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The Biochemical Journal|June 30, 2021
Conformational plasticity of the ULK3 kinase domainSebastian Mathea, Eidarus Salah, Cynthia Tallant, et al.Journal of Medicinal Chemistry|May 29, 2020
Bioisosteric Replacement of Arylamide-Linked Spine Residues with N-Acylhydrazones and Selenophenes as a Design Strategy to Novel Dibenzosuberone Derivatives as Type I 1/2 p38α MAP Kinase InhibitorsJúlia G B Pedreira, Philipp Nahidino, Mark Kudolo, et al.Journal of Medicinal Chemistry|September 22, 2022
Development and Characterization of Type I, Type II, and Type III LIM-Kinase Chemical ProbesThomas Hanke, Sebastian Mathea, Julia Woortman, et al.Journal of Medicinal Chemistry|June 1, 2018
Development, Optimization, and Structure-Activity Relationships of Covalent-Reversible JAK3 Inhibitors Based on a Tricyclic Imidazo[5,4- d]pyrrolo[2,3- b]pyridine ScaffoldMichael Forster, Apirat Chaikuad, Teodor Dimitrov, et al.ACS Chemical Biology|March 17, 2020
A Highly Selective Chemical Probe for Activin Receptor-like Kinases ALK4 and ALK5Thomas Hanke, Jong Fu Wong, Benedict-Tilman Berger, et al.Journal of Medicinal Chemistry|September 20, 2021
Design and Development of a Chemical Probe for Pseudokinase Ca2+/calmodulin-Dependent Ser/Thr KinaseNadine Russ, Martin Schröder, Benedict-Tilman Berger, et al.Journal of Medicinal Chemistry|December 14, 2022
MSC-1186, a Highly Selective Pan-SRPK Inhibitor Based on an Exceptionally Decorated Benzimidazole-Pyrimidine CoreMartin Schröder, Matthias Leiendecker, Ulrich Grädler, et al.Journal of Medicinal Chemistry|June 4, 2021
Structure-Based Design of Selective Salt-Inducible Kinase InhibitorsRoberta Tesch, Marcel Rak, Monika Raab, et al.ACS Chemical Biology|June 13, 2026
p21-Activated Kinase (PAK) Group I-Targeting Inhibitors Promote the Dimeric Conformation in Live CellsTheresa A L Ehret, Benedict-Tilman Berger, Nicolai Raig, et al.ACS Chemical Biology|January 31, 2024
Development of Potent Dual BET/HDAC Inhibitors via Pharmacophore Merging and Structure-Guided OptimizationNicolas Bauer, Dimitrios-Ilias Balourdas, Joel R Schneider, et al.Pageof 6