BIOTRANSFORMATION OF (+)-AND (-)-CLAUSENAMIDE IN RATS / 药学学报
Acta Pharmaceutica Sinica
; (12): 224-228, 2001.
Article
em Zh
| WPRIM
| ID: wpr-410879
Biblioteca responsável:
WPRO
ABSTRACT
AIM To study the metabolic pathway of chiral clausenamide in the rat and understand its stereoselectivity. METHODS The urine, feces and blood of rat were gathered after the drug was administered, the known metabolites were analyzed by HPLC-DAD and one unknown metabolite was elucidated by using LC-MS analysis. Metabolic stereoselectivity was determined by comparing the metabolic results of (+)- and (-)-clausenamide. RESULTS Six known metabolites were determined and one unknown metabolite was elucidated as N-demethylclausenamide. The metabolic stereoselectivity was shown distinctly. CONCLUSION Chiral clausenamide was mainly metabolized by hydroxylation in liver and the biotransformation exhibited pronounced substrate stereoselectivity.
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Base de dados:
WPRIM
Idioma:
Zh
Revista:
Acta Pharmaceutica Sinica
Ano de publicação:
2001
Tipo de documento:
Article