IP Library Granted Patent US 11,980,614
Granted Patent B2
US 11,980,614 · App. 17/228,590 · Granted May 14, 2024

Methods of treating RBP4 related diseases with triazolopyridines

Inventors: Yu-Hsin Tom Lin (San Diego, CA); Cheng-Chi Irene Wang (San Diego, CA); Konstantin Petrukhin (New Windsor, NY)
Assignees: Belite Bio, Inc; The Trustees of Columbia University in the City of New York
A61K31/4545A61K9/0019A61K9/0053A61K31/4985A61K31/519A61K31/5365A61K31/5383A61P3/04A61P3/10
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Quick Facts
Patent No.
US 11,980,614
App. No.
17/228,590
Granted
May 14, 2024
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 (59)

1. A method of treating obesity 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 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.

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 , —(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 obesity 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.

11. A method of treating obesity 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.

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), 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 compound is administered to the subject orally or intravenously.

16. The method of claim 1 , wherein the administration is to treat existing obesity.

17. The method of claim 1 , wherein the administration is provided to reduce the risk of obesity, its chronic complications, or its clinical symptoms.

18. The method of claim 1 , wherein the administration is provided to cause regression, reversal, or amelioration of obesity.

19. The method of claim 1 , wherein the administration improves plasma insulin levels.

20. The method of claim 1 , wherein the administration decreases an inflammatory cytokine.

Assignments (3)
CONFIRMATORY LICENSE Recorded Nov 10, 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 065547/0959 →
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 063420/0905 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 1, 2022
From: LIN, YU-HSIN TOM; WANG, CHENG-CHI IRENE
To: BELITE BIO, INC
Reel/Frame 059745/0585 →
Continuity (4)
Division 16272911 · Feb 11, 2019
Division 16008838 · Jun 14, 2018
Provisional Application 62520420 · Jun 15, 2017
Related Publication 20210228563A1 · Jul 29, 2021