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首页-小分子抑制剂&激动剂-Tyrosine Kinase-PDGFR-Sunitinib
Sunitinib

Chemical Structure : Sunitinib

CAS No.: 557795-19-4

Sunitinib (SU11248, SU-11248)

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.

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500 mg ¥1380 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

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.

物理化学性质&存储条件

分子量 398.4738
分子式 C22H27FN4O2
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

DMSO: 25 mg/mL

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-

参考文献

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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