18 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
26888301	34	Development and Pharmacological Characterization of Selective Blockers of 2-Arachidonoyl Glycerol Degradation with Efficacy in Rodent Models of Multiple Sclerosis and Pain.	University of Siena
23455058	84	(4-Phenoxyphenyl)tetrazolecarboxamides and related compounds as dual inhibitors of fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL).	University of M£Nster
22185522	159	Structure-activity relationship of a new series of reversible dual monoacylglycerol lipase/fatty acid amide hydrolase inhibitors.	Universidad Complutense De Madrid
22056744	16	Benzisothiazolinone as a useful template for the design of new monoacylglycerol lipase inhibitors: investigation of the target residues and comparison with octhilinone.	Universit£
19029917	5	Selective blockade of 2-arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects.	The Scripps Research Institute
19232787	71	The synthesis and biological evaluation of para-substituted phenolic N-alkyl carbamates as endocannabinoid hydrolyzing enzyme inhibitors.	University of Kuopio
18819796	3	A novel monoacylglycerol lipase inhibitor with analgesic and anti-inflammatory activity.	University of Athens
18507372	31	Synthesis and quantitative structure-activity relationship of fatty acid amide hydrolase inhibitors: modulation at the N-portion of biphenyl-3-yl alkylcarbamates.	Università
17764163	61	Structure-activity relationship of a series of inhibitors of monoacylglycerol hydrolysis--comparison with effects upon fatty acid amide hydrolase.	Universidad Complutense
16854070	12	Fatty acid amide hydrolase inhibitors from virtual screening of the endocannabinoid system.	University of Kuopio
32429662	39	Discovery of Aryl Formyl Piperidine Derivatives as Potent, Reversible, and Selective Monoacylglycerol Lipase Inhibitors.	China Pharmaceutical University
30446439	64	Synthesis and evaluation of potent and selective MGL inhibitors as a glaucoma treatment.	Mak Scientific
31714779	37	Benzisothiazolinone Derivatives as Potent Allosteric Monoacylglycerol Lipase Inhibitors That Functionally Mimic Sulfenylation of Regulatory Cysteines.	Universit£
27766867	109	Therapeutic Potential of Fatty Acid Amide Hydrolase, Monoacylglycerol Lipase, and N-Acylethanolamine Acid Amidase Inhibitors.	Universit£
29309142	36	Discovery of 1,5-Diphenylpyrazole-3-Carboxamide Derivatives as Potent, Reversible, and Selective Monoacylglycerol Lipase (MAGL) Inhibitors.	University of Ferrara