U.S. patent application number 10/583573 was filed with the patent office on 2008-11-20 for 4'-substituted carbovir and abacavir-derivatives as well as related compounds with hiv and hcv antiviral activity.
Invention is credited to Maria Fardis, Choung U. Kim.
Application Number | 20080287471 10/583573 |
Document ID | / |
Family ID | 34738778 |
Filed Date | 2008-11-20 |
United States Patent
Application |
20080287471 |
Kind Code |
A1 |
Fardis; Maria ; et
al. |
November 20, 2008 |
4'-Substituted Carbovir And Abacavir-Derivatives As Well As Related
Compounds With Hiv And Hcv Antiviral Activity
Abstract
The application relates to compounds with activity against
infectious viruses. Accordingly, in one embodiment the invention
provides a compound of the invention which is a compound of Formula
I: (I) wherein: B is adenine, guanine cytosine, uracil, thymine,
7-deazaadenine, 7-deazaguanine, 7-deaza-8-azaguanine,
7-deaza-8-azaadenine, inosine, nebularine, nitropyrrole,
nitroindole, 2-aminopurine, 2-amino-6-chloropuriine,
2,6-diaminopurine, hypoxanthine, pseudouridine, pseudo-cytosine,
pseudoisocytosine, 5-propynylcytosine, isocytosines, isoguanine,
7-deazaguanine, 2-thiopyrimidine, 6-thioguanine, 4-thiothymine,
4-thiouracil O.sup.6-methylguanine, N.sup.6-methyladenine,
O.sup.4-methylthymine, 5,6-dihydrothymine, 5,6-dihydroucacil,
4-methylindole, triazole, or pyrazolo[3,4-d]pyrimidine; and B is
optionally substituted with one or more alkyl, alkenyl, alkynyl,
cycloalkyl, (cycloalkyl)alkyl, hydroxy, or halo; and R.sup.1 is
alkyl, alkenyl, alkynyl, cyano, azido, or fluoromethyl; or a
pharmaceutically acceptable salt or solvate thereof.
##STR00001##
Inventors: |
Fardis; Maria; (San Carlos,
CA) ; Kim; Choung U.; (San Carlos, CA) |
Correspondence
Address: |
VIKSNINS HARRIS & PADYS PLLP
P.O BOX 111098
St. Paul
MN
55111-1098
US
|
Family ID: |
34738778 |
Appl. No.: |
10/583573 |
Filed: |
December 22, 2004 |
PCT Filed: |
December 22, 2004 |
PCT NO: |
PCT/US04/43571 |
371 Date: |
January 28, 2008 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
60532256 |
Dec 22, 2003 |
|
|
|
Current U.S.
Class: |
514/263.37 ;
435/375; 544/264; 544/276 |
Current CPC
Class: |
C07H 19/16 20130101;
C07D 473/18 20130101; A61P 31/14 20180101; A61P 31/18 20180101;
A61P 43/00 20180101; C07D 473/16 20130101; C07H 19/06 20130101 |
Class at
Publication: |
514/263.37 ;
544/276; 544/264; 435/375 |
International
Class: |
A61K 31/52 20060101
A61K031/52; C07D 473/00 20060101 C07D473/00; C12N 5/06 20060101
C12N005/06; A61P 31/18 20060101 A61P031/18 |
Claims
1. A compound of Formula I: ##STR00010## wherein: B is adenine,
guanine, cytosine, uracil, thymine, 7-deazaadenine, 7-deazaguanine,
7-deaza-8-azaguanine, 7-deaza-8-azaadenine, inosine, nebularine,
nitropyrrole, nitroindole, 2-aminopurine, 2-amino-6-chloropurine,
2,6-diaminopurine, hypoxanthine, pseudouridine, pseudocytosine,
pseudoisocytosine, 5-propynylcytosine, isocytosine, isoguanine,
2-thiopyrimidine, 6-thioguanine, 4-thiothymine, 4-thiouracil,
O.sup.6-methylguanine, N.sup.6-methyladenine,
O.sup.4-methylthymine, 5,6-dihydrothymine, 5,6-dihydrouracil,
4-methylindole, triazole, or pyrazolo[3,4-d]pyrimidine; and B is
optionally substituted with one or more alkyl, alkenyl, alkynyl,
cycloalkyl, (cycloalkyl)alkyl, hydroxy, or halo; and R.sup.1 is
alkyl, alkenyl, alkynyl, cyano, azido, or fluoromethyl; or a
pharmaceutically acceptable salt or solvate thereof; provided the
compound of formula I is not a compound of formula II: ##STR00011##
wherein R.sup.1 is alkyl.
2. The compound of claim 1 wherein B is adenine, guanine, cytosine,
uracil, or thymine; which B is optionally substituted with one or
more alkyl, alkenyl, alkynyl, cycloalkyl, (cycloalkyl)alkyl,
hydroxy, or halo.
3. The compound of claim 1 wherein B is 7-deazaadenine,
7-deazaguanine, 7-deaza-azaguanine, 7-deaza-8-azaadenine, inosine,
nebularine, nitropyrrole, nitroindole, 2-aminopurine,
2-amino-6-chloropurine, 2,6-diaminopurine, hypoxanthine,
pseudouridine, pseudocytosine, pseudoisocytosine,
5-propynylcytosine, isocytosine, isoguanine, 7-deazaguanine,
2-thiopyrimidine, 6-thioguanine, 4-thiothymine, 4-thiouracil,
O.sup.6-methylguanine, N.sup.6-methyladenine,
O.sup.4-methylthymine, 5,6-dihydrothymine, 5,6-dihydrouracil,
4-methylindole, triazole, or pyrazolo[3,4-d]pyrimidine; and B is
optionally substituted with one or more alkyl, alkenyl, alkynyl,
cycloalkyl, (cycloalkyl)alkyl, hydroxy, or halo
4. The compound of claim 1 wherein B is adenine, guanine, cytosine,
uracil, or thymine.
5. The compound of claim 1 which is a compound of formula II:
##STR00012## wherein R.sup.1 is alkenyl, alkynyl, cyano, azido, or
fluoromethyl.
6. The compound of claim 1 which is a compound of formula III:
##STR00013## wherein R.sup.1 has any of the values defined in claim
1.
7. The compound of claim 1 wherein R.sup.1 is alkyl.
8. The compound of claim 1 wherein R.sup.1 is methyl.
9. The compound of claim 1 wherein R.sup.1 is fluoromethyl.
10. The compound of claim 1 wherein R.sup.1 is alkenyl.
11. The compound of claim 1 wherein R.sup.1 is vinyl.
12. The compound of claim 1 wherein R.sup.1 is alkynyl.
13. The compound of claim 1 wherein R.sup.1 is ethynyl.
14. The compound of claim 1 wherein R.sup.1 is cyano.
15. The compound of claim 1 wherein R.sup.1 is azido.
16. A pharmaceutical composition, comprising an effective amount of
a compound of Formula I as described in claim 1, or a
pharmaceutically acceptable salt or solvate thereof, and a
pharmaceutically acceptable excipient.
17. A pharmaceutical composition comprising an effective amount of
a compound of Formula I as described in claim 1, or a
pharmaceutically acceptable salt or solvate thereof; a
pharmaceutically acceptable excipient; and a therapeutically
effective amount of another therapeutic agent.
18. The pharmaceutical composition of claim 16 which further
comprises an AIDS treatment agent selected from an HIV inhibitor
agent, an anti-infective agent, and an immunomodulator.
19. The pharmaceutical composition of claim 16 which further
comprises an HIV-protease inhibitor.
20. The pharmaceutical composition of claim 16 which further
comprises a reverse transcriptase inhibitor.
21. The pharmaceutical composition of claim 16 which further
comprises a non-nucleoside reverse transcriptase inhibitor.
22. The pharmaceutical composition of claim 16 which further
comprises an HIV integrase inhibitor.
23. A method of inhibiting a viral infection in an animal (e.g. a
mammal), comprising administering to the animal, an effective
amount of a compound of Formula I as described in claim 1, or a
pharmaceutically acceptable salt or solvate thereof.
24. A method for the treatment or prevention of the symptoms or
effects of a viral infection in an animal comprising administering
to the animal, an effective amount of a compound of Formula I as
described in claim 1, or a pharmaceutically acceptable salt or
solvate thereof.
25. A method of inhibiting an HCV infection in an animal comprising
administering to the animal, an effective amount of a compound of
Formula I as described in claim 1, or a pharmaceutically acceptable
salt or solvate thereof.
26. A method for the treatment or prevention of the symptoms or
effects of HCV infection in an infected animal comprising
administering to the animal, an effective amount of a compound of
Formula I as described in claim 1, or a pharmaceutically acceptable
salt or solvate thereof.
27. A method of inhibiting a viral enzyme comprising contacting a
sample suspected of containing viral infected cells or tissues with
an effective amount of a compound of Formula I as described in
claim 1, or a pharmaceutically acceptable salt or solvate
thereof.
28. A method of inhibiting RNA-dependent RNA polymerase in an
animal comprising administering to the animal, an effective amount
of a compound of Formula I as described in claim 1, or a
pharmaceutically acceptable salt or solvate thereof.
29-34. (canceled)
35. A process for making a pharmaceutical composition comprising
combining a compound of Formula I as described in claim 1, or a
pharmaceutically acceptable salt or solvate thereof, and a
pharmaceutically acceptable excipient.
Description
PRIORITY OF INVENTION
[0001] This application claims the benefit of priority under 35
U.S.C. .sctn. 119(e) to U.S. Provisional Patent Application Ser.
No. 60/532,256, filed 22 Dec. 2003. The entirety of this
Provisional Application is incorporated herein by reference.
FIELD OF THE INVENTION
[0002] The invention relates generally to 4'-substituted nucleoside
derivatives with antiviral activity.
BACKGROUND OF THE INVENTION
[0003] Carbovir (EP 00,434,450 and EP 00,349,242) along with
abacavir are well known anti-HIV carbocyclic nucleosides. Abacavir
is the most potent nucleoside reverse transcriptase inhibitor
(NRTI) developed to date. An average reduction in viral load of
more than 1.4 log 10 RNA copies/ml is observed after a short course
of abacavir monotherapy.
##STR00002##
[0004] Dideoxynucleotide use such as dideoxycytidine (ddC) and of
didehydrodideoxythymidine (d4T) is limited by associated painful
sensory-motor peripheral neuropathy. Dideoxyinosine also shares
this complication as well as causing acute pancreatitis, and
hepatotoxicity in some cases (Maag, H. et al., J. Med. Chem., 1992,
35, 1440). Yet another concern about this class of compounds has
been the emergence of resistant HIV strains in patients undergoing
treatment with nucleosides. For instance the ddI-resistant strains
were also shown to be resistant to ddC. In another study, clinical
HIV isolates resistant to AZT displayed marked resistance to d4T.
It appears, then, that some cross resistance is inevitable among
this class of similar nucleoside structures. Therefore, an
important criterion for the design of any new nucleoside drug would
be a distinct dissimilarity of structure to the current family of
dideoxynucleosides.
