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公开(公告)号:US08278329B2
公开(公告)日:2012-10-02
申请号:US11924997
申请日:2007-10-26
申请人: Takashi Yamamoto , Seiji Niwa , Kayo Otani , Seiji Ohno , Hajime Koganei , Satoshi Iwayama , Akira Takahara , Yukitsugu Ono , Tomoko Takeda , Shinichi Fujita , Keiko Moki
发明人: Takashi Yamamoto , Seiji Niwa , Kayo Otani , Seiji Ohno , Hajime Koganei , Satoshi Iwayama , Akira Takahara , Yukitsugu Ono , Tomoko Takeda , Shinichi Fujita , Keiko Moki
IPC分类号: A61K31/445 , C07D211/18
CPC分类号: C07D295/205 , C07C237/06 , C07C271/20 , C07C271/22 , C07D211/70 , C07D401/04 , C07D401/12 , C07D405/12 , C07D409/04 , C07D417/06
摘要: The invention relates to a compound represented by the following general formula (1) or its analogue, which selectively inhibit N-type calcium channels or its analogue, and to a method for treating pain etc. comprising the compound represented by the following general formula (1) or its analogue to a patient in need of such treatment: wherein, A represents CH═CH, etc., a, b, c and d represents CH etc., R1, R2, R3, R4, R5 and R6 represents H etc., V—W represents C═C, etc., n represents 0 to 3, Y1 represents O etc., B represents —(CH2)vCHR21 wherein v is 0 to 3, R21 represents H, a lower alkyl group or the like, etc., G represents —CO—, a covalent bond, etc., m is 0 to 6, R7 and R8 represents H, a lower alkyl group, —COR18a, —COOR20 wherein R18a and R20 each represents a lower alkyl group or the like, etc.
摘要翻译: 本发明涉及由以下通式(1)表示的化合物或其类似物,其选择性地抑制N-型钙通道或其类似物,以及涉及治疗疼痛等的方法,其包含由以下通式表示的化合物 1)或其与需要这种治疗的患者的类似物:其中A表示CH = CH等,a,b,c和d表示CH等,R 1,R 2,R 3,R 4,R 5和R 6表示H 等等,V-W表示C = C等,n表示0〜3,Y 1表示O等,B表示 - (CH 2)v CHR 21,其中v为0〜3,R 21表示H,低级烷基或 G等表示-CO-,共价键等,m为0〜6,R7和R8表示H,低级烷基,-COR18a,-COOR20,其中R18a和R20各自表示低级烷基 或类似物等
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公开(公告)号:US07462630B2
公开(公告)日:2008-12-09
申请号:US10787175
申请日:2004-02-27
申请人: Takashi Yamamoto , Seiji Niwa , Kayo Otani , Seiji Ohno , Hajime Koganei , Satoshi Iwayama , Akira Takahara , Yukitsugu Ono , Tomoko Takeda , Shinichi Fujita , Keiko Moki
发明人: Takashi Yamamoto , Seiji Niwa , Kayo Otani , Seiji Ohno , Hajime Koganei , Satoshi Iwayama , Akira Takahara , Yukitsugu Ono , Tomoko Takeda , Shinichi Fujita , Keiko Moki
IPC分类号: A61K31/445 , C07D409/14
CPC分类号: C07D295/205 , C07C237/06 , C07C271/20 , C07C271/22 , C07D211/70 , C07D401/04 , C07D401/12 , C07D405/12 , C07D409/04 , C07D417/06
摘要: The invention relates to a compound represented by the following general formula (1) or its analogue, which selectively inhibit N-type calcium channels or its analogue, and to a method for treating pain etc. comprising the compound represented by the following general formula (1) or its analogue to a patient in need of such treatment: wherein, A represents CH═CH, etc., a, b, c and d represents CH etc., R1, R2, R3, R4, R5 and R6 represents H etc., V—W represents C═C, etc., n represents 0 to 3, Y1 represents O etc., B represents —(CH2)vCHR21 wherein v is 0 to 3, R21 represents H, a lower alkyl group or the like, etc., G represents —CO—, a covalent bond, etc., m is 0 to 6, R7 and R8 represents H, a lower alkyl group, —COR18a, —COOR20 wherein R18a and R20 each represents a lower alkyl group or the like, etc.
