发明名称 Substituted imidazole derivatives and their use as cytokine inhibitors
摘要 <p>Novel 2,4,5-triarylimidazole compounds of formula: &lt;CHEM&gt; wherein R1 is pyrimidinyl, optionally substituted with one or two substituents each of which is independently selected form C1-4 alkyl, halo, C1-4 alkoxy, C1-4 alkylthio, NH2, mono- or di-C1-6-alkylamino and a N-heterocyclyl ring which ring has from 5 to 7 members, and optionally contains an additional heteroatom selected from oxygen, sulfur and NR22; R2 is R8 or -OR12; R3 is -XaP(Z)(XbR13)2 or Q-(Y1)t; R4 is phenyl, naphth-1-yl or naphth-2-yl; Q is an aryl or heteroaryl group; Y1 is independently selected from hydrogen, C1-5 alkyl, halo-substituted C1-5 alkyl; R8 is hydrogen, heterocyclyl, heterocyclylalkyl or R11; R11 is C1-10 alkyl, halo-substituted C1-10 alkyl, C2-10 alkenyl, C2-10 alkynyl, C3-7 cycloalkyl, C5-7 cycloalkenyl, aryl, arylalkyl, heteroaryl or heteroarylalkyl; processes for the preparation thereof, the use thereof in treating cytokine mediated diseases and pharmaceutical compositions for use in such therapy.</p>
申请公布号 EP0943616(A1) 申请公布日期 1999.09.22
申请号 EP19990201468 申请日期 1993.01.13
申请人 SMITHKLINE BEECHAM CORPORATION 发明人 ADAMS, JERRY LEROY;LEE, JOHN C;WHITE, JOHN RICHARD;GALLAGHER, TIMOTHY F.
分类号 A61K31/4164;A61K31/44;A61K31/4427;A61K31/4433;A61K31/4439;A61K31/4545;A61K31/47;A61K31/4709;A61K31/4725;A61K31/496;A61K31/505;A61K31/506;A61K31/5377;A61P7/02;A61P9/00;A61P11/00;A61P19/02;A61P11/06;A61P13/12;A61P17/06;A61P19/00;A61P19/08;A61P19/10;A61P29/00;A61P31/10;A61P37/00;A61P37/06;A61P43/00;C07D233/56;C07D401/04;C07D401/14;C07D403/04;C07D409/14;C07D413/14;C07D417/14;(IPC1-7):C07D403/04;C07F9/655;C07D403/14 主分类号 A61K31/4164
代理机构 代理人
主权项
地址