IP Library Granted Patent US 11,976,049
Granted Patent B2
US 11,976,049 · App. 18/061,610 · Granted May 7, 2024

Substituted naphthyl p38alpha mitogen-activated protein kinase inhibitors

Inventors: Adam Galan (Alameda, CA); Wendy Luo (Palo Alto, CA); Ritu Lal (Palo Alto, CA)
Assignee: GEN1E LIFESCIENCES INC.
C07D265/32A61P35/00C07D295/135
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Quick Facts
Patent No.
US 11,976,049
App. No.
18/061,610
Granted
May 7, 2024
Kind
B2
Abstract

Substituted naphthyl p38α mitogen-activated protein kinase inhibitors, pharmaceutical compositions thereof, and the use of the substituted naphthyl p38α mitogen-activated protein kinase inhibitors and pharmaceutical compositions thereof for treating diseases are disclosed.

Claims (29)

1. A compound having the structure of Formula (6):

or a pharmaceutically acceptable salt thereof, wherein,

R 1 is selected from C 1-4 alkanediyl, C 1-4 heteroalkanediyl, substituted C 1-4 alkanediyl, and substituted C 1-4 heteroalkanediyl;

R 2 is substituted C 5-12 heterocycloalkyl, wherein

R 2 is bonded to R 1 through a nitrogen heteroatom of the substituted C 5-12 heterocycloalkyl moiety; and

R 2 comprises a heteroatomic group selected from —S—, —NH—, —N(—CH 3 )—, —SO—, and —SO 2 —;

R 3 is selected from —C(═O)— and —SO 2 —;

R 4 is —N(R 5 ) 2 wherein each R 5 is independently selected from hydrogen and C 1-4 alkyl; and

each substituent is independently selected from —OH, ═O, —NH 2 , —NO 2 , C 1-6 alkyl, C 1-6 cycloalkyl, C 6 aryl, C 1-6 heteroalkyl, C 1-6 heterocycloalkyl, and C 5-6 heteroaryl.

2. The compound of claim 1 , wherein R 1 is C 1-4 alkanediyl.

3. The compound of claim 1 , wherein substituted C 5-12 heterocycloalkyl is substituted C 6 heterocycloalkyl.

4. The compound of claim 1 , wherein R 2 comprises the heteroatomic group —SO 2 —.

5. The compound of claim 1 , wherein each R 2 substituent is independently selected from —OH, ═O, and —NH 2 .

6. The compound of claim 1 , wherein each R 2 substituent is ═O.

7. The compound of claim 1 , wherein R 3 is —SO 2 —.

8. The compound of claim 1 , wherein R 4 is bonded to the 5-position of the naphthyl moiety.

9. The compound of claim 1 , wherein,

R 1 is methane-diyl;

R 2 comprises the heteroatomic group —SO 2 —;

R 3 is —SO 2 —; and

R 4 is —N(R 5 ) 2 wherein each R 5 is independently selected from hydrogen and methyl.

10. The compound of claim 1 , wherein in the moiety R 2 , the substituent is ═O.

11. A pharmaceutical composition comprising the compound of claim 1 or a pharmaceutically acceptable salt thereof.

12. A method of treating a disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein the disease is treated by inhibiting the p38α MAPK receptor.

13. A method of treating a disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein the disease is cancer, wherein the cancer is selected from breast cancer and melanoma.

14. A method of treating a disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein the disease is an inflammatory disease, wherein the inflammatory disease is selected from acute respiratory distress syndrome, focal segmental glomerulonephritis, atherosclerosis/acute coronary syndrome, chronic obstructive pulmonary disease, asthma, inflammatory bowel disease, Crohn's disease, psoriasis, lupus, multiple sclerosis, inflammation in hypercholesteremia, pain, diabetes, and rheumatoid arthritis.

15. A method of treating a disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein the disease is an autoimmune disease, wherein the autoimmune disease is selected from lupus, graft-versus-host disease, hepatitis C-induced vasculitis, Type I diabetes, multiple sclerosis, spontaneous loss of pregnancy, an atopic disease, and an inflammatory bowel disease.

16. A method of treating a disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein the disease is an age-related disease, wherein the age-related disease is selected from hearing loss, muscle degeneration, Werner's syndrome, cellular aging, and Alzheimer's disease.

17. A method of treating a disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein the disease is selected from acute lung injury, acute respiratory distress syndrome (ARDS), and chronic obstructive pulmonary disease (COPD).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 13, 2023
From: GALAN, ADAM; LAL, RITU; LUO, WENDY
To: GEN1E LIFESCIENCES INC.
Reel/Frame 062375/0310 →
Continuity (3)
Continuation 17700168 · Mar 21, 2022
Provisional Application 63164664 · Mar 23, 2021
Related Publication 20230227417A1 · Jul 20, 2023