Coupling of UDP-glucuronosyltransferases and multidrug resistance-associated proteins is responsible for the intestinal disposition and poor bioavailability of emodin. [electronic resource]
Producer: 20130424Description: 316-24 p. digitalISSN:- 1096-0333
- Biological Availability
- Biological Transport
- Caco-2 Cells
- Emodin -- pharmacokinetics
- Glucuronosyltransferase -- metabolism
- Humans
- Intestinal Absorption
- Intestinal Mucosa -- metabolism
- Intestines -- enzymology
- Leukotriene C4 -- pharmacology
- Multidrug Resistance-Associated Proteins -- antagonists & inhibitors
- Propionates -- pharmacology
- Quinolines -- pharmacology
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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