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Future Medicinal Chemistry|June 22, 2017
A novel antimicrobial approach based on the inhibition of zinc uptake in Salmonella entericaAndrea Battistoni, Serena Ammendola, Emilia Chiancone, et al.Future Medicinal Chemistry|June 22, 2017
DXS as a target for structure-based drug designRobin Matthias Gierse, Eswar Redeem, Eleonora Diamanti, et al.Future Medicinal Chemistry|May 17, 2018
Identification of small-molecule EGFR allosteric inhibitors by high-throughput dockingFabiana Caporuscio, Annachiara Tinivella, Valentina Restelli, et al.Future Medicinal Chemistry|May 10, 2017
Inhibition of amyloid oligomerization into different supramolecular architectures by small molecules: mechanistic insights and design rulesSayanti Brahmachari, Ashim Paul, Daniel Segal, et al.Future Medicinal Chemistry|July 19, 2018
Synthesis & molecular modeling studies of bronchodilatory active indole-pyridine conjugatesAladdin M Srour, Siva S Panda, Asmaa M M Salman, et al.Future Medicinal Chemistry|July 19, 2018
An efficient formulation based on cationic porphyrins to photoinactivate Staphylococcus aureus and Escherichia coliLúcia Marciel, Mariana Q Mesquita, Rosalina Ferreira, et al.Future Medicinal Chemistry|July 26, 2018
Cancer-targeted delivery systems based on peptidesTheodora Chatzisideri, George Leonidis, Vasiliki SarliFuture Medicinal Chemistry|July 26, 2018
Lead optimization-hit expansion of new asymmetrical pyridinium/quinolinium compounds as choline kinase α1 inhibitorsGianluca Rubbini, Ana Begoña Buades-Martín, María Kimatrai-Salvador, et al.Future Medicinal Chemistry|June 29, 2018
Confident application of a global human liver microsomal activity QSARJonna Stålring, Anna-Karin Sohlenius-Sternbeck, Ylva Terelius, et al.Future Medicinal Chemistry|July 12, 2018
In silico approaches for investigating the binding propensity of apigenin and luteolin against class I HDAC isoformsShabir Ahmad Ganai, Zeenat Farooq, Shahid Banday, et al.Pageof 237