Abstract
The metabolic fate of the anti-Parkinsonian drug budipine was studied in rats after oral administration. The presence of an aromatic hydroxylation product, metabolite Mi, and its O-sulphate conjugate was confirmed. Three new minor metabolites, budipine N-oxide, metabolite M1 N-oxide and a secondary metabolite derived from M1 via hydroxylation of a methyl of the tert-butyl group, were isolated and identified in rat urine. The presence of a metabolite M1-glucuronic acid conjugate, was also established through different enzymatic treatments of the rat urine.
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | 113-118 |
| Numero di pagine | 6 |
| Rivista | European Journal of Drug Metabolism and Pharmacokinetics |
| Volume | 16 |
| Numero di pubblicazione | 2 |
| DOI | |
| Stato di pubblicazione | Pubblicato - apr 1991 |
| Pubblicato esternamente | Sì |