发明名称 LTA4 hydrolase inhibitor pharmaceutical compositions and methods of use
摘要 The present invention provides compounds of the formula Ar1-Q-Ar2-Y-R-Z and pharmaceutically acceptable salts thereof wherein Ar1 and Ar2 are optionally substituted aryl moieties, Z is an optionally substituted nitrogen-containing moiety which may be an acyclic, cyclic or bicyclic amine or an optionally substituted monocyclic or bicyclic nitrogen-containing heteroaromatic moiety; Q is a linking group capable of linking two aryl groups; R is an alkylene moiety; Y is a linking moiety capable of linking an aryl group to an alkylene moiety and wherein Z is bonded to R through a nitrogen atom. The compounds and pharmaceutical compositions of the present invention are useful in the treatment of inflammatory diseases which are mediated by LTB4 production, such as psoriasis, ulcerative colitis, IBD and asthma.
申请公布号 US6506876(B1) 申请公布日期 2003.01.14
申请号 US19940321184 申请日期 1994.10.11
申请人 G.D. SEARLE & CO. 发明人 CHANDRAKUMAR NIZAL SAMUEL;CHEN BARBARA BAOSHENG;CLARE MICHAEL;DESAI BIPINCHANDRA NANUBHAI;DJURIC STEVAN WAKEFIELD;DOCTER STEPHEN HERMANN;GASIECKI ALAN FRANK;HAACK RICHARD ARTHUR;LIANG CHI-DEAN;MIYASHIRO JULIE MARION;PENNING THOMAS DALE;RUSSELL MARK ANDREW;YU STELLA SIU-TZYY
分类号 C07D295/08;A61K31/135;A61K31/138;A61K31/192;A61K31/195;A61K31/197;A61K31/215;A61K31/216;A61K31/34;A61K31/341;A61K31/343;A61K31/357;A61K31/36;A61K31/381;A61K31/40;A61K31/403;A61K31/404;A61K31/415;A61K31/4184;A61K31/435;A61K31/44;A61K31/4427;A61K31/443;A61K31/4433;A61K31/445;A61K31/4465;A61K31/4468;A61K31/4535;A61K31/454;A61K31/46;A61K31/495;A61K31/496;A61K31/535;A61K31/5355;A61K31/5375;A61K31/695;A61P29/00;A61P43/00;C07D207/14;C07D207/16;C07D209/12;C07D211/58;C07D211/62;C07D213/38;C07D215/12;C07D235/08;C07D277/24;C07D295/18;C07D307/42;C07D307/81;C07D307/85;C07D311/58;C07D317/54;C07D333/16;C07D401/12;C07D405/12;C07D409/12;C07D471/04;C07D473/08;C07D491/052;C07D491/107;(IPC1-7):A01N43/40 主分类号 C07D295/08
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