Synthesis and in vitro evaluation of novel highly potent coumarin inhibitors of gyrase B
- 1 July 1999
- journal article
- Published by Elsevier BV in Bioorganic & Medicinal Chemistry Letters
- Vol. 9 (14), 2079-2084
- https://doi.org/10.1016/s0960-894x(99)00329-7
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Design, synthesis and evaluation of a novel series of spiroketals based on the structure of the antibacterial gyrase inhibitor novobiocinJournal of the Chemical Society, Perkin Transactions 1, 1997
- Resolving the role of topoisomerase II in chromatin structure and functionTrends in Cell Biology, 1995
- Structure and function of type II DNA topoisomerasesBiochemical Journal, 1994
- DNA Gyrase: Structure and FunctionCritical Reviews in Biochemistry and Molecular Biology, 1991
- Synthesis and in vitro activity of new semisynthetic coumermycin analogs: Chemical modification at the C-3 amide.The Journal of Antibiotics, 1989
- A selective cleavage of the oxazole moiety in noviosylcoumarin antibiotics. A new process to key intermediates for coumermycin analog synthesisThe Journal of Organic Chemistry, 1988
- Inhibitors of DNA topoisomerasesBiochemistry, 1988
- SEMISYNTHETIC COUMERMYCINS. IThe Journal of Antibiotics, 1968
- SEMISYNTHETIC COUMERMYCINS. IIThe Journal of Antibiotics, 1968
- THE PARTIAL STRUCTURE OF NOVOBIOCIN (STREPTONIVICIN).1 II.Journal of the American Chemical Society, 1956