Potent α-amino-β-lactam carbamic acid ester as NAAA inhibitors. Synthesis and structure–activity relationship (SAR) studies-Reference-Cited by-同舟云学术

Potent α-amino-β-lactam carbamic acid ester as NAAA inhibitors. Synthesis and structure–activity relationship (SAR) studies

Published:2016-03 Issue: Volume:111 Page:138-159
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Nuzzi Andrea,Fiasella Annalisa,Ortega Jose Antonio,Pagliuca Chiara,Ponzano Stefano,Pizzirani Daniela,Bertozzi Sine Mandrup,Ottonello Giuliana,Tarozzo Glauco,Reggiani Angelo,Bandiera Tiziano,Bertozzi Fabio,Piomelli Daniele

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference69 articles.

1. A new definition of neuropathic pain;Jensen;Pain,2011

2. Molecular characterization of n-acylethanolamine-hydrolyzing acid amidase, a novel member of the choloylglycine hydrolase family with structural and functional similarity to acid ceramidase;Tsuboi;J. Biol. Chem.,2005

3. Purification and characterization of an acid amidase selective for n-palmitoylethanolamine, a putative endogenous anti-inflammatory substance;Ueda;J. Biol. Chem.,2001

4. The n-acylethanolamine-hydrolyzing acid amidase (NAAA);Tsuboi;Chem. Biodivers.,2007

5. Selective n-acylethanolamine-hydrolyzing acid amidase inhibition reveals a key role for endogenous palmitoylethanolamide in inflammation;Solorzano;Proc. Natl. Acad. Sci. U.S.A.,2009

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