Synthesis and pharmacological evaluation of 2, 4-dinitroaryldithiocarbamate derivatives as novel monoacylglycerol lipase inhibitors

…, G Labar, GG Muccioli, JH Poupaert…

文献索引：Kapanda, Coco N.; Muccioli, Giulio G.; Labar, Geoffray; Poupaert, Jacques H.; Lambert, Didier M. Journal of Medicinal Chemistry, 2009 , vol. 52, # 22 p. 7310 - 7314

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被引用次数: 17

摘要

Monoacylglycerol lipase (MAGL) is responsible for signal termination of 2- arachidonoylglycerol (2-AG), an endocannabinoid neurotransmitter endowed with several physiological effects. Previously, we showed that the arylthioamide scaffold represents a privileged template for designing MAGL inhibitors. A series of 37 compounds resulting from pharmacomodulations around the arylthioamide template were synthesized and tested to ...