Clopidogrel (hydrogen sulfate)


CAS No. : 120202-66-6

(Synonyms: (S)-(+)-Clopidogrel bisulfate; (S)-(+)-Clopidogrel hydrogen sulfate)

120202-66-6
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Cat. No. : HY-17459
M.Wt: 419.90
Formula: C16H18ClNO6S2
Purity: >98 %
Solubility: H2O : 16.67 mg/mL (ultrasonic);DMSO : ≥ 46.7 mg/mL
Introduction of 120202-66-6 :

Clopidogrel hydrogen sulfate is an antiplatelet agent to prevent blood clots. Clopidogrel hydrogen sulfate inhibits CYP2B6 and CYP2C19 with IC50s of 18.2 nM and 524 nM, respectively[1]. Clopidogrel hydrogen sulfate is a potent antithrombotic agent that inhibits ADP-induced platelet aggregation[2].Clopidogrel hydrogen sulfate also is an orally active P2Y(12) inhibitor[5]. IC50 & Target: IC50: 18.2 nM (CYP2B6)[1].
IC50: 524 nM (CYP2C19)[1] In Vitro: Clopidogrel (1.5 mM;12 and 24 hours) up-regulates the expression of TRIB3 and CHOP in a concentration- and time-dependent manner, as measured by real-time PCR and Western blot analysis[3].
Clopidogrel (1.5 mM; 24 hours) significantly induces human gastric epithelial cell (GES-1) apoptosis[3]. In Vivo: Clopidogrel (5 mg/kg) significantly inhibits thrombus formation compared with vehicle. Acetylsalicylic acid (0.15 mg/kg) can add to the antithrombotic effect of Clopidogrel in mice; Acetylsalicylic acid (0.6 mg/kg) blunts the antithrombotic effect of Clopidogrel[4].

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