发现新型基于噻吩并[2,3 - d ]嘧啶-4-基的Cyclin D1-CDK4抑制剂:合成,生物学评估和结构-活性关系。第2部分
摘要:
描述,设计和合成新型噻吩并[2,3 - d ]嘧啶-4-基类似物作为细胞周期蛋白依赖性激酶4(CDK4)抑制剂。重点研究the上带有取代苯基,4-[((甲基氨基)甲基]苯甲醛(22)和5-异二氢吲哚甲醛(24)(6-叔丁基硫代[2,3- d ]嘧啶-已经鉴定出4-基)hydr衍生物。在本文中,讨论了我们合成化合物的效价,选择性和结构活性关系。
发现新型基于噻吩并[2,3 - d ]嘧啶-4-基的Cyclin D1-CDK4抑制剂:合成,生物学评估和结构-活性关系。第2部分
摘要:
描述,设计和合成新型噻吩并[2,3 - d ]嘧啶-4-基类似物作为细胞周期蛋白依赖性激酶4(CDK4)抑制剂。重点研究the上带有取代苯基,4-[((甲基氨基)甲基]苯甲醛(22)和5-异二氢吲哚甲醛(24)(6-叔丁基硫代[2,3- d ]嘧啶-已经鉴定出4-基)hydr衍生物。在本文中,讨论了我们合成化合物的效价,选择性和结构活性关系。
Arylmethoxy Isoindoline Derivatives and Compositions Comprising and Methods of Using the Same
申请人:Man Hon-Wah
公开号:US20110196150A1
公开(公告)日:2011-08-11
Provided are 4′-arylmethoxy isoindoline compounds, and pharmaceutically acceptable salts, solvates, clathrates, stereoisomers, and prodrugs thereof. Methods of use, and pharmaceutical compositions of these compounds are disclosed.
ARYLMETHOXY ISOINDOLINE DERIVATIVES AND COMPOSITIONS COMPRISING AND METHODS OF USING THE SAME
申请人:Celgene Corporation
公开号:US20180037567A1
公开(公告)日:2018-02-08
Provided are 4′-arylmethoxy isoindoline compounds, and pharmaceutically acceptable salts, solvates, clathrates, stereoisomers, and prodrugs thereof. Methods of use, and pharmaceutical compositions of these compounds are disclosed.
Arylmethoxy isoindoline derivatives and compositions comprising and methods of using the same
申请人:Celgene Corporation
公开号:US10189814B2
公开(公告)日:2019-01-29
Provided are 4′-arylmethoxy isoindoline compounds, and pharmaceutically acceptable salts, solvates, clathrates, stereoisomers, and prodrugs thereof. Methods of use, and pharmaceutical compositions of these compounds are disclosed.