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Curcuminoids inhibit multiple human cytochromes P450 (CYP), UDP-glucuronosyltransferase (UGT), and sulfotransferase (SULT) enzymes, while piperine is a relatively selective CYP3A4 inhibitor
Laurie P Volak, Senait Ghirmai, John R. Cashman and Michael H. Court
Drug Metabolism and Disposition May 14, 2008, DOI: https://doi.org/10.1124/dmd.108.020552
Laurie P Volak
Senait Ghirmai
John R. Cashman
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Curcuminoids inhibit multiple human cytochromes P450 (CYP), UDP-glucuronosyltransferase (UGT), and sulfotransferase (SULT) enzymes, while piperine is a relatively selective CYP3A4 inhibitor
Laurie P Volak, Senait Ghirmai, John R. Cashman and Michael H. Court
Drug Metabolism and Disposition May 14, 2008, DOI: https://doi.org/10.1124/dmd.108.020552
OtherArticle
Curcuminoids inhibit multiple human cytochromes P450 (CYP), UDP-glucuronosyltransferase (UGT), and sulfotransferase (SULT) enzymes, while piperine is a relatively selective CYP3A4 inhibitor
Laurie P Volak, Senait Ghirmai, John R. Cashman and Michael H. Court
Drug Metabolism and Disposition May 14, 2008, DOI: https://doi.org/10.1124/dmd.108.020552
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