In-silico fragment-based identification of novel angiogenesis inhibitors

被引:31
作者
Dakshanamurthy, Sivanesan [1 ]
Kim, Min
Brown, Milton L.
Byers, Stephen W.
机构
[1] Georgetown Univ, Lombardi Comprehens Canc ctr, Dept Oncol, Washington, DC 20057 USA
[2] Georgetown Univ, Lombardi Comprehens Canc Ctr, Drug Discovery Program, Washington, DC USA
关键词
fragment-screening; docking; molecular dynamics; angiogenesis inhibitors; VEGFR2;
D O I
10.1016/j.bmcl.2007.05.104
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Inhibition of vascular endothelial growth factor receptor-2 (VEGFR2) kinase blocks angiogenesis, the process of generating new capillary blood vessels that are important in tumor growth. To identify small molecule inhibitors of the VEGFR2 kinase, we undertook a computer assisted fragment-based screening that used 3-D, structural models of the VEGFR2 kinase, and hinge region as a fragment anchor point. Seven novel non-cytotoxic compounds were identified which limited the induction of capillary networks by human umbilical vein endothelial cells in the low micromolar range. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4551 / 4556
页数:6
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