In vitro effects of racemates, separate enantiomers and major metabolites of mefloquine and halofantrine on metoprolol biotransformation by rat liver microsomes

Xenobiotica

Volumn 29, Issue 6, 1999, Pages 595-601

  Baune, B ^a   Furlan, V ^b   Taburet, A M ^b   Farinotti, R ^a  

^a UNIVERSITÉ PARIS SACLAY   (France)

^b BICÊTRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DRUG METABOLITE; HALOFANTRINE; MEFLOQUINE; METOPROLOL;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DRUG BLOOD LEVEL; DRUG ELIMINATION; DRUG HALF LIFE; DRUG HYDROXYLATION; DRUG METABOLISM; DRUG POTENCY; DRUG TRANSFORMATION; ENANTIOMER; LIVER MICROSOME; MALE; NONHUMAN; RACEMIC MIXTURE; RAT; STRUCTURE ACTIVITY RELATION;

ANIMALS; ANTIMALARIALS; BIOTRANSFORMATION; MALE; MEFLOQUINE; METOPROLOL; MICROSOMES, LIVER; PHENANTHRENES; RATS; RATS, SPRAGUE-DAWLEY; STEREOISOMERISM;

ANIMALIA;

EID: 0032808699     PISSN: 00498254     EISSN: None     Source Type: Journal    
DOI: 10.1080/004982599238416     Document Type: Article

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