发明名称 Bicyclic oxopyridine and oxopyrimidine derivatives
摘要 Compounds of formulae (1a) and (1b) are described: in which the dashed line represents an optional bond; A is a -N=atom or a -N(R<b>)-, -C(R<b>)= or -C(R<b>)(R<C>)- group; R<a>, R<b >and R<c >is each independently a hydrogen atom or an optionally substituted C<1-6>alkyl group; X is an -O- or -S- atom or -NH- group or substituted N atom; each Y is independently a N atom or CH group or substituted C atom; n is zero or the integer 1; Alk<1 >is an optionally substituted aliphatic or heteroaliphatic chain L<1 >is a covalent bond or a linker atom or group; Cy<1 >is a hydrogen atom or an optionally substituted cycloaliphatic, polycycloaliphatic, heterocycloaliphatic, polyheterocycloaliphatic, aromatic or heteroaromatic group; Ar is an optionally substituted aromatic or heteroaromatic group; and the salts, solvates, hydrates and N-oxides thereof; The compounds are potent inhibitors of p38 kinase and are use in the prophylaxis or treatment of p38 kinase mediated diseases or disorders, such as rheumatoid arthritis.
申请公布号 US2004254200(A1) 申请公布日期 2004.12.16
申请号 US20040492466 申请日期 2004.07.20
申请人 DAVIS JEREMY MARTIN;BROOKINGS DANIEL CHRISTOPHER;LANGHAM BARRY JOHN 发明人 DAVIS JEREMY MARTIN;BROOKINGS DANIEL CHRISTOPHER;LANGHAM BARRY JOHN
分类号 A61K31/4365;A61K31/437;A61K31/444;A61K31/4545;A61K31/496;A61K31/5377;A61P1/04;A61P1/16;A61P3/10;A61P5/14;A61P7/02;A61P7/06;A61P9/00;A61P9/04;A61P9/10;A61P11/00;A61P11/06;A61P13/12;A61P17/00;A61P17/06;A61P19/02;A61P19/08;A61P19/10;A61P21/04;A61P25/00;A61P25/16;A61P25/28;A61P29/00;A61P31/04;A61P31/12;A61P31/14;A61P31/18;A61P31/20;A61P35/00;A61P35/02;A61P35/04;A61P37/00;A61P37/02;A61P37/06;A61P37/08;A61P43/00;C07D471/04;C07D495/04;(IPC1-7):A61K31/519;A61K31/522;C07D471/02;C07D491/02;C07D498/02 主分类号 A61K31/4365
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