouse (male, C57BL/6), and after 0.5 hour LPS (055:B5, Sigma)
peritoneally administered to the mouse at a dose of 60 mg/kg. To
the control groups, only the medium may be administered. Sixty min
after LPS treatment, heparin-added blood collection may be
conducted from the abdominal vena cava under ether anesthesia, and
centrifuged (12,000 rpm) at 4.degree. C. for 3 min to provide
plasma (which may be stored at -80.degree. C. before use).
TNF.alpha. in the plasma may be quantified using an ELISA kit
(R&D systems; Minneapolis, Minn.).
[1034] Efficacy of CCR4 Antagonists for Therapeutic
Indications.
[1035] A representative procedure for evaluating the efficacy of
CCR4 antagonists for treatment of septic shock is described herein.
An animal model of endotoxic shock may be induced by injecting mice
with LPS. Three groups (15 mice per group) may be treated with an
i.p. injection of an LPS dose that produces 90% mortality in mice.
One group of mice may also receive PBS and Tween 0.5% i.p. 30 min
before LPS administration. A second group of mice may also receive
different doses of the CCR4 antagonist(s) given either i.p., IV,
SC, IM, PO or via any other mode of administration 30 min before,
or concurrently with, LPS administration. A third group of mice may
serve as a positive control and consist of mice treated with either
mouse IL-10 i.p. or anti-TNF antibodies i.p. 30 min before LPS
administration. Mice are monitored for death for 72 h following the
LPS injection.
[1036] Asthma. Representative procedures for evaluating the
efficacy of CCR4 antagonists for treatment of asthma are as
described herein. Procedure A: An animal model of asthma may be
induced by sensitizing mice to an experimental antigen (e.g. OVA)
by standard immunization techniques, and subsequently introducing
that same antigen into the mice's lungs by aerosolization. Three
groups of mice (10 mice per group) may be actively sensitized on
Day 0 by a single i.p. injection with 100 .mu.g OVA in PBS, along
with an IgE-selective adjuvant (e.g. aluminum hydroxide). Eleven
days' post-sensitization, at the peak of their IgE response, the
mice may be placed in a Plexiglas chamber and challenged with
aerosolized OVA (1%) for 30 min using the ultrasonic nebulizer
(e.g., De Vilbliss; Ingersoll Rand; Dublin, I E). One group of mice
may additionally receive PBS and Tween 0.5% i.p. at the initial
sensitization, and at different dosing schedules thereafter, up
until the aerosolized OVA challenge. A second group of mice may
receive different doses of the CCR4 antagonist(s) given either
i.p., IV, SC, IM, PO or via any other mode of administration at the
initial sensitization, and at different dosing schedules
thereafter, up until the aerosolized OVA challenge. A third group
of mice, serving as a positive control, may be treated with either
mouse IL-10 i.p., anti-IL-4 antibodies i.p., or anti-IL5 antibodies
i.p. at the initial sensitization, and at different dosing
schedules thereafter, up until the aerosolized OVA challenge.
[1037] Following the aerosolized OVA challenge, mice may be
analyzed at different time points for pulmonary function, cellular
infiltrates in bronchoalveolar lavage (BAL), histological
examination of lungs, and measurement of serum OVA-specific IgE
titers.
[1038] Procedure B. Ovalbumin (OVA, 0.2 mg/mL) and Alum (8 mg/mL)
prepared in physiological saline may be intraperitoneally
administered (500 .mu.L) to mice (male, C57BL/6) on Day 1 (test
starting day) and Day 8 (1 week thereafter), to sensitize the mice.
On Days 15 to 21, mice may be placed in an inhalation chamber (W:
240 mm.times.L: 240 mm.times.H: 120 mm), and a 2% OVA solution may
be sprayed with an ultrasonic wave-type nebulizer (NE-U12; Omron,
San Ramon, Calif.) for 20 min to conduct induction. A CCR4
antagonist(s) may be suspended in a medium and administered orally
at 30 min before OVA sensitization on Day 8 and at 30 min before
OVA induction on Days 15 to 21. For a control group, only the
medium may be administered. Three h post-OVA inhalation on Day 21,
the mice may be exsanguinated, catheter tubes inserted into their
trachea, and lungs washed with heparin-containing physiological
saline (10 U/mL) to provide a bronchoalveolar lavage fluid (BALF).
