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Bioorganic & Medicinal Chemistry Letters|July 28, 2007
Identification and characterization of 3-substituted pyrazolyl esters as alternate substrates for cathepsin B: the confounding effects of DTT and cysteine in biological assaysMichael C Myers, Andrew D Napper, Nuzhat Motlekar, et al.Bioorganic & Medicinal Chemistry|December 9, 2009
Identification of triazinoindol-benzimidazolones as nanomolar inhibitors of the Mycobacterium tuberculosis enzyme TDP-6-deoxy-d-xylo-4-hexopyranosid-4-ulose 3,5-epimerase (RmlC)Sharmila Sivendran, Victoria Jones, Dianqing Sun, et al.Antimicrobial Agents and Chemotherapy|June 16, 2010
Discovery of potent small-molecule inhibitors of multidrug-resistant Plasmodium falciparum using a novel miniaturized high-throughput luciferase-based assayEdinson Lucumi, Claire Darling, Hyunil Jo, et al.Molecular Pharmacology|April 12, 2008
Kinetic characterization and molecular docking of a novel, potent, and selective slow-binding inhibitor of human cathepsin LParag P Shah, Michael C Myers, Mary Pat Beavers, et al.Journal of Medicinal Chemistry|December 13, 2005
Discovery of indoles as potent and selective inhibitors of the deacetylase SIRT1Andrew D Napper, Jeffrey Hixon, Thomas McDonagh, et al.The Journal of Biological Chemistry|April 9, 2016
Regulatory T Cell Modulation by CBP/EP300 Bromodomain InhibitionSrimoyee Ghosh, Alexander Taylor, Melissa Chin, et al.Pageof 3