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International Journal of Molecular Sciences|June 20, 2019
Opportunities for Overcoming <i>Mycobacterium tuberculosis</i> Drug Resistance: Emerging Mycobacterial Targets and Host-Directed TherapyEveline Torfs, Tatiana Piller, Paul Cos, et al.Pharmacognosy Magazine|October 21, 2016
Evaluation of the Genotoxicity and Cytotoxicity of Semipurified Fractions from the Mediterranean Brown Algae, <i>Dictyopteris membranacea</i>Najoua Akremi, Davie Cappoen, Roel Anthonissen, et al.Chemical Biology & Drug Design|May 21, 2016
Design, synthesis and biological evaluation of novel quinoline-based carboxylic hydrazides as anti-tubercular agentsSubhash Chander, Penta Ashok, Davie Cappoen, et al.Journal of Cheminformatics|May 25, 2026
Integrating chemical structure and high-throughput transcriptomics for mechanistically interpretable Tox21 bioactivity predictionGuillaume Cattebeke, Anne-Sofie Vermeersch, Davie Cappoen, et al.Organic & Biomolecular Chemistry|February 26, 2019
Synthesis and antitubercular activity of 1- and 3-substituted benzo[g]isoquinoline-5,10-dionesRobert J Smets, Eveline Torfs, Filip Lemière, et al.European Journal of Medicinal Chemistry|November 10, 2019
Novel thiazolidinedione-hydroxamates as inhibitors of Mycobacterium tuberculosis virulence factor Zmp1Veronika Šlachtová, Marek Šebela, Eveline Torfs, et al.Journal of Medicinal Chemistry|March 12, 2014
1,2,3,4,8,9,10,11-octahydrobenzo[j]phenanthridine-7,12-diones as new leads against Mycobacterium tuberculosisDavie Cappoen, Pieter Claes, Jan Jacobs, et al.Immunobiology|December 1, 2016
Comparative analysis of the internalization of the macrophage receptor sialoadhesin in human and mouse primary macrophages and cell linesMarjorie De Schryver, Annelies Leemans, Isabel Pintelon, et al.ACS Medicinal Chemistry Letters|January 21, 2017
Novel Potentiators for Vancomycin in the Treatment of Biofilm-Related MRSA Infections via a Mix and Match ApproachArno Vermote, Gilles Brackman, Martijn D P Risseeuw, et al.European Journal of Medicinal Chemistry|October 15, 2022
Novel heterocyclic hydroxamates as inhibitors of the mycobacterial zinc metalloprotease Zmp1 to probe its mechanism of functionMilan Dak, Veronika Šlachtová, Marek Šebela, et al.Pageof 4