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Chemistry and Physics of Lipids|July 29, 2015
Monoglyceride lipase: Structure and inhibitorsLaura Scalvini, Daniele Piomelli, Marco MorJournal of Enzyme Inhibition and Medicinal Chemistry|July 14, 2021
Different roles for the acyl chain and the amine leaving group in the substrate selectivity of <i>N</i>-Acylethanolamine acid amidaseAndrea Ghidini, Laura Scalvini, Francesca Palese, et al.Journal of Medicinal Chemistry|March 20, 2020
<i>N</i>-Acylethanolamine Acid Amidase (NAAA): Structure, Function, and InhibitionDaniele Piomelli, Laura Scalvini, Yannick Fotio, et al.Scientific Reports|August 9, 2016
Free-energy studies reveal a possible mechanism for oxidation-dependent inhibition of MGLLaura Scalvini, Federica Vacondio, Michele Bassi, et al.Methods in Molecular Biology (Clifton, N.J.)|February 5, 2020
Design and SAR Analysis of Covalent Inhibitors Driven by Hybrid QM/MM SimulationsAlessio Lodola, Donatella Callegari, Laura Scalvini, et al.Journal of Chemical Information and Modeling|May 17, 2022
Mechanistic Modeling of Monoglyceride Lipase Covalent Modification Elucidates the Role of Leaving Group Expulsion and Discriminates Inhibitors with High and Low PotencyFrancesca Galvani, Laura Scalvini, Silvia Rivara, et al.Journal of Chemical Information and Modeling|December 21, 2021
Free-Energy Simulations Support a Lipophilic Binding Route for Melatonin ReceptorsGian Marco Elisi, Laura Scalvini, Alessio Lodola, et al.Pharmacological Research|August 29, 2006
The fatty-acid amide hydrolase inhibitor URB597 does not affect triacylglycerol hydrolysis in rat tissuesJason R Clapper, Andrea Duranti, Andrea Tontini, et al.The Journal of Pharmacology and Experimental Therapeutics|December 8, 2004
Characterization of the fatty acid amide hydrolase inhibitor cyclohexyl carbamic acid 3'-carbamoyl-biphenyl-3-yl ester (URB597): effects on anandamide and oleoylethanolamide deactivationDarren Fegley, Silvana Gaetani, Andrea Duranti, et al.Chemical Communications (Cambridge, England)|September 2, 2005
QM/MM modelling of oleamide hydrolysis in fatty acid amide hydrolase (FAAH) reveals a new mechanism of nucleophile activationAlessio Lodola, Marco Mor, Johannes C Hermann, et al.Pageof 49