GSK-J1
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。
包装与价格:
包装 | 价格(元) |
10mg | 询价 |
25mg | 询价 |
50mg | 询价 |
100mg | 询价 |
CAS: | 1373422-53-7 |
分子式: | C22H23N5O2 |
分子量: | 389.45 |
纯度: | ≥98% |
溶解性: | DMSO |
存储: | Powder -20℃ 3 years; 4℃ 2 years In solvent -80℃ 6 months;-20℃ 1 month |
研究领域: | Cancer |
Target: | IC50: 60 nM (KDM6B)[2] |
描述: | GSK-J1 is a potent inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A, with IC50 of 60 nM towards KDM6B. |