Showing results (101-110 of 179) with videos related to

Sort By:
Pageof 18
Bioorganic & Medicinal Chemistry|July 16, 2010
The structure-activity relationships of A-ring-substituted aromathecin topoisomerase I inhibitors strongly support a camptothecin-like binding modeMaris A Cinelli, Andrew E Morrell, Thomas S Dexheimer, et al.
Acta Crystallographica. Section D, Biological Crystallography|September 9, 2010
Structural study and thermodynamic characterization of inhibitor binding to lumazine synthase from Bacillus anthracisEkaterina Morgunova, Boris Illarionov, Sabine Saller, et al.
Journal of the American Chemical Society|February 11, 2010
Mechanistic insights on riboflavin synthase inspired by selective binding of the 6,7-dimethyl-8-ribityllumazine exomethylene anionRyu-Ryun Kim, Boris Illarionov, Monika Joshi, et al.
Bioorganic & Medicinal Chemistry|February 25, 2016
Synthesis and biological evaluation of new fluorinated and chlorinated indenoisoquinoline topoisomerase I poisonsDaniel E Beck, Wei Lv, Monica Abdelmalak, et al.
Journal of Medicinal Chemistry|October 29, 2004
Synthesis and anticancer activity of simplified indenoisoquinoline topoisomerase I inhibitors lacking substituents on the aromatic ringsMuthukaman Nagarajan, Andrew Morrell, Brian C Fort, et al.
Journal of Molecular Biology|February 13, 2003
Enzyme catalysis via control of activation entropy: site-directed mutagenesis of 6,7-dimethyl-8-ribityllumazine synthaseMarkus Fischer, Ilka Haase, Klaus Kis, et al.
Journal of Medicinal Chemistry|October 13, 2006
Synthesis and evaluation of indenoisoquinoline topoisomerase I inhibitors substituted with nitrogen heterocyclesMuthukaman Nagarajan, Andrew Morrell, Alexandra Ioanoviciu, et al.
Pageof 18