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Biorxiv : the Preprint Server for Biology|January 16, 2026
Degradation of the TEAD•YAP/TAZ Transcription Factor Complex by Heterobifunctional Small Molecules that Bind to the TEAD Allosteric Lipid PocketI-Ju Yeh, Mona K Ghozayel, Khuchtumur Bum-Erdene, et al.
Chemmedchem|April 4, 2017
Structure-Based Target-Specific Screening Leads to Small-Molecule CaMKII InhibitorsDavid Xu, Liwei Li, Donghui Zhou, et al.
Journal of Chemical Information and Modeling|May 27, 2014
Enrichment of chemical libraries docked to protein conformational ensembles and application to aldehyde dehydrogenase 2Bo Wang, Cameron D Buchman, Liwei Li, et al.
ACS Medicinal Chemistry Letters|January 25, 2021
Design and Synthesis of Fragment Derivatives with a Unique Inhibition Mechanism of the uPAR·uPA InteractionKhuchtumur Bum-Erdene, Degang Liu, David Xu, et al.
Journal of the American Chemical Society|August 19, 2004
Strategy in inhibition of cathepsin B, a target in tumor invasion and metastasisIn Taek Lim, Samy O Meroueh, Mijoon Lee, et al.
Journal of the American Chemical Society|June 15, 2006
Thermodynamics of interactions of vancomycin and synthetic surrogates of bacterial cell wallMikhail Rekharsky, Dusan Hesek, Mijoon Lee, et al.
The Journal of Physical Chemistry. B|July 21, 2006
Computational investigation of irreversible inactivation of the zinc-dependent protease carboxypeptidase AJason B Cross, Thom Vreven, Samy O Meroueh, et al.
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