发明名称 NOVEL IMIDAZOLE LIPOXYGENASE INHIBITORS
摘要 <p>PCT No. PCT/IB96/00744 Sec. 371 Date Jun. 29, 1998 Sec. 102(e) Date Jun. 29, 1998 PCT Filed Jul. 24, 1996 PCT Pub. No. WO97/11079 PCT Pub. Date Mar. 27, 1997The present invention provides a compound of formula (I): and a pharmaceutically acceptable salt thereof, wherein Ar is phenylene optionally substituted with halo, hydroxy, cyano, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 halo-substituted alkyl or C1-C4 halo-substituted alkoxy, X is -A-X1- or -X2-A-, where A is a direct bond or C1-C4 alkylene, and X1 is oxy, thio, sulfinyl or sulfonyl; Ar is phenylene, pyridylene or thienylene optionally substituted with halo, hydroxy, cyano, nitro, amino, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkylthio, C1-C4 halo-substituted alkyl, C1-C4 halo-substituted alkoxy, C1-C4 alkylamino or di(C1-C4)alkylamino; Y is CN or CONR1R2 wherein R1 and R2 are independently hydrogen or C1-C4 alkyl; and R is hydrogen or C1-C6 alkyl; W is C2-C3 alkylene, one carbon atom of which may be replaced by an oxygen atom. Further the invention provides a pharmaceutical composition for treating an inflammatory disease, allergy or cardiovascular diseases or the like in a mammalian subject which comprises a compound of formula (I) and a pharmaceutically acceptable carrier.</p>
申请公布号 GR3035279(T3) 申请公布日期 2001.04.30
申请号 GR20010400096T 申请日期 2001.01.22
申请人 PFIZER INC. 发明人 MANO, TAKASHI;STEVENS, RODNEY, W.
分类号 C07D493/08;A61K31/35;A61K31/415;A61P29/00;A61P37/08;A61P43/00;C07D521/00;(IPC1-7):C07D493/08 主分类号 C07D493/08
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