IP Library Granted Patent US 11,084,781
Granted Patent B2
US 11,084,781 · App. 16/612,680 · Granted Aug 10, 2021

Diarylureas as CB1 allosteric modulators

Inventors: Yanan Zhang (Apex, NC); Thuy Nguyen (Morrisville, NC); Nadezhda German (Amarillo, TX)
Assignee: Research Triangle Institute
C07C275/38A61P25/30C07D205/04C07D207/335C07D211/38C07D213/643C07D215/12C07D239/26C07D295/135C07D333/20C07D487/08C07D491/107
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Quick Facts
Patent No.
US 11,084,781
App. No.
16/612,680
Granted
Aug 10, 2021
Kind
B2
Abstract

The present invention provides novel diarylurea derivatives (compounds of formula (I)) and their uses. The compounds of the present invention are demonstrated to be allosteric modulators of the CB1 receptor, and therefore useful for the treatment of diseases and conditions mediated by CB1.

Claims (44)

1. A compound of Formula (I):

wherein:

R 2 is C 1-6 alkyl, C 1-6 alkoxy, halogen, or C 1-6 haloalkyl;

R 3 is H, C 1-6 alkyl, C 1-6 alkenyl, C 1-6 alkynyl, halogen, C 1-6 haloalkyl, NO 2 , or CN; and

n is 1, 2, or 3;

or a pharmaceutically acceptable salt or solvate thereof.

2. The compound of claim 1 , wherein n is 1.

3. The compound of claim 1 , wherein R 3 is halogen or cyano.

4. The compound of claim 1 , wherein R 3 is Cl.

5. The compound of claim 1 , wherein R 2 is halogen.

6. A method for inhibiting the CB1 receptor comprising administering an effective amount of a compound of claim 1 to a patient in need thereof, wherein the patient suffers from a CB1 receptor mediated disorder selected from one or more of substance withdrawal, drug dependence, smoking cessation, opioid addiction, cocaine addiction, relapse of cocaine addiction, tobacco addiction, alcohol addiction, endometrial cancer, hepatocellular carcinoma, ovarian cancer, breast cancer, pancreatic cancer, colorectal cancer, lung cancer, prostate cancer, desmotrophic small round cell tumors, and renal cell carcinoma, analgesia, chronic pain, acute pain, somatic pain, visceral pain, neuropathic pain, inflammatory pain, infertility, memory loss, cognitive dysfunction, Alzheimer's Disease, Tourette's Syndrome, dyskinesia, amyotrophic lateral sclerosis, stroke, atherosclerosis, hypertension, hemorrhagic shock, cardiogenic shock, hypercholesterolemia, dyslipidemia, diabetes, retinopathy, glaucoma, anxiety, gastrointestinal disorders, intestinal hypomotility, obesity, appetite behavior, or weight loss.

7. The method of claim 6 , wherein the disorder is selected from the group consisting of:

(a) substance withdrawal, drug dependence, smoking cessation, opioid addiction, cocaine addiction, tobacco addiction, alcohol addiction, and relapse of addiction;

(b) endometrial cancer, hepatocellular carcinoma, ovarian cancer, breast cancer, pancreatic cancer, colorectal cancer, lung cancer, prostate cancer, desmotrophic small round cell tumors, and renal cell carcinoma;

(c) infertility;

(d) hypercholesterolemia, dyslipidemia, diabetes, gastrointestinal disorders, intestinal hypomotility, obesity, appetite behavior, and weight loss; and

(e) retinopathy and glaucoma.

8. A pharmaceutical compositon comprising a compound of claim 1 and one or more pharmaceutically acceptable carriers.

9. A compound selected from the group consisting of:

3-(4-Chlorophenyl)-1-[3-(4-chlorophenyl)phenyl]urea;

3-(4-Chlorophenyl)-1-[3-(4-fluorophenyl)phenyl]urea;

3-(4-Chlorophenyl)-1-[3-(4-tert-butylphenyl)phenyl]urea;

and pharmaceutically acceptable salts or solvates thereof.

