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GSK-J1 (Free acid)

JMJ H3K27 Demethylase Inhibitor (Cell Imperm)
Catalog No. J48-904B


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Catalog No. Pack Size Price (USD)
J48-904B-5 5 mg $110
J48-904B-25 25 mg $450
J48-904B-BULK BULK Contact Us  


Overview:

Potent and selective inhibitor of jumonji H3K27 histone demethylases JMJD3 and UTX (IC50 = 60 nM, human JMJD3). This is the first known inhibitor selective for the H3K27me3-specific JMJ subfamily which binds to the active catalytic site of the enzyme. The COOH group confers cell impermeability and as such is useful as a standard in in vitro assays. A cell permeable ethyl ester analog is also available.

References:


1. L Kruidenier et al. Nature 2012 488:404


CAS Registry Number:

1373422-53-7


Molecular Formula:

C22H23N5O2


Appearance:

Pale yellow powder


Molecular Weight:

389.5


Purity:

99%


Solubilization:

May be dissolved in DMSO (20 mg/ml, warm)


Aliases:

N-[2-(2-Pyridinyl)-6-(1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl)-4-pyrimidinyl]-β-alanine


Storage and Stability:

Store desiccated as supplied at ambient temperature for up to 2 years. Store solutions at -20oC for up to 3 months.


Molecular Structure:



Product Datasheets



There are no related publications available for this product.


RESEARCH AREAS

Cancer, Cell Cycle, Inflammation



SIGNALCHEM BIOTECH INC.


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