Drug intelligence / Profile preview

ofloxacin + roxithromycin

Development stage
Unknown
Lead developer
Daiichi Sankyo
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, RNA-Targeting Small Molecules → Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Oral
01

Overview

Ofloxacin + roxithromycin is a fixed-dose combination of two antibacterial agents used to treat a variety of bacterial infections. Ofloxacin is a synthetic fluoroquinolone antibiotic that inhibits bacterial DNA gyrase, thereby preventing DNA replication and leading to cell death. Roxithromycin is a macrolide antibiotic that binds to the 50S ribosomal subunit, inhibiting protein synthesis in susceptible bacteria. The combination may be used for respiratory tract infections, skin and soft tissue infections, genitourinary tract infections, and other conditions where both Gram-positive and Gram-negative coverage is desired. In vitro studies suggest potential additive or synergistic effects against certain pathogens when these drugs are combined[1][3]. Both agents are orally bioavailable small molecules.

Other names
ofloxacin and roxithromycinofloxacin plus roxithromycin
02

Targets

Bacterial 50S ribosomal subunitDNA gyraseTopo IV (Bacterial Topoisomerase IV)

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