Mepyramine, a histamine H1 receptor antagonist, inhibits the metabolic activity of rat and human P450 2D forms

Journal of Pharmacology and Experimental Therapeutics

Volumn 272, Issue 2, 1995, Pages 939-944

  Hiroi, T ^a   Ohishi, N ^a   Imaoka, S ^a   Yabusaki, Y ^a   Fukui, H ^a   Funae, Y ^a  

^a OSAKA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIHISTAMINIC AGENT; CHLORPHENIRAMINE; CIMETIDINE; CYTOCHROME P450 ISOENZYME; DEBRISOQUINE; DIPHENHYDRAMINE; HISTAMINE H1 RECEPTOR; HISTAMINE H1 RECEPTOR ANTAGONIST; HISTAMINE H2 RECEPTOR ANTAGONIST; LIDOCAINE; MEPYRAMINE; QUINIDINE; QUININE; RANITIDINE; TESTOSTERONE; THIOPERAMIDE; TRIPROLIDINE;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DRUG ACTIVITY; DRUG HYDROXYLATION; DRUG PROTEIN BINDING; DRUG SPECIFICITY; ENZYME INHIBITION; LIVER MICROSOME; MALE; NONHUMAN; PRIORITY JOURNAL; RAT;

ANIMAL; CYTOCHROME P-450 CYP2D6; CYTOCHROME P-450 ENZYME SYSTEM; HUMAN; MALE; MIXED FUNCTION OXYGENASES; PYRILAMINE; RATS; RATS, SPRAGUE-DAWLEY;

EID: 0028816462     PISSN: 00223565     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)