U.S. patent application number 16/449131 was filed with the patent office on 2020-10-15 for withanolides useful for the treatment of neurodegenerative diseases.
The applicant listed for this patent is ImStar Therapeutics Inc., Universite Laval. Invention is credited to Agnes H. Chan, Jean-Pierre Julien, Anthony A. Shaw.
Application Number | 20200325168 16/449131 |
Document ID | / |
Family ID | 1000005117837 |
Filed Date | 2020-10-15 |
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United States Patent
Application |
20200325168 |
Kind Code |
A9 |
Shaw; Anthony A. ; et
al. |
October 15, 2020 |
WITHANOLIDES USEFUL FOR THE TREATMENT OF NEURODEGENERATIVE
DISEASES
Abstract
Provided herein are synthetic analogs of withanolide natural
products and their pharmaceutical uses in treating
neurodegenerative diseases.
Inventors: |
Shaw; Anthony A.;
(Vancouver, CA) ; Julien; Jean-Pierre; (Quebec
City, CA) ; Chan; Agnes H.; (Vancouver, CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
ImStar Therapeutics Inc.
Universite Laval |
Vancouver
Quebec City |
|
CA
CA |
|
|
Prior
Publication: |
|
Document Identifier |
Publication Date |
|
US 20190315798 A1 |
October 17, 2019 |
|
|
Family ID: |
1000005117837 |
Appl. No.: |
16/449131 |
Filed: |
June 21, 2019 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
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15038927 |
May 24, 2016 |
10351590 |
|
|
PCT/US14/67436 |
Nov 25, 2014 |
|
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16449131 |
|
|
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61908455 |
Nov 25, 2013 |
|
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C07J 71/001
20130101 |
International
Class: |
C07J 71/00 20060101
C07J071/00 |
Claims
1. A method of treating or preventing a neurodegenerative disease
in a patient, the method comprising: administering to the patient a
therapeutically or prophylactically effective amount of a compound
Formula (I): ##STR00008## wherein: R.sup.1 is hydrogen, alkyl,
alkenyl, haloalkyl, aralkyl, heterocyclylalkyl,
--R.sup.a--OR.sup.b, --C(O)R.sup.b, cycloalkylalkyl or
--P(O).sub.2O.sup.2-; R.sup.2 is hydrogen, alkyl, alkenyl,
haloalkyl, --OR.sup.b or --OC(O)R.sup.b; R.sup.3 is hydrogen,
alkyl, alkenyl, haloalkyl, aralkyl, heterocyclylalkyl,
--R.sup.a--OR.sup.b, --C(O)R.sup.b, cycloalkylalkyl or
--P(O).sub.2O.sup.2-; R.sup.4 is hydrogen, alkyl, alkenyl,
haloalkyl, --OR.sup.b or --OC(O)R.sup.b; R.sup.a is an alkylene or
alkenylene chain; and R.sup.b is hydrogen, alkyl, alkenyl,
haloalkyl, aralkyl, cycloalkylalkyl or heterocyclylalkyl, as an
isolated stereoisomer or mixture thereof, or a pharmaceutically
acceptable salt thereof, provided that, when R.sup.2 and R.sup.4
are each hydrogen, R.sup.1 and R.sup.3 cannot both be selected from
the group consisting of hydrogen and --C(O)CH.sub.3; or when
R.sup.1 and R.sup.3 are each --C(O)CH.sub.3, R.sup.2 or R.sup.4
cannot both be selected from the group consisting of hydrogen and
--OC(O)CH.sub.3.
2. The method of claim 1, wherein R.sup.1 and R.sup.3 are each
independently lower alkyl or alkenyl.
3. The method of claim 2 wherein R.sup.1 and R.sup.3 are
independently methyl.
4. The method of claim 1, wherein R.sup.2 and R.sup.4 are each
hydrogens, and the compound has a structure represented by Formula
(Ia): ##STR00009## wherein: R.sup.1 is hydrogen, alkyl or alkenyl;
and R.sup.3 is hydrogen, alkyl or alkenyl.
5. The method of claim 4 wherein R.sup.1 is methyl and R.sup.3 is
hydrogen.
6. The method of claim 4 wherein R.sup.1 is hydrogen and R.sup.3 is
methyl.
7. The method of claim 4 wherein R.sup.1 is methyl and R.sup.3 is
methyl.
8. The method of claim 1 wherein the neurodegenerative disease is
characterized by TDP-43 proteinopathy.
9. The method of claim 1 wherein the neurodegenerative disease is
amyotrophic lateral sclerosis, Alzheimer's disease, Parkinson's
disease, or frontotemporal lobar degeneration.
10. A method of treating or preventing a disease characterized by
TDP-43 proteinopathy in a patient comprising administering to the
patient a therapeutically or prophylactically effective amount of a
compound Formula (I): ##STR00010## wherein: R.sup.1 is hydrogen,
alkyl, alkenyl, haloalkyl, aralkyl, heterocyclylalkyl,
--R.sup.a--OR.sup.b, --C(O)R.sup.b, cycloalkylalkyl or
--P(O).sub.2O.sup.2-; R.sup.2 is hydrogen, alkyl, alkenyl,
haloalkyl, --OR.sup.b or --OC(O)R.sup.b; R.sup.3 is hydrogen,
alkyl, alkenyl, haloalkyl, aralkyl, heterocyclylalkyl,
--R.sup.a--OR.sup.b, --C(O)R.sup.b, cycloalkylalkyl or
--P(O).sub.2O.sup.2-; R.sup.4 is hydrogen, alkyl, alkenyl,
haloalkyl, --OR.sup.b or --OC(O)R.sup.b; R.sup.a is an alkylene or
alkenylene chain; and R.sup.b is hydrogen, alkyl, alkenyl,
haloalkyl, aralkyl, cycloalkylalkyl or heterocyclylalkyl, as an
isolated stereoisomer or mixture thereof, or a pharmaceutically
acceptable salt thereof, provided that, when R.sup.2 and R.sup.4
are each hydrogen, R.sup.1 and R.sup.3 cannot both be selected from
the group consisting of hydrogen and --C(O)CH.sub.3; or when
R.sup.1 and R.sup.3 are each --C(O)CH.sub.3, R.sup.2 or R.sup.4
cannot both be selected from the group consisting of hydrogen and
--OC(O)CH.sub.3.
11. The method of claim 10, wherein R.sup.1 and R.sup.3 are each
independently lower alkyl or alkenyl.
12. The method of claim 11 wherein R.sup.1 and R.sup.3 are
independently methyl.
13. The method of claim 10, wherein R.sup.2 and R.sup.4 are each
hydrogens, and the compound has a structure represented by Formula
(Ia): ##STR00011## wherein: R.sup.1 is hydrogen, alkyl or alkenyl;
and R.sup.3 is hydrogen, alkyl or alkenyl.
14. The method of claim 13 wherein R.sup.1 is methyl and R.sup.3 is
hydrogen.
15. The method of claim 13 wherein R.sup.1 is hydrogen and R.sup.3
is methyl.
16. The method of claim 13 wherein R.sup.1 is methyl and R.sup.3 is
methyl.
17. The method of claim 10 wherein the disease characterized by
TDP-43 proteinopathy is amyotrophic lateral sclerosis, Alzheimer's
disease, Parkinson's disease, or frontotemporal lobar degeneration.
Description
CROSS-REFERENCE TO RELATED APPLICATION
[0001] This application is a divisional of U.S. application Ser.
No. 15/038,927, filed May 24, 2016 (now allowed), which is a 371
national phase application of International Application No.
PCT/US2014/067436 filed Nov. 25, 2014, which claims the benefit
under 35 U.S.C. .sctn. 119(e) of U.S. Provisional Patent
Application No. 61/908,455 filed Nov. 25, 2013, which applications
are incorporated herein by reference in their entirety.
BACKGROUND
Technical Field
[0002] This application relates to synthetic analogs of withanolide
natural products and their pharmaceutical uses.
Description of the Related Art
[0003] Neurodegenerative diseases are characterized by selective
neurodegeneration in specific regions of the brain and spinal cord.
Amyotrophic Lateral Sclerosis (ALS), commonly known as "Lou
Gehrig's disease", is a progressive neurodegenerative disease of
unknown etiology. The disease progressively impairs an individual's
ability to control voluntary muscle movement. The disease tends to
progress rapidly, leading to paralysis and death within 2-5 years
of diagnosis in most cases. There are currently few therapeutic
options for patients suffering from ALS. The only FDA approved drug
for the treatment of ALS is Rilutek.RTM., introduced in 1995, which
extends life expectancy in individuals with ALS for a few
months.