[0005] Substitution at the 4' position of nucleosides has been
reported to exert potent antiviral activity against HIV-1 as
demonstrated by 4'-azido-2'-deoxythymidine (4'-AZT) (Maag, H. et
al., J. Med. Chem., 1992, 35, 1440). In addition, 4'-ethynyl
nucleoside analogs have been shown to be active against a wide
spectrum of HIV viruses, specifically against HIV-1.sub.M184V and
HIV-1.sub.M184I (Kodama, E. I. et al., Antimicrob. Agents
Chemother., 2001, 1539). Recently, Haraguchi et al. reported the
preparation of 4'-substituted d4T analogs. They demonstrated that
contrary to the previous reports, the 3'-hydroxy group is not
necessary for the 4'-substituted nucleosides to be active against
HIV (Haraguchi, K. et al., Bioorg. Med. Chem. Lett., 2003, 13,
3775).
[0006] There is currently a need for therapeutic antiviral agents
having unique structural characteristics. Additionally, there is a
need for antiviral agents with improved pharmacological properties,
e.g., drugs having improved antiviral activity and pharmacokinetic
properties, including improved oral bioavailability, greater
potency and extended effective half-life in vivo.
SUMMARY OF THE INVENTION
[0007] The invention relates to compounds with activity against
infectious viruses. Accordingly, in one embodiment the invention
provides a compound of the invention which is a compound of Formula
I:
##STR00003##
wherein:
[0008] B is adenine, guanine, cytosine, uracil, thymine,
7-deazaadenine, 7-deazaguanine, 7-deaza-8-azaguanine,
7-deaza-8-azaadenine, inosine, nebularine, nitropyrrole,
nitroindole, 2-aminopurine, 2-amino-6-chloropurine,
2,6-diaminopurine, hypoxanthine, pseudouridine, pseudocytosine,
pseudoisocytosine, 5-propynylcytosine, isocytosine, isoguanine,
7-deazaguanine, 2-thiopyrimidine, 6-thioguanine, 4-thiothymine,
4-thiouracil, O.sup.6-methylguanine, N.sup.6-methyladenine,
O.sup.4-methylthymine, 5,6-dihydrothymine, 5,6-dihydrouracil,
4-methylindole, triazole, or pyrazolo[3,4-d]pyrimidine; and B is
optionally substituted with one or more alkyl, alkenyl, alkynyl,
cycloalkyl, (cycloalkyl)alkyl, hydroxy, or halo; and
[0009] R.sup.1 is alkyl, alkenyl, alkynyl, cyano, azido, or
fluoromethyl;
[0010] or a pharmaceutically acceptable salt or solvate
thereof.
[0011] In one embodiment, the invention also provides a
pharmaceutical composition, comprising an effective amount of a
compound of Formula I, or a pharmaceutically acceptable salt or
solvate thereof, and a pharmaceutically acceptable excipient.
[0012] In one embodiment, the invention also provides a
pharmaceutical composition, comprising an effective amount of a
compound of Formula I, or a pharmaceutically acceptable salt or
solvate thereof; a pharmaceutically acceptable excipient; and a
therapeutically effective amount of another therapeutic agent.
[0013] In one embodiment, the invention also provides a
pharmaceutical composition, comprising an effective amount of a
compound of Formula I, or a pharmaceutically acceptable salt or
solvate thereof; a pharmaceutically acceptable excipient; and a
therapeutically effective amount of an AIDS treatment agent
selected from an HIV inhibitor agent, an anti-infective agent, and
an immunomodulator.
[0014] In one embodiment, the invention also provides a
pharmaceutical composition, comprising an effective amount of a
compound of Formula I, or a pharmaceutically acceptable salt or
solvate thereof; a pharmaceutically acceptable excipient; and a
therapeutically effective amount of an HIV-protease inhibitor.
[0015] In one embodiment, the invention also provides a
pharmaceutical composition, comprising an effective amount of a
compound of Formula I, or a pharmaceutically acceptable salt or
solvate thereof; a pharmaceutically acceptable excipient; and a
therapeutically effective amount of a reverse transcriptase
inhibitor.
[0016] In one embodiment, the invention also provides a
pharmaceutical composition, comprising an effective amount of a
compound of Formula I, or a pharmaceutically acceptable salt or
solvate thereof; a pharmaceutically acceptable excipient; and a
therapeutically effective amount of a non-nucleoside reverse
transcriptase inhibitor.
[0017] In one embodiment, the invention also provides a
pharmaceutical composition, comprising an effective amount of a
compound of Formula I, or a pharmaceutically acceptable salt or
solvate thereof; a pharmaceutically acceptable excipient; and a
therapeutically effective amount of an HIV integrase inhibitor.
[0018] In one embodiment, the invention also provides a method of
inhibiting a viral infection in an animal (e.g. a mammal),
comprising administering an effective amount of a compound of
Formula I, or a pharmaceutically acceptable salt or solvate
thereof, to the animal.
[0019] In one embodiment, the invention also provides a method for
the treatment or prevention of the symptoms or effects of a viral
infection in an animal, comprising administering an effective
amount of a compound of Formula I, or a pharmaceutically acceptable
salt or solvate thereof, to the animal.
[0020] In one embodiment, the invention also provides a method of
inhibiting an HCV infection in an animal, comprising administering
an effective amount of a compound of Formula I, or a
pharmaceutically acceptable salt or solvate thereof, to the
animal.
[0021] In one embodiment, the invention also provides a method for
the treatment or prevention of the symptoms or effects of HCV
infection in an infected animal, comprising administering an
effective amount of a compound of Formula I, or a pharmaceutically
acceptable salt or solvate thereof, to the animal.
[0022] In one embodiment, the invention also provides a method of
inhibiting a viral enzyme, comprising contacting a sample suspected
of containing viral infected cells or tissues with a compound of
Formula I, or a pharmaceutically acceptable salt or solvate
thereof.
[0023] In one embodiment, the invention also provides a method of
inhibiting RNA-dependent RNA polymerase in an animal, comprising
administering an effective amount of a compound of Formula I, or a
pharmaceutically acceptable salt or solvate thereof, to the
animal.
[0024] In one embodiment, the invention also provides a compound of
Formula I, or a pharmaceutically acceptable salt or solvate
thereof, for use in medical therapy (preferably for use in treating
a viral infection in an animal).
[0025] In one embodiment, the invention also provides the use of a
compound of Formula I, or a pharmaceutically acceptable salt or
solvate thereof, to prepare a medicament useful for inhibiting a
viral infection in an animal (e.g. a mammal).
[0026] In one embodiment, the invention also provides the use of a
compound of Formula I, or a pharmaceutically acceptable salt or
solvate thereof, to prepare a medicament useful for the treatment
or prevention of the symptoms or effects of a viral infection in an
animal.
[0027] In one embodiment, the invention also provides the use of a
compound of Formula I, or a pharmaceutically acceptable salt or
solvate thereof, to prepare a medicament useful for inhibiting an
HCV infection in an animal.
[0028] In one embodiment, the invention also provides the use of a
compound of Formula I, or a pharmaceutically acceptable salt or
solvate thereof to prepare a medicament useful for the treatment or
prevention of the symptoms or effects of HCV infection in an
infected animal.
[0029] In one embodiment, the invention also provides the use of a
compound of Formula I, or a pharmaceutically acceptable salt or
solvate thereof, to prepare a medicament useful for inhibiting an
RNA-dependent RNA polymerase in an animal.
[0030] In one embodiment, the invention also provides a process for
making a pharmaceutical composition comprising combining a compound
of formula I, or a pharmaceutically acceptable salt or solvate
thereof, and a pharmaceutically acceptable excipient.
[0031] In one embodiment, the invention also provides processes and
novel intermediates disclosed herein which are useful for preparing
compounds of the invention. Some of the compounds of the invention
are useful to prepare other compounds of the invention.
[0032] In one embodiment, the invention also provides a process for
making a pharmaceutical composition comprising combining a compound
of formula I, or a pharmaceutically acceptable salt or solvate
thereof, and a pharmaceutically acceptable excipient.
DETAILED DESCRIPTION OF EXEMPLARY CLAIMS
[0033] Reference will now be made in detail to certain claims of
the invention, examples of which are illustrated in the
accompanying structures and formulas. While the invention will be
described in conjunction with the enumerated claims, it will be
understood that they are not intended to limit the invention to
those claims. On the contrary, the invention is intended to cover
all alternatives, modifications, and equivalents, which may be
included within the scope of the present invention as defined by
the claims.
DEFINITIONS
[0034] Unless stated otherwise, the following terms and phrases as
used herein are intended to have the following meanings:
[0035] When tradenames are used herein, applicants intend to
independently include the tradename product and the active
pharmaceutical ingredient(s) of the tradename product.
[0036] The term "prodrug" as used herein refers to any compound
that when administered to a biological system generates the drug
substance, i.e. active ingredient, as a result of spontaneous
chemical reaction(s), enzyme catalyzed chemical reaction(s),
photolysis, and/or metabolic chemical reaction(s). A prodrug is
thus a covalently modified analog or latent form of a
therapeutically-active compound.
[0037] "Protecting group" refers to a moiety of a compound that
masks or alters the properties of a functional group or the
properties of the compound as a whole. Chemical protecting groups
and strategies for protection/deprotection are well known in the
art. See e.g., Protective Groups in Organic Chemistry, Theodora W.
Greene, John Wiley & Sons, Inc., New York, 1991. Protecting
groups are often utilized to mask the reactivity of certain
functional groups, to assist in the efficiency of desired chemical
reactions, e.g., making and breaking chemical bonds in an ordered
and planned fashion. Protection of functional groups of a compound
alters other physical properties besides the reactivity of the
protected functional group, such as the polarity, lipophilicity
(hydrophobicity), and other properties which can be measured by
common analytical tools. Chemically protected intermediates may
themselves be biologically active or inactive.
[0038] Protected compounds may also exhibit altered, and in some
cases, optimized properties in vitro and in vivo, such as passage
through cellular membranes and resistance to enzymatic degradation
or sequestration. In this role, protected compounds with intended
therapeutic effects may be referred to as prodrugs. Another
function of a protecting group is to convert the parental drug into
a prodrug, whereby the parental drug is released upon conversion of
the prodrug in vivo. Because active prodrugs may be absorbed more
effectively than the parental drug, prodrugs may possess greater
potency in vivo than the parental drug. Protecting groups are
removed either in vitro, in the instance of chemical intermediates,
or in vivo, in the case of prodrugs. With chemical intermediates,
it is not particularly important that the resulting products after
deprotection, e.g., alcohols, be physiologically acceptable,
although in general it is more desirable if the products are
pharmacologically innocuous.
[0039] Any reference to any of the compounds of the invention also
includes a reference to a physiologically acceptable salt thereof.
Examples of physiologically acceptable salts of the compounds of
the invention include salts derived from an appropriate base, such
as an alkali metal (for example, sodium), an alkaline earth (for
example, magnesium), ammonium and NX.sub.4.sup.+ (wherein X is
C.sub.1-C.sub.4 alkyl). Physiologically acceptable salts of an
hydrogen atom or an amino group include salts of organic carboxylic
acids such as acetic, benzoic, lactic, fumaric, tartaric, maleic,
malonic, malic, isethionic, lactobionic and succinic acids; organic
sulfonic acids, such as methanesulfonic, ethanesulfonic,
benzenesulfonic and p-toluenesulfonic acids; and inorganic acids,
such as hydrochloric, sulfuric, phosphoric and sulfamic acids.
