Profile and molecular modeling of 3-(indole-3-yl)-4-(3,4,5-trimethoxyphenyl)-1 H-pyrrole-2,5-dione (1) as a highly selective VEGF-R2/3 inhibitor

J Med Chem. 2006 Dec 14;49(25):7549-53. doi: 10.1021/jm0609871.

Abstract

We report on selectivity profiling of 1 in a panel of 20 protein kinases and molecular modeling indicating 1 to be highly active and selective for VEGF-R2/3. Sequence alignment analysis and detailed insights into the ATP binding pockets of targeted protein kinases from the panel result in a unique structural architecture of VEGF-R2 mainly caused by the hydrophobic pocket I, determining the molecular basis for activity and selectivity of 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Binding Sites
  • Crystallography, X-Ray
  • Hydrophobic and Hydrophilic Interactions
  • Indoles / chemical synthesis*
  • Indoles / chemistry
  • Models, Molecular*
  • Molecular Sequence Data
  • Pyrroles / chemical synthesis*
  • Pyrroles / chemistry
  • Vascular Endothelial Growth Factor Receptor-2 / chemistry*
  • Vascular Endothelial Growth Factor Receptor-3 / chemistry*

Substances

  • Indoles
  • Pyrroles
  • Vascular Endothelial Growth Factor Receptor-2
  • Vascular Endothelial Growth Factor Receptor-3