[0004] A number of hypotheses have been advanced concerning the
pathogenesis of ALS. One is that glutamate, the most abundant
excitatory neurotransmitter in the central nervous system (CNS),
causes neuronal cell death when its levels are chronically
elevated. Glutamate levels have been shown to be elevated in ALS
patients (A. Platitakis and J. T. Caroscio, Ann. Neurol. 1987, 22:
5575-579). Oxidative stress is another area of focus in ALS
research. The potential importance of antioxidant dysfunction was
triggered by the discovery that superoxide dismutase (SOD)1
mutations are associated with the familial form of ALS (D. R. Rosen
et al., 1993, Nature, 362: 59-62) which account for about 20% of
cases. An autoimmune mechanism is another potential ALS
pathogenesis (M. R. Pagani et al. Neurol. Res. Int., 2011,
2011:497080). Abnormal protein mis-folding and aggregation have
recently gained recognition as an underlying pathogenic mechanism
in ALS and several other neurodegenerative diseases. Intracellular
proteins that exhibit conformational mis-folding in ALS include
SOD1 and transactive response (TAR) DNA-binding protein-43
(TDP-43).
[0005] Several years ago it was demonstrated that abnormalities in
TDP-43, a highly-conserved nuclear protein, were closely associated
with ALS (T. Arai et al, 2006, Biochem. Biophys. Res. Commun., 351:
602-611). In healthy nerve cells, TDP-43 intracellular distribution
is restricted to the nuclear region. However, in ALS-affected
neuronal cells, TDP-43 was also prominently present within
cytoplasmic aggregates. Further, it was shown that
neuropathology-associated TDP-43 was atypically phosphorylated,
extensively ubiquitinated, and proteolytically cleaved to generate
carboxyl-terminus fragments in affected brain regions (M. Neumann
et al., 2006, Science 314:130-133). Thus, the modified TDP-43
accumulation patterns as well as intracellular processing
abnormalities were proposed as contributors to degenerative
neuronal cell changes in ALS. These and other abnormalities related
to TDP-43 are referred to herein as TDP-43 proteinopathies.
[0006] A relatively recent discovery related to TDP-43 has provided
fundamental insights into pathogenic mechanisms operative in ALS.
Studies performed at Laval University showed that TDP-43 was
unexpectedly associated with the p65 sub-unit of the nuclear
factor-.kappa.B (NF-.kappa.B) inflammation-regulating transcription
factor in spinal cord samples obtained from ALS patients (V. Swamp
et al., 2011, 1 Exp. Med., 208:2429-2447).
[0007] Activation of the NF-.kappa.B signalling pathway is
triggered by a number of stimuli including reactive oxygen species,
various pro-inflammatory cytokines including interleukin-1 (IL-1)
and tumor necrosis factory.alpha. (TNF.alpha.) as well as different
bacterial products (S. Vallabhapurapu and M. Karin, 2009, Annu.
Rev. Immunol., 27: 693-733; L. Verstrepen et al., 2008, Cell. Mol.
Life Sci. 65: 2964-29678). NF-.kappa.B activity is primarily
restrained by its physical interaction with inhibitory I.kappa.B
proteins. In resting cells, NF-.kappa.B is present as a latent,
inactive, I.kappa.B-bound complex in the cytoplasm. When a cell
receives a threshold level of one of these signals, NF-.kappa.B is
rapidly liberated from I.kappa.B, enters the nucleus and activates
transcription of specific genes, many of which encode
pro-inflammatory and immune-response regulatory proteins. Almost
all signals that trigger the NF-.kappa.B signalling pathway
converge on activation of a molecular complex that contains a
serine residue-specific I.kappa.B kinase (IKK) (M. Adli et al.,
2010, PLoS One, 5: e9428). In the classical NF-.kappa.B pathway,
activation of the IKK complex leads to phosphorylation mediated by
IKK.beta. of two specific serines near the N terminus of
I.kappa.B.alpha., which subsequently targets I.kappa.B.alpha. for
intracellular ubiquitination and degradation by the 26S proteasome
complex (Vallabhapurapu 2009 op cit.; M. Adli 2010 op cit.).
Activation of the NF-.kappa.B signalling pathway is generally a
transient cellular event and tightly regulated (Vallabhapurapu 2009
op cit).
[0008] TDP-43 and the p65 chain of NF-.kappa.B were shown to have
co-immunoprecipitated in cell culture systems, spinal cord extracts
from transgenic TDP-43 mice and spinal cord samples prepared from
post-mortem ALS patients, but not from matched control samples
(Swamp 2011 op. cit.). In mouse and human spinal cord samples, p65
tended to co-localize with TDP-43 in the nuclei of microglia,
astrocytes and neurons. TDP-43 mRNA levels were up-regulated by
2.5-fold while NF-.kappa.B mRNA was up-regulated by approximately
four-fold in ALS spinal cord samples as compared to control subject
material (Swamp 2011 op. cit.). Gel-shift assays confirmed that the
p65 chain of NF-.kappa.B p65 was more likely to bind to its
consensus sequence of reporter DNA in the presence of TDP-43.
Further, TDP-43 over-expression boosted production of
pro-inflammatory cytokines, which heightened neuronal
susceptibility to neurotoxic elements. Deletion mutation
protein-mapping studies revealed that TDP-43 interacted with the
p65 chain component of NF-.kappa.B through its N-terminal domain
and RNA recognition motif (RMM-1) (Swamp 2011 op. cit.).
NF-.kappa.B inhibition attenuated the vulnerability of cultured
neurons over-expressing TDP-43 to glutamate-induced or microglia
cell-mediated toxicity.
[0009] Pharmacological intervention with withaferin A (WA)
attenuated disease symptoms and ameliorated motor dysfunction in
TDP-43 transgenic mice. WA was shown to inhibit TNF.alpha. induced
activation of I.kappa.B kinase .beta. (IKK.beta.) via a
thioalkylation-sensitive redox mechanism (W. Vanden Berghe et al.,
2012, Biochem. Pharmacol., 84: 1282-12891). IKK.beta. Ser-181
hyperphosphorylation induced by WA led to inhibition of
I.kappa.B.alpha. phosphorylation and degradation which prevented
NF-.kappa.B translocation, NF-.kappa.B/DNA binding and gene
transcription (M. Kaileh et al., 2007, J. Biol. Chem., 282:
4253-4264).
[0010] Withaferin A (WA) was the first withanolide-type compound
isolated from leaves of the Withania somifera plant.
##STR00001##
This compound has been noted for its anti-inflammatory, anti-tumor,
anti-angiogenic and immuno-suppressive activities. WA is a member
of withanolides, which are generally described as a group of
naturally occurring C28-steroidal lactone triterpenoids built on an
intact or rearranged ergostane framework, in which C-22 and C-26
are appropriately oxidized to form a six-membered lactone ring (M.
H. Mirjalili et al., Molecules 2009, 14(7): 2373-2393). Numerous
analogs of WA have been purified from withanolide-containing plant
material, synthesized, or semi-synthetically prepared from the WA
starting material (U.S. Pub. No. 2011/0230551).
[0011] WA has been proposed as a treatment for neurodegenerative
diseases, such as ALS, frontotemporal lobar degeneration,
Parkinson's disease and Alzheimer's disease (WO2012/174666) and it
has been shown that WA is effective in ameliorating disease
progression in mouse models of ALS. An in vivo therapeutic effect
of WA through NF-.kappa.B inhibition has been demonstrated in four
recognized transgenic mouse models of ALS.
[0012] Although WA is a promising therapeutic agent for the
treatment of ALS and other neurodegenerative diseases, it has a
short half life when administered in vivo, as well as some
toxicity. Hence there is a need for novel compounds with improved
pharmacokinetic, bio-distribution and safety profiles.
BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS
[0013] FIG. 1A shows bioluminescense imaging of the brains of
GFAP-luciferase transgenic mice after exposure to
lipopolysaccharide (LPS) followed by treatment with saline or the
withanolide compounds 4-O-methyl WA or 27-O-methyl WA.
[0014] FIG. 1B is a bar graph showing the relative intensity of the
bioluminescense of the brain images from FIG. 1A.
[0015] FIG. 2 includes bar graphs showing the effect of different
concentration of withanolides 4-O-methyl WA, 27-O-methyl WA and 4,
27-O-dimethyl A on NF-.kappa.B reporter activity in BV2 microglial
cells stimulated with LPS.
[0016] FIG. 3 includes bar graphs showing the effect of different
concentrations of withanolides 4-O-methyl WA, 27-O-methyl WA and
4,27-O-dimethyl WA on the up-regulation of TNF-.alpha.-induced
signalling activity in the HEK.sup.293-NF-.kappa.B-luciferase
reporter cell line.
[0017] FIG. 4A shows the accelerating rotarod performance of TDP-43
A315T mice treated with vehicle, 4-O-Methyl WA or 27-O-Methyl WA
analogs over a 15 week period.
