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Antibacterial Activities and Inhibitory Effects of Sitafloxacin (DU-6859a) and Its Optical Isomers against Type II Topoisomerases
Author(s) -
Takaaki Akasaka,
Seiko Kurosaka,
Yoko Uchida,
Mayumi Tanaka,
Kenichi Sato,
I Hayakawa
Publication year - 1998
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.42.5.1284
Subject(s) - topoisomerase , dna gyrase , topoisomerase iv , escherichia coli , topoisomerase inhibitor , minimum inhibitory concentration , biology , antibacterial agent , microbiology and biotechnology , staphylococcus aureus , bacteria , in vitro , chemistry , biochemistry , antibiotics , genetics , gene
The in vitro inhibitory effects of sitafloxacin (DU-6859a) and its three stereoisomers on bacterial DNA gyrase from Escherichia coli, topoisomerase IV from Staphylococcus aureus, and topoisomerase II from human placenta were compared. No correlation was observed between the inhibitory activities of quinolones against bacterial type II topoisomerases and those against human topoisomerase II. Sitafloxacin showed the most potent inhibitory activities against bacterial type II topoisomerases and the lowest activity against human type II topoisomerase.

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