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Journal of Medicinal Chemistry|August 31, 2021
Discovery of a Potent Dual SLK/STK10 Inhibitor Based on a Maleimide ScaffoldRicardo A M Serafim, Fiona J Sorrell, Benedict-Tilman Berger, et al.Angewandte Chemie (International Ed. in English)|December 24, 2024
Probing the Protein Kinases' Cysteinome by Covalent FragmentsGuiqun Wang, Nico J Seidler, Sandra Röhm, et al.Nature|September 14, 2022
CDK11 regulates pre-mRNA splicing by phosphorylation of SF3B1Milan Hluchý, Pavla Gajdušková, Igor Ruiz de Los Mozos, et al.Journal of Medicinal Chemistry|December 21, 2023
Synthesis of Pyrazole-Based Macrocycles Leads to a Highly Selective Inhibitor for MST3Jennifer Alisa Amrhein, Lena Marie Berger, Dimitrios-Ilias Balourdas, et al.Oncotarget|February 22, 2020
Identification of molecular targets for the targeted treatment of gastric cancer using dasatinibRaquel Carvalho Montenegro, Alison Howarth, Alessandro Ceroni, et al.Cell Chemical Biology|January 26, 2021
Structure-kinetic relationship reveals the mechanism of selectivity of FAK inhibitors over PYK2Benedict-Tilman Berger, Marta Amaral, Daria B Kokh, et al.Journal of Medicinal Chemistry|September 10, 2021
Development of a Selective Dual Discoidin Domain Receptor (DDR)/p38 Kinase Chemical ProbeSandra Röhm, Benedict-Tilman Berger, Martin Schröder, et al.International Journal of Molecular Sciences|January 21, 2022
Aurora Kinase A Is Involved in Controlling the Localization of Aquaporin-2 in Renal Principal CellsSandrine Baltzer, Timur Bulatov, Christopher Schmied, et al.Journal of Medicinal Chemistry|July 19, 2024
Back-Pocket Optimization of 2-Aminopyrimidine-Based Macrocycles Leads to Potent EPHA2/GAK Kinase InhibitorsJoshua Gerninghaus, Rezart Zhubi, Andreas Krämer, et al.Journal of Medicinal Chemistry|February 29, 2024
Development of Selective Pyrido[2,3-d]pyrimidin-7(8H)-one-Based Mammalian STE20-Like (MST3/4) Kinase InhibitorsMarcel Rak, Amelie Menge, Roberta Tesch, et al.Pageof 6