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Inhibition of fatty acid amide hydrolase and monoacylglycerol lipase by the anandamide uptake inhibitor VDM11: evidence that VDM11 acts as an FAAH substrate

1. There is some dispute concerning the extent to which the uptake inhibitor VDM11 (N-(4-hydroxy-2-methylphenyl) arachidonoyl amide) is capable of inhibiting the metabolism of the endocannabinoid anandamide (AEA) by fatty acid amide hydrolase (FAAH). In view of a recent study demonstrating that the...

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Sonraí Bibleagrafaíochta
Main Authors: Vandevoorde, Séverine, Fowler, Christopher J
Formáid: Artigo
Teanga:Inglês
Foilsithe: 2005
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1576210/
https://ncbi.nlm.nih.gov/pubmed/15895107
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.bjp.0706253
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