A. Fiasella

发表

Exploring the structural requirements for inhibition of the ubiquitin E3 ligase breast cancer associated protein 2 (BCA2) as a treatment for breast cancer.

A. Brancale, A. Westwell, A. Burger, 2010, Journal of medicinal chemistry.

3‐Aminoazetidin‐2‐one Derivatives as N‐Acylethanolamine Acid Amidase (NAAA) Inhibitors Suitable for Systemic Administration

M. Mor, G. Tarzia, D. Piomelli, 2014, ChemMedChem.

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

A. Reggiani, D. Piomelli, T. Bandiera, 2016, European journal of medicinal chemistry.

Synthesis of 6-deoxy-N-Cbz-d,l-iminoglycal-derived vinyl epoxides and examination of their regio- and stereoselectivity in nucleophilic addition reactions

P. Crotti, Lucilla Favero, V. D. Bussolo, 2013 .

Stereoselective synthesis of 4-amino-2,3-unsaturated-N-Cbz-imino-O-glycosides via new diastereoisomeric N-Cbz-imino glycal-derived allyl N-nosyl aziridines.

F. Bertolini, P. Crotti, Lucilla Favero, 2009, Organic letters.

Stereoselective synthesis of 2,3-unsaturated-aza-O-glycosides via new diastereoisomeric N-Cbz-imino glycal-derived allyl epoxides.

M. Romano, M. Pineschi, P. Crotti, 2007, Organic letters.

Stereoselective synthesis of 2-O-MEM-2,3-unsaturated-β-O-glycosides and elaboration to useful synthetic tools

P. Crotti, Lucilla Favero, V. D. Bussolo, 2010 .

Stereoselective Synthesis of β-Phenylselenoglycosides from Glycals and Rationalization of the Selenoglycosylation Processes.

F. Balzano, P. Crotti, V. D. Bussolo, 2010 .

Potent a -amino- b -lactam carbamic acid ester as NAAA inhibitors. Synthesis and structure e activity relationship (SAR) studies European

A. Reggiani, D. Piomelli, T. Bandiera, 2022 .

A Potent Systemically Active N-Acylethanolamine Acid Amidase Inhibitor that Suppresses Inflammation and Human Macrophage Activation.

A. Reggiani, M. Mor, G. Tarzia, 2015, ACS chemical biology.

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 Administration

G. Bottegoni, R. Bertorelli, A. Reggiani, 2021, Journal of medicinal chemistry.

An Important Role for N-Acylethanolamine Acid Amidase in the Complete Freund’s Adjuvant Rat Model of Arthritis

D. Piomelli, E. Romeo, O. Sasso, 2016, The Journal of Pharmacology and Experimental Therapeutics.

A Potent Systemically Active N-Acylethanolamine Acid Amidase Inhibitor that Suppresses Inflammation and Human Macrophage Activation.

A. Reggiani, M. Mor, G. Tarzia, 2015, ACS chemical biology.