发明公开
- 专利标题: IMIDAZOQUINAZOLINE DERIVATIVES
- 专利标题(中): 咪唑喹唑啉衍生物
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申请号: EP97937841.1申请日: 1997-08-29
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公开(公告)号: EP0863144A1公开(公告)日: 1998-09-09
- 发明人: ONODA, Yasuo , NOMOTO, Yuji , OHNO, Tetsuji , YAMADA, Koji , ICHIMURA, Michio
- 申请人: Kyowa Hakko Co., Ltd.
- 申请人地址: 6-1, Ohtemachi 1-chome Chiyoda-ku, Tokyo 100 JP
- 专利权人: Kyowa Hakko Co., Ltd.
- 当前专利权人: Kyowa Hakko Co., Ltd.
- 当前专利权人地址: 6-1, Ohtemachi 1-chome Chiyoda-ku, Tokyo 100 JP
- 代理机构: VOSSIUS & PARTNER
- 优先权: JP230807/96 19960830
- 国际公布: WO9808848 19980305
- 主分类号: C07D487/04
- IPC分类号: C07D487/04
摘要:
The present invention provides imidazoquinazoline derivatives represented by formula (I):
wherein R 1 represents hydrogen, substituted or unsubstituted lower alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted bicycloalkyl, substituted or unsubstituted tricycloalkyl or the like, R 2 represents hydrogen, substituted or unsubstituted lower alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted bicycloalkyl, substituted or unsubstituted tricycloalkyl, substituted or unsubstituted lower alkenyl, substituted or unsubstituted aralkyl or the like, R 3 represents hydrogen, substituted lower alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted bicycloalkyl, substituted or unsubstituted tricycloalkyl, substituted or unsubstituted lower alkenyl, substituted or unsubstituted aralkyl or the like, and R 2 and R 3 are combined to represent a substituted or unsubstituted N-containing heterocyclic group, X represents O or S, or pharmaceutically acceptable salts thereof, which have potent and selective cyclic guanosine 3',5'-monophosphate (cGMP)-specific phosphodiesterase (PDE) inhibitory activity and are useful for treating or ameliorating cardiovascular diseases such as thrombosis, angina pectoris, hypertension, heart failure, arterial sclerosis, as well as asthma, impotence and the like.
wherein R 1 represents hydrogen, substituted or unsubstituted lower alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted bicycloalkyl, substituted or unsubstituted tricycloalkyl or the like, R 2 represents hydrogen, substituted or unsubstituted lower alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted bicycloalkyl, substituted or unsubstituted tricycloalkyl, substituted or unsubstituted lower alkenyl, substituted or unsubstituted aralkyl or the like, R 3 represents hydrogen, substituted lower alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted bicycloalkyl, substituted or unsubstituted tricycloalkyl, substituted or unsubstituted lower alkenyl, substituted or unsubstituted aralkyl or the like, and R 2 and R 3 are combined to represent a substituted or unsubstituted N-containing heterocyclic group, X represents O or S, or pharmaceutically acceptable salts thereof, which have potent and selective cyclic guanosine 3',5'-monophosphate (cGMP)-specific phosphodiesterase (PDE) inhibitory activity and are useful for treating or ameliorating cardiovascular diseases such as thrombosis, angina pectoris, hypertension, heart failure, arterial sclerosis, as well as asthma, impotence and the like.
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