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Chemical Communications (Cambridge, England)|October 17, 2017
Novel activity-based probes for N-acylethanolamine acid amidaseRita Petracca, Elisa Romeo, Marc P Baggelaar, et al.Chemmedchem|January 10, 2014
Synthesis, structure-activity, and structure-stability relationships of 2-substituted-N-(4-oxo-3-oxetanyl) N-acylethanolamine acid amidase (NAAA) inhibitorsRomina Vitale, Giuliana Ottonello, Rita Petracca, et al.European Journal of Medicinal Chemistry|February 12, 2016
Potent α-amino-β-lactam carbamic acid ester as NAAA inhibitors. Synthesis and structure-activity relationship (SAR) studiesAndrea Nuzzi, Annalisa Fiasella, Jose Antonio Ortega, et al.ACS Medicinal Chemistry Letters|June 6, 2014
β-Lactones Inhibit N-acylethanolamine Acid Amidase by S-Acylation of the Catalytic N-Terminal CysteineAndrea Armirotti, Elisa Romeo, Stefano Ponzano, et al.Journal of Medicinal Chemistry|September 3, 2013
Synthesis and structure-activity relationship (SAR) of 2-methyl-4-oxo-3-oxetanylcarbamic acid esters, a class of potent N-acylethanolamine acid amidase (NAAA) inhibitorsStefano Ponzano, Fabio Bertozzi, Luisa Mengatto, et al.Journal of Medicinal Chemistry|September 1, 2021
Discovery and SAR Evolution of Pyrazole Azabicyclo[3.2.1]octane Sulfonamides as a Novel Class of Non-Covalent N-Acylethanolamine-Hydrolyzing Acid Amidase (NAAA) Inhibitors for Oral AdministrationPaolo Di Fruscia, Anna Carbone, Giovanni Bottegoni, et al.Pageof 2