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Comparative Cytochrome P450 In Vitro Inhibition by Atypical Antipsychotic Drugs

The goal of this study was to assess in human liver microsomes the inhibitory capacity of commonly used antipsychotics on the most prominent CYP450 drug metabolizing enzymes (CYP1A2, CYP2C9, CYP2D6, and CYP3A). Chlorpromazine was the only antipsychotic that inhibited CYP1A2 activity (IC(50) = 9.5 μM...

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Detalhes bibliográficos
Main Authors: Gervasini, Guillermo, Caballero, Maria J., Carrillo, Juan A., Benitez, Julio
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3586484/
https://ncbi.nlm.nih.gov/pubmed/23476805
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/792456
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