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FAAH gene

Known as: FAAH, FAAH-1, FATTY ACID AMIDE HYDROLASE 
National Institutes of Health

Related topics

Related topics

3 relations
FA2H genefatty acid alpha-hydroxylasefatty acid amide hydrolase

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2015
Highly Cited
2015
Multitarget fatty acid amide hydrolase/cyclooxygenase blockade suppresses intestinal inflammation and protects against nonsteroidal anti‐inflammatory drug‐dependent gastrointestinal damage
The ability of nonsteroidal anti‐inflammatory drugs (NSAIDs) to inhibit cyclooxygenase (Cox)‐1 and Cox‐2 underlies the… 
2014
2014
Combined inhibition of FAAH and COX produces enhanced anti-allodynic effects in mouse neuropathic and inflammatory pain models
2011
2011
Identification of potent, noncovalent fatty acid amide hydrolase (FAAH) inhibitors.
Review
2007
Review
2007
Therapeutic potential of endocannabinoid-hydrolysing enzyme inhibitors.
The specific protein target of delta9-tetrahydrocannabinol (delta9-THC), the main active ingredient of Cannabis sativa L., was… 
Highly Cited
2006
Highly Cited
2006
Development of the first potent and specific inhibitors of endocannabinoid biosynthesis.
Highly Cited
2006
Highly Cited
2006
Fatty acid amide hydrolase inhibitors from virtual screening of the endocannabinoid system.
The endocannabinoid system consists of two cannabinoid receptors (CB1 and CB2), endogenous ligands (endocannabinoids), and the… 
Highly Cited
2005
Highly Cited
2005
Discovery of an exceptionally potent and selective class of fatty acid amide hydrolase inhibitors enlisting proteome-wide selectivity screening: concurrent optimization of enzyme inhibitor potency…
Highly Cited
2004
Highly Cited
2004
A simple stopped assay for fatty acid amide hydrolase avoiding the use of a chloroform extraction phase.
Highly Cited
1999
Highly Cited
1999
Inhibition of anandamide hydrolysis by the enantiomers of ibuprofen, ketorolac, and flurbiprofen.
The endogenous cannabimimetic anandamide is hydrolyzed by a fatty acid amide hydrolase to yield arachidonic acid and ethanolamine… 
Highly Cited
1998
Highly Cited
1998
An endogenous sleep-inducing compound is a novel competitive inhibitor of fatty acid amide hydrolase.
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