[0018] FIG. 4B shows the linear regression analysis of the data in
FIG. 4A.
SUMMARY
[0019] Described herein are semi-synthetic analogs of withaferin A
and methods for using the analogs for the prophylaxsis or treatment
of neurodegenerative diseases or conditions such as Amyotrophic
Lateral Sclerosis (ALS), frontotemporal lobar degeneration (FTLD),
Parkinson's disease, Alzheimer's disease and mild cognitive
impairment.
[0020] Accordingly, in one aspect, the invention is directed to
compounds of Formula (I):
##STR00002##
wherein:
[0021] R.sup.1 is hydrogen, alkyl, alkenyl, haloalkyl, aralkyl,
heterocyclylalkyl, --R.sup.a--OR.sup.b, --C(O)R.sup.b,
cycloalkylalkyl or --P(O).sub.2O.sup.2-; [0022] R.sup.2 is
hydrogen, alkyl, alkenyl, haloalkyl, --OR.sup.b or --OC(O)R.sup.b;
[0023] R.sup.3 is hydrogen, alkyl, alkenyl, haloalkyl, aralkyl,
heterocyclylalkyl, --R.sup.a--OR.sup.b, --C(O)R.sup.b,
cycloalkylalkyl or --P(O).sub.2O.sup.2-; [0024] R.sup.4 is
hydrogen, alkyl, alkenyl, haloalkyl, --OR.sup.b or --OC(O)R.sup.b;
[0025] R.sup.a is an alkylene or alkenylene chain; and [0026]
R.sup.b is hydrogen, alkyl, alkenyl, haloalkyl, aralkyl,
cycloalkylalkyl or heterocyclylalkyl, [0027] as an isolated
stereoisomer or mixture thereof, or a pharmaceutically acceptable
salt thereof, provided that, [0028] when R.sup.2 and R.sup.4 are
each hydrogen, R.sup.1 and R.sup.3 cannot both be selected from the
group consisting of hydrogen and --C(O)CH.sub.3; or [0029] when
R.sup.1 and R.sup.3 are each --C(O)CH.sub.3, R.sup.2 or R.sup.4
cannot both be selected from the group consisting of hydrogen and
--OC(O)CH.sub.3.
[0030] In some embodiments, the compounds are of formula (I)
wherein R.sup.2 and R.sup.4 are each hydrogens, and the compounds
have a structure represented by Formula (Ia):
##STR00003##
wherein: [0031] R.sup.1 is hydrogen, alkyl or alkenyl; and [0032]
R.sup.3 is hydrogen, alkyl or alkenyl.
[0033] In further embodiments, the compounds are:
27-O-methylwithaferin A (R.sup.1 is hydrogen and R.sup.3 is
methyl), 4-O-methylwithaferin A (R.sup.1 is methyl and R.sup.3 is
hydrogen), and 4,27-O-dimethylwithaferin A (R.sup.1 is methyl and
R.sup.3 is methyl).
[0034] Another aspect of the invention is directed to a
pharmaceutical composition comprising a compound of formula (I) or
formula (Ia) and a pharmaceutically acceptable excipient.
[0035] In another aspect, the invention is directed to a method of
treating or preventing a disease characterized by TDP-43
proteinopathy in a patient comprising administering to a patient in
need thereof a therapeutically or prophylactically effective amount
of a compound of formula (I) or formula (Ia).
[0036] In another aspect, the invention is directed to a method of
treating or preventing amyotrophic lateral sclerosis in a patient
comprising administering to a patient in need thereof a
therapeutically or prophylactically effective amount of a compound
of formula (I) or formula (Ia).
[0037] In a further aspect, the invention is directed to a method
of treating or preventing Alzheimer's disease in a patient
comprising administering to a patient in need thereof a
therapeutically or prophylactically effective amount of a compound
of formula (I) or formula (Ia).
[0038] In a further aspect, the invention is directed to a method
of treating or preventing Parkinson's disease in a patient
comprising administering to a patient in need thereof a
therapeutically or prophylactically effective amount of a compound
of a formula (I) or formula (Ia).
[0039] In another aspect, the invention is directed to method of
treating or preventing motor neuron disease in a patient comprising
administering to a patient in need thereof a therapeutically or
prophylactically effective amount of a compound of formula (I) or
formula (Ia).
[0040] In another aspect, the invention is directed to a method of
treating or preventing frontotemporal lobar degeneration in a
patient comprising administering to a patient in need thereof a
therapeutically or prophylactically effective amount of a compound
of formula (I) or formula (Ia).
[0041] In another aspect, the invention is directed to a method of
treating or preventing mild cognitive impairment or preventing the
development of Alzheimer's disease in a patient exhibiting mild
cognitive impairment comprising administering to a patient in need
thereof a therapeutically or prophylactically effective amount of a
compound of Formula (I) or Formula (Ia).
DETAILED DESCRIPTION
[0042] Disclosed herein are semi-synthetic analogs of Withaferin A
and their various pharmaceutical uses, particularly in treating
neurodegenerative diseases, including amyotrophic Lateral Sclerosis
(ALS), frontotemporal lobar degeneration (FTLD), Parkinson's
disease, mild cognitive impairment (MCI), Alzheimer's disease, and
diseases associated with TPD-43 proteinopathy. One embodiment
provides a compound of Formula (I):
##STR00004##
wherein: [0043] R.sup.1 is hydrogen, alkyl, alkenyl, haloalkyl,
aralkyl, heterocyclylalkyl, --R.sup.a--OR.sup.b, --C(O)R.sup.b,
cycloalkylalkyl or --P(O).sub.2O.sup.2-; [0044] R.sup.2 is
hydrogen, alkyl, alkenyl, haloalkyl, --OR.sup.b or --OC(O)R.sup.b;
[0045] R.sup.3 is hydrogen, alkyl, alkenyl, haloalkyl, aralkyl,
heterocyclylalkyl, --R.sup.a--OR.sup.b, --C(O)R.sup.b,
cycloalkylalkyl or --P(O).sub.2O.sup.2-; [0046] R.sup.4 is
hydrogen, alkyl, alkenyl, haloalkyl, --OR.sup.b or --OC(O)R.sup.b;
[0047] R.sup.a is an alkylene or alkenylene chain; and [0048]
R.sup.b is hydrogen, alkyl, alkenyl, haloalkyl, aralkyl,
cycloalkylalkyl or heterocyclylalkyl, [0049] as an isolated
stereoisomer or mixture thereof, or a pharmaceutically acceptable
salt thereof, provided that, [0050] when R.sup.2 and R.sup.4 are
each hydrogen, R.sup.1 and R.sup.3 cannot both be selected from the
group consisting of hydrogen and --C(O)CH.sub.3; or [0051] when
R.sup.1 and R.sup.3 are each --C(O)CH.sub.3, R.sup.2 or R.sup.4
cannot both be selected from the group consisting of hydrogen and
--OC(O)CH.sub.3.
[0052] In various embodiments, the compound of Formula (I)
comprises one or more alkyl ether moieties, in particular, at the
C-4, C-27 or both locations. In certain embodiments, Wand R.sup.3
are independently lower alkyl or alkenyl. In further embodiments,
R.sup.1 and R.sup.3 are independently methyl.
[0053] In various embodiments, R.sup.2 and R.sup.4 are each
hydrogens, and the compound of Formula (I) has a structure
represented by Formula (Ia):
##STR00005##
wherein: [0054] R.sup.1 is hydrogen, alkyl or alkenyl; and [0055]
R.sup.3 is hydrogen, alkyl or alkenyl.
[0056] In further embodiments, the compounds are:
27-O-methylwithaferin A (R.sup.1 is hydrogen and R.sup.3 is
methyl), 4-O-methylwithaferin A (R.sup.1 is methyl and R.sup.3 is
hydrogen), and 4,27-O-dimethylwithaferin A (R.sup.1 is methyl and
R.sup.3 is methyl)
[0057] Each individual compound disclosed in U.S. Pub. No.
2011/0230551 is expressly excluded from the scope of Formulae (I)
and (IIa).
[0058] Another embodiment provides a pharmaceutical composition
comprising a compound of Formula (I) or Formula (Ia), as defined
herein, and a pharmaceutically acceptable excipient.
[0059] Various embodiments further provide pharmaceutical use of
the compound of Formula (I) or (Ia). More specifically, the
pharmaceutical uses of the compound or composition comprising the
same include the treatment of neurodegenerative diseases, or
prevention of the progression or worsening of neurodegenerative
diseases. In particular, the neurodegenerative disease is
characterized by TDP-43 proteinopathy.
[0060] Thus, one embodiment provides a method of treating or
preventing a disease characterized by TDP-43 proteinopathy in a
patient comprising administering to a patient in need thereof a
therapeutically or prophylactically effective amount of a compound
of Formula (I) or Formula (Ia).
