发明名称 1,4-DIHYDROPYRIDINE COMPOUNDS
摘要 PCT No. PCT/IB97/00058 Sec. 371 Date Feb. 1, 1999 Sec. 102(e) Date Feb. 1, 1999 PCT Filed Jan. 27, 1997 PCT Pub. No. WO97/30048 PCT Pub. Date Aug. 21, 1997A compound of formula (I) and its pharmaceutically acceptable salts, wherein A1 and A2 are each halo; X is direct bond, CH2, CO, O, S, S(O) or S(O)2; R1 is selected from a variety of groups such as hydrogen; substituted or unsubstituted C1-4 alkyl; substituted or unsubstituted piperidinyl; substituted or unsubstituted C5-14 cycloalkyl, bicycloalkyl or tricycloalkyl; substituted or unsubstituted C7-14 azacyclo-, azabicyclo- or azatricyclo-alkyl; bicyclo C7-10 alkenyl; benzocyclo C5-7 alkyl; and heterocyclic; R2 is hydrogen, C1-4 alkyl, substituted or unsubstituted phenyl or heterocyclic; and R3 and R4 are each C1-5 alkyl. The novel dihydropyridine compounds of this invention have excellent bradykinin antagonistic activity and are thus useful for the treatment of inflammation, cardiovascular disease, pain, common cold, allergies, asthma, pancreatitis, burns, virus infection, head injury, multiple trauma or the like in mammalian, especially humans.
申请公布号 HRP970094(A2) 申请公布日期 1998.06.30
申请号 HR1997P000094 申请日期 1997.02.18
申请人 IKEDA TAKAFUMI 发明人 IKEDA TAKAFUMI
分类号 C07D401/04;A61K31/4427;A61K31/4433;A61K31/445;A61P1/08;A61P9/00;A61P11/08;A61P17/02;A61P25/02;A61P29/00;A61P31/12;A61P37/02;A61P43/00;C07D211/90;C07D401/06;C07D405/12;C07D409/04;C07D409/12;C07D451/04;C07D453/02;(IPC1-7):C07D451/04 主分类号 C07D401/04
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