发明名称 Benzimidazole cyclooxygenase-2 inhibitors
摘要 This invention provides a compound of the following formula:or the pharmaceutically acceptable salts thereof, whereinAr is heteroaryl; X1 and X2 are independently selected from halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, amino, C1-C4 alkanoyl, carboxy, carbamoyl, cyano, nitro, mercapto, (C1-C4 alkyl)thio, (C1-C4 alkyl)sulfinyl, (C1-C4 alkyl)sulfonyl, aminosulfonyl, or the like; R1 is selected from hydrogen, straight or branched C1-C4 alkyl, C3-C8 cycloalkyl, C4-C8 cycloalkenyl, phenyl , heteroaryl and the like; R2 and R3 are independently selected from hydrogen, halo, C1-C4 alkyl, phenyl and the like; or R1 and R2 can form, together with the carbon atom to which they are attached, a C5-C7 cycloalkyl ring; and m and n are independently 0, 1, 2 or 3.These compounds and pharmaceutical compositions containing such compounds are useful as analgesics and anti-inflammatory agents.
申请公布号 US6310079(B1) 申请公布日期 2001.10.30
申请号 US19990244875 申请日期 1999.02.05
申请人 PFIZER INC. 发明人 OKUMURA YOSHIYUKI;MURATA YOSHINORI;MANO TAKASHI
分类号 A61K31/00;A61K31/41;A61K31/425;A61K31/427;A61K31/44;A61K31/4427;A61K31/443;A61K31/4433;A61K31/4439;A61K31/495;A61K31/4965;A61K31/497;A61K31/505;A61K31/506;A61K31/53;A61P9/00;A61P9/10;A61P11/00;A61P11/06;A61P13/00;A61P13/12;A61P19/00;A61P19/02;A61P19/10;A61P25/00;A61P25/04;A61P25/28;A61P29/00;A61P35/00;A61P43/00;C07D401/04;C07D401/14;C07D403/04;C07D405/14;C07D409/14;C07D413/14;C07D417/04;C07D417/14;(IPC1-7):A61K31/443 主分类号 A61K31/00
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