Novel Benzohydroxamate-Based Potent and Selective Histone Deacetylase 6 (HDAC6) Inhibitors Bearing a Pentaheterocyclic Scaffold: Design, Synthesis, and Biological Evaluation-Reference-Cited by-同舟云学术

Novel Benzohydroxamate-Based Potent and Selective Histone Deacetylase 6 (HDAC6) Inhibitors Bearing a Pentaheterocyclic Scaffold: Design, Synthesis, and Biological Evaluation

Published:2019-11-11 Issue:23 Volume:62 Page:10711-10739
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Vergani Barbara¹,Sandrone Giovanni¹,Marchini Mattia¹,Ripamonti Chiara¹,Cellupica Edoardo¹,Galbiati Elisabetta¹,Caprini Gianluca¹,Pavich Gianfranco¹,Porro Giulia¹,Rocchio Ilaria¹,Lattanzio Maria¹,Pezzuto Marcello¹,Skorupska Malgorzata¹,Cordella Paola¹,Pagani Paolo¹,Pozzi Pietro¹,Pomarico Roberta¹,Modena Daniela¹,Leoni Flavio¹,Perego Raffaella¹,Fossati Gianluca¹,Steinkühler Christian¹,Stevenazzi Andrea¹^ORCID

Affiliation:

1. Preclinical R&D, Italfarmaco Group, Via dei Lavoratori 54, I-20092 Cinisello Balsamo, Milan, Italy

Funder

Regione Lombardia

European Regional Development Fund

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.9b01194

Reference103 articles.