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Drug metabolism by CYP2C8.3 is determined by substrate dependent interactions with cytochrome P450 reductase and cytochrome b5

Genetic polymorphisms in CYP2C8 can influence the metabolism of important therapeutic agents and cause interindividual variation in drug response and toxicity. The significance of the variant CYP2C8*3 has been controversial with reports of higher in vivo but lower in vitro activity compared to CYP2C...

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Main Authors: Kaspera, Rüdiger, Naraharisetti, Suresh B., Evangelista, Eric A., Marciante, Kristin D., Psaty, Bruce M., Totah, Rheem A.
Formato: Artigo
Idioma:Inglês
Publicado: 2011
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3159548/
https://ncbi.nlm.nih.gov/pubmed/21726541
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bcp.2011.06.027
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