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Organic & Biomolecular Chemistry|August 29, 2018
Semi-syntheses of the 11-hydroxyrotenoids sumatrol and villosinolDavid A Russell, Julien J Freudenreich, Hannah L Stewart, et al.
Chemical Communications (Cambridge, England)|January 28, 2020
Fsp3-rich and diverse fragments inspired by natural products as a collection to enhance fragment-based drug discoveryAbigail R Hanby, Nikolaj S Troelsen, Thomas J Osberger, et al.
Molecular Biosystems|August 2, 2006
Cell-cell communication in Gram-negative bacteriaMartin Welch, Helga Mikkelsen, Jane E Swatton, et al.
Bioorganic & Medicinal Chemistry|May 13, 2017
A fragment-based approach leading to the discovery of a novel binding site and the selective CK2 inhibitor CAM4066Claudia De Fusco, Paul Brear, Jessica Iegre, et al.
Organic & Biomolecular Chemistry|March 6, 2009
Fluoride-free cross coupling using vinyldisiloxanesHannah F Sore, Christine M Boehner, Simon J F MacDonald, et al.
Chemical Science|October 13, 2023
A cell-active cyclic peptide targeting the Nrf2/Keap1 protein-protein interactionJessica Iegre, Sona Krajcovicova, Anders Gunnarsson, et al.
European Journal of Organic Chemistry|October 11, 2019
Cycloaddition Strategies for the Synthesis of Diverse Heterocyclic Spirocycles for Fragment-Based Drug DiscoveryThomas A King, Hannah L Stewart, Kim T Mortensen, et al.
Journal of the American Chemical Society|December 17, 2009
Zn2+-triggered amide tautomerization produces a highly Zn2+-selective, cell-permeable, and ratiometric fluorescent sensorZhaochao Xu, Kyung-Hwa Baek, Ha Na Kim, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 13, 2004
Finding new components of the target of rapamycin (TOR) signaling network through chemical genetics and proteome chipsJing Huang, Heng Zhu, Stephen J Haggarty, et al.
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