IP Library Granted Patent US 11,413,278
Granted Patent B2
US 11,413,278 · App. 15/766,797 · Granted Aug 16, 2022

Compounds and methods for promoting stress resistance

Inventors: Cynthia Kenyon (Nicasio, CA); Peichuan Zhang (Berkeley, CA); James Cregg (San Francisco, CA); Kean-Hooi Ang (San Francisco, CA); Michelle Arkin (San Francisco, CA)
Assignee: The Regents of the University of California
A61K31/443A61K31/12A61K31/341A61K31/404A61K31/4184A61K31/437A61K31/44A61K31/4406A61K31/4439A61K31/45A61K31/519A61K31/55A61P3/10A61P9/00A61P29/00A61P35/00
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,413,278
App. No.
15/766,797
Granted
Aug 16, 2022
Kind
B2
Abstract

Disclosed herein, inter alia, are compounds and methods useful for increasing stress resistance.

Claims (19)

1. A method of treating lung cancer in a subject in need thereof, the method comprising administering to the subject an effective amount of a compound of Formula (Ia) or a pharmaceutically acceptable salt thereof:

wherein:

R 4 is R 29 -substituted or unsubstituted phenyl or R 29 -substituted or unsubstituted 5 or 6 membered heteroaryl;

R 29 is halogen, —CF 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC═(O)NHNH 2 , —NHC═(O)NH 2 , —NHSO 2 H, —NHC═(O)H, —NHC(O)—OH, —NHOH, —OCF 3 , —OCHF 2 , phenoxy, R 30 -substituted or unsubstituted C 1 -C 6 alkyl, R 30 -substituted or unsubstituted 2 to 6 membered heteroalkyl, R 30 -substituted or unsubstituted C 3 -C 6 cycloalkyl, R 30 -substituted or unsubstituted 3 to 6 membered heterocycloalkyl, R 30 -substituted or unsubstituted phenyl, or R 30 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 30 is halogen, —CF 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC═(O)NHNH 2 , —NHC═(O)NH 2 , —NHSO 2 H, —NHC═(O)H, —NHC(O)—OH, —NHOH, —OCF 3 , —OCHF 2 , R 31 -substituted or unsubstituted C 1 -C 6 alkyl, R 31 -substituted or unsubstituted 2 to 6 membered heteroalkyl, R 31 -substituted or unsubstituted C 3 -C 6 cycloalkyl, R 31 -substituted or unsubstituted 3 to 6 membered heterocycloalkyl, R 31 -substituted or unsubstituted phenyl, or R 31 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 31 is halogen, oxo, —CF 3 , —CCl 3 , —CN, —S(O)CH 3 , —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —C(O)CH 3 , —CH 2 CH 2 OH, —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC═(O)NHNH 2 , —NHC═(O)NH 2 , —NHSO 2 H, —NHC═(O)H, —NHC(O)OH, —NHOH, —OCH 3 , —OCF 3 , —OCHF 2 unsubstituted C 1 -C 6 alkyl, unsubstituted 2 to 6 membered heteroalkyl, unsubstituted C 3 -C 6 cycloalkyl, unsubstituted 3 to 6 membered heterocycloalkyl, unsubstituted phenyl, or unsubstituted 5 to 6 membered heteroaryl.

2. The method of claim 1 , wherein the compound of Formula (Ia) is:

3. The method of claim 1 , wherein the lung cancer is non-small cell lung cancer.

4. A method of inhibiting proliferation of lung cancer cells or inhibiting survival of lung cancer cells, the method comprising contacting the lung cancer cells with a compound of formula (Ia) or a pharmaceutically acceptable salt thereof;

wherein:

R 4 is R 29 -substituted or unsubstituted phenyl or R 29 -substituted or unsubstituted 5 or 6 membered heteroaryl;

R 29 is halogen, —CF 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC═(O)NHNH 2 , —NHC═(O)NH 2 , —NHSO 2 H, —NHC═(O)H, —NHC(O)—OH, —NHOH, —OCF 3 , —OCHF 2 , phenoxy, R 30 -substituted or unsubstituted C 1 -C 6 alkyl, R 30 -substituted or unsubstituted 2 to 6 membered heteroalkyl, R 30 -substituted or unsubstituted C 3 -C 6 cycloalkyl, R 30 -substituted or unsubstituted 3 to 6 membered heterocycloalkyl, R 30 -substituted or unsubstituted phenyl, or R 30 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 30 is halogen, —CF 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC═(O)NHNH 2 , —NHC═(O)NH 2 , —NHSO 2 H, —NHC═(O)H, —NHC(O)—OH, —NHOH, —OCF 3 , —OCHF 2 , R 31 -substituted or unsubstituted C 1 -C 6 alkyl, R 31 -substituted or unsubstituted 2 to 6 membered heteroalkyl, R 31 -substituted or unsubstituted C 3 -C 6 cycloalkyl, R 31 -substituted or unsubstituted 3 to 6 membered heterocycloalkyl, R 31 -substituted or unsubstituted phenyl, or R 31 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 31 is halogen, oxo, —CF, —CCl 3 , —CN, —S(O)CH 3 , —OH, —NH, —COOH, —CONH 2 , —NO 2 , —C(O)CH 3 , —CH 2 CH 2 OH, —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC═(O)NHNH 2 , —NHC═(O)NH 2 , —NHSO 2 H, —NHC═(O)H, —NHC(O)OH, —NHOH, —OCH, —OCF 3 , —OCHF 2 , unsubstituted C 1 -C 6 alkyl, unsubstituted 2 to 6 membered heteroalkyl, unsubstituted C 3 -C 6 cycloalkyl, unsubstituted 3 to 6 membered heterocycloalkyl, unsubstituted phenyl, or unsubstituted 5 to 6 membered heteroaryl.

5. The method of claim 4 , wherein the compound of Formula (Ia) is:

6. The method of claim 4 , wherein the lung cancer cells are non-small cell lung cancer cells.

7. The method of claim 2 , wherein the compound of Formula (Ia) is:

8. The method of claim 2 , wherein the compound of Formula (Ia) is:

9. The method of claim 2 , wherein the compound of Formula (Ia) is:

Assignments (1)
CONFIRMATORY LICENSE Recorded Apr 27, 2018
From: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046033/0827 →
Continuity (3)
Provisional Application 62245812 · Oct 23, 2015
Provisional Application 62239244 · Oct 8, 2015
Related Publication 20180289682A1 · Oct 11, 2018