a generic term for any of a wide range of synthetic antibacterial compounds whose molecular structures contain a 4-oxo-1,4-dihydroquinoline or a 4-oxo-1,4-dihydrocinnoline nucleus; e.g. cinoxacin, ciprofloxacin, nalidixic acid, oxolinic acid. Their antibiotic activity derives from interaction with the A subunit of bacterial DNA gyrase (see type II DNA topoisomerase); this results in trapping of bacterial DNA in the complex it forms with the A sububit. Rejoining of the DNA strands broken by the enzyme is thereby arrested.