IP Library Granted Patent US 9,737,512
Granted Patent B2
US 9,737,512 · App. 15/066,416 · Granted Aug 22, 2017

Methods and compositions for treating chronic pain

Inventors: Xiaodong Cheng (Houston, TX); Fang Mei (Houston, TX); Annemieke Kavelaars (Houston, TX); Cobi J. Heijnen (Houston, TX)
Assignee: THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM
A61K31/422A61K31/275A61K31/42A61K31/33
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Quick Facts
Patent No.
US 9,737,512
App. No.
15/066,416
Granted
Aug 22, 2017
Kind
B2
Abstract

Certain embodiments are directed to methods of treating pain, e.g., chronic or neuropathic pain, comprising administering an effective amount of an EPAC inhibitor.

Claims (13)

1. A method of treating pain comprising administering an effective amount of an EPAC inhibitor having a general formula of:

where R 1 and R 2 are independently substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycle, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl to a subject in need of such treatment.

2. The method of claim 1 , wherein R 1 is a substituted isoxazole.

3. The method of claim 2 , wherein the substituted isoxazole has linear alkyl, branched alkyl, or cycloalkyl substitution.

4. The method of claim 2 , wherein the substituted isoxazole is methyl, ethyl, n-propyl, iso-propyl), n-butyl, sec-butyl, iso-butyl, tert-butyl, neo-pentyl, n-pentyl, or isopenyl substituted isoxazole.

5. The method of claim 2 , wherein R 1 is a 5-methyl isoxazole or a 5-tert-butyl isoxazole.

6. The method of claim 1 , wherein R 2 is a substituted or unsubstituted phenyl.

7. The method of claim 6 , wherein R 2 is a substituted phenyl having one or more substituent selected from bromo, fluoro, chloro, iodo, or combinations thereof.

8. The method of claim 6 , wherein R 2 is a 3-chlorophenyl; 2-chlorophenyl; 4-chlorophenyl; phenyl; 3,6-dichlorophenyl; 3-methylphenyl, 3-trifluoromethylphenyl; 3-nitrophenyl; 4-methylphenyl, 3,5-dichlorophenyl; 4-bromophenyl; 3-bromophenyl; 3,6-dimethylphenyl; benzopyridine; 2,3-dichlorophenyl; 3-ethynyl; benzoic acid ethyl ester; 3-benzonitrile; 3-acetylphenyl; 2,3-methylphenyl; 3-ethoxyphenyl; indane; 3,5-di-trifluoromethylphenyl; 6-chloro-benzoic acid; or 3-chloro, 4-hydroxyphenyl.

