VEGFR Tyrosine Kinase Inhibitor II (Synonyms: Vascular Endothelial Growth Factor Tyrosine Kinase Inhibitor II) |
| Katalog-Nr.GC16062 |
VEGFR Tyrosinkinase-Inhibitor II (Verbindung 3) ist ein potenter Angiogenese-Inhibitor mit IC50-Werten von 0,02, 0,18, 0,24 7,3 und 7 ⋼M fÜr KDR, Flt-1, c-Kit, EGF-R bzw. c-Src .
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 269390-69-4
Sample solution is provided at 25 µL, 10mM.
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VEGFR tyrosine kinase inhibitor II is a pyridinyl-anthranilamide compound that inhibits the kinase activities of VEGFR2 (KDR), VEGFR1 (FLT1), and c-Kit (IC50s = 20, 180, and 240 nM, respectively).1 It displays minimal activity against c-Src and EGFR (IC50s = 7 and 7.3 µM, respectively) and is inactive against Cdk1, c-Met, IGF-1R, and PKA (IC50s > 10 µM).1 VEGFR tyrosine kinase inhibitor II has been investigated for its potential to inhibit tumor induced angiogenesis.[1]
Reference:
[1] Furet, P., Bold, G., Hofmann, F., et al. Identification of a new chemical class of potent angiogenesis inhibitors based on conformational considerations and database searching. Bioorganic & Medicinal Chemistry Letters 13(18), 2967-2971 (2003).
Average Rating: 5 (Based on Reviews and 19 reference(s) in Google Scholar.)
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