Physiologically acceptable salts of a compound of an hydroxy group
include the anion of said compound in combination with a suitable
cation such as Na.sup.+ and NX.sub.4.sup.+ (wherein X is
independently selected from H or a C.sub.1-C.sub.4 alkyl
group).
[0040] For therapeutic use, salts of active ingredients of the
compounds of the invention will be physiologically acceptable, i.e.
they will be salts derived from a physiologically acceptable acid
or base. However, salts of acids or bases which are not
physiologically acceptable may also find use, for example, in the
preparation or purification of a physiologically acceptable
compound. All salts, whether or not derived form a physiologically
acceptable acid or base, are within the scope of the present
invention.
[0041] "Alkyl" is C.sub.1-C.sub.18 hydrocarbon containing normal,
secondary, tertiary or cyclic carbon atoms. Examples are methyl
(Me, --CH.sub.3), ethyl (Et, --CH.sub.2CH.sub.3), 1-propyl (n-Pr,
n-propyl, --CH.sub.2CH.sub.2CH.sub.3), 2-propyl (1-Pr, i-propyl,
--CH(CH.sub.3).sub.2), 1-butyl (n-Bu, n-butyl,
--CH.sub.2CH.sub.2CH.sub.2CH.sub.3), 2-methyl-1-propyl (1-Bu,
1-butyl, --CH.sub.2CH(CH.sub.3).sub.2), 2-butyl (s-Bu, s-butyl,
--CH(CH.sub.3)CH.sub.2CH.sub.3), 2-methyl-2-propyl (t-Bu, t-butyl,
--C(CH.sub.3).sub.3), 1-pentyl (n-pentyl,
--CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.3), 2-pentyl
(--CH(CH.sub.3)CH.sub.2CH.sub.2CH.sub.3), 3-pentyl
(--CH(CH.sub.2CH.sub.3).sub.2), 2-methyl-2-butyl
(--C(CH.sub.3).sub.2CH.sub.2CH.sub.3), 3-methyl-2-butyl
(--CH(CH.sub.3)CH(CH.sub.3).sub.2), 3-methyl-1-butyl
(--CH.sub.2CH.sub.2CH(CH.sub.3).sub.2), 2-methyl-1-butyl
(--CH.sub.2CH(CH.sub.3)CH.sub.2CH.sub.3), 1-hexyl
(--CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.3), 2-hexyl
(--CH(CH.sub.3)CH.sub.2CH.sub.2CH.sub.2CH.sub.3), 3-hexyl
(--CH(CH.sub.2CH.sub.3)(CH.sub.2CH.sub.2CH.sub.3)),
2-methyl-2-pentyl (--C(CH.sub.3).sub.2CH.sub.2CH.sub.2CH.sub.3),
3-methyl-2-pentyl (--CH(CH.sub.3)CH(CH.sub.3)CH.sub.2CH.sub.3),
4-methyl-2-pentyl (--CH(CH.sub.3)CH.sub.2CH(CH.sub.3).sub.2),
3-methyl-3-pentyl (--C(CH.sub.3)(CH.sub.2CH.sub.3).sub.2),
2-methyl-3-pentyl (--CH(CH.sub.2CH.sub.3)CH(CH.sub.3).sub.2),
2,3-dimethyl-2-butyl (--C(CH.sub.3).sub.2CH(CH.sub.3).sub.2),
3,3-dimethyl-2-butyl (--CH(CH.sub.3)C(CH.sub.3).sub.3.
[0042] "Alkenyl" is C.sub.2-C.sub.18 hydrocarbon containing normal,
secondary, tertiary or cyclic carbon atoms with at least one site
of unsaturation, i.e. a carbon-carbon, sp.sup.2 double bond.
Examples include, but are not limited to, ethylene or vinyl
(--CH.dbd.CH.sub.2), allyl (--CH.sub.2CH.dbd.CH.sub.2),
cyclopentenyl (--C.sub.5H.sub.7), and 5-hexenyl
(--CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.dbd.CH.sub.2).
[0043] "Alkynyl" is C.sub.2-C.sub.18 hydrocarbon containing normal,
secondary, tertiary or cyclic carbon atoms with at least one site
of unsaturation, i.e. a carbon-carbon, sp triple bond. Examples
include, but are not limited to, acetylenic (--C.ident.CH) and
propargyl (--CH.sub.2C.ident.CH),
[0044] "Alkylene" refers to a saturated, branched or straight chain
or cyclic hydrocarbon radical of 1-18 carbon atoms, and having two
monovalent radical centers derived by the removal of two hydrogen
atoms from the same or two different carbon atoms of a parent
alkane. Typical alkylene radicals include, but are not limited to,
methylene (--CH.sub.2--) 1,2-ethyl (--CH.sub.2CH.sub.2--),
1,3-propyl (--CH.sub.2CH.sub.2CH.sub.2--), 1,4-butyl
(--CH.sub.2CH.sub.2CH.sub.2CH.sub.2--), and the like.
[0045] "Alkenylene" refers to an unsaturated, branched or straight
chain or cyclic hydrocarbon radical of 2-18 carbon atoms, and
having two monovalent radical centers derived by the removal of two
hydrogen atoms from the same or two different carbon atoms of a
parent alkene. Typical alkenylene radicals include, but are not
limited to, 1,2-ethylene (--CH.dbd.CH--).
[0046] "Alkynylene" refers to an unsaturated, branched or straight
chain or cyclic hydrocarbon radical of 2-18 carbon atoms, and
having two monovalent radical centers derived by the removal of two
hydrogen atoms from the same or two different carbon atoms of a
parent alkyne. Typical alkynylene radicals include, but are not
limited to, acetylene (--C.ident.C--), propargyl
(--CH.sub.2C.ident.C--), and 4-pentynyl
(--CH.sub.2CH.sub.2CH.sub.2C.ident.CH--).
[0047] "Aryl" means a monovalent aromatic hydrocarbon radical of
6-20 carbon atoms derived by the removal of one hydrogen atom from
a single carbon atom of a parent aromatic ring system. Typical aryl
groups include, but are not limited to, radicals derived from
benzene, substituted benzene, naphthalene, anthracene, biphenyl,
and the like.
[0048] "Arylalkyl" refers to an acyclic alkyl radical in which one
of the hydrogen atoms bonded to a carbon atom, typically a terminal
or sp.sup.3 carbon atom, is replaced with an aryl radical. Typical
arylalkyl groups include, but are not limited to, benzyl,
2-phenylethan-1-yl, naphthylmethyl, 2-naphthylethan-1-yl,
naphthobenzyl, 2-naphthophenylethan-1-yl and the like. The
arylalkyl group comprises 6 to 20 carbon atoms, e.g., the alkyl
moiety, including alkanyl, alkenyl or alkynyl groups, of the
arylalkyl group is 1 to 6 carbon atoms and the aryl moiety is 5 to
14 carbon atoms.
[0049] "Substituted alkyl", "substituted aryl", and "substituted
arylalkyl" mean alkyl, aryl, and arylalkyl respectively, in which
one or more hydrogen atoms are each independently replaced with a
non-hydrogen substituent. Typical substituents include, but are not
limited to, --X, --R, --O.sup.-, --OR, --SR, --S.sup.-, --NR.sub.2,
--NR.sub.3, .dbd.NR, --CX.sub.3, --CN, --OCN, --SCN,
--N.dbd.C.dbd.O, --NCS, --NO, --NO.sub.2, .dbd.N.sub.2, --N.sub.3,
NC(.dbd.O)R, --C(.dbd.O)R, --C(.dbd.O)NRR,
--S(.dbd.O).sub.2O.sup.-, --S(.dbd.O).sub.2OH, --S(.dbd.O).sub.2R,
--OS(.dbd.O).sub.2OR, --S(.dbd.O).sub.2NR, --S(.dbd.O)R,
--OP(.dbd.O)O.sub.2RR, --P(.dbd.O)O.sub.2RR,
--P(.dbd.O)(O.sup.-).sub.2, --P(.dbd.O)(OH).sub.2, --C(.dbd.O)R,
--C(.dbd.O)X, --C(S)R, --C(O)OR, --C(O)O.sup.-, --C(S)OR, --C(O)SR,
--C(S)SR, --C(O)NRR, --C(S)NRR, --C(NR)NRR, where each X is
independently a halogen: F, Cl, Br, or I; and each R is
independently --H, alkyl, aryl, heterocycle, protecting group or
prodrug moiety. Alkylene, alkenylene, and alkynylene groups may
also be similarly substituted.
[0050] "Heterocycle" as used herein includes by way of example and
not limitation these heterocycles described in Paquette, Leo A.;
Principles of Modern Heterocyclic Chemistry (W. A. Benjamin, New
York, 1968), particularly Chapters 1, 3, 4, 6, 7, and 9; The
Chemistry of Heterocyclic Compounds, A Series of Monographs" (John
Wiley & Sons, New York, 1950 to present), in particular Volumes
13, 14, 16, 19, and 28; and J. Am. Chem. Soc. (1960) 82:5566. In
one specific embodiment of the invention "heterocycle" includes a
"carbocycle" as defined herein, wherein one or more (e.g. 1, 2, 3,
or 4) carbon atoms have been replaced with a heteroatom (e.g. O, N,
or S).
