Date published: 2025-10-2

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Fleroxacin (CAS 79660-72-3)

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Application:
Fleroxacin is an antiproliferative antibacterial agent
CAS Number:
79660-72-3
Purity:
≥99%
Molecular Weight:
369.34
Molecular Formula:
C17H18F3N3O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Fleroxacin, with the CAS number 79660-72-3, is a synthetic antibiotic belonging to the fluoroquinolone class. This chemical is characterized by the presence of a fluorine atom, which is integral to its potent antimicrobial action against a wide range of bacterial pathogens. Fleroxacin operates by targeting bacterial DNA gyrase and topoisomerase IV, two key enzymes involved in DNA replication, transcription, and repair. The mechanism of action involves the formation of a stable, ternary complex between the drug, the enzyme, and DNA, which inhibits the function of these enzymes. This interference prevents the supercoiling of DNA that is necessary for normal bacterial cell processes, leading to the disruption of DNA function, replication, and ultimately bacterial cell death. In research settings, fleroxacin has been extensively used to study the dynamics of bacterial DNA manipulation and the cellular consequences of DNA gyrase and topoisomerase IV inhibition. This research provides insights into the molecular basis of antibiotic action and resistance, helping to explain how modifications to the quinolone structure can impact their efficacy and resistance profiles. Moreover, fleroxacin serves as a model compound for developing newer fluoroquinolones with improved efficacy and reduced resistance potential, contributing to the broader understanding of antibiotic design and bacterial resistance mechanisms.


Fleroxacin (CAS 79660-72-3) References

  1. Effect of fleroxacin on mouse bladder carcinogenesis with N-butyl-N- (4-hydroxybutyl) nitrosamine.  |  Ebisuno, S., et al. 1999. Urol Int. 62: 150-4. PMID: 10529665
  2. Investigation of binding between fluoroquinolones and pepsin by fluorescence spectroscopy and molecular simulation.  |  Lian, SQ., et al. 2019. Luminescence. 34: 595-601. PMID: 31074200
  3. A highly sensitive and selective 'turn-on' fluorescent probe for detection of fleroxacin in human serum and urine based on a lanthanide functionalized metal-organic framework.  |  Liu, TY., et al. 2019. Dalton Trans. 48: 17945-17952. PMID: 31793573
  4. Identification of Binding Epitopes of a Fluorinated Compound Bound to Proteins Using 1H and 19F NMR Spectroscopy.  |  Furihata, K. and Tashiro, M. 2020. Anal Sci. 36: 881-883. PMID: 32037346
  5. Collection and Separation of Fleroxacin and Ciprofloxacin in Ultrasound-Assisted Ionic Liquid Salting-Out Microextraction System.  |  Li, K., et al. 2020. J Chromatogr Sci. 58: 576-584. PMID: 32448888
  6. Establishment of an immunological detection method of fleroxacin by fluorescence-linked immunosorbent assay.  |  Liu, Y., et al. 2021. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 38: 594-601. PMID: 33667148
  7. Comparison of fleroxacin oxidation by chlorine and chlorine dioxide: Kinetics, mechanism and halogenated DBPs formation.  |  He, G., et al. 2022. Chemosphere. 286: 131585. PMID: 34293556
  8. Development of 1H{19F} saturation transfer difference experiments for detection of a fluorinated compound bound to proteins.  |  Furihata, K. and Tashiro, M. 2022. Anal Sci. 38: 825-829. PMID: 35318618
  9. Effects of environmental factors on the fleroxacin photodegradation with the identification of reaction pathways.  |  Huang, R., et al. 2022. Chemosphere. 308: 136373. PMID: 36113649
  10. NMR screening method based on 19F spin-spin relaxation time for analyses of fluorinated compound bound to proteins.  |  Furihata, K. and Tashiro, M. 2024. Anal Sci. 40: 219-223. PMID: 37838626

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Fleroxacin, 5 g

sc-205694
5 g
$192.00

Fleroxacin, 10 g

sc-205694A
10 g
$360.00