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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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Detaylı Bibliyografya
Asıl Yazarlar: Gervasini, Guillermo, Caballero, Maria J., Carrillo, Juan A., Benitez, Julio
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Hindawi Publishing Corporation 2013
Konular:
Online Erişim: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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