IP Library Granted Patent US 11,007,186
Granted Patent B2
US 11,007,186 · App. 16/272,911 · Granted May 18, 2021

Methods of treating RBP4 related diseases with triazolopyridines

Inventors: Yu-Hsin Tom Lin (San Diego, CA); Cheng-Chi Irene Wang (San Diego, CA)
Assignee: Belite Bio, Inc
A61K31/4545A61K9/0019A61K9/0053A61K31/4985A61K31/519A61K31/5365A61K31/5383A61P3/04A61P3/10
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Quick Facts
Patent No.
US 11,007,186
App. No.
16/272,911
Granted
May 18, 2021
Kind
B2
Abstract

Provided herein are heterocyclic derivative compounds and pharmaceutical compositions comprising said compounds that are useful for the treatment of retinal binding protein (RBP4) related diseases, such as obesity and the like.

Claims (61)

1. A method of treating a metabolic disease or disorder in a subject in need thereof, the method comprising administering to the subject a composition comprising a therapeutically effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof:

wherein:

each R 1 is independently halogen, haloalkyl, or alkyl;

R 2 is —H, —OH, or halogen;

p is 0, 1, 2, 3, 4, or 5; and

A has the structure:

wherein:

α, β, χ, and δ are each independently absent or present, and when present each is a bond;

X is N;

Z 1 is S, O, or N;

Z 2 is S, O, N, or NR 3 ;

R 3 is H, C 1 -C 4 alkyl, or oxetane; and

B is a substituted or unsubstituted fused 5-, 6-, or 7-membered ring structure; and

wherein the metabolic disease or disorder is type II diabetes or diabetic retinopathy.

2. The method of claim 1 , wherein:

when α is present, then Z 1 and Z 2 are N, X is N, β is present, and χ and δ are absent.

3. The method of claim 1 , wherein A has the structure

wherein:

n is 0, 1, or 2;

α, β, χ, δ, ϵ, and ϕ are each independently absent or present, and when present each is a bond;

Z 1 is S, O, or N;

Z 2 is S, O, N or NR 3 ,

wherein R 3 is H, C 1 -C 4 alkyl, or oxetane;

X is N;

Y 1 , Y 2 , Y 3 and each occurrence of Y 4 are each independently CR 4 , C(R 5 ) 2 , NR 6 , O, N, SO 2 , or —(C═O)—, wherein:

each R 4 is independently H, halogen, C 1 -C 10 alkyl, C 1 -C 10 cycloalkyl, —O(C 1 -C 10 alkyl), —C(O)OH, —C(O)O(C 1 -C 10 alkyl), —C(O)NH 2 , —C(O)NH (C 1 -C 4 alkyl), —C(O)N(C 1 -C 4 alkyl) 2 , —NHC(O)NH(C 1 -C 10 alkyl), —NHC(O)N(C 1 -C 4 alkyl) 2 , —SO 2 NH(C 1 -C 10 alkyl), —SO 2 N(C 1 -C 10 alkyl) 2 , —CN, or —CF 3 ;

each R 5 is independently H or C 1 -C 10 alkyl; and

each R 6 is independently H, C 1 -C 10 alkyl, C 3 -C 6 cycloalkyl, —(C 1 -C 10 alkyl)CF 3 , —(C 1 -C 10 alkyl)OCH 3 , —(C 1 -C 10 alkyl)-halogen, —SO 2 (C 1 -C 10 alkyl), —SO 2 (C 1 -C 10 alkyl)-CF 3 , —SO 2 (C 1 -C 10 alkyl)OCH 3 , —SO 2 (C 1 -C 10 alkyl)-halogen, —C(O)(C 1 -C 10 alkyl), —C(O)(C 1 -C 10 alkyl)CF 3 , —C(O)(C 1 -C 10 alkyl)OCH 3 , —C(O)(C 1 -C 10 alkyl)-halogen, —C(O)NH(C 1 -C 10 alkyl), —C(O)N(C 1 -C 10 alkyl) 2 , —(C 1 -C 10 alkyl)C(O)OH, —C(O)NH 2 , or oxetane.

