IP Library Granted Patent US 10,137,123
Granted Patent B2
US 10,137,123 · App. 15/583,867 · Granted Nov 27, 2018

Methods and compositions for prevention and treatment of cardiac hypertrophy

Inventor: Alexander Stokes (Honolulu, HI)
Assignee: University of Hawaii
A61K31/496A61K31/00A61K31/497A61P9/04
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Quick Facts
Patent No.
US 10,137,123
App. No.
15/583,867
Granted
Nov 27, 2018
Kind
B2
Abstract

Methods are provided of treating cardiac hypertrophy in a mammalian subject comprising administering to the subject an anti-hypertrophic effective amount of an ion channel TR-PV1 inhibitor. The methods include treatment of a symptom of cardiac hypertrophy in the subject comprises cardiac remodeling, cardiac fibrosis, apoptosis, hypertension, or heart failure.

Claims (95)

1. A method of treating heart failure of any cause in a mammalian subject comprising administering to the subject an effective amount of an ion channel TRPV1 inhibitor, with the proviso that if the heart failure is caused by acute myocardial ischemia, the administering of the ion channel TRPV1 inhibitor occurs after the therapeutic window for protection from acute myocardial ischemia.

2. The method according to claim 1 , wherein the treating of heart failure of any cause further treats cardiac fibrosis.

3. The method according to claim 1 , wherein the treating of heart failure of any cause further induces cardiac remodeling.

4. The method according to claim 1 , wherein the treating of heart failure of any cause further treats apoptosis.

5. The method according to claim 1 wherein the inhibitor is selected from the group consisting of:

N-(4-tertiarybutylphenyl)-4-(3-chloropyridin-2-yl)-tetrahydropyrazine-1(2H)-carboxamide;

N-(3-Methoxyphenyl)-4-chlorocinnamide;

1-lsoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea;

(2E)-N-(2,3-Dihydro-1,4-benzodioxin-6-yl)-3-[4-(1,1-dimethylethyl)phenyl]-2-propenamide;

2-Acetylamino-4-[6′-(4-trifluoromethylphenyl)-pyrimidin-4′-yl-oxy]-benzothiazole;

N-(2-bromophenyl-N′-[((R)-1-(5-trifluoromethyl-2-pyridyl)pyrrolidin-3-yl)]urea;

N-(2-bromophenyl)-N′-{2-[ethyl(3-methylphenyl)amino]ethyl}urea;

(R)-(5-tert-butyl-2,3-dihydro-1H-inden-1-yl)-3-(1H-indazol-4-yl)-urea;

N-(Isoquinolin-5-yl)-N′-[spiro-(cyclobutane-1,2′-(3′,4′-dihydro-benzopyran-4′-yl))]urea;

(2R)-4-(3-chloro-2-pyridinyl)-2-methyl-N-[4-(trifluoromethyl)phenyl]-1-piperazinecarboxamide;

4-(4′-Trifluoromethyl-anilino)-7-(3′-trifluoromethyl-pyridin-2-yl)-quinazoline;

N-[2-(4-chlorophenyl)ethyl]-1,3,4,5-tetrahydro-7,8-dihydroxy-2H-2-benzazepine-2-carbothioamide;

(5R*,8R*,6E,9E)-5,8-Dimethyl-4-methylenetetradeca-6,9-dienoic acid;

1-(3-Fluorobenzyl)-2-(N-(1,2-dimethyl-1,3-isoindazol-5-yl)-acetamido)-{pyridine-[3,4-b]-pyrrole};

N-(4-chlorobenzyl)-N′-(1-methyl-1H-indazol-4-yl)urea;

N-(4-tert-butylbenzyl)-N′-(1-methyl-1H-indazol-4-yl)urea;

N-(3-fluoro-4-(trifluoromethyl)benzyl)-N′-(1-methyl-1H-indazol-4-yl)-urea;

N-(4-fluoro-3-(trifluoromethyl)benzyl)-N′-(1-methyl-1H-indazol-4-yl)-urea;

N-(3,4-dichlorobenzyl)-N′-(1-methyl-1H-indazol-4-yl)urea;

N-(2,4-dichlorobenzyl)-N′-(1-methyl-1H-indazol-4-yl)urea;

N-(4-ethylbenzyl)-N′-(1-methyl-1H-indazol-4-yl)urea;

N-(2-chlorobenzyl)-N′-(1-methyl-1H-indazol-4-yl)urea;

N-(4-fluorobenzyl)-N′-(1-methyl-1H-indazol-4-yl)urea;

N-(2-fluorobenzyl)-N′-(1-methyl-1H-indazol-4-yl)urea;

N-[1-(bromophenyl)ethyl-N′-(1-methyl-1H-Indazol-4-yl)urea;

