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Future Medicinal Chemistry|June 2, 2012
From multiply active natural product to candidate drug? Antibacterial (and other) minor groove binders for DNAColin Suckling
Future Medicinal Chemistry|June 2, 2012
Medicinal chemistry of farnesoid X receptor ligands: from agonists and antagonists to modulatorsDaniel Merk, Dieter Steinhilber, Manfred Schubert-Zsilavecz
Future Medicinal Chemistry|December 23, 2014
Composing compound libraries for hit discovery--rationality-driven preselection or random choice by structural diversity?Elisabeth Weidel, Matthias Negri, Martin Empting, et al.
Future Medicinal Chemistry|November 23, 2013
Recapitulating the α-helix: nonpeptidic, low-molecular-weight ligands for the modulation of helix-mediated protein-protein interactionsMaryanna Lanning, Steven Fletcher
Future Medicinal Chemistry|November 23, 2013
Flavaglines: potent anticancer drugs that target prohibitins and the helicase eIF4AChristine Basmadjian, Frédéric Thuaud, Nigel Ribeiro, et al.
Future Medicinal Chemistry|May 4, 2018
Global medicinal chemistry and GCPR conferenceLaurent Schio
Future Medicinal Chemistry|May 12, 2018
Recent progress of sodium-glucose transporter 2 inhibitors as potential antidiabetic agentsYajing Zhang, Huazhuo Ban, Runan Yu, et al.
Future Medicinal Chemistry|May 24, 2018
Synthesis and biological evaluation of 2-aminothiazole-thiazolidinone conjugates as potential antitubercular agentsMahmoud F Abo-Ashour, Wagdy M Eldehna, Riham F George, et al.
Future Medicinal Chemistry|May 24, 2018
Synthesis & antitumor activity of epothilones B and D and their analogsHao Cheng, Gangliang Huang
Future Medicinal Chemistry|June 21, 2017
Design, synthesis and multitarget biological profiling of second-generation anti-Alzheimer rhein-huprine hybridsFrancisco Javier Pérez-Areales, Nibal Betari, Antonio Viayna, et al.
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