DescriptionInhibitor of vascular endothelial growth factor (VEGF) receptor tyrosine kinase. Inhibits activity of KDR and FLT VEGF receptors (IC50 values are 100 nM and 2 µM respectively) and displays > 3-fold selectivity over FGFR-1. Orally active in vivo.
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|Observed MW: 370.21|
Safety and Handling
Recommended Storage : Desiccate at RT
For Research Use Only
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