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Journal of Medicinal Chemistry|November 7, 2024
Development of <i>N</i>-(4-(1<i>H</i>-Imidazol-1-yl)phenyl)-4-chlorobenzenesulfonamide, a Novel Potent Inhibitor of β-Catenin with Enhanced Antitumor Activity and Metabolic StabilityMichela Puxeddu, Lele Ling, Silvia Ripa, et al.ACS Medicinal Chemistry Letters|May 20, 2017
3-Aroyl-1,4-diarylpyrroles Inhibit Chronic Myeloid Leukemia Cell Growth through an Interaction with TubulinGiuseppe La Regina, Ruoli Bai, Antonio Coluccia, et al.Journal of Medicinal Chemistry|November 3, 2011
Design and synthesis of 2-heterocyclyl-3-arylthio-1H-indoles as potent tubulin polymerization and cell growth inhibitors with improved metabolic stabilityGiuseppe La Regina, Ruoli Bai, Willeke Rensen, et al.ACS Infectious Diseases|August 3, 2024
4-(3-Phenylsulfonylindol-2-yl)-1-(pyridin-2-yl)piperazinyl-methanones as Potent Inhibitors of both SARS-CoV-2 and HCoV-OC43 VirusesMichela Puxeddu, Manuela Donalisio, Joachim Jakob Bugert, et al.Journal of Medicinal Chemistry|July 16, 2014
New pyrrole derivatives with potent tubulin polymerization inhibiting activity as anticancer agents including hedgehog-dependent cancerGiuseppe La Regina, Ruoli Bai, Antonio Coluccia, et al.Journal of Medicinal Chemistry|October 30, 2023
4-(3-Phenyl-4-(3,4,5-trimethoxybenzoyl)-1<i>H</i>-pyrrol-1-yl)benzenesulfonamide, a Novel Carbonic Anhydrase and Wnt/β-Catenin Signaling Pathway Dual-Targeting Inhibitor with Potent Activity against Multidrug Resistant Cancer CellsDomiziana Masci, Michela Puxeddu, Laura Di Magno, et al.ACS Pharmacology & Translational Science|July 20, 2023
Novel <i>N</i>-(Heterocyclylphenyl)benzensulfonamide Sharing an Unreported Binding Site with T-Cell Factor 4 at the β-Catenin Armadillo Repeats Domain as an Anticancer AgentMarianna Nalli, Laura Di Magno, Yichao Wen, et al.ACS Pharmacology & Translational Science|April 17, 2025
Correction to "Novel <i>N</i>-(Heterocyclylphenyl)benzensulfonamide Sharing an Unreported Binding Site with T-Cell Factor 4 at the β-Catenin Armadillo Repeats Domain as Anticancer Agent"Marianna Nalli, Laura Di Magno, Yichao Wen, et al.Journal of Medicinal Chemistry|December 11, 2012
Toward highly potent cancer agents by modulating the C-2 group of the arylthioindole class of tubulin polymerization inhibitorsGiuseppe La Regina, Ruoli Bai, Whilelmina Maria Rensen, et al.Journal of Medicinal Chemistry|July 2, 2015
New Indole Tubulin Assembly Inhibitors Cause Stable Arrest of Mitotic Progression, Enhanced Stimulation of Natural Killer Cell Cytotoxic Activity, and Repression of Hedgehog-Dependent CancerGiuseppe La Regina, Ruoli Bai, Antonio Coluccia, et al.Pageof 9