Results 21 to 30 of about 13,359 (214)
Design and Potency of Dual Soluble Epoxide Hydrolase/Fatty Acid Amide Hydrolase Inhibitors [PDF]
Fatty acid amide hydrolase (FAAH) is responsible for regulating concentrations of the endocannabinoid arachidonoyl ethanolamide. Multiple FAAH inhibitors have been developed for clinical trials and have failed to demonstrate efficacy at treating pain ...
Sean D. Kodani +5 more
doaj +2 more sources
Fatty acid amide hydrolase and 9-lipoxygenase modulate cotton seedling growth by ethanolamide oxylipin levels. [PDF]
Article asserts that polyunsaturated N-acylethanolamines (NAEs) can be hydrolyzed by fatty acid amide hydrolase (FAAH) or oxidized by lipoxygenase (LOX).
Arias-Gaguancela O, Aziz M, Chapman KD.
europepmc +2 more sources
Fatty acid amide hydrolase protein sequences.
The amino acid sequences of Homo sapiens, Schistosoma mekongi, Schistosoma japonicum, Schistosoma mansoni, Schistosoma haematobium, Schistosoma bovis, Fasciola hepatica, Paragonimus westermani, Clonorchis sinensis, and Echinococcus granulosus fatty acid ...
Phornpimon Tipthara (1784512) +7 more
core +1 more source
Polyunsaturated fatty acid-derived lipid mediators and T cell function [PDF]
Copyright © 2014 Nicolaou, Mauro, Urquhart and Marelli-Berg . This is an open- access article distributed under the terms of the Creative Commons Attribution License (CC BY) .
Mauro, Claudio; id_orcid +17 more
core +1 more source
Conformational Effects in Enzyme Catalysis: Reaction via a High Energy Conformation in Fatty Acid Amide Hydrolase [PDF]
Quantum mechanics/molecular mechanics and molecular dynamics simulations of fatty acid amide hydrolase show that reaction (amide hydrolysis) occurs via a distinct, high energy conformation.
Mulholland, Adrian J +20 more
core +1 more source
Given that drug addiction occurs as a result of complex gene-environment interaction, a number of studies claimed that cannabinoid receptor 1 (CNR1), fatty acid amide hydrolase (FAAH), and monoacylglycerol lipase (MGLL) single nucleotide polymorphisms ...
Altun Beril +8 more
doaj +1 more source
R-flurbiprofen reduces neuropathic pain in rodents by restoring endogenous cannabinoids [PDF]
Background: R-flurbiprofen, one of the enantiomers of flurbiprofen racemate, is inactive with respect to cyclooxygenase inhibition, but shows analgesic properties without relevant toxicity. Its mode of action is still unclear.
Geisslinger, Gerd +45 more
core +1 more source
BackgroundThe endocannabinoid ligand anandamide (AEA) is removed from the extracellular space by a process of cellular uptake followed by metabolism. In many cells, such as the RBL-2H3 cell line, inhibition of FAAH activity reduces the observed uptake ...
Emmelie Björklund +4 more
doaj +1 more source
Background Pain relief remains a major subject of inadequately met need of patients. Therapeutic agents designed to treat pain and inflammation so far have low to moderate efficiencies with significant untoward side effects. FAAH-1 has been proposed as a
Julius T. Dongdem +4 more
doaj +1 more source
Discovery of Uracil Derivatives as Potent Inhibitors of Fatty Acid Amide Hydrolase
Fatty Acid Amide Hydrolase (FAAH) is an intracellular serine enzyme involved in the biological degradation of the fatty acid ethanolamide family of signaling lipids, which exerts neuroprotective, anti-inflammatory, and analgesic properties.
Yan Qiu, Yang Zhang, Yuhang Li, Jie Ren
doaj +1 more source

