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ACS Chemical Biology|June 19, 2013
Exhaustive proteome mining for functional MHC-I ligandsChristian P Koch, Anna M Perna, Sabrina Weissmüller, et al.Chemmedchem|October 6, 2015
Aryl Bis-Sulfonamide Inhibitors of IspF from Arabidopsis thaliana and Plasmodium falciparumJonas Thelemann, Boris Illarionov, Konstantin Barylyuk, et al.Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|June 27, 2021
Learning from Nature: From a Marine Natural Product to Synthetic Cyclooxygenase-1 Inhibitors by Automated De Novo DesignLukas Friedrich, Gino Cingolani, Ying-Hui Ko, et al.Scientific Reports|March 18, 2016
Identification of E-cadherin signature motifs functioning as cleavage sites for Helicobacter pylori HtrAThomas P Schmidt, Anna M Perna, Tim Fugmann, et al.Plos One|June 8, 2011
Bioassays to monitor Taspase1 function for the identification of pharmacogenetic inhibitorsShirley K Knauer, Verena Fetz, Jens Rabenstein, et al.Biochemical Pharmacology|October 27, 2011
Molecular characterization of EP6--a novel imidazo[1,2-a]pyridine based direct 5-lipoxygenase inhibitorJoanna M Wisniewska, Carmen B Rödl, Astrid S Kahnt, et al.Angewandte Chemie (International Ed. in English)|June 5, 2014
Deorphaning pyrrolopyrazines as potent multi-target antimalarial agentsDaniel Reker, Michael Seet, Max Pillong, et al.Journal of Immunology (Baltimore, Md. : 1950)|August 4, 2009
Identification of human cathepsin G as a functional target of boswellic acids from the anti-inflammatory remedy frankincenseLars Tausch, Arne Henkel, Ulf Siemoneit, et al.Chemmedchem|May 3, 2014
Binding to large enzyme pockets: small-molecule inhibitors of trypanothione reductaseElke Persch, Steve Bryson, Nickolay K Todoroff, et al.Scientific Reports|July 1, 2020
A novel FRET peptide assay reveals efficient Helicobacter pylori HtrA inhibition through zinc and copper bindingSabine Bernegger, Cyrill Brunner, Matej Vizovišek, et al.Pageof 34