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ACS Chemical Biology|September 8, 2022
Exploring the Surface of the Ectodomain of the PD-L1 Immune Checkpoint with Small-Molecule FragmentsRadoslaw Kitel, Ismael Rodríguez, Xabier Del Corte, et al.Journal of Medicinal Chemistry|December 1, 2023
Discovery of Inhibitory Fragments That Selectively Target Spire2-FMN2 InteractionRadoslaw Kitel, Ewa Surmiak, Jan Borggräfe, et al.International Journal of Molecular Sciences|March 6, 2021
Structural Determinants of Substrate Specificity of SplF Protease from Staphylococcus aureusNatalia Stach, Abdulkarim Karim, Przemyslaw Golik, et al.Chembiochem : a European Journal of Chemical Biology|January 5, 2023
Nutlin-3a-aa: Improving the Bioactivity of a p53/MDM2 Interaction Inhibitor by Introducing a Solvent-Exposed Methylene GroupFlorian Nietzold, Stefan Rubner, Beata Labuzek, et al.ACS Medicinal Chemistry Letters|May 31, 2021
Design, Synthesis, and Biological Evaluation of Imidazopyridines as PD-1/PD-L1 AntagonistsRoberto Butera, Marta Ważyńska, Katarzyna Magiera-Mularz, et al.Structure (London, England : 1993)|March 13, 2018
Unique Substrate Specificity of SplE Serine Protease from Staphylococcus aureusNatalia Stach, Magdalena Kalinska, Michal Zdzalik, et al.Journal of Medicinal Chemistry|July 27, 2021
Terphenyl-Based Small-Molecule Inhibitors of Programmed Cell Death-1/Programmed Death-Ligand 1 Protein-Protein InteractionDamian Muszak, Ewa Surmiak, Jacek Plewka, et al.International Journal of Biological Macromolecules|February 29, 2024
Discovery of bioactive natural products of microbial origin as inhibitors of the PD-1/PD-L1 protein-protein interactionElisabeth Domingo-Contreras, José R Tormo, Victor Gonzalez-Menendez, et al.European Journal of Medicinal Chemistry|February 15, 2026
N-terphenylpicolinamide derivatives designed to target PD-L1 increase activation and proliferation of T cells, and their cytotoxic properties toward cancer cellsDamian Muszak, Justyna Kocik-Krol, Julia Zaber, et al.Pageof 2