N-(1-methyl-1H-indazol-4-yl)-N′-{4-[(trifluoromethyl)thio]benzyl}urea;

1-(2,3-dichlorophenyl)-3-[2-(N-ethyl-3-methylanilino)ethyl]urea;

1-[2-(N-ethyl-3-methylanilino)ethyl]-3-naphthalen-1-ylurea;

1-(4-bromophenyl)-3-[2-(N-ethyl-3-methylanilino)ethyl]urea;

1-(3-bromophenyl)-3-[2-(N-ethyl-3-methylanilino)ethyl]urea;

1-(chlorophenyl)-3-[2-(N-ethyl-3-methylanilino)ethyl]urea;

1-[2-(N-ethyl-3-methylanilino)ethyl]-3-(2-fluorophenyl)urea;

1-[2-{N-ethyl-3-methylanilino)ethyl]-3-(2-methylphenyl)urea;

1-[2-(N-ethyl-3-methylanilino)ethyl]-3-phenylurea;

2-[(2-bromophenyl)carbamoylamino]ethyl-ethylmethyl-(3-methylphenyl)azanium iodide;

1-(2-bromophenyl)-3-[2-(N-ethyl-3-fluoro-4-methylanilino)ethyl]urea;

1-(2-bromophenyl)-3-[2-(N-ethyl-3,4-difluoroanilino)ethyl]urea;

1-(2-bromophenyl)-3-[2-(N-ethyl-3-fluoroanilino)ethyl]urea;

1-(2-bromophenyl)-3-[2-(N-ethyl-4-methylanilino)ethyl]urea;

1-(2-bromophenyl)-3-[2-(N-ethyl-2-methylanilino)ethyl]urea;

1-(2-bromophenyl)-3-[2-(N-ethylanilino)ethyl]urea;

N-[2-[(2-bromophenyl)carbamoylamino]ethyl]-N-(3-methylphenyl)acetamide;

1-[2-{N-benzyl-3-methylanilino)ethyl]-3-(2-bromophenyl)urea;

1-(2-bromophenyl)-3-[2-(2,3-dimethylanilino)ethyl]urea;

1-(2-bromophenyl)-3-[2-(3-methylanilino)ethyl]urea;

1-(2,5-dichlorophenyl)-3-[2-(N-ethyl-3-methylanilino)ethyl]urea;

4-fluoro-4-(3-methylpyridin-2-yl)-N-[4-trifluoromethylphenyl]piperidine-1-carboxamide;

4-fluoro-4(pyridin-2-yl)N-[4-trifluoromethylphenyl]piperidine-1-carboxamide;

4-fluoro-4(pyridine-2-yl)N-[4-trifluoromethylbenzyl]piperidine-1-carboxamide;

2-{4-fluoro-1-[4-trifluoromethylbenzoyl]piperidin-4-yl}pyridine;

2-(4-fluoro-1-{[4-trifluoromethylphenyl]acetyl}piperidin-4-yl)pyridine;

2-(4-fluoro-1-{3-[4-trifluoromethylphenyl]propanoyl}piperidin-4-yl)pyridine;

4-fluoro-4-(1-methyl-1H-imidazol-2-yl)-N-[4-trifluoromethylphenyl]piperidine-1-carboxamide;

4-methoxy-4-pyridin-2-yl-N-[4-trifluoromethylphenyl]piperidine-1-carboxamide;

4-methoxy-4-pyridin-2-yl-N-[4-trifluoromethylbenzyl]piperidine-1-carboxamide;

4-fluoro-N-(4-isopropylphenyl)-4-(3-methylpyridin-2-yl)piperidine-1-carboxamide;

4-fluoro-4-(3-methylpyridin-2-yl)-N-{4-[1,2,2,2-tetrafluoro-1-trifluoromethylethyl]phenyl}piperidine-1-carboxamide;

N-(4-Tert-butylphenyl)-4-fluoro-4-(3-methylpyridin-2-yl)piperidine-1-carboxamide;

4-fluoro-4-(3-methylpyridin-2-yl)-N-[4-(pentafluoro-lambda(sup 6)-sulfanyl)phenyl]piperidine-1-carboxamide;

N-(4-Butylphenyl)-4-fluoro-4-(3-methylpyridin-2-yl)piperidine-1-carboxamide;

N-(4-Benzylphenyl)-4-fluoro-4-(3-methylpyridin-2-yl)piperidine-1-carboxamide;

N-biphenyl-4-yl-4-fluoro-4-(3-methylpyridin-2-yl)piperidine-1-carboxamide;

4-fluoro-4-(3-methylpyridin-2-yl)-N-[5-trifluoromethylpyridin-2-yl]piperidine-1-carboxamide;

