中文名 | SU5408 |
英文名 | SU5408 |
别名 | RAMUCIRUMAB ( 雷莫芦单抗 ) 化合物VEGFR2 KINASE INHIBITOR I 2,4-二甲基-5-((2-氧吲哚-3-亚甲基)甲基)-1H-吡咯-3-羧酸乙酯 |
英文别名 | SU5408 SU-5408 SU 5408 VEGFR2 TK Inhibitor VEGFR2 KISE INHIBITOR I VEGFR2 Kinase Inhibitor I VEGFR2 kinase inhibitor I(SU-5408) 1H-Pyrrole-3-carboxylic acid, 5-[(1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-, ethyl ester |
CAS | 15966-93-5 |
化学式 | C18H18N2O3 |
分子量 | 310.35 |
密度 | 1.271±0.06 g/cm3(Predicted) |
沸点 | 571.4±50.0 °C(Predicted) |
溶解度 | DMSO: 6 mg/mL |
酸度系数 | 12.40±0.20(Predicted) |
存储条件 | Sealed in dry,Store in freezer, under -20°C |
体外研究 | 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 (VEGFR2 Kinase Inhibitor I) is found to be the most potent and selective VEGFR2 inhibitor among the compounds. SU5408 (VEGFR2 Kinase Inhibitor I) shows little or no effect against receptors for platelet-derived growth factor, epidermal growth factor, or insulin-like growth factor (IC 50 >100 µM). |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 3.222 ml | 16.111 ml | 32.222 ml |
5 mM | 0.644 ml | 3.222 ml | 6.444 ml |
10 mM | 0.322 ml | 1.611 ml | 3.222 ml |
5 mM | 0.064 ml | 0.322 ml | 0.644 ml |
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