Giacomo Carenzi

发表

Synthesis and biological characterization of spiro[2H-(1,3)-benzoxazine-2,4'-piperidine] based histone deacetylase inhibitors.

S. Minucci, C. Mercurio, M. Varasi, 2013, European journal of medicinal chemistry.

Synthesis, biological characterization and molecular modeling insights of spirochromanes as potent HDAC inhibitors.

S. Minucci, C. Mercurio, L. Moretti, 2016, European journal of medicinal chemistry.

Discovery, synthesis, and pharmacological evaluation of spiropiperidine hydroxamic acid based derivatives as structurally novel histone deacetylase (HDAC) inhibitors.

A. Mai, S. Minucci, C. Mercurio, 2011, Journal of medicinal chemistry.

Spiro[chromane‐2,4′‐piperidine]‐Based Histone Deacetylase Inhibitors with Improved in vivo Activity

S. Minucci, C. Mercurio, M. Varasi, 2012, ChemMedChem.

Direct chromatographic methods for enantioresolution of amino acids: recent developments

L. Pollegioni, S. Sacchi, Giacomo Carenzi, 2020, Amino Acids.

Construction of highly functionalized medium-sized rings: synthesis of hyperforin and perforatumone model systems.

K. Nicolaou, Giacomo Carenzi, Valer Jeso, 2005, Angewandte Chemie.

Selective synthesis of 14-amino taxanes

G. Fontana, Giacomo Carenzi, A. Guerrini, 2005 .

Cinnamic anilides as new mitochondrial permeability transition pore inhibitors endowed with ischemia-reperfusion injury protective effect in vivo.

S. Minucci, P. Pelicci, R. Amici, 2014, Journal of medicinal chemistry.

E40, a novel microbial protease efficiently detoxifying gluten proteins, for the dietary management of gluten intolerance

C. Gianfrani, R. Troncone, G. Mamone, 2019, Scientific Reports.

Spiro[chromane‐2,4′‐piperidine]‐Based Histone Deacetylase Inhibitors with Improved in vivo Activity

S. Minucci, C. Mercurio, M. Varasi, 2012, ChemMedChem.