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公开(公告)号:EP1427720A1
公开(公告)日:2004-06-16
申请号:EP02772871.6
申请日:2002-09-20
发明人: UEHARA, Fumiaki,MITSUBISHI PHARMA CORPORATION , ARITOMO, Keiichi,MITSUBISHI PHARMA CORPORATION , SHODA, Aya,MITSUBISHI PHARMA CORPORATION , HIKI, Shinsuke,MITSUBISHI PHARMA CORPORATION , OKUYAMA, Masahiro,MITSUBISHI PHARMA CORPORATION , USUI, Yoshihiro,MITSUBISHI PHARMA CORPORATION , OOIZUMI, Mitsuru,MITSUBISHI PHARMA CORPORATION , WATANABE, Kazutoshi,MITSUBISHI PHARMA CORPORATION , YAMAKOSHI, Koichi,MITSUBISHI PHARMA CORPORATION
IPC分类号: C07D401/04 , C07D401/14 , C07D413/14 , A61K31/505 , A61P25/28
CPC分类号: C07D401/04 , C07D239/34 , C07D239/47 , C07D239/56 , C07D401/14 , C07D413/14
摘要: A pyrimidone derivative represented by formula (I) or a salt thereof, or a solvate thereof or a hydrate thereof having inhibitory activity against tau protein kinase 1:wherein R1 represents a C¿1?-C12 alkyl group which may be substituted; R represents, for example, a group represented by the following formula (II):wherein R?2 and R3¿ independently represent a hydrogen atom or a C¿1?-C8 alkyl group; R?4¿ represents a benzene ring which may be substituted, a naphthalene ring which may be substituted, an indan ring which may be substituted, a tetrahydronaphthalene ring which may be substituted, or an optionally substituted heterocyclic ring having 1 to 4 hetero atoms selected from the group consisting of oxygen atom, sulfur atom and nitrogen atom, and having 5 to 10 ring-constituting atoms in total.
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公开(公告)号:EP1427709A1
公开(公告)日:2004-06-16
申请号:EP02772870.8
申请日:2002-09-20
发明人: UEHARA, Fumiaki,MITSUBISHI PHARMA CORPORATION , ARITOMO, Keiichi,MITSUBISHI PHARMA CORPORATION , SHODA, Aya,MITSUBISHI PHARMA CORPORATION , HIKI, Shinsuke,MITSUBISHI PHARMA CORPORATION , OKUYAMA, Masahiro,MITSUBISHI PHARMA CORPORATION , USUI, Yoshihiro,MITSUBISHI PHARMA CORPORATION , OOIZUMI, Mitsuru,MITSUBISHI PHARMA CORPORATION , WATANABE, Kazutoshi,MITSUBISHI PHARMA CORPORATION
IPC分类号: C07D239/46 , C07D239/56 , C07D239/34 , C07D413/14 , C07D401/14 , A61K31/505 , A61P25/28
CPC分类号: A61K31/535 , C07D239/34 , C07D239/47 , C07D239/56 , C07D401/04 , C07D401/14 , C07D413/14
摘要: A pyrimidone derivative represented by formula (I) or a salt thereof, or a solvate thereof or a hydrate thereof having inhibitory activity against tau protein kinase 1:wherein R1 represents a C1-C12 alkyl group which may be substituted;R represents, for example, a group represented by the following formula (II):wherein R2 and R3 independently represent a hydrogen atom or a C1-C8 alkyl group; R4 represents a benzene ring which may be substituted, a naphthalene ring which may be substituted, an indan ring which may be substituted, a tetrahydronaphthalene ring which may be substituted, or an optionally substituted heterocyclic ring having 1 to 4 hetero atoms selected from the group consisting of oxygen atom, sulfur atom and nitrogen atom, and having 5 to 10 ring-constituting atoms in total.
摘要翻译: 由式(I)表示的嘧啶酮衍生物或其盐,或其溶剂合物或其水合物对tau蛋白激酶1具有抑制活性:其中R1表示可被取代的C1-C12烷基; R表示例如由下式(II)表示的基团:其中R2和R3独立地表示氢原子或C1-C8烷基; R4表示可被取代的苯环,可被取代的萘环,可被取代的茚满环,可被取代的四氢萘环,或具有1-4个选自下述基团的杂原子的任意取代的杂环 由氧原子,硫原子和氮原子构成,并且总共具有5〜10个构成环的原子。
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