Volak, Laurie P <br/><br/>
Curcuminoids inhibit multiple human cytochromes P450, UDP-glucuronosyltransferase, and sulfotransferase enzymes, whereas piperine is a relatively selective CYP3A4 inhibitor.  [electronic resource] 

 -  Drug metabolism and disposition: the biological fate of chemicals  Aug 2008 
 - 1594-605 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1521-009X 
<br/><br/><label>Standard No.: </label>10.1124/dmd.108.020552  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acetaminophen--metabolism<br/>Alkaloids--pharmacology<br/>Benzodioxoles--pharmacology<br/>Chromatography, High Pressure Liquid<br/>Curcumin--pharmacology<br/>Cytochrome P-450 Enzyme Inhibitors<br/>Enzyme Inhibitors--pharmacology<br/>Glucuronosyltransferase--antagonists & inhibitors<br/>Humans<br/>Liver--drug effects<br/>Piperidines--pharmacology<br/>Polyunsaturated Alkamides--pharmacology<br/>Recombinant Proteins--antagonists & inhibitors<br/>Spectrometry, Fluorescence<br/>Spectrometry, Mass, Electrospray Ionization<br/>Spectrophotometry, Ultraviolet<br/>Sulfotransferases--antagonists & inhibitors