Name | ethyl 2,4-dimethyl-5-[(2-oxo-1H-indol-3-ylidene)methyl]-1H-pyrrole-3-carboxylate |
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Synonyms |
VEGFR2 Kinase Inhibitor I
IN1018 SU5408 |
Description | SU5408 is a potent and cell-permeable inhibitor of VEGFR2 kinase with an IC50 of 70 nM. |
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Related Catalog | |
Target |
VEGFR2:70 nM (IC50) |
In Vitro | 3-Substituted indolin-2-ones have been designed and synthesized as a novel class of tyrosine kinase inhibitors which exhibit selectivity toward different receptor tyrosine kinases (RTKs). These compounds have been evaluated for their relative inhibitory properties against a panel of RTKs in intact cells. SU5408 is found to be the most potent and selective VEGFR2 inhibitor among the compounds. SU5408 shows little or no effect against receptors for platelet-derived growth factor, epidermal growth factor, or insulin-like growth factor (IC50>100 µM)[1]. |
References |
Molecular Formula | C18H18N2O3 |
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Molecular Weight | 310.34700 |
Exact Mass | 310.13200 |
PSA | 71.19000 |
LogP | 3.43890 |
Storage condition | 2-8℃ |