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公开(公告)号:US09790212B2
公开(公告)日:2017-10-17
申请号:US15292200
申请日:2016-10-13
发明人: Charles William Blackledge, Jr. , Joelle Lorraine Burgess , Neil W. Johnson , Jiri Kasparec , Steven David Knight , Louis V. LaFrance, III , Juan I. Luengo , William Henry Miller , Kenneth Allen Newlander , Stuart Paul Romeril , Mark Schulz , Dai-Shi Su , Xinrong Tian
IPC分类号: C07D401/12 , A61K31/4412 , C07D409/14 , C07D405/14 , C07D413/14 , C07D409/12 , C07D403/12 , C07D409/06
CPC分类号: C07D409/14 , C07D401/12 , C07D403/12 , C07D405/14 , C07D409/06 , C07D409/12 , C07D413/14
摘要: This invention relates to novel compounds according to Formula (III)(a) which are inhibitors of Enhancer of Zeste Homolog 2 (EZH2), and to pharmaceutical compositions containing them.
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公开(公告)号:US09556157B2
公开(公告)日:2017-01-31
申请号:US14898178
申请日:2014-07-09
IPC分类号: C07D409/12 , C07D409/14 , A61K31/4436
CPC分类号: C07D409/14 , C07D409/12
摘要: This invention relates to novel compounds according to Formula (I) which are inhibitors of Enhancer of Zeste Homolog 2 (EZH2), to pharmaceutical compositions containing them, to processes for their preparation, and to their use in therapy for the treatment of cancers.
摘要翻译: 本发明涉及式(I)的新化合物,其为Zeste同系物2(EZH2)的增效剂的抑制剂,含有它们的药物组合物,其制备方法及其在治疗癌症中的用途。
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公开(公告)号:US09505745B2
公开(公告)日:2016-11-29
申请号:US14787866
申请日:2014-04-25
发明人: Charles William Blackledge, Jr. , Joelle Lorraine Burgess , Neil W. Johnson , Jiri Kasparec , Steven David Knight , Louis V. LaFrance, III , Juan I. Luengo , William Henry Miller , Kenneth Allen Newlander , Stuart Paul Romeril , Mark Schulz , Dai-Shi Su , Xinrong Tian
IPC分类号: C07D401/12 , C07D403/12 , C07D409/12 , C07D409/14 , C07D405/14 , C07D413/14
CPC分类号: C07D409/14 , C07D401/12 , C07D403/12 , C07D405/14 , C07D409/06 , C07D409/12 , C07D413/14
摘要: This invention relates to novel compounds according to Formula (I) which are inhibitors of Enhancer of Zeste Homolog 2 (EZH2), to pharmaceutical compositions containing them, to processes for their preparation, and to their use in therapy for the treatment of cancers.
摘要翻译: 本发明涉及式(I)的新化合物,其为Zeste同系物2(EZH2)的增效剂的抑制剂,含有它们的药物组合物,其制备方法及其在治疗癌症中的用途。
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