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Bioorganic Chemistry|February 27, 2007
A high-throughput screening approach to anthrax lethal factor inhibitionSherida L Johnson, Li-Hsing Chen, Maurizio PellecchiaChemical Biology & Drug Design|June 25, 2010
A novel pharmacophore model for the design of anthrax lethal factor inhibitorsHongbin Yuan, Sherida L Johnson, Li-Hsing Chen, et al.Bioorganic & Medicinal Chemistry|April 11, 2009
Structure-activity relationship studies of a novel series of anthrax lethal factor inhibitorsSherida L Johnson, Li-Hsing Chen, Elisa Barile, et al.Chemical Biology & Drug Design|January 29, 2008
Rhodanine derivatives as selective protease inhibitors against bacterial toxinsSherida L Johnson, Li-Hsing Chen, Rebecca Harbach, et al.Journal of Medicinal Chemistry|May 23, 2008
Development of paramagnetic probes for molecular recognition studies in protein kinasesJesus Vazquez, Surya K De, Li-Hsing Chen, et al.Journal of Medicinal Chemistry|August 6, 2011
Design and characterization of a potent and selective dual ATP- and substrate-competitive subnanomolar bidentate c-Jun N-terminal kinase (JNK) inhibitorJohn L Stebbins, Surya K De, Petra Pavlickova, et al.Bioorganic & Medicinal Chemistry|March 14, 2009
Discovery of 2-(5-nitrothiazol-2-ylthio)benzo[d]thiazoles as novel c-Jun N-terminal kinase inhibitorsSurya K De, Li-Hsing Chen, John L Stebbins, et al.Journal of Medicinal Chemistry|March 11, 2009
Design, synthesis, and structure-activity relationship of substrate competitive, selective, and in vivo active triazole and thiadiazole inhibitors of the c-Jun N-terminal kinaseSurya K De, John L Stebbins, Li-Hsing Chen, et al.Chemical Biology & Drug Design|May 14, 2011
Targeting metalloproteins by fragment-based lead discoverySherida Johnson, Elisa Barile, Biancamaria Farina, et al.Proceedings of the National Academy of Sciences of the United States of America|October 17, 2008
Identification of a new JNK inhibitor targeting the JNK-JIP interaction siteJohn L Stebbins, Surya K De, Thomas Machleidt, et al.Pageof 2