Chemical Structure : Sunitinib
CAS No.: 557795-19-4
货号: PC-42490Not For Human Use, Lab Use Only.
A multi-targeted RTK inhibitor that targets VEGFR2 (Flk-1) and PDGFRβ with Ki of 8 nM and 9 nM respectively.
规格 | 价格 | 库存 | 数量 |
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100 mg | ¥580 | In stock | |
250 mg | ¥880 | In stock | |
500 mg | ¥1380 | In stock | |
1 g | Get quote |
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Sunitinib (SU11248) is a multi-targeted RTK inhibitor that targets VEGFR2 (Flk-1) and PDGFRβ with Ki of 8 nM and 9 nM respectively.
Sunitinib displays >10-fold higher selectivity over FGFR-1, EGFR, Cdk2, Met, IGFR-1, Abl, and Src.
Sunitinib also inhibits phosphorylation of wild-type FLT3, FLT3-ITD, and FLT3-Asp835 with IC50 of 250 nM, 50 nM, and 30 nM.
Sunitinib regresses FLT3-ITD tumors in the subcutaneous tumor xenograft model.
分子量 | 398.4738 | |
分子式 | C22H27FN4O2 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
DMSO: 25 mg/mL |
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Chemical Name/SMILES |
1H-Pyrrole-3-carboxamide, N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl- |
1. Sun L, et al. J Med Chem. 2003 Mar 27;46(7):1116-9.
2. O'Farrell AM, et al. Blood. 2003 May 1;101(9):3597-605.
3. Mendel DB, et al. Clin Cancer Res. 2003 Jan;9(1):327-37.
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