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公开(公告)号:US07718801B2
公开(公告)日:2010-05-18
申请号:US11661486
申请日:2005-08-30
申请人: Mikako Kawamura , Takashi Hashihayata , Satoshi Sunami , Tetsuya Sugimoto , Fuyuki Yamamoto , Yoshiyuki Sato , Kaori Kamijo , Morihiro Mitsuya , Yoshikazu Iwasawa , Hideya Komatani
发明人: Mikako Kawamura , Takashi Hashihayata , Satoshi Sunami , Tetsuya Sugimoto , Fuyuki Yamamoto , Yoshiyuki Sato , Kaori Kamijo , Morihiro Mitsuya , Yoshikazu Iwasawa , Hideya Komatani
IPC分类号: C07D239/00 , C07D239/02
CPC分类号: C07D471/04 , C07D487/04
摘要: The present invention relates to a compound represented by Formula [I] or a pharmaceutically acceptable salt or ester thereof: wherein: X1, X2, X3, and X4, which may be identical or different, are each C or N, provided that none to two of X1, X2, X3, and X4 is/are N; Y is CH or N; R1, R1′, R2, R2′, R3, R3′, R4, and R4′, which may be identical or different, are each a hydrogen atom, a lower alkyl group, or the like; R5 is a hydrogen atom or a methyl group; R6 and R7, which may be identical or different, are each a hydrogen atom, a lower alkyl group, or the like; R8 and R8′, which may be identical or different, are each a hydrogen atom, a lower alkyl group, or the like; R9 is an aryl group or a heteroaryl group which may be substituted; and n is an integer from 1 to 3, and a PLK1 inhibitor or an anticancer agent containing the same.
摘要翻译: 本发明涉及由式[I]表示的化合物或其药学上可接受的盐或酯:其中:X 1,X 2,X 3和X 4可以相同或不同,各自为C或N,条件是 X1,X2,X3和X4中的两个为N; Y是CH或N; R1,R1',R2,R2',R3,R3',R4和R4'可以相同或不同,分别为氢原子,低级烷基等; R5是氢原子或甲基; R 6和R 7可以相同或不同,分别为氢原子,低级烷基等; R 8和R 8'可以相同或不同,分别为氢原子,低级烷基等; R9是可以被取代的芳基或杂芳基; n为1〜3的整数,PLK1抑制剂或含有该PLK1抑制剂的抗癌剂。
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公开(公告)号:US20080070894A1
公开(公告)日:2008-03-20
申请号:US11661486
申请日:2005-08-30
申请人: Mikako Kawamura , Takashi Hashihayata , Satoshi Sunami , Tetsuya Sugimoto , Fuyuki Yamamoto , Yoshiyuki Sato , Kaori Kamijo , Morihiro Mitsuya , Yoshikazu Iwasawa , Hideya Komatani
发明人: Mikako Kawamura , Takashi Hashihayata , Satoshi Sunami , Tetsuya Sugimoto , Fuyuki Yamamoto , Yoshiyuki Sato , Kaori Kamijo , Morihiro Mitsuya , Yoshikazu Iwasawa , Hideya Komatani
IPC分类号: A61K31/397 , A61K31/496 , A61K31/497 , A61K31/501 , A61K31/506 , A61K31/52 , A61K31/5377 , A61K31/5513 , A61P35/00 , C07D237/06 , C07D239/24 , C07D243/14 , C07D295/00 , C07D473/00
CPC分类号: C07D471/04 , C07D487/04
摘要: The present invention relates to a compound represented by Formula [I] or a pharmaceutically acceptable salt or ester thereof: wherein: X1, X2, X3, and X4, which may be identical or different, are each C or N, provided that none to two of X1, X2, X3, and X4 is/are N; Y is CH or N; R1, R1′, R2, R2′, R3, R3′, R4, and R4′, which may be identical or different, are each a hydrogen atom, a lower alkyl group, or the like; R5 is a hydrogen atom or a methyl group; R6 and R7, which may be identical or different, are each a hydrogen atom, a lower alkyl group, or the like; R8 and R8′, which may be identical or different, are each a hydrogen atom, a lower alkyl group, or the like; R9 is an aryl group or a heteroaryl group which may be substituted; and n is an integer from 1 to 3, and a PLK1 inhibitor or an anticancer agent containing the same.
