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Antiviral Research|February 6, 2013
Computer-aided identification, design and synthesis of a novel series of compounds with selective antiviral activity against chikungunya virusMarcella Bassetto, Tine De Burghgraeve, Leen Delang, et al.Journal of Medicinal Chemistry|June 21, 2012
New nitrogen containing substituents at the indole-2-carboxamide yield high potent and broad spectrum indolylarylsulfone HIV-1 non-nucleoside reverse transcriptase inhibitorsGiuseppe La Regina, Antonio Coluccia, Andrea Brancale, et al.Bioorganic Chemistry|May 21, 2023
Targeting the Grb2 cSH3 domain: Design, synthesis and biological evaluation of the first series of modulatorsMarianna Bufano, Michela Puxeddu, Marianna Nalli, et al.European Journal of Medicinal Chemistry|June 17, 2019
Switching on the activity of 1,5-diaryl-pyrrole derivatives against drug-resistant ESKAPE bacteria: Structure-activity relationships and mode of action studiesDomiziana Masci, Charlotte Hind, Mohammad K Islam, et al.Chemmedchem|December 6, 2019
Design, Synthesis and Discovery of N,N'-Carbazoyl-aryl-urea Inhibitors of Zika NS5 Methyltransferase and Virus ReplicationSharon Spizzichino, Giulio Mattedi, Kate Lauder, et al.Journal of Medicinal Chemistry|December 4, 2013
Design, synthesis, and biological evaluation of 1-phenylpyrazolo[3,4-e]pyrrolo[3,4-g]indolizine-4,6(1H,5H)-diones as new glycogen synthase kinase-3β inhibitorsValeria La Pietra, Giuseppe La Regina, Antonio Coluccia, et al.ACS Chemical Neuroscience|April 4, 2017
Bax Activation Blocks Self-Renewal and Induces Apoptosis of Human Glioblastoma Stem CellsSimona Daniele, Deborah Pietrobono, Barbara Costa, et al.Journal of Medicinal Chemistry|March 14, 2009
Indolylarylsulfones bearing natural and unnatural amino acids. Discovery of potent inhibitors of HIV-1 non-nucleoside wild type and resistant mutant strains reverse transcriptase and coxsackie B4 virusFrancesco Piscitelli, Antonio Coluccia, Andrea Brancale, et al.Traffic (Copenhagen, Denmark)|November 10, 2022
Multiplexed cellular profiling identifies an organoselenium compound as an inhibitor of CRM1-mediated nuclear exportLucia Jimenez, Victor Mayoral-Varo, Carlos Amenábar, et al.Journal of Medicinal Chemistry|October 27, 2015
Discovery of 1,1'-Biphenyl-4-sulfonamides as a New Class of Potent and Selective Carbonic Anhydrase XIV InhibitorsGiuseppe La Regina, Antonio Coluccia, Valeria Famiglini, et al.Pageof 16