发明申请
US20090192174A1 Novel Aminopyridine Derivatives Having Aurora a Selective Inhibitory Action
有权
具有极光选择性抑制作用的新型氨基吡啶衍生物
- 专利标题: Novel 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新型氨基吡啶衍生物
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申请号: US12226639申请日: 2007-04-25
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公开(公告)号: US20090192174A1公开(公告)日: 2009-07-30
- 发明人: Tetsuya Kato , Nobuhiko Kawanishi , Takashi Mita , Keita Nagai , Katsumasa Nonoshita , Mitsuru Ohkubo
- 申请人: Tetsuya Kato , Nobuhiko Kawanishi , Takashi Mita , Keita Nagai , Katsumasa Nonoshita , Mitsuru Ohkubo
- 申请人地址: JP Kudankita, 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 Kudankita, Chiyoda-ku, Tokyo
- 优先权: JP2006-124475 20060427
- 国际申请: PCT/JP2007/059413 WO 20070425
- 主分类号: A61K31/506
- IPC分类号: A61K31/506 ; C07D487/04
摘要:
The present invention relates to a compound of general formula I: wherein: n1 and n2 are the same or different, and are 0 or 1; R is aryl, heteroaryl, etc.; Re is hydrogen atom or lower alkyl; two groups selected from four groups consisting of (i) either one of Ra1 and Ra1′, (ii) either one of Ra2 and Ra2′, (iii) either one of Rb1 and Rb1′, and (iv) either one of Rb2 and Rb2′, are combined to form —(CH2)n— where n is 1, 2 or 3; and among Ra1, Ra1′, Ra2, Ra2′, Rb1, Rb1′, Rb2 and Rb2′, the groups which do not form —(CH2)n— are each independently hydrogen atom, etc.; X1, X2, X3 and X4 are each independently CH, N, etc.; Y1, Y2, Y3 and Y4 are the same or different and are CH or N, etc.; W is a 5-membered aromatic heterocyclic group, or a pharmaceutically acceptable salt or ester thereof.
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