Journal
DRUG METABOLISM AND PHARMACOKINETICS
Volume 23, Issue 6, Pages 412-420Publisher
JAP SOC STUDY XENOBIOTICS
DOI: 10.2133/dmpk.23.412
Keywords
prasugrel; antiplatelet; thienopyridine; cytochrome P450; active metabolite
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Differences in the inhibition of cytochrome P450 activities among thienopyridine antiplatelet agents, ticlopidine, clopidogrel, prasugrel, and the metabolites, 2-oxo-clopidogrel, clopidogrel acid metabolite, deacetylated metabolite of prasugrel (R-95913) and the pharmacologically active metabolites of clopidogrel and prasugrel, were examined using recombinant cytochromes P450 and fluorescent probe substrates. Ticlopidine and clopidogrel inhibited CYP2B6 with IC(50) values of 0.0517 +/- 0.0323 mu M and 0.0182 +/- 0.0069 mu M, respectively, and inhibited CYP2C19 with IC(50) values of 0.203 +/- 0.124 mu M and 0.524 +/- 0.160 mu M, respectively. Ticlopidine also inhibited CYP2D6 (IC(50) of 0.354 +/- 0.158 mu M). In contrast, 2-oxoclopidogrel, prasugrel and R-95913 were much weaker inhibitors of CYP2B6, CYP2C19 and CYP2D6. The inhibitory effects of all the compounds tested were much weaker on the isoforms other than those indicated above. The active metabolites of clopidogrel and prasugrel and clopidogrel acid metabolite also did not affect the activities of the P450s examined.
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