IP Library › Granted Patent US 12,213,971
Granted Patent B2
US 12,213,971 · App. 18/310,387 · Granted Feb 4, 2025

Histone deacetylase inhibitors for immunomodulation in tumor microenvironment

Inventors: Jia-Shiong Chen (Taipei, TW); Mu-Hsuan Yang (Taipei, TW); Yi-Hong Wu (Taipei, TW); Sz-Hao Chu (Taipei, TW); Cheng-Han Chou (Taipei, TW); Ye-Su Chao (Taipei, TW); Chia-Nan Chen (Taipei, TW)
Assignee: GREAT NOVEL THERAPEUTICS BIOTECH & MEDICALS CORPORATION
A61K31/444A61K31/44A61K31/4406A61P35/00C07D213/56C07D401/12
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Quick Facts
Patent No.
US 12,213,971
App. No.
18/310,387
Granted
Feb 4, 2025
Kind
B2
Abstract

The present disclosure generally relates to compounds class I HDAC inhibitors, their production and applications. The compounds possess epigenetic immunomodulatory activities in the tumor microenvironment (TME) and thus inhibit growth of tumor cells.

Claims (41)

1. A method for epigenetic immunomodulation of tumor microenvironment (TME) and/or treatment of cancer in a subject in need thereof, the method comprising administrating an effective amount of a compound of formula (I) to the subject:

wherein W and Y are each independently selected from CH and N;

R 1 is each independently selected from hydrogen, halogen, C 1 -C 3 alkyl and halogenated C 1 -C 3 alkyl, and can be mono-, di-, tri- or tetra-substitution;

C 1 and C 2 are C atoms linked by a double bond;

Ar is selected from the group consisting of the following:

wherein Ar is linked to C 2 via the solid line;

R 2 has the same meaning as described for R 1 ; and

R 3 is hydrogen or C 1 -C 3 alkyl;

or a pharmaceutically acceptable salt, hydrate, stereoisomer or solvate thereof.

2. The method of claim 1 , wherein the compound has the formula (Ia):

wherein W, Y, R 1 , C 1 , C 2 and Ar have the same meaning as described in formula (I), or a pharmaceutically acceptable salt, hydrate, stereoisomer or solvate thereof.

3. The method of claim 1 , wherein in Formula (I) Ar is selected from the six-membered rings, and R 2 and the atom of Ar linked to C 2 are at para-positions.

4. The method of claim 1 , wherein in Formula (I) W and Y are selected from the following combinations: (1) W is N and Y is CH, (2) W is CH and Y is N, and (3) W and Y are CH.

5. The method of claim 1 , wherein in Formula (I) W is N and Y is CH.

6. The method of claim 1 , wherein in Formula (I) R 1 is F or fluorinated C 1 -C 3 alkyl.

7. The method of claim 1 , wherein in Formula (I) R 2 is C 1 -C 3 alkyl or fluorinated C 1 -C 3 alkyl.

8. The method of claim 1 , wherein the compound is selected from the group consisting of:

or a pharmaceutically acceptable salt, hydrate, stereoisomer or solvate thereof.

9. The method of claim 1 , wherein one or more second agent can be further administered in combination with the compound of formula (I).

10. The method of claim 9 , wherein the one or more second agent is an immune checkpoint inhibitor, an NSAID, a TKI or an anti-cancer agent or a combination thereof.

11. The method of claim 1 , wherein the method is for inducing cell cycle arrest of tumor cells, for inducing apoptosis of tumor cells, for inducing histone H3 acetylation, for inducing immune memory, for activating CTL, for decreasing immunosuppressive cells.

12. A method for treating or preventing the disease associated with class I HDAC in a subject in need thereof comprising administrating an effective amount of a compound of formula (I) to the subject:

wherein W and Y are each independently selected from CH and N;

R 1 is each independently selected from hydrogen, halogen, C 1 -C 3 alkyl and halogenated C 1 -C 3 alkyl, and can be mono-, di-, tri- or tetra-substitution;

C 1 and C 2 are C atoms linked by a double bond;

Ar is selected from the group consisting of the following:

wherein Ar is linked to C 2 via the solid line;

R 2 has the same meaning as described for R 1 ; and

R 3 is hydrogen or C 1 -C 3 alkyl;

or a pharmaceutically acceptable salt, hydrate, stereoisomer or solvate thereof.

13. The method of claim 12 , wherein the compound has the formula (Ia):

wherein W, Y, R 1 , C 1 , C 2 and Ar have the same meaning as described in formula (I), or a pharmaceutically acceptable salt, hydrate, stereoisomer or solvate thereof.

14. The method of claim 12 , wherein in Formula (I) Ar is selected from the six-membered rings, and R 2 and the atom of Ar linked to C 2 are at para-positions.

15. The method of claim 12 , wherein in Formula (I) W and Y are selected from the following combinations: (1) W is N and Y is CH, (2) W is CH and Y is N, and (3) W and Y are CH.

16. The method of claim 12 , wherein in Formula (I) W is N and Y is CH.

17. The method of claim 12 , wherein in Formula (I) R 1 is F or fluorinated C 1 -C 3 alkyl.

18. The method of claim 12 , wherein in Formula (I) R 2 is C 1 -C 3 alkyl or fluorinated C 1 -C 3 alkyl.

19. The method of claim 12 , wherein the compound is selected from the group consisting of:

or a pharmaceutically acceptable salt, hydrate, stereoisomer or solvate thereof.

20. The method of claim 12 , wherein one or more second agent can be further administered in combination with the compound of formula (I).

21. The method of claim 20 , wherein the one or more second agent is an immune checkpoint inhibitor, an NSAID, a TKI or an anti-cancer agent or a combination thereof.

Assignments (1)
NUNC PRO TUNC ASSIGNMENT Recorded Jul 27, 2023
From: CHEN, JIA-SHIONG; YANG, MU-HSUAN; WU, YI-HONG; CHU, SZ-HAO; CHOU, CHENG-HAN; CHAO, YE-SU; CHEN, CHIA-NAN
To: GREAT NOVEL THERAPEUTICS BIOTECH & MEDICALS CORPORATION
Reel/Frame 064410/0361 →
Continuity (3)
Division 17243378 · Apr 28, 2021
Provisional Application 63018427 · Apr 30, 2020
Related Publication 20230263790A1 · Aug 24, 2023
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