[0061] A further embodiment provides a method of treating or
preventing amyotrophic lateral sclerosis in a patient comprising
administering to a patient in need thereof a therapeutically or
prophylactically effective amount of a compound of Formula (I) or
Formula (Ia).
[0062] Another embodiment provides a method of treating or
preventing Alzheimer's disease in a patient comprising
administering to a patient in need thereof a therapeutically or
prophylactically effective amount of a compound of Formula (I) or
Formula (Ia).
[0063] Another embodiment provides a method of treating or
preventing Parkinson's disease in a patient comprising
administering to a patient in need thereof a therapeutically or
prophylactically effective amount of a compound of Formula (I) or
Formula (Ia).
[0064] Another embodiment provides a method of treating or
preventing motor neuron disease in a patient comprising
administering to a patient in need thereof a therapeutically or
prophylactically effective amount of a compound of Formula (I) or
Formula (Ia).
[0065] Another embodiment provides a method of treating or
preventing frontotemporal lobar degeneration in a patient
comprising administering to a patient in need thereof a
therapeutically or prophylactically effective amount of a compound
of Formula (I) or Formula (Ia).
[0066] Another embodiment provides a method of treating or
preventing mild cognitive impairment or preventing the development
of Alzheimer's disease in a patient exhibiting mild cognitive
impairment comprising administering to a patient in need thereof a
therapeutically or prophylactically effective amount of a compound
of Formula (I) or Formula (Ia).
Definitions
[0067] As used in the specification and appended claims, unless
specified to the contrary, the following terms have the meaning
indicated:
[0068] "Amino" refers to the --NH.sub.2 radical.
[0069] "Carboxy" refers to the --C(O)OH radical.
[0070] "Cyano" refers to the --CN radical.
[0071] "Nitro" refers to the --NO.sub.2 radical.
[0072] "Oxo" refers to the .dbd.O radical.
[0073] "Thioxo" refers to the .dbd.S radical.
[0074] "Alkyl" refers to a straight or branched hydrocarbon chain
radical consisting solely of carbon and hydrogen atoms, containing
no unsaturation, having from one to twelve carbon atoms, preferably
one to eight carbon atoms or one to six carbon atoms and which is
attached to the rest of the molecule by a single bond, for example,
methyl, ethyl, n-propyl, 1-methylethyl (iso-propyl), n-butyl,
n-pentyl, 1,1-dimethylethyl (t-butyl), 3-methylhexyl,
2-methylhexyl, and the like. For purposes of this invention, the
term "lower alkyl" refers to an alkyl radical having one to four
carbon atoms.
[0075] "Alkenyl" refers to a straight or branched hydrocarbon chain
radical consisting solely of carbon and hydrogen atoms, containing
at least one double bond, having from two to twelve carbon atoms,
preferably one to eight carbon atoms and which is attached to the
rest of the molecule by a single bond, for example, ethenyl,
prop-1-enyl, but-1-enyl, pent-1-enyl, penta-1,4-dienyl, and the
like.
[0076] "Alkylene chain" refers to a straight or branched divalent
hydrocarbon chain linking the rest of the molecule to a radical
group, consisting solely of carbon and hydrogen, containing no
unsaturation and having from one to twelve carbon atoms, for
example, methylene, ethylene, propylene, n-butylene, and the like.
The alkylene chain is attached to the rest of the molecule through
a single bond and to the radical group through a single bond. The
points of attachment of the alkylene chain to the rest of the
molecule and to the radical group can be through one carbon in the
alkylene chain or through any two carbons within the chain.
[0077] "Alkenylene chain" refers to a straight or branched divalent
hydrocarbon chain linking the rest of the molecule to a radical
group, consisting solely of carbon and hydrogen, containing at
least one double bond and having from two to twelve carbon atoms,
for example, ethenylene, propenylene, n-butenylene, and the like.
The alkenylene chain is attached to the rest of the molecule
through a double bond or a single bond and to the radical group
through a double bond or a single bond. The points of attachment of
the alkenylene chain to the rest of the molecule and to the radical
group can be through one carbon or any two carbons within the
chain.
[0078] "Aryl" refers to a hydrocarbon ring system radical
comprising hydrogen, 6 to 14 carbon atoms and at least one aromatic
ring. For purposes of this invention, the aryl radical may be a
monocyclic, bicyclic, or tricyclic system and which may include
spiro ring systems. An aryl radical is commonly, but not
necessarily, attached to the parent molecule via an aromatic ring
of the aryl radical. Aryl radicals include, but are not limited to,
aryl radicals derived from acenaphthylene, anthracene, azulene,
benzene, 6,7,8,9-tetrahydro-5H-benzo[7]annulene, fluorene,
as-indacene, s-indacene, indane, indene, naphthalene, phenalene,
and phenanthrene.
[0079] "Aralkyl" refers to a radical of the formula
--R.sub.a--R.sub.c where R.sub.a is an alkylene chain as defined
above and R.sub.c is one or more aryl radicals as defined above.
Examples of aralkyl include, without limitation, benzyl,
diphenylmethyl and the like.
[0080] "Cycloalkyl" refers to a stable non-aromatic monocyclic or
polycyclic hydrocarbon radical consisting solely of carbon and
hydrogen atoms, which includes fused, spiro or bridged ring
systems, having from three to fifteen carbon atoms, preferably
having from three to ten carbon atoms, more preferably from five to
seven carbons and which is saturated or unsaturated and attached to
the rest of the molecule by a single bond. For purposes of this
invention, a bridged ring system is a system wherein two
non-adjacent ring atoms thereof are connected through an atom or a
group of atoms, wherein the atom or the group of atoms are the
bridging element. Examples of cycloalkyl include, without
limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl,
cycloheptyl, and cyclooctyl. Polycyclic radicals include fused,
spiro or bridged cycloalkyl radicals, for example, C.sub.10
radicals such as adamantanyl (bridged) and decalinyl (fused), and
C.sub.7 radicals such as bicyclo[3.2.0]heptanyl (fused),
norbornanyl and norbornenyl (bridged), as well as substituted
polycyclic radicals, for example, substituted C.sub.7 radicals such
as 7,7-dimethylbicyclo[2.2.1]heptanyl (bridged), and the like.
[0081] "Cycloalkylalkyl" refers to a radical of the formula
--R.sub.aR.sub.d where R.sub.a is an alkylene chain as defined
above and R.sub.d is a cycloalkyl radical as defined above.
[0082] "Halo" refers to fluoro, chloro, bromo or iodo.
[0083] "Haloalkyl" refers to an alkyl radical, as defined above,
that is substituted by one or more halo radicals, as defined above,
for example, trifluoromethyl, difluoromethyl, trichloromethyl,
2,2,2-trifluoroethyl, 1-fluoromethyl-2-fluoroethyl,
3-bromo-2-fluoropropyl, 1-bromomethyl-2-bromoethyl, and the
like.
[0084] "Heterocyclyl" refers to a stable 3- to 18-membered
non-aromatic ring system radical which comprises one to twelve
carbon atoms and from one to six heteroatoms selected from the
group consisting of nitrogen, oxygen and sulfur. Unless stated
otherwise specifically in the specification, the heterocyclyl
radical may be a monocyclic, bicyclic, tricyclic or tetracyclic
ring system, which may include spiro or bridged ring systems; and
the nitrogen, carbon or sulfur atoms in the heterocyclyl radical
may be optionally oxidized; the nitrogen atom may be optionally
quaternized; and the heterocyclyl radical may be partially or fully
saturated. Examples of a bridged heterocyclyl include, but are not
limited to, azabicyclo[2.2.1]heptanyl, diazabicyclo[2.2.1]heptanyl,
diazabicyclo[2.2.2]octanyl, diazabicyclo[3.2.1]octanyl,
diazabicyclo[3.3.1]nonanyl, diazabicyclo[3.2.2]nonanyl and
oxazabicyclo[2.2.1]heptanyl. A "bridged N-heterocyclyl" is a
bridged heterocyclyl containing at least one nitrogen, but which
optionally contains up to four additional heteroatoms selected from
O, N and S. For purposes of this invention, a non-bridged ring
system is a system wherein no two non-adjacent ring atoms thereof
are connected through an atom or a group of atoms. Examples of
heterocyclyl radicals include, but are not limited to, dioxolanyl,
1,4-diazepanyl, decahydroisoquinolyl, imidazolinyl, imidazolidinyl,
isothiazolidinyl, isoxazolidinyl, morpholinyl, octahydroindolyl,
octahydroisoindolyl, octahydro-1H-pyrrolo[3,2-c]pyridinyl,
octahydro-1H-pyrrolo[2,3-c]pyridinyl,
octahydro-1H-pyrrolo[2,3-b]pyridinyl,
octahydro-1H-pyrrolo[3,4-b]pyridinyl,
octahydropyrrolo[3,4-c]pyrrolyl,
octahydro-1H-pyrido[1,2-a]pyrazinyl, 2-oxopiperazinyl,
2-oxopiperidinyl, 2-oxopyrrolidinyl, oxazolidinyl,
3,7-diazabicyclo[3.3.1]nonan-3-yl, piperidinyl, piperazinyl,
4-piperidonyl, pyrrolidinyl, pyrazolidinyl, quinuclidinyl,
thiazolidinyl, tetrahydrofuranyl, thienyl[1,3]dithianyl,
trithianyl, tetrahydropyranyl, thiomorpholinyl, thiamorpholinyl,
1-oxo-thiomorpholinyl, 1,1-dioxo-thiomorpholinyl, azetidinyl,
octahydropyrrolo[3,4-c]pyrrolyl, octahydropyrrolo[3,4-b]pyrrolyl,
decahydroprazino[1,2-a]azepinyl, azepanyl, azabicyclo[3.2.1]octyl,
and 2,7-diazaspiro[4.4]nonanyl.
