AZD-9056

• Description :

  A potent, selective, orally bioavailable P2X7 receptor antagonist; inhibits release of pro-inflammatory mediators from isolated human peripheral monocytes (IL-1β and IL-18) and human alveolar macrophages (IL-1β) with IC50 values of 10-13 nM.

• Stability :

  ≥ 2 years

• Purity :

  >98% (HPLC)

• Weight :

  419.006

• Molecular Formula :

  C24H35ClN2O2

• Notes :

  Research use only, not for human use.

• Receptor :

  P2X Receptor

• CAS Number :

  345304-65-6