[0051] Examples of heterocycles include by way of example and not
limitation pyridyl, dihydroypyridyl, tetrahydropyridyl (piperidyl),
thiazolyl, tetrahydrothiophenyl, sulfur oxidized
tetrahydrothiophenyl, pyrimidinyl, furanyl, thienyl, pyrrolyl,
pyrazolyl, imidazolyl, tetrazolyl, benzofuranyl, thianaphthalenyl,
indolyl, indolenyl, quinolinyl, isoquinolinyl, benzimidazolyl,
piperidinyl, 4-piperidonyl, pyrrolidinyl, 2-pyrrolidonyl,
pyrrolinyl, tetrahydrofuranyl, tetrahydroquinolinyl,
tetrahydroisoquinolinyl, decahydroquinolinyl,
octahydroisoquinolinyl, azocinyl, triazinyl, 6H-1,2,5-thiadiazinyl,
2H,6H-1,5,2-dithiazinyl, thienyl, thianthrenyl, pyranyl,
isobenzofuranyl, chromenyl, xanthenyl, phenoxathinyl, 2H-pyrrolyl,
isothiazolyl, isoxazolyl, pyrazinyl, pyridazinyl, indolizinyl,
isoindolyl, 3H-indolyl, 1H-indazoly, purinyl, 4H-quinolizinyl,
phthalazinyl, naphthyridinyl, quinoxalinyl, quinazolinyl,
cinnolinyl, pteridinyl, 4aH-carbazolyl, carbazolyl,
.beta.-carbolinyl, phenanthridinyl, acridinyl, pyrimidinyl,
phenanthrolinyl, phenazinyl, phenothiazinyl, furazanyl,
phenoxazinyl, isochromanyl, chromanyl, imidazolidinyl,
imidazolinyl, pyrazolidinyl, pyrazolinyl, piperazinyl, indolinyl,
isoindolinyl, quinuclidinyl, morpholinyl, oxazolidinyl,
benzotriazolyl, benzisoxazolyl, oxindolyl, benzoxazolinyl,
isatinoyl, and bis-tetrahydrofuranyl:
##STR00004##
[0052] By way of example and not limitation, carbon bonded
heterocycles are bonded at position 2, 3, 4, 5, or 6 of a pyridine,
position 3, 4, 5, or 6 of a pyridazine, position 2, 4, 5, or 6 of a
pyrimidine, position 2, 3, 5, or 6 of a pyrazine, position 2, 3, 4,
or 5 of a furan, tetrahydrofuran, thiofuran, thiophene, pyrrole or
tetrahydropyrrole, position 2, 4, or 5 of an oxazole, imidazole or
thiazole, position 3, 4, or 5 of an isoxazole, pyrazole, or
isothiazole, position 2 or 3 of an aziridine, position 2, 3, or 4
of an azetidine, position 2, 3, 4, 5, 6, 7, or 8 of a quinoline or
position 1, 3, 4, 5, 6, 7, or 8 of an isoquinoline. Still more
typically, carbon bonded heterocycles include 2-pyridyl, 3-pyridyl,
4-pyridyl, 5-pyridyl, 6-pyridyl, 3-pyridazinyl, 4-pyridazinyl,
5-pyridazinyl, 6-pyridazinyl, 2-pyrimidinyl, 4-pyrimidinyl,
5-pyrimidinyl, 6-pyrimidinyl, 2-pyrazinyl, 3-pyrazinyl,
5-pyrazinyl, 6-pyrazinyl, 2-thiazolyl, 4-thiazolyl, or
5-thiazolyl.
[0053] By way of example and not limitation, nitrogen bonded
heterocycles are bonded at position 1 of an aziridine, azetidine,
pyrrole, pyrrolidine, 2-pyrroline, 3-pyrroline, imidazole,
imidazolidine, 2-imidazoline, 3-imidazoline, pyrazole, pyrazoline,
2-pyrazoline, 3-pyrazoline, piperidine, piperazine, indole,
indoline, 1H-indazole, position 2 of a isoindole, or isoindoline,
position 4 of a morpholine, and position 9 of a carbazole, or
.beta.-carboline. Still more typically, nitrogen bonded
heterocycles include 1-aziridyl, 1-azetedyl, 1-pyrrolyl,
1-imidazolyl, 1-pyrazolyl, and 1-piperidinyl.
[0054] "Carbocycle" refers to a saturated, unsaturated or aromatic
ring having 3 to 7 carbon atoms as a monocycle, 7 to 12 carbon
atoms as a bicycle, and up to about 20 carbon atoms as a polycycle.
Monocyclic carbocycles have 3 to 6 ring atoms, still more typically
5 or 6 ring atoms. Bicyclic carbocycles have 7 to 12 ring atoms,
e.g., arranged as a bicyclo [4,5], [5,5], [5,6] or [6,6] system, or
9 or 10 ring atoms arranged as a bicyclo [5,6] or [6,6] system.
Examples of monocyclic carbocycles include cyclopropyl, cyclobutyl,
cyclopentyl, 1-cyclopent-1-enyl, 1-cyclopent-2-enyl,
1-cyclopent-3-enyl, cyclohexyl, 1-cyclohex-1-enyl,
1-cyclohex-2-enyl, 1-cyclohex-3-enyl, phenyl, spiryl and
naphthyl.
[0055] The term "chiral" refers to molecules which have the
property of non-superimposability of the mirror image partner,
while the term "achiral" refers to molecules which are
superimposable on their mirror image partner.
[0056] The term "stereoisomers" refers to compounds which have
identical chemical constitution, but differ with regard to the
arrangement of the atoms or groups in space.
[0057] "Diastereomer" refers to a stereoisomer with two or more
centers of chirality and whose molecules are not mirror images of
one another. Diastereomers have different physical properties,
e.g., melting points, boiling points, spectral properties, and
reactivities. Mixtures of diastereomers may separate under high
resolution analytical procedures such as electrophoresis and
chromatography.
[0058] "Enantiomers" refer to two stereoisomers of a compound which
are non-superimposable mirror images of one another.
[0059] The term "treatment" or "treating," to the extent it relates
to a disease or condition includes preventing the disease or
condition from occurring, inhibiting the disease or condition,
eliminating the disease or condition, and/or relieving one or more
symptoms of the disease or condition.
[0060] Stereochemical definitions and conventions used herein
generally follow S. P. Parker, Ed., McGraw-Hill Dictionary of
Chemical Terms (1984) McGraw-Hill Book Company, New York; and
Eliel, E. and Wilen, S., Stereochemistry of Organic Compounds
(1994) John Wiley & Sons, Inc., New York. Many organic
compounds exist in optically active forms, i.e., they have the
ability to rotate the plane of plane-polarized light. In describing
an optically active compound, the prefixes D and L or R and S are
used to denote the absolute configuration of the molecule about its
chiral center(s). The prefixes d and l or (+) and (-) are employed
to designate the sign of rotation of plane-polarized light by the
compound, with (-) or l meaning that the compound is levorotatory.
A compound prefixed with (+) or d is dextrorotatory. For a given
chemical structure, these stereoisomers are identical except that
they are mirror images of one another. A specific stereoisomer may
also be referred to as an enantiomer, and a mixture of such isomers
is often called an enantiomeric mixture. A 50:50 mixture of
enantiomers is referred to as a racemic mixture or a racemate,
which may occur where there has been no stereoselection or
stereospecificity in a chemical reaction or process. The terms
"racemic mixture" and "racemate" refer to an equimolar mixture of
two enantiomeric species, devoid of optical activity.
Protecting Groups
[0061] In the context of the present invention, protecting groups
include prodrug moieties and chemical protecting groups.
[0062] Protecting groups are available, commonly known and used,
and are optionally used to prevent side reactions with the
protected group during synthetic procedures, i.e. routes or methods
to prepare the compounds of the invention. For the most part the
decision as to which groups to protect, when to do so, and the
nature of the chemical protecting group "PG" will be dependent upon
the chemistry of the reaction to be protected against (e.g.,
acidic, basic, oxidative, reductive or other conditions) and the
intended direction of the synthesis. The PG groups do not need to
be, and generally are not, the same if the compound is substituted
with multiple PG. In general, PG will be used to protect functional
groups such as carboxyl, hydroxyl, thio, or amino groups and to
thus prevent side reactions or to otherwise facilitate the
synthetic efficiency. The order of deprotection to yield free,
deprotected groups is dependent upon the intended direction of the
synthesis and the reaction conditions to be encountered, and may
occur in any order as determined by the artisan.
[0063] Various functional groups of the compounds of the invention
may be protected. For example, protecting groups for --OH groups
(whether hydroxyl, carboxylic acid, phosphonic acid, or other
functions) include "ether- or ester-forming groups". Ether- or
ester-forming groups are capable of functioning as chemical
protecting groups in the synthetic schemes set forth herein.
However, some hydroxyl and thio protecting groups are neither
ether- nor ester-forming groups, as will be understood by those
skilled in the art, and are included with amides, discussed
below.
[0064] A very large number of hydroxyl protecting groups and
amide-forming groups and corresponding chemical cleavage reactions
are described in Protective Groups in Organic Synthesis, Theodora
W. Greene (John Wiley & Sons, Inc., New York, 1991, ISBN
0-471-62301-6) ("Greene"). See also Kocienski, Philip J.;
Protecting Groups (Georg Thieme Verlag Stuttgart, New York, 1994),
which is incorporated by reference in its entirety herein. In
particular Chapter 1, Protecting Groups: An Overview, pages 1-20,
Chapter 2, Hydroxyl Protecting Groups, pages 21-94, Chapter 3, Diol
Protecting Groups, pages 95-117, Chapter 4, Carboxyl Protecting
Groups, pages 118-154, Chapter 5, Carbonyl Protecting Groups, pages
155-184. For protecting groups for carboxylic acid, phosphonic
acid, phosphonate, sulfonic acid and other protecting groups for
acids see Greene as set forth below. Such groups include by way of
example and not limitation, esters, amides, hydrazides, and the
like. Another set of protecting groups include any of the typical
amino protecting groups described by Greene at pages 315-385.
Specific Embodiments of the Invention
[0065] Specific values described for radicals, substituents, and
ranges, as well as specific embodiments of the invention described
herein, are for illustration only; they do not exclude other
defined values or other values within defined ranges.
[0066] For a compound of Formula I, in one specific embodiment,
C.sub.1-C.sub.8 substituted alkyl, C.sub.1-C.sub.8 substituted
alkenyl, C.sub.1-C.sub.8 substituted alkynyl, C.sub.6-C.sub.20
substituted aryl, and C.sub.2-C.sub.20 substituted heterocycle are
independently substituted with one or more substituents selected
from F, Cl, Br, I, OH, --NH.sub.2, --NH.sub.3.sup.+, --NHR,
--NR.sub.2, --NR.sub.3.sup.+, C.sub.1-C.sub.8 alkylhalide,
carboxylate, sulfate, sulfamate, sulfonate, 5-7 membered ring
sultam, C.sub.1-C.sub.8 alkylsulfonate, C.sub.1-C.sub.8 alkylamino,
4-dialkylaminopyridinium, C.sub.1-C.sub.8 alkylhydroxyl,
C.sub.1-C.sub.8 alkylthiol, --SO.sub.2R, --SO.sub.2Ar, --SOAr,
--SAr, --SO.sub.2NR.sub.2, --SOR, --CO.sub.2R, --C(.dbd.O)NR.sub.2,
5-7 membered ring lactam, 5-7 membered ring lactone, --CN,
--N.sub.3, --NO.sub.2, C.sub.1-C.sub.8 alkoxy, C.sub.1-C.sub.8
trifluoroalkyl, C.sub.1-C.sub.8 alkyl, C.sub.3-C.sub.12 carbocycle,
C.sub.6-C.sub.20 aryl, C.sub.2-C.sub.20 heterocycle,
polyethyleneoxy, phosphonate, phosphate, and a prodrug moiety.
[0067] For a compound of Formula I, in one specific embodiment,
"protecting group" is selected from a carboxyl ester, a
carboxamide, an aryl ether, an alkyl ether, a trialkylsilyl ether,
a sulfonic acid ester, a carbonate, and a carbamate.
Antiviral Compounds
[0068] The compounds of the invention include those with antiviral
activity.
[0069] Typically, compounds of the invention have a molecular
weight of from about 200 amu to about 10,000 amu; in a specific
embodiment of the invention, compounds have a molecular weight of
less than about 5000 amu; in another specific embodiment of the
invention, compounds have a molecular weight of less than about
2500 amu; in another specific embodiment of the invention,
compounds have a molecular weight of less than about 1000 amu; in
another specific embodiment of the invention, compounds have a
molecular weight of less than about 800 amu; in another specific
embodiment of the invention, compounds have a molecular weight of
less than about 600 amu; and in another specific embodiment of the
invention, compounds have a molecular weight of less than about 400
amu and a molecular weight of greater than about 200 amu.