[0085] "Heterocyclylalkyl" refers to a radical of the formula
--R.sub.a--R.sub.e where R.sub.a is an alkylene chain as defined
above and R.sub.e is a heterocyclyl radical as defined above, and
when the heterocyclyl is a nitrogen-containing heterocyclyl, the
heterocyclyl may be attached to the alkylene chain at the nitrogen
atom.
[0086] As used herein, unless specified otherwise, each one of
alkyl, alkenyl, haloalkyl, aralkyl, heterocyclylalkyl, alkylene
chain, alkenylene chain, cycloalkylalkyl moieties may be optionally
substituted, whereby one or more hydrogens are replaced by one or
more of the following substituents: amino, halo, cyano, nitro, oxo,
thioxo, trialkylsilanyl (including trimethylsilanyl), --OR.sup.f,
--OC(O)--R.sup.f, --N(R.sup.f).sub.2, --C(O)R.sup.f,
--C(O)OR.sup.f, --C(O)N(R.sup.f).sub.2, --N(R.sup.f)C(O)OR.sup.f,
--N(R.sup.f)C(O)R.sup.f, --N(R.sup.f)S(O).sub.2R,
--S(O).sub.tOR.sup.f (where t is 1 or 2), --S(O).sub.pR.sup.f
(where p is 0, 1 or 2), and --S(O).sub.2N(R.sup.f).sub.2 where each
R.sup.f is independently selected from the group consisting of
alkyl, alkenyl, haloalkyl, aralkyl, heterocyclylalkyl,
cycloalkylalkyl.
[0087] "Patient" means a mammal who has been diagnosed with a
neurodegenerative disease or who is genetically predisposed to such
diseases.
[0088] "Mammal" means any vertebrate of the class Mammalia. Humans
and domestic animals, such as cats, dogs, swine, cattle, sheep,
goats, horses, rabbits, and the like are a particular focus.
Preferably, for purposes of this invention, the mammal is a primate
(e.g., monkey, baboon, chimpanzee and human), and more preferably,
the mammal is a human.
[0089] "Pharmaceutically acceptable excipient" includes without
limitation any adjuvant, carrier, excipient, glidant, sweetening
agent, diluent, preservative, dye/colorant, flavor enhancer,
surfactant, wetting agent, dispersing agent, suspending agent,
stabilizer, isotonic agent, solvent, or emulsifier which has been
approved by the United States Food and Drug Administration as being
acceptable for use in humans or domestic animals.
[0090] "Pharmaceutically acceptable salt" includes both acid and
base addition salts.
[0091] "Pharmaceutically acceptable acid addition salt" refers to
those salts which retain the biological effectiveness and
properties of the free bases, which are not biologically or
otherwise undesirable, and which are formed with inorganic acids
such as, but not limited to, hydrochloric acid, hydrobromic acid,
sulfuric acid, nitric acid, phosphoric acid and the like, and
organic acids such as, but not limited to, acetic acid,
2,2-dichloroacetic acid, adipic acid, alginic acid, ascorbic acid,
aspartic acid, benzenesulfonic acid, benzoic acid,
4-acetamidobenzoic acid, camphoric acid, camphor-10-sulfonic acid,
capric acid, caproic acid, caprylic acid, carbonic acid, cinnamic
acid, citric acid, cyclamic acid, dodecylsulfonic acid,
ethane-1,2-disulfonic acid, ethanesulfonic acid,
2-hydroxyethanesulfonic acid, formic acid, fumaric acid, galactaric
acid, gentisic acid, glucoheptonic acid, gluconic acid, glucuronic
acid, glutamic acid, glutaric acid, 2-oxo-glutaric acid,
glycerophosphoric acid, glycolic acid, hippuric acid, isobutyric
acid, lactic acid, lactobionic acid, lauric acid, maleic acid,
malic acid, malonic acid, mandelic acid, methanesulfonic acid,
mucic acid, naphthalene-1,5-disulfonic acid, naphthalene-2-sulfonic
acid, 1-hydroxy-2-naphthoic acid, nicotinic acid, oleic acid,
orotic acid, oxalic acid, palmitic acid, pamoic acid, propionic
acid, pyroglutamic acid, pyruvic acid, salicylic acid,
4-aminosalicylic acid, sebacic acid, stearic acid, succinic acid,
tartaric acid, thiocyanic acid, p-toluenesulfonic acid,
trifluoroacetic acid, undecylenic acid, and the like.
[0092] "Pharmaceutically acceptable base addition salt" refers to
those salts which retain the biological effectiveness and
properties of the free acids, which are not biologically or
otherwise undesirable. These salts are prepared from addition of an
inorganic base or an organic base to the free acid. Salts derived
from inorganic bases include, but are not limited to, the sodium,
potassium, lithium, ammonium, calcium, magnesium, iron, zinc,
copper, manganese, aluminum salts and the like. Preferred inorganic
salts are the ammonium, sodium, potassium, calcium, and magnesium
salts. Salts derived from organic bases include, but are not
limited to, salts of primary, secondary, and tertiary amines,
substituted amines including naturally occurring substituted
amines, cyclic amines and basic ion exchange resins, such as
ammonia, isopropylamine, trimethylamine, diethylamine,
triethylamine, tripropylamine, diethanolamine, ethanolamine,
2-dimethylaminoethanol, 2-diethylaminoethanol, dicyclohexylamine,
lysine, arginine, histidine, caffeine, procaine, hydrabamine,
choline, betaine, benethamine, benzathine, ethylenediamine,
glucosamine, methylglucamine, theobromine, triethanolamine,
tromethamine, purines, piperazine, piperidine, N-ethylpiperidine,
polyamine resins and the like. Particularly preferred organic bases
are isopropylamine, diethylamine, ethanolamine, trimethylamine,
dicyclohexylamine, choline and caffeine.
[0093] A "pharmaceutical composition" refers to a formulation of a
compound of formula (I) or a formulation of a therapeutic agent
described herein and a medium generally accepted in the art for the
delivery of the biologically active compound to mammals, for
example, humans. Such a medium includes all pharmaceutically
acceptable carriers, diluents or excipients therefor.
[0094] "Neurodegenerative disease" refers to a progressive loss of
structure or function of neurons, including death of neurons.
Examples of the neurodegenerative diseases include, without
limitation, Parkinson's, Alzheimer's, ALS, motor neuron disease and
frontotemporal lobar degeneration (FTLD). In particular, the
neurodegenerative disease may be characterized by TDP-43
proteinopathy. Neurodegenerative disease also includes mild
cognitive impairment (MCI) (described in S. Gautier et al., 2006,
The Lancet 351: 1262-1270).
[0095] "Therapeutically effective amount" refers to that amount of
the therapeutic agent sufficient to delay, forestall or minimize
the progress of neurodegeneration, or to provide a therapeutic
benefit in the treatment or management of neurodegenerative
diseases, including the amelioration of symptoms associated with
neurodegenerative diseases.
[0096] "Prophylactically effective amount" refers to that amount of
the prophylactic agent sufficient to result in preventing or
forestalling neurodegenerative diseases, particularly in patients
who may be genetically predisposed to such diseases. A
prophylactically effective amount may refer to the amount of
prophylactic agent sufficient to prevent the age-related or early
on-set of neurodegenerative diseases.
[0097] As used herein, the terms "prevent", preventing" and
"prevention" refer to the prevention of the spread or onset of
neurodegenerative diseases in a patient.
[0098] As used herein, the terms "treat", "treating" and
"treatment" refer to delay, forestall or minimize the
neurodegenerative process, preferably prior to neurodegenerative
diseases such as ALS, Parkinson's, Alzheimer's, FTLD or mild
cognitive impairment (MCI) could develop from the
neurodegeneration. The terms also refer to management of
neurodegenerative diseases, including the amelioration of symptoms
associated with neurodegenerative diseases.
