Title : Role of the equine CYP3A94, CYP3A95 and CYP3A97 in ketamine metabolism in presence of medetomidine, diazepam and methadone studied by enantioselective capillary electrophoresis.

Pub. Date : 2018 Aug

PMID : 29614330






5 Functional Relationships(s)
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1 Role of the equine CYP3A94, CYP3A95 and CYP3A97 in ketamine metabolism in presence of medetomidine, diazepam and methadone studied by enantioselective capillary electrophoresis. Ketamine cytochrome P450 3A97 Equus caballus
2 Role of the equine CYP3A94, CYP3A95 and CYP3A97 in ketamine metabolism in presence of medetomidine, diazepam and methadone studied by enantioselective capillary electrophoresis. Methadone cytochrome P450 3A97 Equus caballus
3 Enzyme kinetics for ketamine N-demethylation were determined using equine CYP3A94, CYP3A95 and CYP3A97, and the effect of medetomidine, diazepam and methadone on the ketamine metabolism was studied in vitro. Ketamine cytochrome P450 3A97 Equus caballus
4 In contrast to diazepam and methadone, the alpha2-recepor agonist medetomidine diminished the norketamine formation significantly in CYP3A94 and CYP3A97. Medetomidine cytochrome P450 3A97 Equus caballus
5 In contrast to diazepam and methadone, the alpha2-recepor agonist medetomidine diminished the norketamine formation significantly in CYP3A94 and CYP3A97. norketamine cytochrome P450 3A97 Equus caballus