[0070] The compounds of the invention also typically have a logD
(polarity) less than about 5. In one embodiment the invention
provides compounds having a logD less than about 4; in another one
embodiment the invention provides compounds having a logD less than
about 3; in another one embodiment the invention provides compounds
having a logD greater than about -5; in another one embodiment the
invention provides compounds having a logD greater than about -3;
and in another one embodiment the invention provides compounds
having a logD greater than about 0 and less than about 3.
[0071] Selected substituents within the compounds of the invention
are present to a recursive degree. In this context, "recursive
substituent" means that a substituent may recite another instance
of itself. Because of the recursive nature of such substituents,
theoretically, a large number may be present in any given claim.
For example, R.sup.x contains a R.sup.y substituent. R.sup.y can be
R.sup.2, which in turn can be R.sup.3. If R.sup.3 is selected to be
R.sup.3c, then a second instance of R.sup.x can be selected. One of
ordinary skill in the art of medicinal chemistry understands that
the total number of such substituents is reasonably limited by the
desired properties of the compound intended. Such properties
include, by of example and not limitation, physical properties such
as molecular weight, solubility or log P, application properties
such as activity against the intended target, and practical
properties such as ease of synthesis.
[0072] Whenever a compound described herein is substituted with
more than one of the same designated group, it will be understood
that the groups may be the same or different, i.e., each group is
independently selected. Wavy lines indicate the site of covalent
bond attachments to the adjoining groups, moieties, or atoms.
Stereoisomers
[0073] The compounds of the invention may have chiral centers. The
compounds of the invention thus include racemic mixtures of all
stereoisomers, including enantiomers, diastereomers, and
atropisomers. In addition, the compounds of the invention include
enriched or resolved optical isomers at any or all asymmetric,
chiral atoms. In other words, the chiral centers apparent from the
depictions are provided as the chiral isomers or racemic mixtures.
Both racemic and diastereomeric mixtures, as well as the individual
optical isomers isolated or synthesized, substantially free of
their enantiomeric or diastereomeric partners, are all within the
scope of the invention. The racemic mixtures are separated into
their individual, substantially optically pure isomers through
well-known techniques such as, for example, the separation of
diastereomeric salts formed with optically active adjuncts, e.g.,
acids or bases followed by conversion back to the optically active
substances. In most instances, the desired optical isomer is
synthesized by means of stereospecific reactions, beginning with
the appropriate stereoisomer of the desired starting material.
[0074] The compounds of the invention can also exist as tautomeric
isomers in certain cases. All though only one delocalized resonance
structure may be depicted, all such forms are contemplated within
the scope of the invention. For example, ene-amine tautomers can
exist for purine, pyrimidine, imidazole, guanidine, amidine, and
tetrazole systems and all their possible tautomeric forms are
within the scope of the invention.
Salts and Hydrates
[0075] The compositions of this invention optionally comprise salts
of the compounds herein, especially pharmaceutically acceptable
non-toxic salts containing, for example, Na.sup.+, Li.sup.+,
K.sup.+, Ca.sup.+2 and Mg.sup.+2. Such salts may include those
derived by combination of appropriate cations such as alkali and
alkaline earth metal ions or ammonium and quaternary amino ions
with an acid anion moiety, typically a carboxylic acid. Monovalent
salts are preferred if a water soluble salt is desired.
[0076] Metal salts typically are prepared by reacting the metal
hydroxide with a compound of this invention. Examples of metal
salts which are prepared in this way are salts containing Li.sup.+,
Na.sup.+, and K.sup.+. A less soluble metal salt can be
precipitated from the solution of a more soluble salt by addition
of the suitable metal compound.
[0077] In addition, salts may be formed from acid addition of
certain organic and inorganic acids, e.g., HCl, HBr,
H.sub.2SO.sub.4, H.sub.3PO.sub.4 or organic sulfonic acids, to
basic centers, typically amines, or to acidic groups. Finally, it
is to be understood that the compositions herein comprise compounds
of the invention in their un-ionized, as well as zwitterionic form,
and combinations with stoichiometric amounts of water as in
hydrates.
[0078] Also included within the scope of this invention are the
salts of the parental compounds with one or more amino acids. Any
of the amino acids described above are suitable, especially the
naturally-occurring amino acids found as protein components,
although the amino acid typically is one bearing a side chain with
a basic or acidic group, e.g., lysine, arginine or glutamic acid,
or a neutral group such as glycine, serine, threonine, alanine,
isoleucine, or leucine.
Methods of Inhibition of Viral Infections
[0079] Another aspect of the invention relates to methods of
inhibiting viral infections, comprising the step of treating a
sample or subject suspected of needing such inhibition with a
composition of the invention.
[0080] Compositions of the invention may act as inhibitors of viral
infections, or as intermediates for such inhibitors or have other
utilities as described below. The inhibitors will bind to locations
on the surface or in a cavity of a cell having a unique geometry.
Compositions binding a cell may bind with varying degrees of
reversibility. Those compounds binding substantially irreversibly
are ideal candidates for use in this method of the invention. Once
labeled, the substantially irreversibly binding compositions are
useful as probes for the detection of viruses. Accordingly, the
invention relates to methods of detecting viruses in a sample or
subject suspected of containing a virus, comprising the steps of:
treating such a sample or subject with a composition comprising a
compound of the invention bound to a label; and observing the
effect of the sample on the activity of the label. Suitable labels
are well known in the diagnostics field and include stable free
radicals, fluorophores, radioisotopes, enzymes, chemiluminescent
groups and chromogens. The compounds herein are labeled in
conventional fashion using functional groups such as hydroxyl or
amino.
[0081] Within the context of the invention samples suspected of
containing a virus include natural or man-made materials such as
living organisms; tissue or cell cultures; biological samples such
as biological material samples (blood, serum, urine, cerebrospinal
fluid, tears, sputum, saliva, tissue samples, and the like);
laboratory samples; food, water, or air samples; bioproduct samples
such as extracts of cells, particularly recombinant cells
synthesizing a desired glycoprotein; and the like. Typically the
sample will be suspected of containing an organism which induces a
viral infection, frequently a pathogenic organism such as an tumor
virus. Samples can be contained in any medium including water and
organic solvent\water mixtures. Samples include living organisms
such as humans, and man made materials such as cell cultures.
[0082] The treating step of the invention comprises adding the
composition of the invention to the sample or it comprises adding a
precursor of the composition to the sample. The addition step
comprises any method of administration as described above.
[0083] If desired, the anti-virus activity of a compound of the
invention after application of the composition can be observed by
any method including direct and indirect methods of detecting such
activity. Quantitative, qualitative, and semiquantitative methods
of determining such activity are all contemplated. Typically one of
the screening methods described above are applied, however, any
other method such as observation of the physiological properties of
a living organism are also applicable.
Screens for Antiviral Compounds
[0084] Compositions of the invention are screened for antiviral
activity by any of the conventional techniques for evaluating
enzyme activity. Within the context of the invention, typically
compositions are first screened for inhibitory activity in vitro
and compositions showing inhibitory activity are then screened for
activity in vivo. Compositions having in vitro Ki (inhibitory
constants) of less then about 5.times.10.sup.-6 M, typically less
than about 1.times.10.sup.-7 M and preferably less than about
5.times.10.sup.-8 M are preferred for in vivo use.
[0085] Useful in vitro screens have been described in detail and
will not be elaborated here.
Pharmaceutical Formulations
[0086] The compounds of this invention are formulated with
conventional carriers and excipients, which will be selected in
accord with ordinary practice. Tablets will contain excipients,
glidants, fillers, binders and the like. Aqueous formulations are
prepared in sterile form, and when intended for delivery by other
than oral administration generally will be isotonic. All
formulations will optionally contain excipients such as those set
forth in the Handbook of Pharmaceutical Excipients (1986).
Excipients include ascorbic acid and other antioxidants, chelating
agents such as EDTA, carbohydrates such as dextrin,
hydroxyalkylcellulose, hydroxyalkylmethylcellulose, stearic acid
and the like. The pH of the formulations ranges from about 3 to
about 11, but is ordinarily about 7 to 10.
[0087] While it is possible for the active ingredients to be
administered alone it may be preferable to present them as
pharmaceutical formulations. The formulations, both for veterinary
and for human use, of the invention comprise at least one active
ingredient, as above defined, together with one or more acceptable
carriers therefor and optionally other therapeutic ingredients. The
carrier(s) must be "acceptable" in the sense of being compatible
with the other ingredients of the formulation and physiologically
innocuous to the recipient thereof.
[0088] The formulations include those suitable for the foregoing
administration routes. The formulations may conveniently be
presented in unit dosage form and may be prepared by any of the
methods well known in the art of pharmacy. Techniques and
formulations generally are found in Remington's Pharmaceutical
Sciences (Mack Publishing Co., Easton, Pa.). Such methods include
the step of bringing into association the active ingredient with
the carrier which constitutes one or more accessory ingredients. In
general the formulations are prepared by uniformly and intimately
bringing into association the active ingredient with liquid
carriers or finely divided solid carriers or both, and then, if
necessary, shaping the product.
[0089] Formulations of the present invention suitable for oral
administration may be presented as discrete units such as capsules,
cachets or tablets each containing a predetermined amount of the
active ingredient; as a powder or granules; as a solution or a
suspension in an aqueous or non-aqueous liquid; or as an
oil-in-water liquid emulsion or a water-in-oil liquid emulsion. The
active ingredient may also be administered as a bolus, electuary or
paste.
[0090] A tablet is made by compression or molding, optionally with
one or more accessory ingredients. Compressed tablets may be
prepared by compressing in a suitable machine the active ingredient
in a free-flowing form such as a powder or granules, optionally
mixed with a binder, lubricant, inert diluent, preservative,
surface active or dispersing agent. Molded tablets may be made by
molding in a suitable machine a mixture of the powdered active
ingredient moistened with an inert liquid diluent. The tablets may
optionally be coated or scored and optionally are formulated so as
to provide slow or controlled release of the active ingredient
therefrom.
[0091] For administration to the eye or other external tissues
e.g., mouth and skin, the formulations are preferably applied as a
topical ointment or cream containing the active ingredient(s) in an
amount of, for example, 0.075 to 20% w/w (including active
ingredient(s) in a range between 0.1% and 20% in increments of 0.1%
w/w such as 0.6% w/w, 0.7% w/w, etc.), preferably 0.2 to 15% w/w
and most preferably 0.5 to 10% w/w. When formulated in an ointment,
the active ingredients may be employed with either a paraffinic or
a water-miscible ointment base. Alternatively, the active
ingredients may be formulated in a cream with an oil-in-water cream
base.