摘要翻译: 本发明涉及由以下通式(1)表示的化合物或其类似物,其选择性地抑制N-型钙通道或其类似物,以及涉及治疗疼痛等的方法,其包含由以下通式表示的化合物 1)或其与需要这种治疗的患者的类似物:其中A表示CH-CH等,a,b,c和d表示CH等,R 1,R 2,R 3,R 4,R 5和R 6表示H 等等,VW表示CC等,n表示0〜3,Y1表示O等,B表示 - (CH2)vCHR21,其中v为0-3,R21表示H,低级烷基等。 ,G表示-CO-,共价键等,m为0〜6,R7和R8表示H,低级烷基,-COR18a,-COOR20,其中R18a和R20各自表示低级烷基等, 等等
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3.
公开(公告)号:US20080058311A1
公开(公告)日:2008-03-06
申请号:US11924997
申请日:2007-10-26
申请人: Takashi YAMAMOTO , Seiji Niwa , Kayo Otani , Seiji Ohno , Hajime Koganei , Satoshi Iwayama , Akira Takahara , Yukitsugu Ono , Tomoko Takeda , Shinichi Fujita , Keiko Moki
发明人: Takashi YAMAMOTO , Seiji Niwa , Kayo Otani , Seiji Ohno , Hajime Koganei , Satoshi Iwayama , Akira Takahara , Yukitsugu Ono , Tomoko Takeda , Shinichi Fujita , Keiko Moki
IPC分类号: A61K31/55 , A61K31/215 , A61K31/40 , A61K31/445 , A61P25/00 , C07C69/00 , C07D221/00 , C07D295/00 , C07D223/02 , C07D207/00 , A61P43/00 , A61P11/06 , A61K31/4523 , A61K31/495
CPC分类号: C07D295/205 , C07C237/06 , C07C271/20 , C07C271/22 , C07D211/70 , C07D401/04 , C07D401/12 , C07D405/12 , C07D409/04 , C07D417/06
摘要: The invention relates to a compound represented by the following general formula (1) or its analogue, which selectively inhibit N-type calcium channels or its analogue, and to a method for treating pain etc. comprising the compound represented by the following general formula (1) or its analogue to a patient in need of such treatment: wherein, A represents CH═CH, etc., a, b, c and d represents CH etc., R1, R2, R3, R4, R5 and R6 represents H etc., V—W represents C═C, etc., n represents 0 to 3, Y1 represents O etc., B represents —(CH2)vCHR21 wherein v is 0 to 3, R21 represents H, a lower alkyl group or the like, etc., G represents —CO—, a covalent bond, etc., m is 0 to 6, R7 and R8 represents H, a lower alkyl group, —COR18a, —COOR20 wherein R18a and R20 each represents a lower alkyl group or the like, etc.
摘要翻译: 本发明涉及由以下通式(1)表示的化合物或其类似物,其选择性地抑制N-型钙通道或其类似物,以及涉及治疗疼痛等的方法,其包含由以下通式表示的化合物 1)或其与需要这种治疗的患者的类似物:其中A表示CH-CH等,a,b,c和d表示CH等,R 1,R 2,R 3,R 4,R 5和R 6表示H 等等,VW表示CC等,n表示0〜3,Y1表示O等,B表示 - (CH2)vCHR21,其中v为0-3,R21表示H,低级烷基等。 ,G表示-CO-,共价键等,m为0〜6,R7和R8表示H,低级烷基,-COR18a,-COOR20,其中R18a和R20各自表示低级烷基等, 等等
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