4-(3-chloropyridin-2-yl)-4-fluoro-N-[4-trifluoromethylphenyl]piperidine-1-carboxamide;

4-fluoro-4-(3-fluoropyridin-2-yl)-N-[4-trifluoromethylphenyl]piperidine-1-carboxamide;

4-fluoro-4-(3-methoxypyridin-2-yl)-N-[4-trifluoromethylphenyl]piperidine-1-carboxamide;

4-fluoro-4-(3-methylpyridin-2-yl)-N-[4-trifluoromethylphenyl]piperidine-1-carbothioamide;

N′-cyano-4-fluoro-4-(3-methylpyridin-2-yl)-N-[4-trifluoromethylphenyl]piperidine-1-carboximidamide;

4-fluoro-4-(3-methylpyridin-2-yl)-N′-(1-phenylpiperidin-4-yl)-N-[4-trifluoromethylphenyl]piperidine-1-carboximidamide;

4-fluoro-4-phenyl-N-[4-trifluoromethylphenyl]piperidine-1-carboxamide;

(+/−)-(syn)-4-fluoro-2-methyl-4-(3-methylpyridin-2-yl)-N-[4-trifluoromethylphenyl]piperidine-1-carboxamide;

4-(fluoromethyl)-4-pyridin-2-yl-N-[4-trifluoromethylphenyl]piperidine-1-carboxamide;

syn- and anti-3-fluoro-3-pyridin-2-yl-N-[4-trifluoromethylphenyl]-8-azabicyclo[3.2-]octane-8-carboxamide;

3-fluoro-3-pyridin-2-yl-N-[4-trifluoromethylphenyl]-8-azabicyclo[3.2.1]octane-8-carboxamide;

4-fluoro-4-pyrimidin-2-yl-N-[4-trifluoromethylphenyl]piperidine-1-carboxamide;

4-fluoro-4-(3-phenylpropyl)-N-[4-trifluoromethylphenyl]piperidine-1-carboxamide;

2-[4-fluoro-4-(3-methylpyridin-2-yl)piperidin-1-yl]-6-trifluoromethyl-1H-benzimidazole;

2-(4-fluoro-4-pyridin-2-ylpiperidin-1-yl)-6-(trifluoromethyl)-1H-benzimidazole;

4-fluoro-N-[4-trifluoromethylphenyl]-4-[3-trifluoromethylpyridin-2-yl]piperidine-1-carboxamide;

4-fluoro-N-(4-methylphenyl)-4-(3-methylpyridin-2-yl)piperidine-1-carboxamide;

N-(4-ethylphenyl)-4-fluoro-4-(3-methylpyridin-2-yl)piperidine-1-carboxamide;

N-(4-chlorophenyl)-4-fluoro-4-(3-methylpyridin-2-yl)piperidine-1-carboxamide;

4-fluoro-4-(3-methylpyridin-2-yl)-N-[4-trifluoromethoxyphenyl]piperidine-1-carboxamide;

N-(4-cyanophenyl)-4-fluoro-4-(3-methylpyridin-2-yl)piperidine-1-carboxamide;

N-[4-dimethylaminophenyl]-4-fluoro-4-(3-methylpyridin-2-yl)piperidine-1-carboxamide;

1-(2-(3,3-dimethylbutyl)-4-(trifluoromethyl)benzyl)-3-(1-methyl-1H-indazo-1-4-yl)urea;

N-acetyl-1-phenylalanyl-1-leucinamide; and pharmaceutically acceptable salts thereof.

6. The method according to claim 2 wherein the inhibitor is N-(4-t-butyl-phenyl)-4-(3-chloropyridin-2-yl)-tetrahydropyrazine-1(2H)-carboxamide or a pharmaceutically acceptable salt thereof.

7. The method according to claim 1 wherein the inhibitor is N-(4-t-butyl-phenyl)-4-(3-chloropyridin-2-yl)-tetrahydropyrazine-1(2H)-carboxamide or a pharmaceutically acceptable salt thereof.

8. The method according to claim 3 wherein the inhibitor is N-(4-t-butyl-phenyl)-4-(3-chloropyridin-2-yl)-tetrahydropyrazine-1(2H)-carboxamide or a pharmaceutically acceptable salt thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 17, 2018
From: STOKES, ALEXANDER
To: UNIVERSITY OF HAWAII
Reel/Frame 047196/0276 →
CONFIRMATORY LICENSE Recorded Jun 25, 2018
From: UNIVERSITY OF HAWAII
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046419/0342 →
Continuity (4)
Continuation 14745060 · Jun 19, 2015
Division 13824912
Provisional Application 61409781 · Nov 3, 2010
Related Publication 20170231982A1 · Aug 17, 2017
Cited By (1)
US 12,403,139