10. A method for inhibiting the CB1 receptor comprising administering an effective amount of a compound of claim 9 to a patient in need thereof, wherein the patient suffers from a CB1 receptor mediated disorder selected from one or more of substance withdrawal, drug dependence, smoking cessation, opioid addiction, cocaine addiction, relapse of cocaine addiction, tobacco addiction, alcohol addiction, endometrial cancer, hepatocellular carcinoma, ovarian cancer, breast cancer, pancreatic cancer, colorectal cancer, lung cancer, prostate cancer, desmotrophic small round cell tumors, and renal cell carcinoma, analgesia, chronic pain, acute pain, somatic pain, visceral pain, neuropathic pain, inflammatory pain, infertility, memory loss, cognitive dysfunction, Alzheimer's Disease, Tourette's Syndrome, dyskinesia, amyotrophic lateral sclerosis, stroke, atherosclerosis, hypertension, hemorrhagic shock, cardiogenic shock, hypercholesterolemia, dyslipidemia, diabetes, retinopathy, glaucoma, anxiety, gastrointestinal disorders, intestinal hypomotility, obesity, appetite behavior, or weight loss.

11. The method of claim 10 , wherein the disorder is selected from the group consisting of:

(a) substance withdrawal, drug dependence, smoking cessation, opioid addiction, cocaine addiction, tobacco addiction, alcohol addiction, and relapse of addiction;

(b) endometrial cancer, hepatocellular carcinoma, ovarian cancer, breast cancer, pancreatic cancer, colorectal cancer, lung cancer, prostate cancer, desmotrophic small round cell tumors, and renal cell carcinoma;

(c) infertility;

(d) hypercholesterolemia, dyslipidemia, diabetes, anxiety, gastrointestinal disorders, intestinal hypomotility, obesity, appetite behavior, and weight loss; and

(e) retinopathy and glaucoma.

12. A pharmaceutical compositon comprising a compound of claim 9 and one or more pharmaceutically acceptable carriers.

13. The compound of claim 9 , wherein the compound is 3-(4-Chlorophenyl)-1-[3-(4-fluorophenyl)phenyl]urea or a pharmaceutically acceptable salt or solvate thereof.

14. The compound of claim 1 , wherein R 3 is halogen.

15. The compound of claim 1 , wherein n is 2.

16. The compound of claim 1 , wherein n is 3.

17. The compound of claim 1 , wherein R 2 is C 1-6 alkyl or C 1-6 alkoxy.

18. The compound of claim 1 , wherein R 2 is C 1-6 haloalkyl.

19. The compound of claim 1 , wherein R 2 is fluorine.

20. The compound of claim 19 , wherein R 3 is halogen.

21. The compound of claim 19 , wherein R 3 is chlorine.

22. The compound of claim 21 , wherein n is 1.

23. The pharmaceutical composition of claim 12 , wherein the compound is 3-(4-Chlorophenyl)-1-[3-(4-fluorophenyl)phenyl]urea or a pharmaceutically acceptable salt or solvate thereof.

24. The method of claim 6 , wherein the disorder is selected from the group consisting of substance withdrawal, drug dependence, smoking cessation, opioid addiction, cocaine addiction, tobacco addiction, alcohol addiction, and relapse of addiction.

25. The method of claim 10 , wherein the disorder is selected from the group consisting of substance withdrawal, drug dependence, smoking cessation, opioid addiction, cocaine addiction, tobacco addiction, alcohol addiction, and relapse of addiction.

Assignments (3)
CONFIRMATORY LICENSE Recorded Jan 31, 2023
From: RESEARCH TRIANGLE INSTITUTE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 062559/0346 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INADVERTENTLY OMITTED ASSIGNOR:NADEZHDA GERMAN DOC DATE: 11/10/2019 PREVIOUSLY RECORDED ON REEL 051834 FRAME 0583. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNOR INADVERTENTLY OMITTED WHEN RECORDING - SEE SIGNED ASSIGNMENT. Recorded Feb 19, 2020
From: ZHANG, YANAN; NGUYEN, THUY; GERMAN, NADEZHDA
To: RESEARCH TRIANGLE INSTITUTE
Reel/Frame 051969/0180 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 17, 2020
From: ZHANG, YANAN; NGUYEN, THUY
To: RESEARCH TRIANGLE INSTITUTE
Reel/Frame 051834/0583 →
Continuity (2)
Provisional Application 62505383 · May 12, 2017
Related Publication 20200062699A1 · Feb 27, 2020