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Methods in Molecular Biology (Clifton, N.J.)|August 7, 2026
In Silico Methodology for Human Carboxylesterases 1 and 2 Isoforms Substrate Selectivity StudySergio R RiboneJournal of Xenobiotics|January 21, 2026
Experimental and In Silico Approaches to Study Carboxylesterase Substrate SpecificitySergio R Ribone, Mario Alfredo QuevedoJournal of Molecular Graphics & Modelling|June 6, 2017
Structural basis for the potent inhibition of the HIV integrase-LEDGF/p75 protein-protein interactionSergio R Ribone, Mario A QuevedoBiochimica Et Biophysica Acta. Proteins and Proteomics|April 10, 2025
Exploring human carboxylesterases 1 and 2 selectivity of two families of substrates at an atomistic levelSergio R Ribone, Dario A Estrin, Mario A QuevedoJournal of Molecular Graphics & Modelling|July 16, 2014
Development of a receptor model for efficient in silico screening of HIV-1 integrase inhibitorsMario A Quevedo, Sergio R Ribone, Margarita C Briñón, et al.European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|January 18, 2018
Stability and plasmatic protein binding of novel zidovudine prodrugs: Targeting site ii of human serum albuminEsteban M Schenfeld, Sergio R Ribone, Mario A QuevedoJournal of Computer-Aided Molecular Design|November 26, 2021
Target identification for repurposed drugs active against SARS-CoV-2 via high-throughput inverse dockingSergio R Ribone, S Alexis Paz, Cameron F Abrams, et al.Journal of Chemical Information and Modeling|December 8, 2010
Rational approaches for the design of effective human immunodeficiency virus type 1 nonnucleoside reverse transcriptase inhibitorsSergio R Ribone, Mario A Quevedo, Marcela Madrid, et al.Bioorganic & Medicinal Chemistry|February 6, 2008
Binding to human serum albumin of zidovudine (AZT) and novel AZT derivatives. Experimental and theoretical analysesMario A Quevedo, Sergio R Ribone, Guillermo N Moroni, et al.European Journal of Medicinal Chemistry|November 20, 2012
Synthesis, biological evaluation and molecular modeling of 4,6-diarylpyrimidines and diarylbenzenes as novel non-nucleosides HIV-1 reverse transcriptase inhibitorsSergio R Ribone, Volker Leen, Marcela Madrid, et al.Pageof 2