发明授权
US07834018B2 Aminopyridine derivatives having aurora a selective inhibitory action
有权
具有极光选择性抑制作用的氨基吡啶衍生物
- 专利标题: Aminopyridine derivatives having aurora a selective inhibitory action
- 专利标题(中): 具有极光选择性抑制作用的氨基吡啶衍生物
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申请号: US12315425申请日: 2008-12-03
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公开(公告)号: US07834018B2公开(公告)日: 2010-11-16
- 发明人: Mitsuru Ohkubo , Tetsuya Kato , Nobuhiko Kawanishi , Takashi Mita , Toshiyasu Shimomura
- 申请人: Mitsuru Ohkubo , Tetsuya Kato , Nobuhiko Kawanishi , Takashi Mita , Toshiyasu Shimomura
- 申请人地址: JP Chiyoda-Ku Tokyo
- 专利权人: Banyu Pharmaceutical Co., Ltd
- 当前专利权人: Banyu Pharmaceutical Co., Ltd
- 当前专利权人地址: JP Chiyoda-Ku Tokyo
- 代理商 Matthew A. Leff; David A. Muthard
- 优先权: JP2004-315152 20041029; JP2005-161156 20050601
- 主分类号: A61K31/497
- IPC分类号: A61K31/497 ; C07D241/04 ; C07D295/00
摘要:
The present invention relates to a compound represented by the general formula (I): wherein m1 and m2 are 1, 2, or 3; n1 and n2 are 0 or 1; i is an integer of any of 1 to m1; j is an integer of 1 to m2; R is aryl, heteroaryl, or cycloalkyl any of which may be substituted; Rai and Rai′ is hydrogen atom, etc. and Rbj and Rbj′ is hydrogen atom, etc.; Rc, Rd, and Re are hydrogen atom, etc; X1 is CH, CX1a, or N; X2 is CH, N, etc.; X3 is CH, N, etc.; X4 is CH or N; Y1, Y2, and Y3 are each independently CH or N; Z1 and Z2 are each independently CH or N; W is a 5-membered aromatic heterocyclic group such as pyrazolyl, thiazolyl, etc., or a pharmaceutically acceptable salt or ester thereof; a pharmaceutical composition or antitumor agent containing the same; and combinations of the antitumor agent with other antitumor agent(s).
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