摘要翻译: 本发明涉及由式[I]表示的化合物或其药学上可接受的盐或酯:其中:X 1,X 2,X 3, / SUB>和X 4可以相同或不同,各自为C或N,条件是X 1,X 2, / SUB>,X 3和X 4是N; Y是CH或N; R 1,R 1,R 2,R 2,R 3,N 3, R 3,R 4,R 4,R 4和R 4可以相同或不同,分别为氢原子,低级 烷基等; R 5是氢原子或甲基; R 6和R 7可以相同或不同,分别为氢原子,低级烷基等; R 8和R 8可以相同或不同,分别为氢原子,低级烷基等; R 9是可以被取代的芳基或杂芳基; n为1〜3的整数,PLK1抑制剂或含有该PLK1抑制剂的抗癌剂。
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公开(公告)号:US08030327B2
公开(公告)日:2011-10-04
申请号:US11667282
申请日:2005-11-07
申请人: Yoshiyuki Sato , Hideki Kurihara , Kaori Kamijo , Yu Onozaki , Toshiaki Tsujino , Tetsuya Sugimoto , Akiko Watanabe , Morihiro Mitsuya , Hideya Komatani
发明人: Yoshiyuki Sato , Hideki Kurihara , Kaori Kamijo , Yu Onozaki , Toshiaki Tsujino , Tetsuya Sugimoto , Akiko Watanabe , Morihiro Mitsuya , Hideya Komatani
IPC分类号: A01N43/42 , A01N43/38 , A01N43/06 , A61K31/44 , A61K31/40 , A61K31/38 , C07D513/02 , C07D515/02 , C07D333/02 , C07D333/34 , C07D333/22
CPC分类号: C07D471/04 , C07D487/04
摘要: The present invention relates to a compound represented by the Formula [I]: Wherein: the A ring is a 5-membered aromatic heterocyclic group containing at least one hetero atom selected from a nitrogen atom, and the like; A1 and A2, are each a nitrogen atom, and the like; X2, X3, X4, and X5 are all carbon atoms, or alternatively any one of X2, X3, X4, and X5 is a nitrogen atom and the rest are all carbon atoms; R1 is a hydrogen atom, or the like; R2, R3, R4, and R5, are each a hydrogen atom, or the like; R6 and R6′, are each a hydrogen atom, and the like; R7 is an aryl group and the like; and R8 is an amino group or a hydroxy group, or a pharmaceutically acceptable salt or ester thereof.
摘要翻译: 本发明涉及由式[I]表示的化合物:其中:A环是含有至少一个选自氮原子的杂原子的5元芳族杂环基等; A1和A2各自为氮原子等; X2,X3,X4和X5都是碳原子,或者X2,X3,X4和X5中的任何一个是氮原子,其余全部是碳原子; R1是氢原子等; R2,R3,R4和R5各自为氢原子等; R6和R6'各自为氢原子等; R7是芳基等; 并且R 8是氨基或羟基,或其药学上可接受的盐或酯。
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公开(公告)号:US20080103136A1
公开(公告)日:2008-05-01
申请号:US11667282
申请日:2005-11-07
申请人: Yoshiyuki Sato , Hideki Kurihara , Kaori Kamijo , Yu Onozaki , Toshiaki Tsujino , Tetsuya Sugimoto , Akiko Watanabe , Morihiro Mitsuya , Hideya Komatani
发明人: Yoshiyuki Sato , Hideki Kurihara , Kaori Kamijo , Yu Onozaki , Toshiaki Tsujino , Tetsuya Sugimoto , Akiko Watanabe , Morihiro Mitsuya , Hideya Komatani
IPC分类号: A61K31/5377 , C07D471/04 , C07D413/14 , A61K31/497 , A61P35/00 , C07D401/14 , A61K31/437
CPC分类号: C07D471/04 , C07D487/04
摘要: The present invention relates to a compound represented by the Formula [I]: Wherein: the A ring is a 5-membered aromatic heterocyclic group containing at least one hetero atom selected from a nitrogen atom, and the like; A1 and A2, are each a nitrogen atom, and the like; X2, X3, X4, and X5 are all carbon atoms, or alternatively any one of X2, X3, X4, and X5 is a nitrogen atom and the rest are all carbon atoms; R1 is a hydrogen atom, or the like; R2, R3, R4, and R5, are each a hydrogen atom, or the like; R6 and R6′, are each a hydrogen atom, and the like; R7 is an aryl group and the like; and R8 is an amino group or a hydroxy group, or a pharmaceutically acceptable salt or ester thereof.
摘要翻译: 本发明涉及由式[I]表示的化合物:其中:A环是含有至少一个选自氮原子的杂原子的5元芳族杂环基等; A 1和A 2分别是氮原子等; X 2,X 3,X 4和X 5都是碳原子,或者任意一个 X 2,X 3,X 4和X 5是氮原子,其余全部是碳 原子 R 1是氢原子等; R 2,R 3,R 4和R 5各自为氢原子等 ; R 6和R 6'各自为氢原子等; R 7是芳基等; 并且R 8是氨基或羟基,或其药学上可接受的盐或酯。
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