Date published: 2025-9-8

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Pefloxacin mesylate dihydrate (CAS 149676-40-4)

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Application:
Pefloxacin mesylate dihydrate is an analog of norfloxacin that inhibits topoisomerase
CAS Number:
149676-40-4
Purity:
≥98%
Molecular Weight:
465.50
Molecular Formula:
C17H20FN3O3 CH4O3S 2H2O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Pefloxacin mesylate dihydrate, a derivative of quinolone antibiotic pefloxacin, has garnered interest in research due to its antimicrobial properties. Its mechanism involves inhibition of bacterial DNA gyrase, crucial for DNA replication, thus impeding bacterial growth. Research has explored its efficacy against various bacterial strains, particularly those exhibiting resistance to other antibiotics. Studies have investigated its role in treating infections in animal models, assessing pharmacokinetics, and exploring potential synergistic effects with other antimicrobial agents. Furthermore, research delves into elucidating its molecular interactions with bacterial enzymes and DNA, shedding light on its mode of action and potential for drug development. Additionally, investigations into its pharmacological profile, including absorption, distribution, metabolism, and excretion, contribute to understanding its suitability for diverse research applications. Ongoing studies aim to expand knowledge of pefloxacin mesylate dihydrate′s antimicrobial activity, pharmacokinetics, and mechanism of action, fostering its utility as a valuable tool in microbiological and pharmacological research endeavors.


Pefloxacin mesylate dihydrate (CAS 149676-40-4) References

  1. Spectrophotometric determination of ciprofloxacin, enrofloxacin and pefloxacin through charge transfer complex formation.  |  Mostafa, S., et al. 2002. J Pharm Biomed Anal. 27: 133-42. PMID: 11682219
  2. Spectrophotometric determination of enrofloxacin and pefloxacin through ion-pair complex formation.  |  Mostafa, S., et al. 2002. J Pharm Biomed Anal. 28: 173-80. PMID: 11861121
  3. Generic nonextractive spectrophotometric method for determination of 4-quinolone antibiotics by formation of ion-pair complexes with beta-naphthol.  |  Darwish, IA., et al. 2006. J AOAC Int. 89: 334-40. PMID: 16640281
  4. Spectrophotometric determination of pefloxacin mesylate in pharmaceuticals.  |  Basavaiah, K., et al. 2007. Acta Pharm. 57: 221-30. PMID: 17507318
  5. Evaluation of N-bromosuccinimide as a new analytical reagent for the spectrophotometric determination of fluoroquinolone antibiotics.  |  Askal, H., et al. 2007. Chem Pharm Bull (Tokyo). 55: 1551-6. PMID: 17978510
  6. Oral toxicity of pefloxacin, norfloxacin, ofloxacin and ciprofloxacin: comparison of biomechanical and histopathological effects on Achilles tendon in rats.  |  Olcay, E., et al. 2011. J Toxicol Sci. 36: 339-45. PMID: 21628961
  7. Quantitative determination of ofloxacin, ciprofloxacin, norfloxacin and pefloxacin in serum by high pressure liquid chromatography.  |  Groeneveld, AJ. and Brouwers, JR. 1986. Pharm Weekbl Sci. 8: 79-84. PMID: 2938073
  8. Validation of two UHPLC-MS/MS methods for fast and reliable determination of quinolone residues in honey.  |  İsmail Emir, A., et al. 2021. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 38: 807-819. PMID: 33760693
  9. Spectroscopic Analyses and Antimicrobial Activity of Novel Ciprofloxacin and 7-Hydroxy-4-methylcoumarin, the Plant-Based Natural Benzopyrone Derivative.  |  El-Attar, MS., et al. 2022. Int J Mol Sci. 23: PMID: 35887366
  10. Cytofluorometric analysis of chondrotoxicity of fluoroquinolone antimicrobial agents.  |  Hayem, G., et al. 1994. Antimicrob Agents Chemother. 38: 243-7. PMID: 8192451
  11. Determination of pefloxacin and its main active metabolite in human serum by high-performance liquid chromatography.  |  Abanmi, N., et al. 1996. Ther Drug Monit. 18: 158-63. PMID: 8721279

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Pefloxacin mesylate dihydrate, 5 g

sc-204838
5 g
$61.00