FGFR3-IN-2

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-2 

FGFR3-IN-2 (compound 18b) 是一种有效和选择性的 FGFR3 抑制剂,抑制 FGFR3VEGFR2IC50 值分别为 4.1 nM 和 570 nM。FGFR3-IN-2 可用于膀胱癌的研究。

FGFR3-IN-2

FGFR3-IN-2 Chemical Structure

CAS No. : 2428742-58-7

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生物活性

FGFR3-IN-2 (compound 18b) is a potent and selective FGFR3 inhibitor, with IC50s of 4.1 nM and 570 nM for FGFR3 and VEGFR2, respectively. FGFR3-IN-2 can be used for the research of bladder cancer[1].

IC50 & Target[1]

FGFR3

4.1 nM (IC50)

VEGFR2

570 nM (IC50)

分子量

597.73

Formula

C28H39N9O4S

CAS 号

2428742-58-7

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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