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In vitro metabolism and drug interaction potential of a new highly potent anti‐cytomegalovirus molecule, CMV423 (2‐chloro 3‐pyridine 3‐yl 5,6,7,8‐tetrahydroindolizine 1‐carboxamide)
Author(s) -
Bournique Bruno,
Lambert Nicole,
Boukaiba Rachid,
Martinet Michel
Publication year - 2001
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1046/j.0306-5251.2001.01413.x
Subject(s) - in vitro , carboxamide , pharmacology , drug , chemistry , drug interaction , metabolism , biochemistry , medicine
Aims To identify the enzymes involved in the metabolism of CMV423, a new anticytomegalovirus molecule, to evaluate its in vitro clearance and to investigate its potential involvement in drug/drug interactions that might occur in the clinic.Methods The enzymes involved in and the kinetics of CMV423 biotransformation were determined using pools of human liver subcellular fractions and heterologously expressed human cytochromes P450 (CYP) and FMO. The effect of CMV423 on CYP probe activities as well as on indinavir and AZT metabolism was determined, and 26 drugs were tested for their potential to inhibit or activate CMV423 metabolism.Results CMV423 was oxidized by CYP and not by FMO or cytosolic enzymes. The K m values for 8‐hydroxylation to rac ‐RPR 127025, an active metabolite, and subsequent ketone formation by human liver microsomes were 44 ± 13 µ m and 47 ± 11 µ m , respectively, with corresponding V max / K m ratios of 14 and 4 µl min −1 nmol −1 P450. Inhibition with selective CYP inhibitors indicated that CYP1A2 was the main isoform involved, with some participation from CYP3A. Expressed human CYP1A1, 1A2, 2C9, 3A4 and 2C8 catalysed rac ‐RPR 127025 formation with K m values of < 10 µ m , 50 ± 21 µ m , 55 ± 19 µ m , circa 282 ± 61 µ m and circa 1450 µ m , respectively. CYP1B1, 2A6, 2B6, 2C19, 2D6, 2E1 or 3A5 did not catalyse the reaction to any detectable extent. CYP1A1 and 3A4 also catalysed ketone formation from rac‐ RPR 127025. In human liver microsomes, CMV423 at 1 and 10 µ m inhibited CYP1A2 activity up to 31% and 63%, respectively, CYP3A4 activity up to 40% (10 µ m ) and CYP2C9 activity by 35% (1 and 10 µ m ). No effect was observed on CYP2A6, 2D6 and 2E1 activities. CMV423 had no effect on indinavir and AZT metabolism. Amongst 26 drugs tested, none inhibited CMV423 metabolism in vitro at therapeutic concentrations.Conclusions CMV423 is mainly metabolized by CYP1A2 and 3A4. Its metabolism should not be saturable at the targeted therapeutic concentrations range ( C max < 1 µ m ). CMV423 will probably affect CYP1A2 and 1A1 activities in vivo to some extent, but no other drug–drug interactions are expected.