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首页-小分子抑制剂&激动剂-Tyrosine Kinase-EGFR-(Rac)-JBJ-04-125-02
(Rac)-JBJ-04-125-02

Chemical Structure : (Rac)-JBJ-04-125-02

CAS No.: 2140807-05-0

(Rac)-JBJ-04-125-02 (JBJ-04-125-02)

货号: PC-72985Not For Human Use, Lab Use Only.

(Rac)-JBJ-04-125-02 is a potent, mutant-selective, allosteric inhibitor of EGFR T790M/L858R with IC50 of 0.26 nM.

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

生物&药学活性

(Rac)-JBJ-04-125-02 is a potent, mutant-selective, allosteric inhibitor of EGFR T790M/L858R with IC50 of 0.26 nM.
JBJ-04-125-02 displays excellent selectivity against a panel of 468 kinases using the KINOMEscan approach (S-Score (35)=0.02).
JBJ-04-125-02 increases apoptosis and efficacy in vitro and in vivo compared with either single agent alone when combined with osimertinib.

物理化学性质&存储条件

分子量 543.617
分子式 C29H26FN5O3S
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

10 mM in DMSO

Chemical Name/SMILES

2-(5-fluoro-2-hydroxyphenyl)-2-(1-oxo-6-(4-(piperazin-1-yl)phenyl)isoindolin-2-yl)-N-(thiazol-2-yl)acetamide

参考文献

1. To C, et al. Cancer Discov. 2019 Jul;9(7):926-943.

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