[0099] The compounds of formula (I) and (Ia), or their
pharmaceutically acceptable salts, may contain one or more
asymmetric centers and may thus give rise to enantiomers,
diastereomers, and other stereoisomeric forms that may be defined,
in terms of absolute stereochemistry, as (R)- or (S)- or, as (D)-
or (L)- for amino acids. The present invention is meant to include
all such possible isomers, as well as their racemic and optically
pure forms. Optically active (+) and (-), (R)- and (S)-, or (D)-
and (L)-isomers may be prepared using chiral synthons or chiral
reagents, or resolved using conventional techniques, such as HPLC
using a chiral column. When the compounds described herein contain
olefinic double bonds or other centers of geometric asymmetry, and
unless specified otherwise, it is intended that the compounds
include both E and Z geometric isomers. Likewise, all tautomeric
forms are also intended to be included.
[0100] A "stereoisomer" refers to a compound made up of the same
atoms bonded by the same bonds but having different
three-dimensional structures, which are not interchangeable. The
present invention contemplates various stereoisomers and mixtures
thereof and includes "enantiomers", which refers to two
stereoisomers whose molecules are nonsuperimposeable mirror images
of one another.
Preparation of the Compound of Formula (I)
[0101] The following reaction scheme shows a semi-synthetic
approach to preparing the compound of Formula (Ia) by using
Withaferin A as a starting material. More specifically, Withaferin
A (available from Sigma-Aldrich Canada) can be treated with one or
more alkylating agents to alkylate the --OH groups of Withaferin
A.
##STR00006##
[0102] The reaction may produce a mixture of mono-alkylated
compounds at C-4 or C-27 locations, as well as di-alkylated WA at
both C-4 and C-27 locations. The alkylated compounds may be
separated and isolated by known methods in the art. Where R.sup.1
and R.sup.3 are identical, a single alkylation step can be carried
out. Where R.sup.1 and R.sup.3 are different, two alkylation steps
may be carried out. For example, a step-wise reaction using
alkylating agents R.sup.1--X and R.sup.3--X (X being a leaving
group) may be carried out to separately alkylate the hydroxy groups
of Withaferin A.
[0103] Selective protection of the hydroxy groups at C-4 or C-27 of
Withaferin A can direct the alkylation step to a particular
location. For instance, the C-4 hydroxy group may be first
protected such that the alkylation step only takes place at the
C-27 hydroxy group.
[0104] Functionalization at the C-12 and C-15 locations of a
compound of Formula (I) may be carried out according to the methods
disclosed in U.S. Pub. No. 2011/0230551, which reference is
incorporated herein by reference in its entirety.
[0105] It will be appreciated by those skilled in the art that in
the processes described below the functional groups of intermediate
compounds may need to be protected by suitable protecting groups.
Such functional groups include hydroxy, amino, mercapto and
carboxylic acid. Suitable protecting groups for hydroxy include
trialkylsilyl or diarylalkylsilyl (for example,
t-butyldimethylsilyl, t-butyldiphenylsilyl or trimethylsilyl),
tetrahydropyranyl, benzyl, and the like. Suitable protecting groups
for amino, amidino and guanidino include benzyl, t-butoxycarbonyl,
benzyloxycarbonyl, and the like. Suitable protecting groups for
mercapto include --C(O)--R'' (where R'' is alkyl, aryl or
arylalkyl), p-methoxybenzyl, trityl and the like. Suitable
protecting groups for carboxylic acids include alkyl, aryl or
arylalkyl esters.
[0106] Protecting groups may be added or removed in accordance with
standard techniques, which are known to one of ordinary skill in
the art and as described herein. The use of protecting groups is
described in detail in Greene, T. W. and P. G. M. Wuts, Greene's
Protective Groups in Organic Synthesis (1999), 3rd Ed., Wiley. As
one of skill in the art would appreciate, the protecting group may
also be a polymer resin such as, but not limited to, a Wang resin,
Rink resin or a 2-chlorotrityl-chloride resin.
Dosage
[0107] The amount of the withanolide compounds required for use in
treatment will vary not only with the particular compound selected
but also with the route of administration, the nature of the
condition for which treatment is required and the age and condition
of the patient and will be ultimately determined by a physician. In
general, the amount of a compound required for use in treatment
will vary not only with the particular compound selected but also
with the route of administration, the nature of the condition for
which treatment is required and the age and condition of the
patient and will be ultimately be determined by a physician.
Generally, a suitable dose will be for example in the range of 0.01
to 1000 mg/kg of body weight per day, or for example, in the range
of 0.1 to 100 mg/kg/day, or, for example, in the range of 0.5 to 50
mg/kg/day, or for example, in the range of 1 to 25 mg/kg/day. Doses
may be administered at appropriate intervals, for example as one,
two, three, four or more doses per day. In some cases doses may be
administered every day, every two to three days, every four to five
days, or every five to seven days. Dosing may continue for days,
weeks, months or years, as required.
EXAMPLES
Example 1
Preparation of WA Methyl Ether Analogs from WA
##STR00007##
[0108] Preparation
[0109] 150 mg of Withaferin A (available from Sigma-Aldrich Canada)
(WA 1) were treated with sodium hydride in methyl iodide. The
reaction produced a mixture of both mono-methylated compounds and
di-methylated WA. The reaction mixture was filtered to remove
excess sodium hydride and sodium iodide. The filtrate was dried and
the residue re-dissolved in dichloromethane. The resulting solution
was chromatographed on a silica gel column. Fractions containing
the mono-methyl ethers (2 and 3) and dimethyl ether (4) were
combined and the compounds separated by reversed phase
chromatography.
[0110] Pure fractions of each compound were pooled, concentrated,
extracted into dichloromethane and dried. Approximately 5-10 mg of
each compound was thus obtained, each as a white solid.
Spectroscopic data of these compounds are provided in Table 1
below.
TABLE-US-00001 TABLE 1 m/z .differential. ppm (CDCl.sub.3) [M + H-
H- OH- 4- 27- Compound H].sup.+ H-4 27a 27b OH-4 27 OMe OMe
Withaferin A 471 3.78 4.41 4.35 2.52 2.86 -- -- (1) (dd) (dd) (dd)
(d) (t) 27-O-methyl 485 3.77 4.29 4.17 2.50 -- -- 3.39 withaferin A
(dd) (d) (d) (d) (s) (2) 4-O-methyl 485 3.27 4.41 4.35 -- 2.86 3.45
-- withaferin A (d) (dd) (dd) (t) (s) -- (3) 4,27-O- 499 3.27 4.29
4.17 -- -- 3.46 3.39 dimethyl (d) (d) (d) (s) (s) withaferin A
(4)
Example 2
Brain Bioluminescence in GFAP-Luciferase Mice Exposed to LPS
[0111] Two of the novel withanolides were tested for their
therapeutic activity in vivo using a transgenic mouse model.
Transgenic GFAP-luciferase mice generated in the laboratory of Dr.
J. P. Julien were used to assess the ability of the withanolides to
inhibit astrogliosis associated with inflammation induced by
lipopolysaccharide (LPS) exposure. In vivo bioluminescence imaging
was performed to asses the inflammatory response in the cranial
region. A decrease in bioluminescense signals in the evaluated
region in comparison to the control (saline) indicated that the
withanolides had crossed the blood brain barrier and subsequently
inhibited gliosis.
[0112] Withanolides [4-O-methyl withaferin A (4-O-methyl WA) and
27-O-methyl withaferin A (27-O-methyl WA)] were diluted in 100%
dimethyl sulfoxide (DMSO) at a final concentration of 2 mg/ml.
GFAP-luc transgenic mice were used to test in vivo the efficacy of
these analogs. In these transgenic mice, the firefly luciferase
reporter gene is under the control of a 12 kb DNA fragment of the
glial fibrillary acidic protein (GFAP) promoter (Caliper Life
Sciences). The luciferase reporter is inducible following LPS
administration resulting in GFAP transcriptional regulation. If the
administration of test compounds following the injection of LPS
decreases LPS-induced astrogliosis in GFAP-luc mice, this is
visualized as a reduced bioluminescent signal upon imaging.
[0113] Transgenic mice under anesthesia were induced to inhale
either 5 ul of a solution of LPS (1 mg/ml in 0.9% saline) or a
solution of 0.9% saline alone followed 2 h later by an
intraperitoneal (i.p.) injection of 0.5 ml of the test compounds
(10% dilution in 0.9% saline) at a final concentration of 4 mg/kg.
