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首页-小分子抑制剂&激动剂-Tyrosine Kinase-FGFR-ASP5878
ASP5878

Chemical Structure : ASP5878

CAS No.: 1453208-66-6

ASP5878 (ASP-5878, ASP 5878)

货号: PC-70221Not For Human Use, Lab Use Only.

ASP-5878 (ASP5878) is a novel potent, selective pan-FGFR inhibitor with IC50 of 0.47/0.60/0.74/3.5 nM for FGFR1/2/3/4, respectively.

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5 mg ¥1980 In stock
10 mg ¥2980 In stock
25 mg ¥4980 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

ASP-5878 (ASP5878) is a novel potent, selective pan-FGFR inhibitor with IC50 of 0.47/0.60/0.74/3.5 nM for FGFR1/2/3/4, respectively.
ASP-5878 also inhibits FGFR3 (K650E), FGFR3 (K650M), VEGFR2, FGFR4 (N535K), FMS with IC50 of 1.6, 4.2, 25, 78, 150 nM, respectively.
ASP-5878 potently suppressed the growth of the FGF19-expressing hepatocellular carcinoma cell lines Hep3B2.1-7, HuH-7, and JHH-7 with IC50 of 8.5-27 nM.
ASP-5878 induces sustained tumor regression in a xenograft mouse model using Hep3B2.1-7. Orally bioactive.

物理化学性质&存储条件

分子量 407.378
分子式 C18H19F2N5O4
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: 250 mg/mL

Chemical Name/SMILES

2-(4-((5-((2,6-difluoro-3,5-dimethoxybenzyl)oxy)pyrimidin-2-yl)amino)-1H-pyrazol-1-yl)ethan-1-ol

参考文献

1. Futami T, et al. Mol Cancer Ther. 2017 Jan;16(1):68-75.

2. Kikuchi A, et al. Cancer Sci. 2017 Feb;108(2):236-242.

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