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Zifaxaban

Chemical Structure : Zifaxaban

CAS No.: 1378266-98-8

Zifaxaban

Catalog No.: PC-35604Not For Human Use, Lab Use Only.

Zifaxaban is a novel, potent, selective, direct and oral factor Xa (FXa) inhibitor with IC50 of 11.1 nM (human FXa), displays >10,000-fold selectivity than other serine proteases.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

    Biological Activity

    Zifaxaban is a novel, potent, selective, direct and oral factor Xa (FXa) inhibitor with IC50 of 11.1 nM (human FXa), displays >10,000-fold selectivity than other serine proteases.
    Zifaxaban also deoes not impair platelet aggregation induced by collagen, adenosine diphosphate (ADP) or arachidonic acid.
    Zifaxaban significantly prolongs clotting time, prothrombin time (PT), and activated partial thromboplastin time (APTT) in the plasma of humans, rabbits, and rats, with a relatively weak effect on thrombin time.
    Zifaxaban strongly suppresses thrombus formation with ED50 values of 3.09 mg/kg in venous thrombosis models in rats.

    Physicochemical Properties

    M.Wt 429.875
    Formula C20H16ClN3O4S
    Appearance Solid
    CAS No.
    Storage
    Solide Powder
    -20 °C 12 Months; 4°C 6 Months
    In Solvent
    -80 °C 6 Months; -20°C 6 Months
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    (S)-5-chloro-N-((2-oxo-3-(4-(2-oxopyridin-1(2H)-yl)phenyl)oxazolidin-5-yl)methyl)thiophene-2-carboxamide

    References

    1. Qiu X, et al. Eur J Pharmacol. 2018 Aug 17. pii: S0014-2999(18)30469-2.

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