The design and synthesis of novel 3-[2-indol-1-yl-ethyl]-1-H-indole derivatives as selective inhibitors of CDK4

被引:54
作者
Aubry, C
Patel, A
Mahale, S
Chaudhuri, B
Maréchal, JD
Suteliffe, MJ
Jenkins, PR [1 ]
机构
[1] Univ Leicester, Dept Chem, Leicester LE1 7RH, Leics, England
[2] De Montfort Univ, Leicester Sch Pharm, Leicester LE1 9BH, Leics, England
[3] Univ Leicester, Dept Biochem & Chem, Leicester LE1 7RH, Leics, England
关键词
indole; CDK4; fascaplysin; 3-[2-indol-l-yl-ethyl]-1H-indole; molecular modelling; IC50;
D O I
10.1016/j.tetlet.2005.01.054
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We present the design, synthesis and biological activity of novel 3-[2-indol-1-yl-ethyl]-1H-indole selective inhibitors of CDK4. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1423 / 1425
页数:3
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