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GSK J2
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
GSK J2图片
CAS NO:1394854-52-4
规格:98%
分子量:389.45
包装与价格:
包装价格(元)
10mg电议
50mg电议

产品介绍
inactive control of GSK J1, JMJD3 (KDM6B) and UTX (KDM6A) inhibitor
CAS:1394854-52-4
分子式:C22H23N5O2
分子量:389.45
纯度:98%
存储:Store at -20°C

Background:

GSK-J2 is an isomer of GSK-J1 that does not have any specific activity. GSK-J1 is a potent inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A.


GSK-J2 is an isomer of GSK-J1, and shows poor activity towards KDM6A and KDM6B, with IC50 of >100 μM and 49 μM, respectively[1].


参考文献:
[1]. Heinemann B, et al. Inhibition of demethylases by GSK-J1/J4. Nature. 2014 Oct 2;514(7520):E1-2.