4-Aryl-5-cyano-2-aminopyrimidines as VEGF-R2 inhibitors: Synthesis and biological evaluation
摘要:
A novel series of 4-aryl-5-cyano-2-aminopyrimidines were synthesized and found to have potent VEGF-R2 kinase inhibitory activity. Structure-activity relationships were investigated and compound 14a was shown to be efficacious in a mouse model of corneal neovascularization. (c) 2007 Elsevier Ltd. All rights reserved.
4-Aryl-5-cyano-2-aminopyrimidines as VEGF-R2 inhibitors: Synthesis and biological evaluation
作者:Terry V. Hughes、Stuart L. Emanuel、Amanda K. Beck、Steven K. Wetter、Peter J. Connolly、Prabha Karnachi、Michael Reuman、Jabed Seraj、Angel R. Fuentes-Pesquera、Robert H. Gruninger、Steven A. Middleton、Ronghui Lin、Jeremy M. Davis、David F.C. Moffat
DOI:10.1016/j.bmcl.2007.04.021
日期:2007.6
A novel series of 4-aryl-5-cyano-2-aminopyrimidines were synthesized and found to have potent VEGF-R2 kinase inhibitory activity. Structure-activity relationships were investigated and compound 14a was shown to be efficacious in a mouse model of corneal neovascularization. (c) 2007 Elsevier Ltd. All rights reserved.