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公开(公告)号:US10292960B2
公开(公告)日:2019-05-21
申请号:US15878057
申请日:2018-01-23
发明人: Nobuharu Andoh , Osamu Sanpei , Tetsuo Toga , David Morris , Roger Aston , Koji Tanaka , Tomokazu Hino
IPC分类号: A61K31/277 , A61K31/341 , A61K31/5377 , A61K31/5383 , A61K31/381 , A61K31/415 , A61K31/4196 , A61K31/42 , A61K31/421 , A61K31/426 , A61K31/4245 , A61K31/433 , A61K31/437 , A61K31/44 , A61K31/4965 , A61K31/465 , A61K31/505
摘要: The present invention relates to an anticancer agent having a high safety and a superior anticancer activity, and an anticancer agent containing, as an active ingredient, an aminoacetonitrile compound represented by the formula (I) wherein R1 is a hydrogen atom, an alkyl group and the like, R2, R3, and R4 are the same or different and each is a hydrogen atom, an alkyl group and the like, R5 and R6 are the same or different and each is a hydrogen atom, a halogen atom and the like, m is 0 or 1, R is a halogen atom, a cyano group, a nitro group, a phenyl group optionally substituted by an alkyl group and the like, an alkyl group and the like, Ar1 is a phenyl group, a naphthyl group, a pyridyl group, a pyrazolyl group, or the like, each of which is optionally substituted by a halogen atom, a cyano group, a nitro group, alkyl group and the like, and W is —O—, —S—, —SO2—, or —N(R7)— wherein R7 is a hydrogen atom, a (C1-C6) alkyl group and the like, or a pharmacologically acceptable salt thereof.
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公开(公告)号:US10391076B2
公开(公告)日:2019-08-27
申请号:US15552907
申请日:2016-02-24
发明人: Nobuharu Andoh , Osamu Sanpei , Tetsuo Toga , David Lawson Morris , Roger Aston , Koji Tanaka , Tomokazu Hino
IPC分类号: A61K31/277 , A61K31/433 , A61K31/4245 , A61K31/5383 , A61K31/4196 , A61K31/437 , A61K31/381 , A61P35/00 , A61K31/40 , A61K31/415 , A61K31/4192 , A61K31/42 , A61K31/425 , A61K31/44 , A61K31/4433 , A61K31/4436 , A61K31/496 , A61K31/4965 , A61K31/505 , A61K31/535
摘要: The present invention relates to an anticancer agent having a high safety and a superior anticancer activity, and anticancer agent containing, as an active ingredient, an aminoacetonitrile compound represented by the formula (I) wherein R1 is a hydrogen atom, an alkyl group and the like, R2, R3, and R4 are the same or different and each is a hydrogen atom, an alkyl group and the like, R5 and R6 are the same or different and each is a hydrogen atom, a halogen atom and the like, m is 0 or 1, R is a halogen atom, a cyano group, a nitro group, a phenyl group optionally substituted by an alkyl group and the like, an alkyl group and the like, Ar1 is a phenyl group, a naphthyl group, a pyridyl group, a pyrazolyl group, or the like, each of which is optionally substituted by a halogen atom, a cyano group, a nitro group, alkyl group and the like, and W is —O—, —S—, —SO2—, or —N(R7)— wherein R7 is a hydrogen atom, a (C1-C6)alkyl group and the like, or a pharmacologically acceptable salt thereof.
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公开(公告)号:US09907778B2
公开(公告)日:2018-03-06
申请号:US14917724
申请日:2014-09-12
发明人: Nobuharu Andoh , Osamu Sanpei , Tetsuo Toga , David Lawson Morris , Roger Aston , Koji Tanaka , Tomokazu Hino
IPC分类号: A61K31/341 , A61K31/4245 , A61K31/5383 , A61K31/4196 , A61K31/437 , A61K31/381 , A61K31/5377 , A61K31/415 , A61K31/277 , A61K31/42 , A61K31/421 , A61K31/426 , A61K31/433 , A61K31/44 , A61K31/4965 , A61K31/505
CPC分类号: A61K31/277 , A61K31/341 , A61K31/381 , A61K31/415 , A61K31/4196 , A61K31/42 , A61K31/421 , A61K31/4245 , A61K31/426 , A61K31/433 , A61K31/437 , A61K31/44 , A61K31/4965 , A61K31/505 , A61K31/5377 , A61K31/5383
摘要: The present invention relates to an anticancer agent having a high safety and a superior anticancer activity, and an anticancer agent containing, as an active ingredient, an aminoacetonitrile compound represented by the formula (I) wherein R1 is a hydrogen atom, an alkyl group and the like, R2, R3, and R4 are the same or different and each is a hydrogen atom, an alkyl group and the like, R5 and R6 are the same or different and each is a hydrogen atom, a halogen atom and the like, m is 0 or 1, R is a halogen atom, a cyano group, a nitro group, a phenyl group optionally substituted by an alkyl group and the like, an alkyl group and the like, Ar1 is a phenyl group, a naphthyl group, a pyridyl group, a pyrazolyl group, or the like, each of which is optionally substituted by a halogen atom, a cyano group, a nitro group, alkyl group and the like, and W is —O—, —S—, —SO2—, or —N(R7)— wherein R7 is a hydrogen atom, a (C1-C6)alkyl group and the like, or a pharmacologically acceptable salt thereof.
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