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