The following day, 2 h before imaging (24 h after the
administration of the LPS solution), the transgenic mice were again
injected with the withanolides as previously. Twenty minutes prior
to imaging, the mice received an i.p. injection of the luciferase
substrate D-luciferin (150 mg/kg). D-luciferin was dissolved in
0.9% saline to a final concentration of 20 mg/ml. Mice were
anesthetized and imaged using an IVIS 200 imaging system
(CaliperLS-Xenogen).
[0114] The results showed a significant decrease in the
bioluminescent signal in mice treated with either 4-O-methyl WA or
27-O-methyl WA compared to mice treated with saline-DMSO alone
(FIG. 1A). FIG. 1B shows a summary graph of the quantification of
the luciferase activity expressed as counts of total photon
emission in the brain of the GFAP-transgenic mice shown in FIG. 1A.
This experiment demonstrated a significant reduction in
astrogliosis in GFAP-transgenic mice treated with either 4-O-methyl
WA or 27-O-methyl WA.
Example 3
[0115] Novel withanolides inhibit NF-.kappa.B reporter activity in
BV2 microglial cells stimulated with LPS. The withanolides
4-O-methyl WA, 27-O-methyl WA and 4,27-O-dimethyl WA were tested
for their ability to inhibit NF-.kappa.B activation. An NF-.kappa.B
specific luciferase reporter system in BV-2 microglial cells was
first established. This cell line was generated by stable
transfection of BV-2 cells with stable insertion of a luciferase
reporter 4 kBwt luciferase plasmid and subsequent selection with
hygomycin. LPS was used to stimulate NF-.kappa.B activity in these
cells. Twenty-five thousand hygromycin B-resistant BV-2 cells were
seeded per well in 24-well dishes and allowed to adhere overnight.
The next morning, the culture medium (DMEM+10% FBS) was removed and
1 ml of fresh medium (DMEM without FBS) added to each well. The
stock solutions of withanolides (2 mg/ml in DMSO) were diluted in
1.times.PBS to various concentration (0.05 to 5 uM) and added to
the wells. LPS was added one hour later at a final concentration of
100 ng/ml. Four hours later, the BV-2 cells were rinsed with
1.times.PBS prior to proceeding with the luciferase assay that was
performed according to the manufacturer's instructions
(Bright-Glo.TM. luciferase assay system, Promega, Wis.).
[0116] The results, provided in FIG. 2, showed that all of the
withanolides tested had the ability to inhibit NF-.kappa.B
expression. Table 2 below shows the IC50 of certain compounds of
Formula (Ia).
TABLE-US-00002 TABLE 2 Compounds IC.sub.50 (.mu.M) 4-O-methyl WA
0.97 27-O-methyl WA 0.71 4,27-O-dimethyl WA 0.80 WA 0.50
Example 4
Novel Withanolides Inhibit Up-Regulation of TNF-.alpha.-Induced
Signalling Activity in the HEK293-NF-.kappa.B-Luciferase Reporter
Cell Line
[0117] Ten thousand hygromycin B-resistant HEK-293 cells were
seeded per well in a 96-well plate (Corning, New-York) and allowed
to adhere overnight. The next morning, the culture medium (DMEM+10%
FBS) was removed and 100 ml of fresh medium (DMEM without FBS)
added to each well. The stock solutions of withanolides 4-O-methyl
WA, 27-O-methyl WA and 4,27-O-dimethyl WA (2 mg/ml in DMSO) were
diluted in 1.times.PBS to various concentration (0.05 to 5 uM) and
added to the wells. Human recombinant TNF-alpha (R&D Systems,
Minneapolis) was added one hour later at a final concentration of
40 ng/ml. Four hours later, the HEK-293 cells were rinsed with
1.times.PBS prior to the luciferase assay, which was performed
according to the manufacturer's instructions (Bright-Glo.TM.
luciferase assay system, Promega, Wis.).
[0118] The results of the assay, shown in FIG. 3, confirmed that
4-O-methyl WA, 27-O-methyl WA and 4,27-O-dimethyl WA inhibited
NF-.kappa.B expression. The IC.sub.50s for 4-O-methyl WA,
27-O-methyl WA and 4,27-O-dimethyl WA are shown in Table 3.
TABLE-US-00003 TABLE 3 Compounds IC.sub.50 (.mu.M) 4-O-methyl WA
0.32 27-O-methyl WA 0.26 4,27-O-dimethyl WA 0.45 WA 0.34
Example 5
Safety Comparison of WA, 4-O-Methyl WA and 27-O-Methyl WA
[0119] An acute dose-escalation study was carried out to compare
the tolerability in vivo of WA, 4-0 methyl WA and 27-0 methyl WA.
Normal C57BL/6 female mice were injected intraperitoneally with WA,
4-O-methyl WA or 27-O-methyl WA at doses ranging from 20 to 65
mg/kg (20, 25, 30, 35, 45, 55 and 65 mg/kg). Animals were observed
for signs of morbidity, mortality and clinical changes in behavior,
breathing, heartbeat, hydration and other conditions (such as
ascites, shock, severe diarrhea and hemorrhage) at 1 h, 6 h and 24
hours post-dosing. Body weight was measured pre-dosing and at 24
h.
[0120] The withanolides 4-O-methyl WA and 27-O-methyl WA both
showed a much better safety profile than WA. The LD50 (lethal dose,
50%) was found to be 55 mg/Kg for WA. The same LD50 value (54
mg/kg) for WA was previously reported (Patwardhan et al., Drug
Discovery and Development, (2006), edited by M. S. Chorghade,
Wiley). In contrast, no mortality was observed when mice were
administered 55 mg/kg of either 4-O-methyl WA or 27-O-methyl WA. At
the highest dose tested in the study, 65 mg/kg, no mortality was
observed for mice injected with either 4-O-methyl WA or 27-O-methyl
WA. However, the animals in these groups did exhibit some weakness
and a decrease in activity post-dosing.
Example 6
Withaferin a Analogs Inhibit Neurological Disease Development in a
TDP-43 A315T Transgenic Mouse Model of ALS
[0121] The impact of repeated dosing with 4-O-Methyl WA and
27-O-Methyl WA on the development of neurological disease in the
TDP-43 A315T transgenic mouse model of ALS was evaluated. The
TDP-43 A315T mouse model for ALS is fully described in Swamp, V et
al., Brain 134: 2610-2626 2011. TDP-43 A315T mice begin to exhibit
neurological deficits at about 9 months of age, as measured by
their performance in a number of behavioral and motor function
tests (Barnes maze test, accelerating rotarod test and passive
avoidance test).
[0122] Male and female TDP-43 A315T mice of approximately 9 months
and 25-55 gm were included in the study, and were randomly assigned
to three groups, as follows:
[0123] Group 1 (n=6) received 4-O-Methyl WA at 5 mg/kg;
[0124] Group 2 (n=7) (the control group) received vehicle (2%
polysorbate [Tween-80]/5% DMSO/93% saline); and
[0125] Group 3 (n=7) received 27-O-Methyl WA at 5 mg/kg.
[0126] All animals received i.p. injections of either vehicle or 5
mg/kg of the test WA analogs every 2 days for 15 weeks. The
injection volume at 12.5 mL/kg was based on the body weight of each
individual animal at the start of the study.
[0127] All animals were observed at least once daily throughout the
study for clinical signs, and were individually weighed weekly
before the rotarod test. There were no significant changes in body
weight or clinical signs over the study period. After 15 weeks, the
mice were sacrificed, and the expression of the mutant TPD-43A315T
protein in the spinal cord of each mouse was confirmed by an
antibody immunofluorescence or western blot test.
[0128] Accelerating rotarod (as described in Gros-Louis, F., et al.
Hum Mol Genet 17, 2691-2702 (2008)) was performed prior to first
dosing and at weekly interval during the study. Testing was
performed at 4-rpm speed with 0.25 rpm/s acceleration. Each mouse
was subjected to three trials per session. The number of seconds
each mouse remained on the rotarod apparatus for each trial was
recorded.
[0129] The results are shown in FIGS. 4A and 4B. FIG. 4A shows the
best scores (of the three trials) for individual mice in each
group. FIG. 4B shows a regression analysis of the data in FIG. 4A.
The data show that the rotarod performance of the vehicle-treated
group declined over the 15 week period. However, the performance of
both the 4-O-Methyl WA- and 27-O-Methyl WA groups actually improved
over that time period. The linear regression analysis showed
statistical significance for both 4-O-Methyl WA (p value of 0.02)
and 27-O-Methyl WA (p value of 0.02), but not for the vehicle (p
value of 0.2).
[0130] The results also demonstrate that the mice were able to
tolerate the administration of 5 mg/kg of the WA analogs every
other day for 15 weeks, providing further evidence for the safety
of the compounds.
Example 7
Larger-Scale Synthesis and Purification of 27-O-Methyl Withaferin
A
[0131] 27-O-methyl withaferin was prepared from withaferin A
starting material and purified using the procedures outlined
below.
