Results 131 to 140 of about 6,342 (159)
Comparative analysis of sex-based, vendor-based, and species differences in cytochrome P450 metabolism. [PDF]
Kinatukara N, Xu X, Shah P.
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CYP2D6-Guided Opioid Management and Postoperative Pain Control: A Randomized Clinical Trial.
Cavallari LH +32 more
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Risk of Seizure Associated With Concomitant Use of Tramadol and Antidepressants in Older Nursing Home Residents. [PDF]
Wei YJ +6 more
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Population Pharmacokinetic Model Assessment of the Effects of Body Weight on Risk of Drug-Drug Interactions After Posaconazole Discontinuation. [PDF]
Wrishko RE +3 more
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Exploring the roles of cytochrome P450 enzymes and their inhibitors in cancers and non-neoplastic human diseases. [PDF]
Lee H, Kwon YJ, Chun YJ.
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AbstractAn enantioselective CE method was used to identify the ability of CYP450 enzymes and their stereoselectivity in catalyzing the transformation of propafenone (PPF) to 5‐hydroxy‐propafenone (5OH‐PPF) and N‐despropyl‐propafenone (NOR‐PPF). Using in vitro incubations with single CYP450 enzymes (SUPERSOMES), 5OH‐PPF is shown to be selectively ...
Afshar, Minoo, Thormann, Wolfgang
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Involvement of CYP2D6, CYP3A4, and other cytochrome P-450 isozymes in N-dealkylation reactions
Journal of Pharmacological and Toxicological Methods, 1994Metabolic N-dealkylation is a commonly observed biotransformation with tertiary and secondary amine drugs and related N-alkylated amides, but surprisingly little is known about the cytochrome P-450 isozymes involved in these dealkylation reactions.
R T Coutts, Glen B Baker
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Drug Metabolism and Disposition, 1999
The ability of antipsychotic drugs to inhibit the catalytic activity of five cytochrome P-450 (CYP) isoforms was compared using in vitro human liver microsomal preparations to evaluate the relative potential of these drugs to inhibit drug metabolism. The apparent kinetic parameters for enzyme inhibition were determined by nonlinear regression analysis ...
Jae-Gook Shin
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The ability of antipsychotic drugs to inhibit the catalytic activity of five cytochrome P-450 (CYP) isoforms was compared using in vitro human liver microsomal preparations to evaluate the relative potential of these drugs to inhibit drug metabolism. The apparent kinetic parameters for enzyme inhibition were determined by nonlinear regression analysis ...
Jae-Gook Shin
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Drug Metabolism and Disposition, 1999
Azelastine, an antiallergy and antiasthmatic drug, has been reported to be mainly N-demethylated to desmethylazelastine in humans. In the present study, Eadie-Hofstee plots of azelastine N-demethylation in human liver microsomes were biphasic. In microsomes from human B-lymphoblast cells, recombinant cytochrome P-450 (CYP)2D6 and CYP1A1 exhibited ...
Hiroshi Yamazaki, Tsuyoshi Yokoi
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Azelastine, an antiallergy and antiasthmatic drug, has been reported to be mainly N-demethylated to desmethylazelastine in humans. In the present study, Eadie-Hofstee plots of azelastine N-demethylation in human liver microsomes were biphasic. In microsomes from human B-lymphoblast cells, recombinant cytochrome P-450 (CYP)2D6 and CYP1A1 exhibited ...
Hiroshi Yamazaki, Tsuyoshi Yokoi
exaly +3 more sources