Leukocyte number in BALF may be counted using hemocyte counter
(SF-3000; Sysmex, Kobe, J P).
[1039] Dermatitis. Representative procedures for evaluating the
efficacy of CCR4 antagonists for treatment of dermatitis are as
described herein. Mouse DTH Model. Mice (male, Balb/c) may be
shaved on the abdomen with hair clippers, and to the abdomen may be
applied ethanol solution (100 L) of 7% (w/v)
2,4,6-trinitrochlrobenzene (TNCB), to sensitize the mice. Seven
days' post-sensitization, a 1% (w/v) TNCB solution in olive oil (20
.mu.L) may be applied to the auricle of the mice (both sides of the
right ear), to conduct induction. A CCR4 antagonist(s) may be
dissolved in a medium, applied to both sides of the right ear (20
.mu.L) 2 h before applying TNCB. To the control groups, only the
medium may be applied. Immediately following compound(s)
administration and 24 h after TNCB application, the thickness of
the mice auricles may be measured with Dialthickness gauge (Ozaki
Seisakusho, JP), which may be used as indicator for efficacy in
mouse DTH model.
[1040] Dermatitis Model to which Hapten is Applied. To the auricle
(both sides of the right ear) of the mice (male, Balb/c), 1% (w/v)
TNCB solution (acetone:olive oil=4:1) (20 .mu.L) may be applied to
conduct first sensitization. Seven days' post-sensitization, 1%
(w/v) TNCB (acetone:olive oil=4:1) (20 .mu.L) may be applied to the
auricle of the mice, to conduct induction (Day 0); this procedure
may be repeated on Days 2, 4, 6, 8, 10, 12, 14 and 16. A CCR4
antagonist(s) may be dissolved in a medium, and applied to both
sides of the right ear (20 .mu.La) two h before applying TNCB. To
the control groups, medium only may be applied. Immediately
following compound(s) administration and 24 h post-TNCB
application, the thickness of the mice auricles may be measured
with Dialthickness gauge, which may be used as an indicator of
efficacy in mouse dermatitis model to which hapten is continuously
applied.
[1041] Infection. A representative procedure for evaluating the
efficacy of CCR4 antagonists for augmenting protective immunity
against viruses, bacteria and parasites is as described herein.
Protective immunity to microbial pathogens is frequently mediated
by Th1 regulatory T cells. Because CCR4 antagonists are believed to
be inhibitors of Th2 regulatory cells, they may alter the
cross-regulation that normally exists between Th1 and Th2 cells and
potentiate Th1 cells, thereby augmenting protection against
infectious disease.
[1042] Three groups of mice (15 mice per group) may be infected
with the intracellular parasite Leishmania major (L. major) by
injecting L. major promastigotes SC into their left hind footpads.
Four weeks after infection, the mice may be challenged with either
Leishmania freeze-thawed antigen, or PBS as a negative control, in
the contra-lateral footpad. One group of mice may also receive PBS
and Tween 0.5% i.p. at the initial sensitization, and at different
dosing schedules thereafter, up until the Leishmania antigen
challenge. A second group of mice may receive different doses of
the CCR4 antagonist(s) given either i.p., IV, SC, IM, PO or via any
other mode of administration at the initial sensitization, and at
different dosing schedules thereafter, up until the Leishmania
antigen challenge. A third group of mice, serving as positive
control, may consist of mice treated with either IL-12, anti-IL-4
antibodies i.p., or anti-IL-5 antibodies i.p. at the initial
sensitization, and at different dosing schedules thereafter, up
until the Leishmania antigen challenge.
