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Bioorganic & Medicinal Chemistry Letters|January 27, 2004
Fluorinated dihydroquinolines as potent n-NOS inhibitorsStefan Jaroch, Hartmut Rehwinkel, Peter Hölscher, et al.Bioorganic & Medicinal Chemistry Letters|March 8, 2016
Identification of novel GLUT inhibitorsHolger Siebeneicher, Marcus Bauser, Bernd Buchmann, et al.ACS Omega|June 18, 2020
Structural Evidence for Isoform-Selective Allosteric Inhibition of Lactate Dehydrogenase AAnders Friberg, Hartmut Rehwinkel, Duy Nguyen, et al.Proceedings of the National Academy of Sciences of the United States of America|December 25, 2003
Dissociation of transactivation from transrepression by a selective glucocorticoid receptor agonist leads to separation of therapeutic effects from side effectsHeike Schäcke, Arndt Schottelius, Wolf-Dietrich Döcke, 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.Journal of Medicinal Chemistry|October 19, 2022
BAY-069, a Novel (Trifluoromethyl)pyrimidinedione-Based BCAT1/2 Inhibitor and Chemical ProbeJudith Günther, Roman C Hillig, Katja Zimmermann, et al.Journal of Medicinal Chemistry|August 24, 2021
BAY-8400: A Novel Potent and Selective DNA-PK Inhibitor which Shows Synergistic Efficacy in Combination with Targeted Alpha TherapiesMarkus Berger, Lars Wortmann, Philipp Buchgraber, et al.Acta Neuropathologica|January 27, 2017
Pan-mutant IDH1 inhibitor BAY 1436032 for effective treatment of IDH1 mutant astrocytoma in vivoStefan Pusch, Sonja Krausert, Viktoria Fischer, et al.Journal of Medicinal Chemistry|September 23, 2017
Selective Nonsteroidal Glucocorticoid Receptor Modulators for the Inhaled Treatment of Pulmonary DiseasesMartin Hemmerling, Stinabritt Nilsson, Karl Edman, et al.Pageof 2