GSK-J1 (Free acid)


  • Specification
  • Related Products
Cat.No.:  BSM-0137
Product Name:  GSK-J1 (Free acid)
CAS No.:  1373422-53-7
Figure: 
Synonyms:  N-[2-(2-Pyridinyl)-6-(1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl)-4-pyrimidinyl]-β-alanine
Description:  GSK-J1 is a 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.
Appearance:  Pale yellow powder.
Molecular Weight:  398.45
Purity:  ≥98% by TLC
Storage:  -20°C
Targets:  JMJD3/UTX
Molecular Formula:  C22H23N5O2
MDL Number:  MFCD22683851
Solubility:  DMSO (~ 20 mg/ml)
Shipping Conditions:  Gel Pack
Warning:  For Research Use Only! Not For Use in Humans.

Online Inquiry

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

USA

Enter your email here to subscribe.

Follow us on

Easy access to products and services you need from our library via powerful searching tools

Copyright © Creative BioMart. All Rights Reserved.