Liu, Wei <br/><br/>
Coupling of UDP-glucuronosyltransferases and multidrug resistance-associated proteins is responsible for the intestinal disposition and poor bioavailability of emodin.  [electronic resource] 

 -  Toxicology and applied pharmacology  Dec 2012 
 - 316-24 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1096-0333 
<br/><br/><label>Standard No.: </label>10.1016/j.taap.2012.08.032  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Biological Availability<br/>Biological Transport<br/>Caco-2 Cells<br/>Emodin--pharmacokinetics<br/>Glucuronosyltransferase--metabolism<br/>Humans<br/>Intestinal Absorption<br/>Intestinal Mucosa--metabolism<br/>Intestines--enzymology<br/>Leukotriene C4--pharmacology<br/>Multidrug Resistance-Associated Proteins--antagonists & inhibitors<br/>Propionates--pharmacology<br/>Quinolines--pharmacology