Title of article :
In-silico fragment-based identification of novel angiogenesis inhibitors
Author/Authors :
Sivanesan Dakshanamurthy، نويسنده , , Min Kim، نويسنده , , Milton L. Brown، نويسنده , , Stephen W. Byers، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
6
From page :
4551
To page :
4556
Abstract :
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.
Keywords :
Fragment-screening , Docking , Angiogenesis inhibitors , VEGFR2 , Molecular dynamics
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
2007
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
798461
Link To Document :
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