-
公开(公告)号:US07494989B2
公开(公告)日:2009-02-24
申请号:US11856339
申请日:2007-09-17
申请人: Seiji Ohno , Kayo Otani , Seiji Niwa , Satoshi Iwayama , Akira Takahara , Hajime Koganei , Yukitsugu Ono , Shinichi Fujita , Tomoko Takeda , Masako Hagihara , Akiko Okajima
发明人: Seiji Ohno , Kayo Otani , Seiji Niwa , Satoshi Iwayama , Akira Takahara , Hajime Koganei , Yukitsugu Ono , Shinichi Fujita , Tomoko Takeda , Masako Hagihara , Akiko Okajima
IPC分类号: C07D213/82 , C07D213/80 , C07D401/06 , A61K31/455 , A61K31/496
CPC分类号: C07D213/80 , A61K31/455 , A61K31/496 , A61K31/505 , A61K31/506 , A61K31/5377 , A61K31/55 , A61K31/551 , C07D213/82 , C07D239/28 , C07D239/34 , C07D239/38 , C07D239/42 , C07D401/04 , C07D403/04 , C07D409/04 , C07D417/04
摘要: Achiral pyrimidine derivatives and pyridine derivatives of the following formulae or analogs thereof have selective N-type calcium channel antagonistic activity and showed analgesic action when they were taken orally. They are useful as therapeutic agents for pains and various diseases associated with the N-type calcium channels.
摘要翻译: 下列通式或其类似物的手性嘧啶衍生物和吡啶衍生物具有选择性的N型钙通道拮抗活性,口服时显示镇痛作用。 它们可用作与N型钙通道相关的疼痛和各种疾病的治疗剂。
-
公开(公告)号:US20080070903A1
公开(公告)日:2008-03-20
申请号:US11856339
申请日:2007-09-17
申请人: Seiji OHNO , Kayo Otani , Seiji Niwa , Satoshi Iwayama , Akira Takahara , Hajime Koganei , Yukitsugu Ono , Shinichi Fujita , Tomoko Takeda , Masako Hagihara , Akiko Okajima
发明人: Seiji OHNO , Kayo Otani , Seiji Niwa , Satoshi Iwayama , Akira Takahara , Hajime Koganei , Yukitsugu Ono , Shinichi Fujita , Tomoko Takeda , Masako Hagihara , Akiko Okajima
IPC分类号: A61K31/55 , A61K31/44 , A61K31/445 , A61K31/496 , A61P9/00 , C07D221/00 , C07D239/24 , C07D295/00 , C07D223/02 , C07D213/02 , A61P25/00 , A61K31/505 , A61K31/506
CPC分类号: C07D213/80 , A61K31/455 , A61K31/496 , A61K31/505 , A61K31/506 , A61K31/5377 , A61K31/55 , A61K31/551 , C07D213/82 , C07D239/28 , C07D239/34 , C07D239/38 , C07D239/42 , C07D401/04 , C07D403/04 , C07D409/04 , C07D417/04
摘要: Achiral pyrimidine derivatives and pyridine derivatives of the following formulae or analogs thereof have selective N-type calcium channel antagonistic activity and showed analgesic action when they were taken orally. They are useful as therapeutic agents for pains and various diseases associated with the N-type calcium channels.
摘要翻译: 下列通式或其类似物的手性嘧啶衍生物和吡啶衍生物具有选择性的N型钙通道拮抗活性,口服时显示镇痛作用。 它们可用作与N型钙通道相关的疼痛和各种疾病的治疗剂。
-
3.
公开(公告)号:US07288544B2
公开(公告)日:2007-10-30
申请号:US10387543
申请日:2003-03-14
申请人: Seiji Ohno , Kayo Otani , Seiji Niwa , Satoshi Iwayama , Akira Takahara , Hajime Koganei , Yukitsugu Ono , Shinichi Fujita , Tomoko Takeda , Masako Hagihara , Akiko Okajima
发明人: Seiji Ohno , Kayo Otani , Seiji Niwa , Satoshi Iwayama , Akira Takahara , Hajime Koganei , Yukitsugu Ono , Shinichi Fujita , Tomoko Takeda , Masako Hagihara , Akiko Okajima
IPC分类号: C07D239/338 , C07D403/04 , A61K31/505
CPC分类号: C07D213/80 , A61K31/455 , A61K31/496 , A61K31/505 , A61K31/506 , A61K31/5377 , A61K31/55 , A61K31/551 , C07D213/82 , C07D239/28 , C07D239/34 , C07D239/38 , C07D239/42 , C07D401/04 , C07D403/04 , C07D409/04 , C07D417/04
摘要: Achiral pyrimidine derivatives and pyridine derivatives of the following formulae or analogs thereof have selective N-type calcium channel antagonistic activity and showed analgesic action when they were taken orally. They are useful as therapeutic agents for pains and various diseases associated with the N-type calcium channels
摘要翻译: 下列通式或其类似物的手性嘧啶衍生物和吡啶衍生物具有选择性的N型钙通道拮抗活性,口服时显示镇痛作用。 它们可用作与N型钙通道相关的疼痛和各种疾病的治疗剂
-
公开(公告)号:US06855716B2
公开(公告)日:2005-02-15
申请号:US10025589
申请日:2001-12-26
申请人: Seiji Ohno , Akiko Okajima , Seiji Niwa , Morikazu Kito , Akira Takahara , Yukitsugu Ono , Yuki Kajigaya , Tomoko Takeda , Hajime Koganei
发明人: Seiji Ohno , Akiko Okajima , Seiji Niwa , Morikazu Kito , Akira Takahara , Yukitsugu Ono , Yuki Kajigaya , Tomoko Takeda , Hajime Koganei
IPC分类号: A61P25/00 , A61P25/28 , C07D239/20 , C07D239/22 , C07D401/04 , C07D401/12 , C07D521/00 , A61K31/505 , A61K31/506 , C07D403/04
CPC分类号: C07D239/22 , C07D231/12 , C07D233/56 , C07D239/20 , C07D249/08 , C07D401/04 , C07D401/12
摘要: Dihydropyrimidine derivatives of the following formula or analogs thereof have selective N-type calcium channel antagonistic activity, and they are used as therapeutic agents for various diseases participating in the N-type calcium channels.
摘要翻译: 下式的二氢嘧啶衍生物或其类似物具有选择性的N型钙通道拮抗活性,并且它们用作参与N型钙通道的各种疾病的治疗剂。
-
-
-