[1043] Over the next 48 h, footpad swelling, caused by a
Delayed-Type Hypersensitivity reaction to the Leishmania antigen
challenge, may be monitored with a metric caliper. The response of
draining lymph node T cells to Leishmania antigen stimulation in
vitro may also be measured, both at the level of proliferation,
cytokine production, and other phenotypic criteria.
[1044] Rheumatoid Arthritis. Rheumatoid Arthritis (RA), which is
generally characterized by chronic inflammation in the membrane
lining (the synovium) of the joints, affects approximately 1% of
the U.S. population, or 2.1 million people in the U.S. Further
understanding of the role of cytokines, including TNF-.alpha. and
IL-1, in the inflammatory process has enabled the development and
introduction of a new class of disease-modifying antirheumatic
drugs (DMARDs). Agents (some of which overlap with treatment
modalities for RA) include ENBREL (etanercept), REMICADE
(infliximab), HUMIRA (adalimumab) and KINERET (anakinra). Though
some of these agents relieve symptoms, inhibit progression of
structural damage, and improve physical function in particular
patient populations, there is still a need for alternative agents
with improved efficacy, complementary mechanisms of action, and
fewer/less severe adverse effects.
[1045] A representative procedure for evaluating the efficacy of
CCR4 antagonists for treatment of rheumatoid arthritis is as
described herein. An animal model of rheumatoid arthritis may be
induced in rodents by injecting them with type II collagen in
selected adjuvants. Three rodent groups, each consisting of 15
genetically-susceptible mice or rats, may be injected SC or
intra-dermally with type II collagen emulsified in Complete
Freund's Adjuvant at days 0 and 21. One group of rodents may
additionally receive PBS and Tween 0.5% i.p. at the initial
sensitization, and at different dosing schedules thereafter. A
second group of rodents may receive different doses of the CCR4
antagonist(s) given either i.p., IV, SC, IM, PO or via any other
mode of administration at the initial sensitization, and at
different dosing schedules thereafter. A third group, serving as
positive control, may consist of rodents treated with either mouse
IL-10 i.p., or anti-TNF antibodies i.p. at the initial
sensitization, and at different dosing schedules thereafter.
[1046] Animals may be monitored from weeks 3 until 8 for the
development of swollen joints or paws, and graded on a standard
disease-severity scale. Disease severity may be confirmed by
histological analysis of joints.
[1047] Systemic Lupus Erythematosus. A representative procedure for
evaluating the efficacy of CCR4 antagonists for treatment of
Systemic Lupus Erythematosus (SLE) is as described herein. Female
NZB/W F1 mice spontaneously develop an SLE-like pathology
commencing at 6 months of age that is characterized by proteinuria,
serum autoantibodies, glomerulonephritis, and eventually death.
[1048] Three groups of NZB/W mice, each comprising 20 mice per
group, may be evaluated. One group of mice may receive PBS and
Tween 0.5% i.p. soon after weaning, and thereafter at varying
dosing schedules. A second group of mice may receive different
doses of the CCR4 antagonist(s) given either i.p., IV, SC, IM, PO
or via any other mode of administration soon after weaning, and
thereafter at varying dosing schedules. A third group of mice,
serving as positive control, may comprise mice treated with
anti-IL-10 antibodies given soon after weaning, and thereafter at
varying dosing schedules. Disease development may be monitored in
terms of eventual mortality, kidney histology, serum autoantibody
levels, and proteinuria.
[1049] Cancer-related Malignancy. A representative procedure for
evaluating the efficacy of CCR4 antagonists for treatment of cancer
is as described herein. Mice homozygous for the severe combined
immune deficiency spontaneous mutation Prkdc.sup.scid(SCID mice),
are characterized by an absence of functional T cells and B cells,
lymphopenia, hypogammaglobulinemia, and a normal hematopoietic
microenvironment. Additional mouse genetic backgrounds can result
in lack of natural killer cells (in NOD-SCID); while the addition
of mutations in IL2 receptor gamma chain results in loss of much
cytokine signaling resulting in highly immune-deficient mice (NSG).
Immuno-defi