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Chemmedchem|September 17, 2013
X-ray structural analysis of tau-tubulin kinase 1 and its interactions with small molecular inhibitorsYafeng Xue, Paul T Wan, Per Hillertz, et al.Bioorganic & Medicinal Chemistry Letters|January 4, 2017
Discovery of new selective glucocorticoid receptor agonist leadsMarkus Berger, Hartmut Rehwinkel, Norbert Schmees, et al.Journal of Synchrotron Radiation|February 18, 2012
Solutions for the storage and handling of SPINE standard pucksCristian Bodin, Fredrik Mauritzson, Rob Horsefield, et al.Chemical Science|October 13, 2023
A cell-active cyclic peptide targeting the Nrf2/Keap1 protein-protein interactionJessica Iegre, Sona Krajcovicova, Anders Gunnarsson, et al.Journal of Medicinal Chemistry|December 18, 2020
Mining Natural Products for Macrocycles to Drug Difficult TargetsFabio Begnini, Vasanthanathan Poongavanam, Björn Over, et al.Journal of Medicinal Chemistry|November 9, 2017
X-ray Characterization and Structure-Based Optimization of Striatal-Enriched Protein Tyrosine Phosphatase InhibitorsMichael R Witten, Lisa Wissler, Melanie Snow, et al.Bioorganic & Medicinal Chemistry Letters|November 5, 2016
Discovery of indazole ethers as novel, potent, non-steroidal glucocorticoid receptor modulatorsMartin Hemmerling, Karl Edman, Matti Lepistö, et al.The Journal of Biological Chemistry|March 21, 2021
Glucocorticoid receptor Thr524 phosphorylation by MINK1 induces interactions with 14-3-3 protein regulatorsClaire C Munier, Leonardo De Maria, Karl Edman, et al.Bioorganic & Medicinal Chemistry Letters|May 17, 2015
Identification of indole inhibitors of human hematopoietic prostaglandin D2 synthase (hH-PGDS)Fredrik Edfeldt, Johan Evenäs, Matti Lepistö, et al.Journal of Medicinal Chemistry|February 2, 2022
Importance of Binding Site Hydration and Flexibility Revealed When Optimizing a Macrocyclic Inhibitor of the Keap1-Nrf2 Protein-Protein InteractionFabio Begnini, Stefan Geschwindner, Patrik Johansson, et al.Pageof 3