[0132] 1. Preparation of 4,27-bis-O-triethylsilylwithaferin A.
[0133] To a stirred solution of withaferin A (4.0 g) in
N,N-dimethylformamide (40 mL) at 0.degree. C. was added imidazole
(2.31 g 4 eq.). Triethylchlorosilane (4.28 mL, 3 eq.) was added in
small portions over approximately 5 minutes, and the resulting
mixture was stirred under nitrogen at 0.degree. C. for
approximately 2 hrs. After the reaction was complete as determined
by HPLC, methanol (2 mL) was added and the mixture was stirred for
another 5-10 min. The reaction mixture was diluted with ethyl
acetate (250 mL) and washed with brine (4.times.100 mL). The
aqueous washings were combined and back extracted with ethyl
acetate (2.times.100 mL). All ethyl acetate extracts were combined,
washed again with brine (3.times.100 mL), dried with anhydrous
sodium sulfate and concentrated to obtain 10 g of crude 4,
27-bis-O-triethylsilylwithaferin A as a pale oil.
[0134] 2. Preparation of 4-O-Triethylsilylwithaferin A
[0135] Crude 4, 27-bis-O-triethylsilylwithaferin A (10 g) was
dissolved in aqueous tetrahydrofuran (120 mL, THF/water, 9/1) at
room temperature. Pyridinium p-toluenesulfonate (PPTS, 120 mg) was
added. The mixture was stirred for approximately 13 hours, during
which additional PPTS (approximately 145 mg) was added in 6-30 mg
portions to the reaction in 1 hour intervals. The reaction progress
was closely monitored by HPLC. After the reaction was complete, the
mixture was diluted with ethyl acetate (300 mL) and washed with
brine (5.times.100 mL). The aqueous washings were combined and back
extracted with ethyl acetate (2.times.50 mL). All ethyl acetate
extracts were combined, washed with brine (100 mL), dried with
anhydrous sodium sulfate, and concentrated to yield a crude product
(11.5 g) as a pale gum. The crude product was purified by silica
gel column chromatography (dichloromethane/acetone 95-93/5-7) to
afford 4.2 g of pure 4-O-triethylsilylwithaferin A.
[0136] 3. Preparation of 27-O-Methyl-4-O-Triethylsilylwithaferin
A
[0137] 4-O-triethylsilylwithaferin A (1.0 g) was dissolved in a
mixture of anhydrous THF (40 mL) and methyl iodide (8 mL) and
cooled in an ice-water bath under nitrogen. Sodium hydride (60% in
mineral oil, 108 mg, 1.58 eq.) was added and the mixture was
stirred at room temperature for 4 minutes. The mixture was then
stirred at room temperature for approximately 1 hour 40 minutes,
during which the reaction was closely monitored by HPLC. After the
product had reached 20-30%, the mixture was diluted with ethyl
acetate (200 mL) and washed with brine (3.times.80 mL). All
washings were combined and back extracted with ethyl acetate
(2.times.50 mL). All ethyl acetate extracts were combined, washed
with 10% aqueous sodium thiosulfate (50 mL), brine (2.times.80 mL),
dried over anhydrous magnesium sulfate, and concentrated.
[0138] The crude product, pooled with another batch started with
0.5 g 4-O-triethylsilylwithaferin A, was purified by column
(dichloromethane/acetone 95-93/5-7) to give 413 mg of
27-O-methyl-4-O-triethylsilylwithaferin A and 756 mg of recovered
starting material. The average yield was about 27%.
[0139] 4. Preparation of 27-O-Methylwithaferin A
[0140] 27-O-methyl-4-O-triethylsilylwithaferin A (413 mg) was
dissolved in a mixture of THF (9.5 mL) and pyridine (1.2 mL) and
stirred in an ice-water bath. Pyridine hydrofluoride (0.85 mL) was
added dropwise, and after 5 minutes at 0.degree. C., the mixture
was stirred at room temperature for 1.5 hr. The mixture was diluted
with ethyl acetate (150 mL), washed with 0.1 N hydrochloric acid
(50 mL) and brine (2.times.50 mL). The washings were combined and
back extracted with ethyl acetate (2.times.50 mL). All ethyl
acetate extracts were combined and washed with saturated sodium
bicarbonate (50 mL), brine (2.times.50 mL), dried over sodium
sulfate, and concentrated. The crude product was purified by
silicagel column chromatography (hexane/acetone, 70-65/30-35) to
yield 275 mg of 27-O-methylwithaferin A (>95% purity; 82%
yield). The purified product was further recrystallized in acetone
and hexane to increase the purity to approximately 99% as assessed
by HPLC.
Example 8
Larger-Scale Synthesis and Purification of 4-O-Methylwithaferin
A
[0141] 4-O-methylwithaferin A was prepared from withaferin A
starting material and purified using the following procedures.
[0142] 1. Preparation of 27-O-(tert-butyldimethylsilyl)withaferin
A
[0143] Withaferin A 5.6 g were dissolved in 60 mL of
dichloromethane. Triethylamine (4.0 mL) was added to the mixing
solution followed by the addition of 4.01 g of
tert-butyldimethylchlorosilane. The solution was stirred at ambient
temperature for approximately 80 hrs. The solution was washed with
water and concentrated to give 6.95 g of crude
27-O-(tert-butyldimethylsilylwithaferin A. This was crystallized
from methanol and dried to give 5.6 g of
27-O-(tert-butyl.dimethylsilywithaferin A with an HPLC purity of
99.5%. Shorter reaction times can be achieved by the addition of
0.5 g of dimethylaminopyridine leading to 95% completion in 12
hours.
[0144] 2. Methylation of 27-O-(tert-butyldimethylsilyl)withaferin
A
[0145] 4.0 g of 27-O-(tert-butyldimethylsilyl)withaferin A was
placed in a round bottom flask under nitrogen. 20 mL of anhydrous
N,N-dimethylformamide were added to the flask. Dissolution of the
solids was incomplete, but addition of 10 mL of methyl iodide
yielded a clear solution. Sodium hydride (0.32 g, 60% in mineral
oil) was added into the mixing solution over 10 minutes. HPLC
showed approximately 80% completion. An additional 0.5 g of sodium
hydride was added to achieve 99% completion. Acetic acid was used
to quench remaining sodium hydride. The mixture was diluted with
dichloromethane and washed with water. The organic layer was
concentrated to 20 mL. HPLC showed 88% purity of
4-O-methyl-27-O-(tert-butyldimethylsilyl)withaferin A.
[0146] 3. Preparation of 4-O-Methylwithaferin A
[0147] The solution of
4-O-methyl-27-O-(tert-butyldimethylsilyl)withaferin A obtained
above was transferred to a PTFE flask rinsing forward with 30 mL of
dichloromethane. Pyridine (3 mL) was added, followed by 1 mL of
pyridine hydrofluoride. The reaction was monitored by HPLC. After
5.5 hours, an additional 0.5 mL of pyridine hydrofluoride was
added. The reaction continued for another 3 hours to 92%
completion. The reaction was worked up by washing the organic
solution with water, then sodium bicarbonate solution, and finally
sodium chloride solution. The dichloromethane layer was
concentrated on a rotary evaporator to give a viscous liquid. This
was diluted with 36.5 mL of dichloromethane and 36.5 mL methanol
and washed with 73 mL water. The organic layer was concentrated
under vacuum to give 3.9 g of crude 4-O-methylwithaferin A.
[0148] 4. Purification of the 4-O-Methylwithaferin A
[0149] The crude 4-O-methylwithaferin A obtained above was
dissolved in dichloromethane and loaded onto a 100 g silicagel
column packed with dichloromethane. The column was eluted with 30%
v/v acetone in dichloromethane. The fractions were analyzed by HPLC
and those containing pure product were combined and evaporated to
give 1.8 g of solids at 97% purity. The solids were crystallized
from a mixture of 5 mL methanol and 10 mL methy-tert-butylether.
The solids were dried in a vacuum oven to give 0.61 g of
4-O-methylwithaferin A at 98% HPLC purity.
[0150] The various embodiments described above can be combined to
provide further embodiments. All of the U.S. patents, U.S. patent
application publications, U.S. patent application, foreign patents,
foreign patent application and non-patent publications referred to
in this specification and/or listed in the Application Data Sheet
are incorporated herein by reference, in their entirety. Aspects of
the embodiments can be modified, if necessary to employ concepts of
the various patents, application and publications to provide yet
further embodiments.
[0151] These and other changes can be made to the embodiments in
light of the above-detailed description. In general, in the
following claims, the terms used should not be construed to limit
the claims to the specific embodiments disclosed in the
specification and the claims, but should be construed to include
all possible embodiments along with the full scope of equivalents
to which such claims are entitled. Accordingly, the claims are not
limited by the disclosure.
* * * * *