Drug intelligence / Profile preview

moxifloxacin

Development stage
Approved
Lead developer
Bayer
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Oral, Intravenous, Ophthalmic
01

Overview

Moxifloxacin is a fourth-generation synthetic fluoroquinolone antibiotic (8-methoxy-fluoroquinolone) developed by Bayer. It exerts its bactericidal effect primarily by inhibiting bacterial DNA gyrase (gyrA subunit) and topoisomerase IV (parC or parE subunits), enzymes essential for DNA replication and transcription. This inhibition leads to disruption of DNA synthesis and ultimately bacterial cell death. Moxifloxacin demonstrates broad-spectrum activity against Gram-positive bacteria, Gram-negative bacteria, anaerobes, atypical pathogens such as Mycoplasma and Chlamydia species, as well as Mycobacterium tuberculosis. It is used clinically to treat respiratory tract infections (including community-acquired pneumonia), acute bacterial sinusitis, acute exacerbations of chronic bronchitis, intra-abdominal infections, skin and soft tissue infections, conjunctivitis (as ophthalmic solution), anthrax exposure prophylaxis/treatment, endocarditis adjunctive therapy in some cases, meningitis adjunctive therapy in some cases and tuberculosis[1][4][5]. The drug is available orally or intravenously as moxifloxacin hydrochloride; ophthalmic formulations are also available.

Brand names
AveloxAvaloxAvelonVigamoxMoxeza
Other names
莫西沙星moxifloxacin hydrochloride
02

Targets

DNA gyraseTopo IV (Bacterial Topoisomerase IV)

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