Drug intelligence / Profile preview

rosoxacin

Development stage
Unknown
Lead developer
Sterling Winthrop
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules
Administration
Oral
01

Overview

Rosoxacin is a first-generation quinolone antibiotic used primarily for the treatment of urinary tract infections and certain sexually transmitted diseases, including uncomplicated acute gonococcal urethritis. It is effective against both Gram-positive and Gram-negative bacteria, including penicillin-resistant strains. The drug acts by binding to and inhibiting bacterial topoisomerase II (DNA gyrase) and topoisomerase IV, enzymes essential for DNA replication, transcription, repair, and recombination in bacteria. Rosoxacin was developed in 1978 by George Lesher and colleagues at Winthrop-Stearns (now part of Sanofi), as an extension of research on nalidixic acid. It is administered orally as a single dose regimen[1][2][4][6][7].

Brand names
Eradacil
Other names
Winuron40034-42-2
02

Targets

Topo IV (Bacterial Topoisomerase IV)DNA gyrase

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