IP Library Granted Patent US 9,682,981
Granted Patent B2
US 9,682,981 · App. 14/556,709 · Granted Jun 20, 2017

Compounds and methods for kinase modulation, and indications therefor

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Quick Facts
Patent No.
US 9,682,981
App. No.
14/556,709
Granted
Jun 20, 2017
Kind
B2
Abstract

Compounds and salts thereof, formulations thereof, conjugates thereof, derivatives thereof, forms thereof and uses thereof are described, wherein the compounds have formula Ia: In certain aspects and embodiments, the described compounds or salts thereof, formulations thereof, conjugates thereof, derivatives thereof, forms thereof are active on one or more of Fms, Kit, Flt3, TrkA, TrkB and TrkC kinase protein. Also described are methods of use thereof to treat diseases and conditions, including diseases and conditions associated with activity of one or more of Fms, Kit, Flt3, TrkA, TrkB and TrkC, including rheumatoid arthritis, osteoarthritis, osteoporosis, peri-prosthetic osteolysis, systemic sclerosis, demyelinating disorders, multiple sclerosis, Charcot Marie Tooth syndrome, amyotrophic lateral sclerosis, Alzheimer's disease, Parkinson's disease, global ischemia, ulcerative colitis, Crohn's disease, immune thrombocytopenic purpura, atherosclerosis, systemic lupus erythematosis, myelopreparation for autologous transplantation, transplant rejection, glomerulonephritis, interstitial nephritis, Lupus nephritis, tubular necrosis, diabetic nephropathy, renal hypertrophy, type I diabetes, acute pain, inflammatory pain, neuropathic pain, acute myeloid leukemia, melanoma, multiple myeloma, breast cancer, prostate cancer, pancreatic cancer, lung cancer, ovarian cancer, gliomas, glioblastoma, neurofibromatosis, osteolytic bone metastases, brain metasteses, gastrointestinal stromal tumors, and giant cell tumors.

Claims (28)

1. A compound of Formula Ia,

or a salt thereof,

wherein:

Y 2 is —N═ and R 15 is hydrogen; or Y 2 is —C(H)═ and R 15 is fluoro or chloro;

L 2 is —CH 2 — or —C(O)—;

Cy 2 is cycloalkyl optionally substituted with one or more R 16 ;

R 14 is —N(R 9a )(R 9b );

R 9a is H and R 9b is selected from the group consisting of (i) H, lower alkyl, lower alkyl substituted with one or more fluoro, lower alkyl substituted with lower alkoxy or lower alkyl substituted with hydroxyl and (ii) cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, arylalkyl, or heteroarylalkyl, each of which is optionally substituted with one to three members selected from lower alkyl, haloalkyl, lower alkoxy or fluoro; or

R 9a and R 9b together with the nitrogen to which they are attached form a 5- or 6-membered ring having from 0 to 1 additional heteroatom selected from O, N or S, each of which is optionally substituted with one to three members selected from lower alkyl, haloalkyl, lower alkoxy or fluoro; and

each R 16 is independently selected from the group consisting of fluoro, —OH, lower alkyl optionally substituted with one or more fluoro, and lower alkoxy optionally substituted with one or more fluoro.

2. A compound selected from the group consisting of:

3. A compound having the formula:

or a salt thereof.

4. A compound having the formula:

or a salt thereof.

5. A compound having the formula:

or a salt thereof.

6. A compound having the formula:

or a salt thereof.

7. A compound having the formula:

or a salt thereof.

8. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier.

9. A pharmaceutical composition comprising a compound of claim 2 and a pharmaceutically acceptable carrier.

10. A pharmaceutical composition comprising a compound of claim 3 and a pharmaceutically acceptable carrier.

11. A pharmaceutical composition comprising a compound of claim 4 and a pharmaceutically acceptable carrier.

12. A pharmaceutical composition comprising a compound of claim 5 and a pharmaceutically acceptable carrier.

13. A pharmaceutical composition comprising a compound of claim 6 and a pharmaceutically acceptable carrier.

14. A pharmaceutical composition comprising a compound of claim 7 and a pharmaceutically acceptable carrier.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE 16TH PATENT NUMBER PREVIOUSLY RECORDED AT REEL: 062856 FRAME: 0846. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Mar 28, 2023
From: OPNA IMMUNO-ONCOLOGY SA
To: OPNA BIO SA
Reel/Frame 063588/0355 →
CHANGE OF NAME Recorded Mar 2, 2023
From: OPNA IMMUNO-ONCOLOGY SA
To: OPNA BIO SA
Reel/Frame 062856/0846 →
CORRECTION OF AN ERROR IN ASSIGNOR'S NAME IN A COVER SHEET PREVIOUSLY RECORDED AT REEL 059925 FRAME 0772. Recorded May 20, 2022
From: PLEXXIKON INC.
To: OPNA IMMUNO-ONCOLOGY SA
Reel/Frame 060131/0148 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 10, 2022
From: PLEXXICON INC.
To: OPNA IMMUNO-ONCOLOGY SA
Reel/Frame 059925/0772 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 17, 2016
From: ZHANG, JIAZHONG; IBRAHIM, PRABHA N.; SPEVAK, WAYNE; TSAI, JAMES; EWING, TODD; ZHANG, YING; ZHANG, CHAO
To: PLEXXIKON INC.
Reel/Frame 037757/0474 →