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首页-小分子抑制剂&激动剂-Tyrosine Kinase-VEGFR-Ki8751
Ki8751

Chemical Structure : Ki8751

CAS No.: 228559-41-9

Ki8751 (Ki 8751, Ki-8751)

货号: PC-42853Not For Human Use, Lab Use Only.

Ki8751 is a potent, selective and orally active VEGFR-2 inhibitor that inhibits VEGFR-2 phosphorylation with IC50 of 0.6 nM.

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5 mg (Free Sample) ¥280 In stock
25 mg ¥1280 In stock
50 mg ¥1980 In stock
100 mg ¥2980 In stock
250 mg Get quote

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

Ki8751 is a potent, selective and orally active VEGFR-2 inhibitor that inhibits VEGFR-2 phosphorylation with IC50 of 0.6 nM.
Ki8751 also inhibits PDGFR family members such as PDGFRα and c-Kit at 67 nM and 40 nM, does not have any inhibitory activity against other kinases such as EGFR, HGFR, InsulinR (IC50>10 uM).
Ki8751  suppressed the growth of the VEGF-stimulated HUVEC on nanomolar level, shows significant antitumor activity against human tumor xenografts such as glioma, stomach carcinoma), lung carcinoma, colon carcinoma and melanoma in nude mice.

物理化学性质&存储条件

分子量 469.4126
分子式 C24H18F3N3O4
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: ≥92mg/mL; Water: <1.2mg/mL; Ethanol: <1.2mg/mL

Chemical Name/SMILES

Urea, N-(2,4-difluorophenyl)-N'-[4-[(6,7-dimethoxy-4-quinolinyl)oxy]-2-fluorophenyl]-

参考文献

1. Kubo K, et al. J Med Chem. 2005 Mar 10;48(5):1359-66.

2. Arao T, et al. Anticancer Res. 2011 Sep;31(9):2787-96.

3. Hasan MR, et al. Int J Cancer. 2011 Nov 1;129(9):2115-23.

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