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Journal of Biomolecular Screening|December 9, 2015
An Alternative Thiol-Reactive Dye to Analyze Ligand Interactions with the Chemokine Receptor CXCR2 Using a New Thermal Shift Assay FormatChristian Bergsdorf, Cédric Fiez-Vandal, David A Sykes, et al.Scientific Reports|June 17, 2020
Gene-signature-derived IC<sub>50</sub>s/EC<sub>50</sub>s reflect the potency of causative upstream targets and downstream phenotypesSteffen Renner, Christian Bergsdorf, Rochdi Bouhelal, et al.Cell Reports|February 21, 2020
A High-Throughput Screening Identifies MICU1 Targeting CompoundsGiulia Di Marco, Francesca Vallese, Benjamin Jourde, et al.Scientific Reports|October 21, 2017
Feasibility and physiological relevance of designing highly potent aminopeptidase-sparing leukotriene A4 hydrolase inhibitorsShin Numao, Franziska Hasler, Claire Laguerre, et al.Chemmedchem|July 10, 2018
X-ray Structures and Feasibility Assessment of CLK2 Inhibitors for Phelan-McDermid SyndromeJoerg Kallen, Christian Bergsdorf, Bertrand Arnaud, et al.Journal of Medicinal Chemistry|February 16, 2021
Discovery of LYS006, a Potent and Highly Selective Inhibitor of Leukotriene A<sub>4</sub> HydrolaseChristian Markert, Gebhard Thoma, Honnappa Srinivas, et al.ACS Medicinal Chemistry Letters|December 20, 2023
Discovery of Ligands for TRIM58, a Novel Tissue-Selective E3 LigaseKlemens Hoegenauer, Shaojian An, Jake Axford, et al.Pageof 2