9. The method of claim 1 , wherein the compound is selected from N-(5-tert-Butyl-isoxazol-3-yl)-2-[(3-chlorophenyl)-hydrazono]-2-cyanoacetamide (HJC0683); 2-[(3-Chlorophenyl)-hydrazono]-2-cyano-N-(5-methyl-isoxazol-3-yl)acetamide (HJC0692); 3-(5-tert-Butyl-isoxazol-3-yl)-2-[(2-chlorophenyl)-hydrazono]-3-oxo-propionitrile (HJC0693); 3-(5-tert-Butyl-isoxazol-3-yl)-2-[(4-chlorophenyl)-hydrazono]-3-oxo-propionitrile (HJC0694); 3-(5-tert-Butyl-isoxazol-3-yl)-3-oxo-2-(phenyl-hydrazono)-propionitrile (HJC0695); 3-(5-tert-Butyl-isoxazol-3-yl)-2-[(2,5-dichlorophenyl)-hydrazono]-3-oxo-propionitrile (HJC0696); 3-(5-tert-Butyl-isoxazol-3-yl)-3-oxo-2-(m-tolyl-hydrazono)propionitrile (HJC0712); 3-(5-tert-Butyl-isoxazol-3-yl)-3-oxo-2-[(3-trifluoromethyl-phenyl)-hydrazono]propionitrile (HJC0720); 3-(5-tert-Butyl-isoxazol-3-yl)-2-[(3-nitrophenyl)-hydrazono]-3-oxo-propionitrile (HJC0721); 3-(5-tert-Butyl-isoxazol-3-yl)-3-oxo-2-(p-tolyl-hydrazono)propionitrile (HJC0724); 3-(5-tert-Butyl-isoxazol-3-yl)-2-[(3,5-dichlorophenyl)-hydrazono]-3-oxo-propionitrile (HJC0726); 2-[(4-Bromophenyl)-hydrazono]-3-(5-tert-butyl-isoxazol-3-yl)-3-oxo-propionitrile (HJC0742); 2-[(3-Bromophenyl)-hydrazono]-3-(5-tert-butyl-isoxazol-3-yl)-3-oxo-propionitrile (HJC0743); 3-(5-tert-Butyl-isoxazol-3-yl)-2-[(2,5-dimethylphenyl)-hydrazono]-3-oxo-propionitrile (HJC0744); 3-(5-tert-Butyl-isoxazol-3-yl)-3-oxo-2-(quinolin-6-yl-hydrazono)propionitrile (HJC0745); 3-(5-tert-Butyl-isoxazol-3-yl)-2-[(2,3-dichlorophenyl)-hydrazono]-3-oxo-propionitrile (HJC0750); 3-(5-tert-Butyl-isoxazol-3-yl)-2-[(3-ethynyl-phenyl)-hydrazono]-3-oxo-propionitrile (HJC0751); 3-{N-[2-(5-tert-Butyl-isoxazol-3-yl)-1-cyano-2-oxo-ethylidene]-hydrazino}benzoic acid ethyl ester (HJC0752); 3-{N-[2-(5-tert-Butyl-isoxazol-3-yl)-1-cyano-2-oxo-ethylidene]-hydrazino}benzonitrile (HJC0753); 2-[(3-Acetyl-phenyl)-hydrazono]-3-(5-tert-butyl-isoxazol-3-yl)-3-oxo-propionitrile (HJC0754); 3-(5-tert-Butyl-isoxazol-3-yl)-2-[(2,3-dimethylphenyl)-hydrazono]-3-oxo-propionitrile (HJC0755); 3-(5-tert-Butyl-isoxazol-3-yl)-2-[(3-hydroxymethylphenyl)-hydrazono]-3-oxo-propionitrile (HJC0756); 3-(5-tert-Butyl-isoxazol-3-yl)-2-(indan-5-yl-hydrazono)-3-oxo-propionitrile (HJC0757); 2-[(3,5-Bis-trifluoromethyl-phenyl)-hydrazono]-3-(5-tert-butyl-isoxazol-3-yl)-3-oxo-propionitrile (HJC0758); 2-{N-[2-(5-tert-Butyl-isoxazol-3-yl)-1-cyano-2-oxo-ethylidene]-hydrazino}-6-chloro-benzoic acid (HJC0759); 3-(5-tert-Butyl-isoxazol-3-yl)-2-[(3-chloro-4-hydroxy-phenyl)-hydrazono]-3-oxo-propionitrile (HJC0760); 2-[(3-Chloro-phenyl)-hydrazono]-3-(5-methyl-isoxazol-3-yl)-3-oxo-propionitrile (HJC0768); or 2-[(3,5-Dichlorophenyl)-hydrazono]-3-(5-methyl-isoxazol-3-yl)-3-oxo-propionitrile (HJC0770).

10. The method of claim 1 , wherein the EPAC inhibitor is 3-(5-tert-Butyl-isoxazol-3-yl)-2-[(3-chlorophenyl)-hydrazono]-3-oxo-propionitrile (HJC0680, ESI-09).

11. The method of claim 1 , wherein the pain is chronic or neuropathic pain.

12. The method of claim 11 , wherein the chronic pain is chemotherapy-associated chronic pain.

Assignments (1)
CONFIRMATORY LICENSE Recorded Jan 3, 2017
From: UNIVERSITY OF TEXAS MEDICAL BR GALVESTON
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 041231/0133 →
Continuity (2)
Provisional Application 62131821 · Mar 11, 2015
Related Publication 20160263088A1 · Sep 15, 2016