Potent and selective inhibitor of VEGFR-2 (Flk-1, KDR). It displays a 100-fold greater potency for the unactivated form of the kinase (Ki=0.04µM) compared to the activated form (Ki=4µM).
Molecular Weight:
264.3
Purity:
98%
CAS Number:
[5812-07-7]
Formula:
C17H16N2O
Target:
VEGFR-2
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