GSK J2

• Description :

  inactive control of GSK J1, JMJD3 (KDM6B) and UTX (KDM6A) inhibitor

• Product Name Alternative :

  3-((6-(4,5-dihydro-1H-benzo[d]azepin-3(2H)-yl)-2-(pyridin-3-yl)pyrimidin-4-yl)amino)propanoate

• Field of Research :

  Chromatin Epigenetics Histone Demethylases

• Purity :

  0.9988

• Form :

  A solid

• Solubility :

  insoluble in H2O; insoluble in EtOH; ≥15.2 mg/mL in DMSO with gentle warming

• Smiles :

  [O-]C(CCNC1=CC(N2CCC3=CC=CC=C3CC2)=NC(C4=CC=CN=C4)=N1)=O

• Molecular Formula :

  C22H23N5O2

• Molecular Weight :

  389.45

• Shipping Conditions :

  Blue ice

• Storage Conditions :

  Desiccate at RT.

• CAS Number :

  1394854-52-4