Publications by authors named "Giovanni Sandrone"

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Mechanistic and Structural Insights on Difluoromethyl-1,3,4-oxadiazole Inhibitors of HDAC6.
Edoardo Cellupica, Aureliano Gaiassi, Ilaria Rocchio, Grazia Rovelli, Roberta Pomarico, Giovanni Sandrone

Int J Mol Sci· May 2024

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The Importance of the "Time Factor" for the Evaluation of Inhibition Mechanisms: The Case of Selected HDAC6 Inhibitors.
Edoardo Cellupica, Gianluca Caprini, Gianluca Fossati, Doris Mirdita, Paola Cordella, Giovanni Sandrone

Biology (Basel)· July 2023

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Identification of a Novel SSTR3 Full Agonist for the Treatment of Nonfunctioning Pituitary Adenomas.
Daniela Modena, Maria Luisa Moras, Giovanni Sandrone, Andrea Stevenazzi, Barbara Vergani

Cancers (Basel)· June 2023

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Difluoromethyl-1,3,4-oxadiazoles are slow-binding substrate analog inhibitors of histone deacetylase 6 with unprecedented isotype selectivity.
Edoardo Cellupica, Gianluca Caprini, Paola Cordella, Cyprian Cukier, Gianluca Fossati, Giovanni Sandrone

J Biol Chem· January 2023

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HDAC Inhibition as Potential Therapeutic Strategy to Restore the Deregulated Immune Response in Severe COVID-19.
Chiara Ripamonti, Valeria Spadotto, Pietro Pozzi, Andrea Stevenazzi, Barbara Vergani, Giovanni Sandrone

Front Immunol· May 2022

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Role of Fluorination in the Histone Deacetylase 6 (HDAC6) Selectivity of Benzohydroxamate-Based Inhibitors.
Giovanni Sandrone, Cyprian D Cukier, Karol Zrubek, Mattia Marchini, Barbara Vergani

ACS Med Chem Lett· November 2021

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Novel Benzohydroxamate-Based Potent and Selective Histone Deacetylase 6 (HDAC6) Inhibitors Bearing a Pentaheterocyclic Scaffold: Design, Synthesis, and Biological Evaluation.
Barbara Vergani, Giovanni Sandrone, Mattia Marchini, Chiara Ripamonti, Edoardo Cellupica

J Med Chem· December 2019

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Amino acidic scaffolds bearing unnatural side chains: an old idea generates new and versatile tools for the life sciences.
Andrea Stevenazzi, Mattia Marchini, Giovanni Sandrone, Barbara Vergani, Maria Lattanzio

Bioorg Med Chem Lett· December 2014

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The Mycobacterium tuberculosis chaperonin 10 monomer exhibits structural plasticity.
Gianluca Fossati, Pietro Cremonesi, Gaetano Izzo, Emanuele Rizzi, Giovanni Sandrone

Biopolymers· October 2004

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