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ACS Pharmacology & Translational Science|August 17, 2023
Rigid Scaffolds Are Promising for Designing Macrocyclic Kinase InhibitorsZheng Zhao, Philip E BourneDrug Discovery Today|January 17, 2018
Progress with covalent small-molecule kinase inhibitorsZheng Zhao, Philip E BournePharmaceuticals (Basel, Switzerland)|November 10, 2022
Systematic Exploration of Privileged Warheads for Covalent Kinase Drug DiscoveryZheng Zhao, Philip E BourneACS Medicinal Chemistry Letters|November 17, 2023
How Ligands Interact with the Kinase HingeZheng Zhao, Philip E BourneDrug Discovery Today|July 19, 2022
Harnessing systematic protein-ligand interaction fingerprints for drug discoveryZheng Zhao, Philip E BourneEuropean Journal of Medicinal Chemistry|April 19, 2026
Deciphering covalent kinase inhibitor binding landscape through structural kinome profilingZheng Zhao, Philip E BourneJournal of Chemical Theory and Computation|April 14, 2020
Revealing Acquired Resistance Mechanisms of Kinase-Targeted Drugs Using an on-the-Fly, Function-Site Interaction Fingerprint ApproachZheng Zhao, Philip E BourneJournal of Chemical Information and Modeling|December 10, 2024
Exploring Extended Warheads toward Developing Cysteine-Targeted Covalent Kinase InhibitorsZheng Zhao, Philip E BourneMedicinal Research Reviews|September 17, 2024
Advances in reversible covalent kinase inhibitorsZheng Zhao, Philip E BourneJournal of Proteome Research|September 18, 2020
Structural Insights into the Binding Modes of Viral RNA-Dependent RNA Polymerases Using a Function-Site Interaction Fingerprint Method for RNA Virus Drug DiscoveryZheng Zhao, Philip E BournePageof 128