4. The method of claim 1 , wherein:

when α is present, then Z 1 and Z 2 are N, X is N, β is present, and χ and δ are absent;

when ϵ and ϕ are each present, then n=1, and each of Y 1 , Y 2 , Y 3 , and Y 4 , are independently —CR 4 — or N; or

when ϵ and ϕ are each absent, then n=0, 1 or 2, each of Y 1 , Y 2 , Y 3 , and each occurrence of Y 4 are independently C(R 5 ) 2 , NR 6 , O, or SO 2 .

5. The method of claim 1 , wherein:

α, β, ϵ, and ϕ are present;

χ and δ are absent;

Z 1 is N;

Z 2 is N; and

X is N.

6. The method of claim 1 , wherein A has the structure:

wherein:

Y 1 , Y 2 , Y 3 and Y 4 are each independently CR 4 or N; and

each R 4 is independently H, halogen, C 1 -C 10 alkyl, C 1 -C 10 cycloalkyl, —O(C 1 -C 10 alkyl), —C(O)OH, —C(O)O(C 1 -C 10 alkyl), —C(O)NH 2 , —C(O)NH (C 1 -C 4 alkyl), —C(O)N(C 1 -C 4 alkyl) 2 , —NHC(O)NH(C 1 -C 10 alkyl), —NHC(O)N(C 1 -C 4 alkyl) 2 , —SO 2 NH(C 1 -C 10 alkyl), —SO 2 N(C 1 -C 10 alkyl) 2 , —CN, or —CF 3 .

7. The method of claim 1 , wherein A has the structure

wherein:

each R 4 is independently H, halogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —O(C 1 -C 4 alkyl), —CN, —CF 3 , —C(O)OH, —C(O)NH 2 , —C(O)N(CH 3 ) 2 , —C(O)NHCH 3 , or —NHC(O)N(CH 3 ) 2 .

8. The method of claim 1 , wherein each R 1 is independently F, Br, Cl, C 1-6 haloalkyl, or C 1-6 alkyl.

9. The method of claim 1 , wherein each R 1 is independently F or CF 3 .

10. A method of treating a metabolic disease or disorder in a subject in need thereof, the method comprising administering to the subject a composition comprising a therapeutically effective amount of a compound having the structure:

or a pharmaceutically acceptable salt thereof; and

wherein the metabolic disease or disorder is type II diabetes or diabetic retinopathy.

11. A method of treating a metabolic disease or disorder in a subject in need thereof, the method comprising administering to the subject a composition comprising a therapeutically effective amount of a compound having the structure:

or a pharmaceutically acceptable salt thereof; and

wherein the metabolic disease or disorder is type II diabetes or diabetic retinopathy.

12. The method of claim 1 , wherein the therapeutically effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof is up to 25 mg per day, up to 50 mg per day, up to 75 mg per day, up to 100 mg per day, up to 150 mg per day, up to 200 mg per day, up to 400 mg per day, up to 600 mg per day, up to 800 mg per day, or up to 1000 mg per day.

13. The method of claim 1 , wherein 24 hours after administration of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, the serum or plasma levels of RBP4 are reduced by at least 50% from baseline.

14. The method of claim 1 , wherein 24 hours after administration of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, the serum or plasma levels of RBP4 are reduced by at least 1 mg/dL.

15. The method of claim 1 , wherein the disease or disorder is type II diabetes.

16. The method of claim 1 , wherein the disease or disorder is diabetic retinopathy.

17. The method of claim 1 , wherein the compound is administered to the subject orally or intravenously.

18. The method of claim 1 , wherein the administration is to treat an existing disease or disorder.

19. The method of claim 1 , wherein the administration is provided to reduce the risk of type II diabetes, its chronic complications, or its clinical symptoms.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2023
From: PETRUKHIN, KONSTANTIN
To: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Reel/Frame 063420/0873 →
CONFIRMATORY LICENSE Recorded Feb 7, 2023
From: COLUMBIA UNIV NEW YORK MORNINGSIDE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 062668/0496 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 17, 2019
From: LIN, YU-HSIN TOM; WANG, CHENG-CHI IRENE
To: BELITE BIO, INC
Reel/Frame 050399/0565 →
Continuity (3)
Division 16008838 · Jun 14, 2018
Provisional Application 62520420 · Jun 15, 2017
Related Publication 20190240212A1 · Aug 8, 2019
Cited By (2)
US 12,364,693 US 12,714,700