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Journal of Medicinal Chemistry|May 8, 2014
Discovery of biarylaminoquinazolines as novel tubulin polymerization inhibitorsGiovanni Marzaro, Antonio Coluccia, Alessandro Ferrarese, et al.Antiviral Chemistry & Chemotherapy|October 18, 2006
Indolyl aryl sulphones as HIV-1 non-nucleoside reverse transcriptase inhibitors: synthesis, biological evaluation and binding mode studies of new derivatives at indole-2-carboxamideGabriella De Martino, Giuseppe La Regina, Rino Ragno, et al.European Journal of Medicinal Chemistry|February 22, 2025
Design and synthesis of novel thioether analogs as promising antiviral agents: In vitro activity against enteroviruses of interestHugo Roux, Franck Touret, Antonio Coluccia, et al.Oncotarget|February 5, 2017
Mitotic cell death induction by targeting the mitotic spindle with tubulin-inhibitory indole derivative moleculesErica Di Cesare, Annalisa Verrico, Andrea Miele, et al.Journal of Medicinal Chemistry|November 30, 2004
Arylthioindoles, potent inhibitors of tubulin polymerizationGabriella De Martino, Giuseppe La Regina, Antonio Coluccia, et al.Molecules (Basel, Switzerland)|May 8, 2019
Small Molecule Inhibitors of KDM5 Histone Demethylases Increase the Radiosensitivity of Breast Cancer Cells Overexpressing JARID1BSimone Pippa, Cecilia Mannironi, Valerio Licursi, et al.Chemmedchem|September 18, 2020
Sulfonamide Inhibitors of β-Catenin Signaling as Anticancer Agents with Different Output on c-MYCLaura Di Magno, Fiorella Di Pastena, Michela Puxeddu, et al.Journal of Medicinal Chemistry|September 7, 2007
Indolyl aryl sulfones as HIV-1 non-nucleoside reverse transcriptase inhibitors: role of two halogen atoms at the indole ring in developing new analogues with improved antiviral activityGiuseppe La Regina, Antonio Coluccia, Francesco Piscitelli, et al.International Journal of Biological Macromolecules|April 9, 2025
Unveiling an unexpected redox regulation of the folding, function and inhibition in the phosphotyrosine binding domain of FRS2Valeria Pennacchietti, Livia Pagano, Mariana Di Felice, et al.Plos One|February 4, 2014
An high-throughput in vivo screening system to select H3K4-specific histone demethylase inhibitorsCecilia Mannironi, Marco Proietto, Francesca Bufalieri, et al.Pageof 9