[0092] If desired, the aqueous phase of the cream base may include,
for example, at least 30% w/w of a polyhydric alcohol, i.e. an
alcohol having two or more hydroxyl groups such as propylene
glycol, butane 1,3-diol, mannitol, sorbitol, glycerol and
polyethylene glycol (including PEG 400) and mixtures thereof. The
topical formulations may desirably include a compound which
enhances absorption or penetration of the active ingredient through
the skin or other affected areas. Examples of such dermal
penetration enhancers include dimethyl sulphoxide and related
analogs.
[0093] The oily phase of the emulsions of this invention may be
constituted from known ingredients in a known manner. While the
phase may comprise merely an emulsifier (otherwise known as an
emulgent), it desirably comprises a mixture of at least one
emulsifier with a fat or an oil or with both a fat and an oil.
Preferably, a hydrophilic emulsifier is included together with a
lipophilic emulsifier which acts as a stabilizer. It is also
preferred to include both an oil and a fat. Together, the
emulsifier(s) with or without stabilizer(s) make up the so-called
emulsifying wax, and the wax together with the oil and fat make up
the so-called emulsifying ointment base which forms the oily
dispersed phase of the cream formulations.
[0094] Emulgents and emulsion stabilizers suitable for use in the
formulation of the invention include Tween.RTM. 60, Span.RTM. 80,
cetostearyl alcohol, benzyl alcohol, myristyl alcohol, glyceryl
mono-stearate and sodium lauryl sulfate.
[0095] The choice of suitable oils or fats for the formulation is
based on achieving the desired cosmetic properties. The cream
should preferably be a non-greasy, non-staining and washable
product with suitable consistency to avoid leakage from tubes or
other containers. Straight or branched chain, mono- or dibasic
alkyl esters such as di-isoadipate, isocetyl stearate, propylene
glycol diester of coconut fatty acids, isopropyl myristate, decyl
oleate, isopropyl palmitate, butyl stearate, 2-ethylhexyl palmitate
or a blend of branched chain esters known as Crodamol CAP may be
used, the last three being preferred esters. These may be used
alone or in combination depending on the properties required.
Alternatively, high melting point lipids such as white soft
paraffin and/or liquid paraffin or other mineral oils are used.
[0096] Pharmaceutical formulations according to the present
invention comprise one or more compounds of the invention together
with one or more pharmaceutically acceptable carriers or excipients
and optionally other therapeutic agents. Pharmaceutical
formulations containing the active ingredient may be in any form
suitable for the intended method of administration. When used for
oral use for example, tablets, troches, lozenges, aqueous or oil
suspensions, dispersible powders or granules, emulsions, hard or
soft capsules, syrups or elixirs may be prepared. 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 including
sweetening agents, flavoring agents, coloring agents and preserving
agents, in order to provide a palatable preparation. Tablets
containing the active ingredient in admixture with non-toxic
pharmaceutically acceptable excipient which are suitable for
manufacture of tablets are acceptable. These excipients may be, for
example, inert diluents, such as calcium or sodium carbonate,
lactose, lactose monohydrate, croscarmellose sodium, povidone,
calcium or sodium phosphate; granulating and disintegrating agents,
such as maize starch, or alginic acid; binding agents, such as
cellulose, microcrystalline cellulose, starch, gelatin or acacia;
and lubricating agents, such as magnesium stearate, stearic acid or
talc. Tablets may be uncoated or may be coated by known techniques
including microencapsulation to delay disintegration and adsorption
in the gastrointestinal tract and thereby provide a sustained
action over a longer period. For example, a time delay material
such as glyceryl monostearate or glyceryl distearate alone or with
a wax may be employed.
[0097] Formulations for oral use may be also presented as hard
gelatin capsules where the active ingredient is mixed with an inert
solid diluent, for example calcium phosphate or kaolin, or as soft
gelatin capsules wherein the active ingredient is mixed with water
or an oil medium, such as peanut oil, liquid paraffin or olive
oil.
[0098] Aqueous suspensions of the invention contain the active
materials in admixture with excipients suitable for the manufacture
of aqueous suspensions. Such excipients include a suspending agent,
such as sodium carboxymethylcellulose, methylcellulose,
hydroxypropyl methylcelluose, sodium alginate,
polyvinylpyrrolidone, gum tragacanth and gum acacia, and dispersing
or wetting agents such as a naturally occurring phosphatide (e.g.,
lecithin), a condensation product of an alkylene oxide with a fatty
acid (e.g., polyoxyethylene stearate), a condensation product of
ethylene oxide with a long chain aliphatic alcohol (e.g.,
heptadecaethyleneoxycetanol), a condensation product of ethylene
oxide with a partial ester derived from a fatty acid and a hexitol
anhydride (e.g., polyoxyethylene sorbitan monooleate). The aqueous
suspension may also contain one or more preservatives such as ethyl
or n-propyl p-hydroxy-benzoate, one or more coloring agents, one or
more flavoring agents and one or more sweetening agents, such as
sucrose or saccharin.
[0099] Oil suspensions may be formulated by suspending the active
ingredient in a vegetable oil, such as arachis oil, olive oil,
sesame oil or coconut oil, or in a mineral oil such as liquid
paraffin. The oral suspensions may contain a thickening agent, such
as 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. These compositions may be
preserved by the addition of an antioxidant such as ascorbic
acid.
[0100] Dispersible powders and granules of the invention suitable
for preparation of an aqueous suspension by the addition of water
provide the active ingredient in admixture with a dispersing or
wetting agent, a suspending agent, and one or more preservatives.
Suitable dispersing or wetting agents and suspending agents are
exemplified by those disclosed above. Additional excipients, for
example sweetening, flavoring and coloring agents, may also be
present.
[0101] The pharmaceutical compositions of the invention may also be
in the form of oil-in-water emulsions. The oily phase may be a
vegetable oil, such as olive oil or arachis oil, a mineral oil,
such as liquid paraffin, or a mixture of these. Suitable
emulsifying agents include naturally-occurring gums, such as gum
acacia and gum tragacanth, naturally occurring phosphatides, such
as soybean lecithin, esters or partial esters derived from fatty
acids and hexitol anhydrides, such as sorbitan monooleate, and
condensation products of these partial esters with ethylene oxide,
such as polyoxyethylene sorbitan monooleate. The emulsion may also
contain sweetening and flavoring agents. Syrups and elixirs may be
formulated with sweetening agents, such as glycerol, sorbitol or
sucrose. Such formulations may also contain a demulcent, a
preservative, a flavoring or a coloring agent.
[0102] The pharmaceutical compositions of the invention may be in
the form of a sterile injectable preparation, such as a sterile
injectable aqueous or oleaginous suspension. This suspension may be
formulated according to the known art using those suitable
dispersing or wetting agents and suspending agents which have been
mentioned above. The sterile injectable preparation may also be a
sterile injectable solution or suspension in a non-toxic
parenterally acceptable diluent or solvent, such as a solution in
1,3-butane-diol or prepared as a lyophilized powder. Among the
acceptable vehicles and solvents that may be employed are water,
Ringer's solution and isotonic sodium chloride solution. In
addition, sterile fixed oils may conventionally be employed as a
solvent or suspending medium. For this purpose any bland fixed oil
may be employed including synthetic mono- or diglycerides. In
addition, fatty acids such as oleic acid may likewise be used in
the preparation of injectables.
[0103] The amount of active ingredient that may be combined with
the carrier material to produce a single dosage form will vary
depending upon the host treated and the particular mode of
administration. For example, a time-release formulation intended
for oral administration to humans may contain approximately 1 to
1000 mg of active material compounded with an appropriate and
convenient amount of carrier material which may vary from about 5
to about 95% of the total compositions (weight:weight). The
pharmaceutical composition can be prepared to provide easily
measurable amounts for administration. For example, an aqueous
solution intended for intravenous infusion may contain from about 3
to 500 .mu.g of the active ingredient per milliliter of solution in
order that infusion of a suitable volume at a rate of about 30
mL/hr can occur.
[0104] Formulations suitable for administration to the eye include
eye drops wherein the active ingredient is dissolved or suspended
in a suitable carrier, especially an aqueous solvent for the active
ingredient. The active ingredient is preferably present in such
formulations in a concentration of 0.5 to 20%, advantageously 0.5
to 10% particularly about 1.5% w/w.
[0105] Formulations suitable for topical administration in the
mouth include lozenges comprising the active ingredient in a
flavored basis, usually sucrose and acacia or tragacanth; pastilles
comprising the active ingredient in an inert basis such as gelatin
and glycerin, or sucrose and acacia; and mouthwashes comprising the
active ingredient in a suitable liquid carrier.
[0106] Formulations for rectal administration may be presented as a
suppository with a suitable base comprising for example cocoa
butter or a salicylate.
[0107] Formulations suitable for intrapulmonary or nasal
administration have a particle size for example in the range of 0.1
to 500 microns (including particle sizes in a range between 0.1 and
500 microns in increments microns such as 0.5, 1, 30 microns, 35
microns, etc.), which is administered by rapid inhalation through
the nasal passage or by inhalation through the mouth so as to reach
the alveolar sacs. Suitable formulations include aqueous or oily
solutions of the active ingredient. Formulations suitable for
aerosol or dry powder administration may be prepared according to
conventional methods and may be delivered with other therapeutic
agents such as compounds heretofore used in the treatment or
prophylaxis of viral infections as described below.
[0108] Formulations suitable for vaginal administration may be
presented as pessaries, tampons, creams, gels, pastes, foams or
spray formulations containing in addition to the active ingredient
such carriers as are known in the art to be appropriate.
[0109] Formulations suitable for parenteral administration include
aqueous and non-aqueous sterile injection solutions which may
contain anti-oxidants, buffers, bacteriostats and solutes which
render the formulation isotonic with the blood of the intended
recipient; and aqueous and non-aqueous sterile suspensions which
may include suspending agents and thickening agents.
[0110] The formulations are presented in unit-dose or multi-dose
containers, for example sealed ampoules and vials, and may be
stored in a freeze-dried (lyophilized) condition requiring only the
addition of the sterile liquid carrier, for example water for
injection, immediately prior to use. Extemporaneous injection
solutions and suspensions are prepared from sterile powders,
granules and tablets of the kind previously described. Preferred
unit dosage formulations are those containing a daily dose or unit
daily sub-dose, as herein above recited, or an appropriate fraction
thereof, of the active ingredient.
[0111] It should be understood that in addition to the ingredients
particularly mentioned above the formulations of this invention may
include other agents conventional in the art having regard to the
type of formulation in question, for example those suitable for
oral administration may include flavoring agents.
[0112] The invention further provides veterinary compositions
comprising at least one active ingredient as above defined together
with a veterinary carrier therefor.
[0113] Veterinary carriers are materials useful for the purpose of
administering the composition and may be solid, liquid or gaseous
materials which are otherwise inert or acceptable in the veterinary
art and are compatible with the active ingredient. These veterinary
compositions may be administered orally, parenterally or by any
other desired route.
[0114] Compounds of the invention can also be formulated to provide
controlled release of the active ingredient to allow less frequent
dosing or to improve the pharmacokinetic or toxicity profile of the
active ingredient. Accordingly, the invention also provided
compositions comprising one or more compounds of the invention
formulated for sustained or controlled release.
