Date published: 2026-4-5

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Ofloxacin (CAS 82419-36-1)

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Application:
Ofloxacin is an antibacterial Topo II and Topo IV inhibitor
CAS Number:
82419-36-1
Purity:
≥98%
Molecular Weight:
361.37
Molecular Formula:
C18H20FN3O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Ofloxacin is a fluoroquinolone antibiotic widely studied for its potent antibacterial activity and distinct mechanism of action. It functions by inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes critical for DNA replication, transcription, repair, and recombination. By stabilizing the DNA-enzyme complexes and preventing the relegation of the cleaved DNA strands, ofloxacin induces double-strand breaks, leading to the disruption of DNA synthesis and cell death. This mode of action is particularly effective against a broad range of Gram-negative and Gram-positive bacteria. In scientific research, ofloxacin is extensively utilized to investigate the mechanisms of bacterial resistance, focusing on mutations in the target enzymes that reduce drug binding and the role of efflux pumps that expel the antibiotic from bacterial cells. Researchers employ ofloxacin to study the structure-activity relationships of fluoroquinolones, aiming to develop new derivatives with improved efficacy and reduced resistance potential. It serves as a model compound in pharmacokinetic and pharmacodynamic studies to understand the drug′s behavior in biological systems, including absorption, distribution, metabolism, and excretion. Ofloxacin is also used in molecular biology to investigate the regulation of DNA repair pathways and the cellular responses to DNA damage. Its ability to induce specific DNA lesions makes it a valuable tool for studying genotoxic stress and the mechanisms involved in maintaining genomic integrity.


Ofloxacin (CAS 82419-36-1) References

  1. Study on the impurity profile and influencing factors of photodegradation in non-aqueous ofloxacin ear drops using liquid chromatography combined with ion trap/time-of-flight mass spectrometry.  |  Xu, B., et al. 2023. J Pharm Biomed Anal. 233: 115476. PMID: 37245330
  2. Atomic-Scale Resolution Insights into Structural and Dynamic Differences between Ofloxacin and Levofloxacin.  |  Pradhan, BL., et al. 2023. ACS Omega. 8: 24093-24105. PMID: 37426250
  3. Toxicity of ciprofloxacin and ofloxacin to Moina macrocopa and investigation of p-value adjustments for (eco)toxicological studies.  |  Nguyen, TD., et al. 2023. Drug Chem Toxicol. 1-12. PMID: 37491899
  4. The co-presence of polystyrene nanoplastics and ofloxacin demonstrates combined effects on the structure, assembly, and metabolic activities of marine microbial community.  |  Liu, M., et al. 2023. J Hazard Mater. 459: 132315. PMID: 37604038
  5. High frequency of ofloxacin resistance patterns of Mycobacterium leprae from India: An indication to revisit second line anti-leprosy treatment regimen.  |  Chhabra, S., et al. 2023. J Glob Antimicrob Resist. 35: 262-267. PMID: 37852372
  6. Ofloxacin-Induced Genital Bullous Fixed Drug Eruption: A Rare Case of Cross-Reactivity to Multiple Fluoroquinolones.  |  Slim, R., et al. 2024. Dermatitis. 35: 194-195. PMID: 37910787
  7. A Review of the Categorizations of Mild, Moderate, and Severe Bacterial Keratitis Ulcers and Day-1 Treatment Regimen When Using the Topical Fluoroquinolones 0.3% Ciprofloxacin and 0.3% Ofloxacin.  |  Pearce, JG., et al. 2023. Curr Ther Res Clin Exp. 99: 100729. PMID: 38090721
  8. Quantitative monitoring ofloxacin in beef by TLC-SERS combined with machine learning analysis.  |  Lu, X., et al. 2024. Spectrochim Acta A Mol Biomol Spectrosc. 308: 123790. PMID: 38142496
  9. Ofloxacin weakened treatment performance of rural domestic sewage in an aerobic biofilm system by affecting biofilm resistance, bacterial community, and functional genes.  |  Feng, B., et al. 2024. Environ Res. 246: 118036. PMID: 38163543

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ofloxacin, 10 g

sc-219475
10 g
$245.00