oleoylethanolamide

fatty-acid amide hydrolase-like ; Rattus norvegicus







13 Article(s)
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1 32075117 Chronic Cannabidiol Administration Fails to Diminish Blood Pressure in Rats with Primary and Secondary Hypertension Despite Its Effects on Cardiac and Plasma Endocannabinoid System, Oxidative Stress and Lipid Metabolism. 2020 Feb 14 1
2 30251159 Effects of fatty acid amide hydrolase inhibitor URB597 in a rat model of trauma-induced long-term anxiety. 2018 Nov 4
3 26642910 Decreased anxiety in juvenile rats following exposure to low levels of chlorpyrifos during development. 2017 Mar 1
4 24433863 Heteroarylureas with spirocyclic diamine cores as inhibitors of fatty acid amide hydrolase. 2014 Feb 1 2
5 25245162 FAAH-mediated modulation of TLR3-induced neuroinflammation in the rat hippocampus. 2014 Nov 15 1
6 23573230 Full inhibition of spinal FAAH leads to TRPV1-mediated analgesic effects in neuropathic rats and possible lipoxygenase-mediated remodeling of anandamide metabolism. 2013 1
7 22029844 The cytoprotective effects of oleoylethanolamide in insulin-secreting cells do not require activation of GPR119. 2012 Apr 5
8 20801430 Blockade of nicotine reward and reinstatement by activation of alpha-type peroxisome proliferator-activated receptors. 2011 Apr 1 2
9 21779318 Administration of URB597, oleoylethanolamide or palmitoylethanolamide increases waking and dopamine in rats. 2011 2
10 20353771 Palmitoylethanolamide and other anandamide congeners. Proposed role in the diseased brain. 2010 Jul 1
11 19403796 Fatty acid amide hydrolase (FAAH) inhibition enhances memory acquisition through activation of PPAR-alpha nuclear receptors. 2009 May 4
12 17336288 Effects of the fatty acid amide hydrolase inhibitor URB597 on the sleep-wake cycle, c-Fos expression and dopamine levels of the rat. 2007 May 7 3
13 12773040 Design, synthesis, and structure-activity relationships of alkylcarbamic acid aryl esters, a new class of fatty acid amide hydrolase inhibitors. 2003 Jun 5 1