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Metabolism of nicousamide in rat and human liver in vitro / 药学学报
Acta Pharmaceutica Sinica ; (12): 912-916, 2008.
Article in Chinese | WPRIM | ID: wpr-232669
ABSTRACT
This paper is aimed to study the metabolic kinetics of nicousamide in rat liver microsomes and cytosol and to identify the major metabolite and drug metabolizing enzymes involved in the metabolism of nicousamide in rat and human liver microsomes by selective inhibitors in vitro. The concentration of nicousamide was determined by HPLC-UV method. The metabolite of nicousamide in rat and human liver microsomes was isolated and identified by LC-MS/MS. The major metabolite of nicousamide in rat and human liver microsomes was identified to be 3-(3'-carboxy-4'-hydroxy-anilino-carbo-)-6-amino-7-hydroxy-8-methyl-coumarin (M1). The metabolite of nicousamide in rat plasma, urine, bile and liver was consistent with M1. The metabolism of nicousamide can be catalyzed by several reductases, including CYP450 reductases, cytochrome b5 reductases and CYP2C6 in rat liver microsomes, as well as xanthine oxidase and DT-diaphorase in rat liver cytosol.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Propylthiouracil / Xanthine Oxidase / Dicumarol / Microsomes, Liver / Mitochondria, Liver / Steroid 21-Hydroxylase / Adenosine Monophosphate / Allopurinol / Cimetidine Limits: Animals / Female / Humans / Male Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2008 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Propylthiouracil / Xanthine Oxidase / Dicumarol / Microsomes, Liver / Mitochondria, Liver / Steroid 21-Hydroxylase / Adenosine Monophosphate / Allopurinol / Cimetidine Limits: Animals / Female / Humans / Male Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2008 Type: Article