生物活性 | |||
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描述 | Vatalanib succinate is a potent, orally active VEGFR inhibitor with IC50s of 37 nM, 77 nM, 270 nM, 660 nM, 730 nM, 1,400 nM, and 580 nM for KDR, Flt-1, Flk, Flt-4, c-Kit, c-Fms, and PDGFR-β, respectively. Vatalanib succinate inhibits vascular endothelial growth factor-induced autophosphorylation of KDR and inhibits endothelial cell proliferation, migration and survival. At concentrations up to 1 µM, Vatalanib succinate does not have any cytotoxic or antiproliferative effects on cells that do not express VEGFR[1]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.15mL 0.43mL 0.22mL |
10.76mL 2.15mL 1.08mL |
21.51mL 4.30mL 2.15mL |