AZD-5438

• Description :

  A potent and oral inhibitor of CDK1/2/9 with IC50 of 16/6/20 nM, respectively; also inhibits the kinase activity of p25-Cdk5 (IC50=14 nM) and GSK-3β (IC50=17 nM) in vitro.

• Stability :

  ≥ 2 years

• Purity :

  >98% (HPLC)

• Weight :

  371.4566

• Molecular Formula :

  C18H21N5O2S

• Notes :

  Research use only, not for human use.

• Receptor :

  CDK1|CDK2|CDK9

• CAS Number :

  602306-29-6