FGFR3-IN-3

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

FGFR3-IN-3 

FGFR3-IN-3 (化合物 40a) 是一种有效的 FGFR 泛型抑制剂,抑制 FGFR1234IC50 值分别为 2.1 nM,3.1 nM,4.3 nM 和 74 nM。FGFR3-IN-3 可用于膀胱癌的研究。

FGFR3-IN-3

FGFR3-IN-3 Chemical Structure

CAS No. : 2428738-41-2

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生物活性

FGFR3-IN-3 (compound 40a) is a potent and pan-FGFR inhibitor, with IC50s of 2.1 nM, 3.1 nM, 4.3 nM and 74 nM for FGFR1, 2, 3, and 4, respectively. FGFR3-IN-3 can be used for the research of bladder cancer[1].

IC50 & Target[1]

FGFR1

2.1 nM (IC50)

FGFR2

3.1 nM (IC50)

FGFR3

4.3 nM (IC50)

FGFR4

74 nM (IC50)

分子量

759.92

Formula

C38H49N9O6S

CAS 号

2428738-41-2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Kuriwaki I, et, al. Structure-based drug design of 1,3,5-triazine and pyrimidine derivatives as novel FGFR3 inhibitors with high selectivity over VEGFR2. Bioorg Med Chem. 2020 May 15;28(10):115453.

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