GSK J1

目录号: A12918

Histone demethylase inhibitor

GSK J1 Chemical Structure

CAS NO. 1373422-53-7

GSK J1 is a potent and selective inhibitor of the H3K27 histone demethylases JMJD3 and UTX

库存: 现货

规格 价格 数量
10 mg
¥ 800.00
25 mg
¥ 1,300.00
50 mg
¥ 2,300.00
100 mg
¥ 3,800.00
Warning 产品仅用于科学研究,不针对患者销售,望谅解.

详情

GSK J1 is a potent and selective inhibitor of the H3K27 histone demethylases JMJD3 and UTX
Targets
JMJD3 (KDM6B) UTX (KDM6A)
28 nM53 nM
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 25.68 mL 128.39 mL 256.77 mL
0.5 mM 5.14 mL 25.68 mL 51.35 mL
1 mM 2.57 mL 12.84 mL 25.68 mL
5 mM 0.51 mL 2.57 mL 5.14 mL

*The above data is based on the productmolecular weight 389.45. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

目录号 A12918
MECHANISM OF ACTION Inhibitor
M. Wt 389.45
Formula C22H23N5O2
Solubility DMSO
Purity >98%
Storage at -20°C 3 years Powder
CAS No. 1373422-53-7
Synonyms 0
SMILES C1CN(CCC2=CC=CC=C21)C3=CC(=NC(=N3)C4=CC=CC=N4)NCCC(=O)O

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