Discovery of N-phenyl nicotinamides as potent inhibitors of Kdr

被引:21
作者
Dominguez, Celia
Smith, Leon
Huang, Qi
Yuan, Chester
Ouyang, Xiaohu
Cai, Lynn
Chen, Paul
Kim, Joseph
Harvey, Timothy
Syed, Rashid
Kim, Tae-Seong
Tasker, Andrew
Wang, Ling
Zhang, Michael
Coxon, Angela
Bready, James
Starnes, Charles
Chen, Danlin
Gan, Yongmei
Neervannan, Sesha
Kumar, Gondi
Polverino, Anthony
Kendall, Richard
机构
[1] Chem Res Discovery, Thousand Oaks, CA 91320 USA
[2] Canc Biol, Thousand Oaks, CA 91320 USA
[3] Canc Pharmacol, Thousand Oaks, CA 91320 USA
[4] Pharmacokinet & Drug Metabol, Thousand Oaks, CA 91320 USA
[5] Pharmaceut Amgen Inc, Thousand Oaks, CA 91320 USA
[6] Bristol Myers Squibb Co, Pharmaceut Res Inst, Princeton, NJ 08543 USA
关键词
VEGF; VEGFR-2; inhibitor; Kdr inhibitor; angiogenesis inhibitor; kinase inhibitor;
D O I
10.1016/j.bmcl.2007.07.077
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Inhibition of tumor-induced angiogenesis is a promising strategy in anticancer research. Neovascularization is a process required for both tumor growth and metastasis. Enhanced understanding of the underlying molecular mechanisms has led to the discovery of a variety of pharmaceutically attractive targets. Decades of investigation suggest that vascular endothelial growth factor (VEGF) and its receptors, in particular VEGFR2 or kinase insert-domain-containing receptor (Kdr), play a critical role in the growth and survival of endothelial cells in newly forming vasculature. The clinical utility of inhibitors of this receptor tyrosine kinase is currently under intense investigation. Herein we report our efforts in this arena. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6003 / 6008
页数:6
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