GSK-J1 (sodium salt)


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Cat.No.:  BSM-0295
Product Name:  GSK-J1 (sodium salt)
CAS No.:  1797832-71-3
Figure: 
Product Overview:  A dual inhibitor of JMJD3 and UTX
Description:  GSK-J1 is a potent inhibitor of the H3K27 histone demethylases JMJD3 and UTX. It is inactive against a panel of additional JMJ family demethylases, including several variants of JMJD2 and JMJD1 and, at concentrations up to 30 μM, has no effect on more than 100 different kinases or other unrelated proteins, including other chromatin-modifying enzymes such as histone deacetylases. Since the highly polar carboxylate group of GSK-J1 restricts its cellular permeability, a prodrug ethyl ester, GSK-J4 has also been developed.
Appearance:  A crystalline solid
Molecular Weight:  411.4
Purity:  ≥95%
Storage:  -20°C
Targets:  JMJD3; UTX
Molecular Formula:  C22H22N5O2 • Na
Chemical Name:  N-[2-(2-pyridinyl)-6-(1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl)-4-pyrimidinyl]-β-alanine, monosodium salt
Warning:  For Research Use Only! Not For Use in Humans.

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