[0115] Effective dose of active ingredient depends at least on the
nature of the condition being treated, toxicity, whether the
compound is being used prophylactically (lower doses) or against an
active viral infection, the method of delivery, and the
pharmaceutical formulation, and will be determined by the clinician
using conventional dose escalation studies. It can be expected to
be from about 0.0001 to about 100 mg/kg body weight per day.
Typically, from about 0.01 to about 10 mg/kg body weight per day.
More typically, from about 0.01 to about 5 mg/kg body weight per
day. More typically, from about 0.05 to about 0.5 mg/kg body weight
per day. For example, the daily candidate dose for an adult human
of approximately 70 kg body weight will range from 1 mg to 1000 mg,
preferably between 5 mg and 500 mg, and may take the form of single
or multiple doses.
Routes of Administration
[0116] One or more compounds of the invention (herein referred to
as the active ingredients) are administered by any route
appropriate to the condition to be treated. Suitable routes include
oral, rectal, nasal, topical (including buccal and sublingual),
vaginal and parenteral (including subcutaneous, intramuscular,
intravenous, intradermal, intrathecal and epidural), and the like.
It will be appreciated that the preferred route may vary with for
example the condition of the recipient. An advantage of the
compounds of this invention is that they are orally bioavailable
and can be dosed orally.
Combination Therapy
[0117] Active ingredients of the invention can also be used in
combination with other therapeutic agents (i.e. active
ingredients). Such combinations are selected based on the condition
to be treated, cross-reactivities of ingredients and
pharmaco-properties of the combination. For example, when treating
a viral infection the compositions of the invention can be combined
with other therapeutic agents that are effective to treat a viral
infection (such as other antiviral agents) or they can be combined
with other therapeutic agents that are effective to ameliorate
symptoms associated with a viral infection.
[0118] It is also possible to combine any compound of the invention
with one or more other active ingredients in a unitary dosage form
for simultaneous or sequential administration to a patient. The
combination therapy may be administered as a simultaneous or
sequential regimen. When administered sequentially, the combination
may be administered in two or more administrations.
[0119] The combination therapy may provide "synergy" and
"synergistic effect", i.e. the effect achieved when the active
ingredients used together is greater than the sum of the effects
that results from using the compounds separately. A synergistic
effect may be attained when the active ingredients are: (1)
co-formulated and administered or delivered simultaneously in a
combined formulation; (2) delivered by alternation or in parallel
as separate formulations; or (3) by some other regimen. When
delivered in alternation therapy, a synergistic effect may be
attained when the compounds are administered or delivered
sequentially, e.g., in separate tablets, pills or capsules, or by
different injections in separate syringes. In general, during
alternation therapy, an effective dosage of each active ingredient
is administered sequentially, i.e. serially, whereas in combination
therapy, effective dosages of two or more active ingredients are
administered together.
Metabolites of the Compounds of the Invention
[0120] Also falling within the scope of this invention are the in
vivo metabolic products of the compounds described herein. Such
products may result for example from the oxidation, reduction,
hydrolysis, amidation, esterification and the like of the
administered compound, primarily due to enzymatic processes.
Accordingly, the invention includes compounds produced by a process
comprising contacting a compound of this invention with a mammal
for a period of time sufficient to yield a metabolic product
thereof. Such products typically are identified by preparing a
radiolabelled (e.g., C.sup.14 or H.sup.3) compound of the
invention, administering it parenterally in a detectable dose
(e.g., greater than about 0.5 mg/kg) to an animal such as rat,
mouse, guinea pig, monkey, or to man, allowing sufficient time for
metabolism to occur (typically about 30 seconds to 30 hours) and
isolating its conversion products from the urine, blood or other
biological samples. These products are easily isolated since they
are labeled (others are isolated by the use of antibodies capable
of binding epitopes surviving in the metabolite). The metabolite
structures are determined in conventional fashion, e.g., by MS or
NMR analysis. In general, analysis of metabolites is done in the
same way as conventional drug metabolism studies well-known to
those skilled in the art. The conversion products, so long as they
are not otherwise found in vivo, are useful in diagnostic assays
for therapeutic dosing of the compounds of the invention even if
they possess no antiviral activity of their own.
[0121] Recipes and methods for determining stability of compounds
in surrogate gastrointestinal secretions are known. Compounds are
defined herein as stable in the gastrointestinal tract where less
than about 50 mole percent of the protected groups are deprotected
in surrogate intestinal or gastric juice upon incubation for 1 hour
at 37.degree. C. Simply because the compounds are stable to the
gastrointestinal tract does not mean that they cannot be hydrolyzed
in vivo. The phosphonate prodrugs of the invention typically will
be stable in the digestive system but are substantially hydrolyzed
to the parental drug in the digestive lumen, liver or other
metabolic organ, or within cells in general.
Antiviral Activity and Cytotoxicity
[0122] The antiviral activity and cytotoxicity of a compound of the
invention can be measured using standard screening protocols that
are known. For example, the antiviral activity of a compound can be
measured in a cell culture assay using the following general
protocol.
[0123] Antiviral Cell Culture Assay
[0124] The assay is based on quantification of the antiviral effect
by a colorimetric detection of the viability of virus-infected
cells in the presence or absence of tested inhibitors. The
compound-induced cell death is determined using a metabolic
substrate
2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide
(XTT) which is converted only by intact cells into a product with
specific absorption characteristics as described by Weislow O S,
Kiser R, Fine D L, Bader J, Shoemaker R H and Boyd M R (1989) J
Natl Cancer Inst 81, 577.
[0125] Assay Protocol for Determination of EC50: [0126] 1. Maintain
MT2 cells in RPMI-1640 medium supplemented with 5% fetal bovine
serum and antibiotics. [0127] 2. Infect the cells with the viral
agent for 3 hours at 37.degree. C. using the virus inoculum
corresponding to a multiplicity of infection equal to 0.01. [0128]
3. Distribute the infected cells into a 96-well plate (20,000 cells
in 100 .mu.l/well) and add various concentrations of the tested
inhibitor in triplicate (100 .mu.l/well in culture media). Include
untreated infected and untreated mock-infected control cells.
[0129] 4. Incubate the cells for 5 days at 37.degree. C. [0130] 5.
Prepare a compound solution (6 ml per assay plate) at a
concentration of 2 mg/ml in a phosphate-buffered saline pH 7.4.
Heat the solution in water-bath for 5 min at 55.degree. C. Add 50
.mu.l of N-methylphenazonium methasulfate (5 .mu.g/ml) per 6 ml of
XTT solution. [0131] 6. Remove 100 .mu.l media from each well on
the assay plate. [0132] 7. Add 100 .mu.l of the XTT substrate
solution per well and incubate at 37.degree. C. for 45 to 60 min in
a CO.sub.2 incubator. [0133] 8. Add 20 .mu.l of 2% Triton X-100 per
well to inactivate the virus. [0134] 9. Read the absorbance at 450
nm with subtracting off the background absorbance at 650 nm. [0135]
10. Plot the percentage absorbance relative to untreated control
and estimate the EC50 value as drug concentration resulting in a
50% protection of the infected cells.
[0136] Cytotoxicity Cell Culture Assay (Determination of CC50):
[0137] The cytotoxicity of a compound of the invention can be
determined using the following general protocol. The assay is based
on the evaluation of cytotoxic effect of tested compounds using a
metabolic substrate.
Assay Protocol for Determination of CC50:
[0138] 1. Maintain MT-2 cells in RPMI-1640 medium supplemented with
5% fetal bovine serum and antibiotics. [0139] 2. Distribute the
cells into a 96-well plate (20,000 cell in 100 .mu.l media per
well) and add various concentrations of the tested compound in
triplicate (100 .mu.l/well). Include untreated control. [0140] 3.
Incubate the cells for 5 days at 37.degree. C. [0141] 4. Prepare
XTT solution (6 ml per assay plate) in dark at a concentration of 2
mg/ml in a phosphate-buffered saline pH 7.4. Heat the solution in a
water-bath at 55.degree. C. for 5 min. Add 50 .mu.l of
N-methylphenazonium methasulfate (5 .mu.g/ml) per 6 ml of XTT
solution. [0142] 5. Remove 100 .mu.l media from each well on the
assay plate and add 100 .mu.l of the XTT substrate solution per
well. Incubate at 37.degree. C. for 45 to 60 min in a CO.sub.2
incubator. [0143] 6. Add 20 .mu.l of 2% Triton X-100 per well to
stop the metabolic conversion of XTT. [0144] 7. Read the absorbance
at 450 nm with subtracting off the background at 650 nm. [0145] 8.
Plot the percentage absorbance relative to untreated control and
estimate the CC50 value as drug concentration resulting in a 50%
inhibition of the cell growth. Consider the absorbance being
directly proportional to the cell growth.
Exemplary Methods of Making the Compounds of the Invention
[0146] The invention also relates to methods of making the
compounds of the invention. The compounds are prepared by any of
the applicable techniques of organic synthesis. Many such
techniques are well known in the art. However, many of the known
techniques are elaborated in Compendium of Organic Synthetic
Methods (John Wiley & Sons, New York), Vol. 1, Ian T. Harrison
and Shuyen Harrison, 1971; Vol. 2, Ian T. Harrison and Shuyen
Harrison, 1974; Vol. 3, Louis S. Hegedus and Leroy Wade, 1977; Vol.
4, Leroy G. Wade, jr., 1980; Vol. 5, Leroy G. Wade, Jr., 1984; and
Vol. 6, Michael B. Smith; as well as March, J., Advanced Organic
Chemistry, Third Edition, (John Wiley & Sons, New York, 1985),
Comprehensive Organic Synthesis, Selectivity, Strategy &
Efficiency in Modern Organic Chemistry. In 9 Volumes, Barry M.
Trost, Editor-in-Chief (Pergamon Press, New York, 1993
printing).
[0147] A number of exemplary methods for the preparation of the
compounds of the invention are provided below. These methods are
intended to illustrate the nature of such preparations are not
intended to limit the scope of applicable methods.
[0148] Generally, the reaction conditions such as temperature,
reaction time, solvents, work-up procedures, and the like, will be
those common in the art for the particular reaction to be
performed. The cited reference material, together with material
cited therein, contains detailed descriptions of such conditions.
Typically the temperatures will be -100.degree. C. to 200.degree.
C., solvents will be aprotic or protic, and reaction times will be
10 seconds to 10 days. Work-up typically consists of quenching any
unreacted reagents followed by partition between a water/organic
layer system (extraction) and separating the layer containing the
product.
[0149] Oxidation and reduction reactions are typically carried out
at temperatures near room temperature (about 20.degree. C.),
although for metal hydride reductions frequently the temperature is
reduced to 0.degree. C. to -100.degree. C., solvents are typically
aprotic for reductions and may be either protic or aprotic for
oxidations. Reaction times are adjusted to achieve desired
conversions.
[0150] Condensation reactions are typically carried out at
temperatures near room temperature, although for non-equilibrating,
kinetically controlled condensations reduced temperatures
(0.degree. C. to -100.degree. C.) are also common. Solvents can be
either protic (common in equilibrating reactions) or aprotic
(common in kinetically controlled reactions).
