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Physiologically Based Pharmacokinetic Model of Mechanism-Based Inhibition of CYP3A by Clarithromycin

The prediction of clinical drug-drug interactions (DDIs) due to mechanism-based inhibitors of CYP3A is complicated when the inhibitor itself is metabolized by CYP3Aas in the case of clarithromycin. Previous attempts to predict the effects of clarithromycin on CYP3A substrates, e.g., midazolam, faile...

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Bibliografische gegevens
Hoofdauteurs: Quinney, Sara K., Zhang, Xin, Lucksiri, Aroonrut, Gorski, J. Christopher, Li, Lang, Hall, Stephen D.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: The American Society for Pharmacology and Experimental Therapeutics 2010
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2812061/
https://ncbi.nlm.nih.gov/pubmed/19884323
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1124/dmd.109.028746
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