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The Journal of Organic Chemistry|July 12, 2012
O-Nucleoside, S-nucleoside, and N-nucleoside probes of lumazine synthase and riboflavin synthaseArindam Talukdar, Yujie Zhao, Wei Lv, et al.The Journal of Organic Chemistry|August 3, 2002
Design, synthesis, and evaluation of 6-carboxyalkyl and 6-phosphonoxyalkyl derivatives of 7-oxo-8-ribitylaminolumazines as inhibitors of riboflavin synthase and lumazine synthaseMark Cushman, Donglai Yang, Stefan Gerhardt, et al.European Journal of Medicinal Chemistry|December 4, 2012
Synthesis, antibacterial activity and docking of 14-membered 9-O-(3-arylalkyl) oxime 11,12-cyclic carbonate ketolidesJian-Hua Liang, Kun An, Wei Lv, et al.The Journal of Biological Chemistry|April 21, 2007
Lumazine synthase from Candida albicans as an anti-fungal target enzyme: structural and biochemical basis for drug designEkaterina Morgunova, Sabine Saller, Ilka Haase, et al.Antimicrobial Agents and Chemotherapy|August 15, 2018
Activity of Aromathecins against African TrypanosomesNathaniel P Nenortas, Maris A Cinelli, Andrew E Morrell, et al.Bioorganic & Medicinal Chemistry|May 27, 2011
An investigation of phenylthiazole antiflaviviral agentsAbdelrahman S Mayhoub, Mansoora Khaliq, Carolyn Botting, et al.Journal of Medicinal Chemistry|July 10, 2008
Design, synthesis, and biological evaluation of antiviral agents targeting flavivirus envelope proteinsZe Li, Mansoora Khaliq, Zhigang Zhou, et al.Plos One|December 14, 2012
Binding of an Indenoisoquinoline to the topoisomerase-DNA complex induces reduction of linker mobility and strengthening of protein-DNA interactionGiordano Mancini, Ilda D'Annessa, Andrea Coletta, et al.Journal of Molecular Biology|April 10, 2003
A structure-based model of the reaction catalyzed by lumazine synthase from Aquifex aeolicusXiaofeng Zhang, Winfried Meining, Mark Cushman, et al.Journal of Medicinal Chemistry|August 7, 2007
Optimization of the indenone ring of indenoisoquinoline topoisomerase I inhibitorsAndrew Morrell, Michael Placzek, Seth Parmley, et al.Pageof 18