[0151] Standard synthetic techniques such as azeotropic removal of
reaction by-products and use of anhydrous reaction conditions
(e.g., inert gas environments) are common in the art and will be
applied when applicable.
Schemes and Examples
[0152] General aspects of these exemplary methods are described
below and in the Examples. Each of the products of the following
processes is optionally separated, isolated, and/or purified prior
to its use in subsequent processes.
[0153] The terms "treated", "treating", "treatment", and the like,
when used in connection with a chemical synthetic operation, mean
contacting, mixing, reacting, allowing to react, bringing into
contact, and other terms common in the art for indicating that one
or more chemical entities is treated in such a manner as to convert
it to one or more other chemical entities. This means that
"treating compound one with compound two" is synonymous with
"allowing compound one to react with compound two", "contacting
compound one with compound two", "reacting compound one with
compound two", and other expressions common in the art of organic
synthesis for reasonably indicating that compound one was
"treated", "reacted", "allowed to react", etc., with compound two.
For example, treating indicates the reasonable and usual manner in
which organic chemicals are allowed to react. Normal concentrations
(0.01M to 10M, typically 0.1M to 1M), temperatures (-100.degree. C.
to 250.degree. C., typically -78.degree. C. to 150.degree. C., more
typically -78.degree. C. to 100.degree. C., still more typically
0.degree. C. to 100.degree. C.), reaction vessels (typically glass,
plastic, metal), solvents, pressures, atmospheres (typically air
for oxygen and water insensitive reactions or nitrogen or argon for
oxygen or water sensitive), etc., are intended unless otherwise
indicated. The knowledge of similar reactions known in the art of
organic synthesis are used in selecting the conditions and
apparatus for "treating" in a given process. In particular, one of
ordinary skill in the art of organic synthesis selects conditions
and apparatus reasonably expected to successfully carry out the
chemical reactions of the described processes based on the
knowledge in the art.
[0154] Modifications of each of the exemplary schemes and in the
examples (hereafter "exemplary schemes") leads to various analogs
of the specific exemplary materials produce. The above-cited
citations describing suitable methods of organic synthesis are
applicable to such modifications.
[0155] In each of the exemplary schemes it may be advantageous to
separate reaction products from one another and/or from starting
materials. The desired products of each step or series of steps is
separated and/or purified (hereinafter separated) to the desired
degree of homogeneity by the techniques common in the art.
Typically such separations involve multiphase extraction,
crystallization from a solvent or solvent mixture, distillation,
sublimation, or chromatography. Chromatography can involve any
number of methods including, for example: reverse-phase and normal
phase; size exclusion; ion exchange; high, medium, and low pressure
liquid chromatography methods and apparatus; small scale
analytical; simulated moving bed (SMB) and preparative thin or
thick layer chromatography, as well as techniques of small scale
thin layer and flash chromatography.
[0156] Another class of separation methods involves treatment of a
mixture with a reagent selected to bind to or render otherwise
separable a desired product, unreacted starting material, reaction
by product, or the like. Such reagents include adsorbents or
absorbents such as activated carbon, molecular sieves, ion exchange
media, or the like. Alternatively, the reagents can be acids in the
case of a basic material, bases in the case of an acidic material,
binding reagents such as antibodies, binding proteins, selective
chelators such as crown ethers, liquid/liquid ion extraction
reagents (LIX), or the like.
[0157] Selection of appropriate methods of separation depends on
the nature of the materials involved. For example, boiling point,
and molecular weight in distillation and sublimation, presence or
absence of polar functional groups in chromatography, stability of
materials in acidic and basic media in multiphase extraction, and
the like. One skilled in the art will apply techniques most likely
to achieve the desired separation.
[0158] A single stereoisomer, e.g., an enantiomer, substantially
free of its stereoisomer may be obtained by resolution of the
racemic mixture using a method such as formation of diastereomers
using optically active resolving agents (Stereochemistry of Carbon
Compounds, (1962) by E. L. Eliel, McGraw Hill; Lochmuller, C. H.,
(1975) J. Chromatogr., 113:(3) 283-302). Racemic mixtures of chiral
compounds of the invention can be separated and isolated by any
suitable method, including: (1) formation of ionic, diastereomeric
salts with chiral compounds and separation by fractional
crystallization or other methods, (2) formation of diastereomeric
compounds with chiral derivatizing reagents, separation of the
diastereomers, and conversion to the pure stereoisomers, and (3)
separation of the substantially pure or enriched stereoisomers
directly under chiral conditions.
[0159] Under method (1), diastereomeric salts can be formed by
reaction of enantiomerically pure chiral bases such as brucine,
quinine, ephedrine, strychnine,
.alpha.-methyl-.beta.-phenylethylamine (amphetamine), and the like
with asymmetric compounds bearing acidic functionality, such as
carboxylic acid and sulfonic acid. The diastereomeric salts may be
induced to separate by fractional crystallization or ionic
chromatography. For separation of the optical isomers of amino
compounds, addition of chiral carboxylic or sulfonic acids, such as
camphorsulfonic acid, tartaric acid, mandelic acid, or lactic acid
can result in formation of the diastereomeric salts.
[0160] Alternatively, by method (2), the substrate to be resolved
is reacted with one enantiomer of a chiral compound to form a
diastereomeric pair (Eliel, E. and Wilen, S. (1994) Stereochemistry
of Organic Compounds, John Wiley & Sons, Inc., p. 322).
Diastereomeric compounds can be formed by reacting asymmetric
compounds with enantiomerically pure chiral derivatizing reagents,
such as menthyl derivatives, followed by separation of the
diastereomers and hydrolysis to yield the free, enantiomerically
enriched xanthene. A method of determining optical purity involves
making chiral esters, such as a menthyl ester, e.g., (-) menthyl
chloroformate in the presence of base, or Mosher ester,
.alpha.-methoxy-.alpha.-(trifluoromethyl)phenyl acetate (Jacob III.
(1982) J. Org. Chem. 47:4165), of the racemic mixture, and
analyzing the NMR spectrum for the presence of the two
atropisomeric diastereomers. Stable diastereomers of atropisomeric
compounds can be separated and isolated by normal- and
reverse-phase chromatography following methods for separation of
atropisomeric naphthyl-isoquinolines (Hoye, T., WO 96/15111). By
method (3), aracemic mixture of two enantiomers can be separated by
chromatography using a chiral stationary phase (Chiral Liquid
Chromatography (1989) W. J. Lough, Ed. Chapman and Hall, New York;
Okamoto, (1990) J. of Chromatogr. 513:375-378). Enriched or
purified enantiomers can be distinguished by methods used to
distinguish other chiral molecules with asymmetric carbon atoms,
such as optical rotation and circular dichroism.
EXAMPLES GENERAL SECTION
[0161] A number of exemplary methods for the preparation of
compounds of the invention are provided herein, for example, in the
Examples hereinbelow. These methods are intended to illustrate the
nature of such preparations and are not intended to limit the scope
of applicable methods. Certain compounds of the invention can be
used as intermediates for the preparation of other compounds of the
invention.
[0162] The invention will now be illustrated by the following
non-limiting Examples.
Example 1
Preparation of a Representative Compound of the Invention
##STR00005##
[0164] The intermediate epoxide 1.11 can be prepared as follows.
Selective iodination of carbovir 1.8 (Crimmins, M. T. et al., J.
Org. Chem., 1996, 61, 4192) at the 5'-position using
triphenylphosphine, iodine, and either pyridine or imidazole in
dioxane (Maag, H. et al., J. Med. Chem., 1992, 35, 1440) provides
compound 1.9. Dehydrohalogenation of 5'-halonucleosides has been
well-described (Ueda, T. In Chemistry of Nucleosides and
Nucleotides; Townsend, L. B., Ed.; Plenum Press; New York, 1988;
83). Use of sodium methoxide provides product 1.10. Epoxidation of
the exocyclic olefin using m-chloroperbenzoic acid or Corey's
reagent (dimethylsulfoxonium methylide) (Gololobov, Y. G. et al.,
Tetrahedron, 1997, 43, 12, 2609) proceeds without stereoselection
to provide a mixture of two diastereomeric epoxides 1.11.
[0165] A representative compound of the invention 1 can be prepared
from the epoxides 1.11 as illustrated below.
##STR00006##
[0166] The mixture of diastereomers can be opened using
ethynyl-trimethyl-silane in the presence of titanium acetylide at
the more highly substituted carbon atom exclusively as reported by
Krause, N. et al., Chem. Ber., 1988, 121, 7, 1315 to provide the
desired product 1.
[0167] Compound 1.12 from the epoxidation reaction can readily be
converted to the related diastereomer using the four step sequence
illustrated below. The epoxide 1.12 is opened using basic condition
such as sodium hydroxide in water and DMSO (Lepage, O. et al., J.
Org. Chem., 2003, 68, 6, 2183) to provide a diol. The primary
alcohol is then protected with a silyl group and the 3' alcohol is
converted into a leaving group (such as a mesylate). Release of the
silyl group followed by exposure of the primary alcohol to base
leads to ring closure to form the diastereomer 1.15.
##STR00007##
Example 2
Preparation of a Representative Compound of the Invention
##STR00008## ##STR00009##
[0169] Abacavir 2.8 can be prepared from compound 1.7 as described
by Crimmins, M. T. et al., J. Org. Chem., 1996, 61, 4192. Selective
iodination at the 5'-position using triphenylphosphine, iodine, and
either pyridine or imidazole in dioxane (Maag, H. et al., J. Med.
Chem., 1992, 35, 1440) provides compound 2.9. Dehydrohalogenation
of 5'-halonucleosides has been well-described (Ueda, T. In
Chemistry of Nucleosides and Nucleotides; Townsend, L. B., Ed.;
Plenum Press; New York, 1988; 83). Use of sodium methoxide proceeds
to generate compound 2.10. Epoxidation of the exocyclic olefin of
2.10 proceeds without a stereoselection to provide a mixture of two
diastereomers. Such reactions may be performed using
m-chloroperbenzoic acid or Corey's reagent (dimethylsulfoxonium
methylide) (Gololobov, Y. G. et al., Tetrahedron, 1997, 43, 12,
2609). The mixture of diastereomers can be opened using
ethynyl-trimethyl-silane in the presence of titanium acetylide at
the more highly substituted carbon atom exclusively as reported by
Krause, N. et al., Chem. Ber., 1988, 121, 7, 1315 to provide the
desired product 2.
[0170] The same reaction scheme can be used to prepare 4' cyano and
azido analogs of carbovir and abacavir. In order to prepare the 4'
ethylene analog, a reduction of the acetylene to ethylene can be
performed (for an example see Shinjiro, S., et al., Org. Lett.,
2003, 5, 11, 1891).
[0171] All literature and patent citations above are hereby
expressly incorporated by reference at the locations of their
citation. Specifically cited sections or pages of the above cited
works are incorporated by reference with specificity. The invention
has been described in detail sufficient to allow one of ordinary
skill in the art to make and use the subject matter of the
following Embodiments. It is apparent that certain modifications of
the methods and compositions of the following Embodiments can be
made within the scope and spirit of the invention.
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