PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 18448569-2 2008 Pactimibe has two equally dominant clearance pathways forming R-125528 by CYP3A4 and M-1 by CYP2D6 in vitro. pactimibe 0-9 cytochrome P450 family 2 subfamily D member 6 Homo sapiens 92-98 18524873-9 2008 The effect of the N-alkyl chain length of pactimibe analogs on their CYP2D6 metabolic stability was plausibly explained by the docking model. pactimibe 42-51 cytochrome P450 family 2 subfamily D member 6 Homo sapiens 69-75 19000552-2 2008 The pharmacokinetics of pactimibe and its pharmacologically inactive plasma metabolite, R-125528, of which the main clearance pathway is CYP2D6, was affected by coadministration of quinidine. pactimibe 24-33 cytochrome P450 family 2 subfamily D member 6 Homo sapiens 137-143 19000552-3 2008 The aim of this study was to investigate the influence of CYP2D6 polymorphism on pharmacokinetics of pactimibe and R-125528. pactimibe 101-110 cytochrome P450 family 2 subfamily D member 6 Homo sapiens 58-64 19000552-4 2008 In addition, exposure was examined after multiple doses of pactimibe sulfate in CYP2D6 poor metabolizer (PMs). pactimibe 59-76 cytochrome P450 family 2 subfamily D member 6 Homo sapiens 80-86 19000552-8 2008 After multiple doses of 100 mg pactimibe to CYP2D6 PMs, the accumulation ratio of R-125528 reached 8.8-fold, however, the exposure of R-125528 in CYP2D6 PMs was covered by the exposure in additional metabolite safety testing. pactimibe 31-40 cytochrome P450 family 2 subfamily D member 6 Homo sapiens 44-50 19000552-8 2008 After multiple doses of 100 mg pactimibe to CYP2D6 PMs, the accumulation ratio of R-125528 reached 8.8-fold, however, the exposure of R-125528 in CYP2D6 PMs was covered by the exposure in additional metabolite safety testing. pactimibe 31-40 cytochrome P450 family 2 subfamily D member 6 Homo sapiens 146-152 19000552-9 2008 CONCLUSIONS: Although CYP2D6 polymorphism greatly affected the pharmacokinetics of R-125528 rather than pactimibe, the exposure in CYP2D6 PMs after a multiple dose of 100 mg pactimibe sulfate was covered by additional non-clinical metabolite safety testing. pactimibe 174-191 cytochrome P450 family 2 subfamily D member 6 Homo sapiens 22-28 19000552-9 2008 CONCLUSIONS: Although CYP2D6 polymorphism greatly affected the pharmacokinetics of R-125528 rather than pactimibe, the exposure in CYP2D6 PMs after a multiple dose of 100 mg pactimibe sulfate was covered by additional non-clinical metabolite safety testing. pactimibe 174-191 cytochrome P450 family 2 subfamily D member 6 Homo sapiens 131-137 18056254-0 2008 CYP2D6-Mediated metabolism of a novel acyl coenzyme A:cholesterol acyltransferase inhibitor, pactimibe, and its unique plasma metabolite, R-125528. pactimibe 93-102 cytochrome P450 family 2 subfamily D member 6 Homo sapiens 0-6