US2021353602A1PendingUtilityA1
Compounds and methods for kinase modulation, and indications therefor
Est. expiryJul 17, 2027(~1 yrs left)· nominal 20-yr term from priority
Inventors:Guoxian WuJiazhong ZhangYong-Liang ZhuChao ZhangPrabha N. IbrahimSongyuan ShiWayne SpevakDean R. ArtisJames Tsai
A61K 31/506C07D 401/12A61P 31/14A61P 17/00A61P 9/00C07D 409/12A61P 31/16A61P 15/00A61K 31/433A61P 7/02C07D 405/12A61P 25/06A61K 31/44A61P 17/06A61P 5/14C07D 231/40A61P 31/20C07D 213/82A61K 31/4436A61P 5/00A61P 3/06A61K 31/5377A61K 31/549A61P 15/10C07D 215/38A61K 31/47C07D 239/48A61P 17/04A61P 1/16A61P 9/08C07D 215/12A61P 19/00A61P 13/12C07D 213/75C07D 285/135A61K 31/415A61P 29/00A61K 31/444A61K 31/42A61P 31/04A61P 3/04C07D 213/76A61P 9/04C07D 215/14A61P 11/06C07D 417/12A61P 11/00A61P 43/00A61P 25/04C07D 261/14C07D 263/48C07D 239/49A61P 19/10A61P 25/16A61P 9/10A61P 19/08A61P 37/08A61P 1/04C07D 285/16A61K 31/4439C07D 213/74A61P 11/02A61P 19/02C07D 417/04A61K 31/4545A61P 35/02A61P 25/00C07D 471/04A61P 21/04A61P 25/14A61P 31/12A61K 31/505A61P 3/00A61P 17/02A61K 31/437A61P 27/02A61P 17/14A61P 25/28A61P 35/04A61P 1/18A61P 37/00A61P 37/06C07D 215/20A61P 3/10A61P 7/00A61P 25/02A61K 45/06A61P 35/00A61P 21/00A61P 13/08
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Claims
Abstract
Compounds active on protein kinases are described, as well as methods of using such compounds to treat diseases and conditions associated with aberrant activity of protein kinases.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . A compound of formula (Ia):
or a pharmaceutically acceptable salt thereof,
wherein:
L 1 is a bond or —N(H)C(O)—;
each R 1 is R 16 ;
R 2 is hydrogen or halogen;
R 3 is lower alkyl or phenyl substituted with one or more substituents selected from the group consisting of fluoro, lower alkyl, fluoro substituted lower alkyl, lower alkoxy, fluoro substituted lower alkoxy, lower alkylthio, and fluoro substituted lower alkylthio;
R 4 is hydrogen;
m is 0, 1, 2, or 3;
Ar is
each X is independently N or CH, provided that at least one and no more than 2 of X in any ring is N;
Y is NH, O, or S;
each R 16 is independently —N(R 19 )—C(O)—R 17 , lower alkyl, or heteroaryl, wherein:
the heteroaryl is optionally substituted with one or more substituents selected from the group consisting of —OH, —NH 2 , —CN, —NO 2 , —C(O)—OH, —S(O) 2 —NH 2 , —C(O)—NH 2 , —O—R 18 , —S—R 18 , —N(R 19 )—R 18 , —N(R 19 )—C(O)—R 18 , —N(R 19 )—S(O) 2 —R 18 , —S(O) 2 —R 18 , —C(O)—R 18 , —C(O)—O—R 18 , —C(O)—N(R 19 )—R 18 , —S(O) 2 —N(R 19 )—R 18 , halogen, lower alkyl, fluoro substituted lower alkyl, and cycloalkylamino;
R 17 is lower alkyl;
R 18 is lower alkyl; and
R 19 at each occurrence is hydrogen or lower alkyl.
3 . The compound of claim 2 , wherein R 2 is hydrogen.
4 . The compound of claim 2 , wherein R 2 is halogen.
5 . The compound of claim 2 , wherein R 3 is phenyl substituted with one or more fluoro.
6 . A pharmaceutical composition comprising a compound of claim 2 and a pharmaceutically acceptable carrier or excipient.Join the waitlist — get patent alerts
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