Atopaxar hydrobromide

• Description:

  A potent, reversible PAR-1 antagonist with IC50 of 19 nM; shows potent inhibitory effects on human platelet aggregation induced by thrombin and TRAP with IC50 of 64 nM and 31 nM, respectively.

• Stability:

  ≥ 2 years

• Purity:

  >98% (HPLC)

• Weight:

  608.54

• Molecular Formula:

  C29H38FN3O5.HBr

• Notes:

  Research use only, not for human use.

• Receptor:

  PAR-1

• CAS Number:

  474550-69-1