Name | tafetinib |
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Synonyms |
SIM-010603
SIM010603 |
Description | Tafetinib (SIM010603) is an oral multi-targets receptor tyrosine kinases inhibitor. Tafetinib inhibitsstem cell factor receptor (Kit),vascular endothelial growth factor receptor-2 (VEGFR-2),platelet-derived growth factor receptor-β (PDGFR-β),glial cell line-derived neurotrophic factor receptor (Rearranged during Transfection; RET), andFms-like tyrosine kinase-3 (FLT3)withIC50values between 5.0 and 68.1 nmol/l. Tafetinib inhibits the phosphorylation ofPDGFR-βandVEGFR-2. Tafetinib inhibits endothelial cell proliferation, endothelial cells chemotaxis, and corneal angiogenesis[1]. |
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Related Catalog | |
References |
Density | 1.251±0.06 g/cm3(Predicted) |
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Boiling Point | 618.2±55.0 °C(Predicted) |
Molecular Formula | C24H29FN4O2 |
Molecular Weight | 424.51 |