Date published: 2025-12-6

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Gatifloxacin sesquihydrate (CAS 180200-66-2)

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Alternate Names:
1-Cyclopropyl-6-fluoro-8-methoxy-7-(3-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid sesquihydrate
CAS Number:
180200-66-2
Purity:
≥98%
Molecular Weight:
402.42
Molecular Formula:
C19H22FN3O4.1.5(H2O)
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Gatifloxacin sesquihydrate, a fluoroquinolone antibiotic, has been extensively studied in scientific research for its antimicrobial properties and mechanisms of action. Its mechanism primarily involves inhibition of bacterial DNA gyrase and topoisomerase IV, essential enzymes involved in DNA replication and repair processes in bacteria. By targeting these enzymes, gatifloxacin disrupts DNA synthesis and leads to bacterial cell death. Research investigations have focused on elucidating the structural basis of gatifloxacin′s interaction with DNA gyrase and topoisomerase IV, providing insights into its high potency and broad-spectrum activity against various bacterial pathogens, including gram-positive and gram-negative bacteria. Furthermore, studies have explored the mechanisms underlying bacterial resistance to gatifloxacin, highlighting the importance of understanding resistance mechanisms for developing strategies to combat antimicrobial resistance. Additionally, gatifloxacin sesquihydrate has been utilized in research aimed at exploring novel drug delivery systems and formulations to enhance its efficacy and bioavailability. Its role as a valuable tool in microbiology and pharmaceutical research underscores gatifloxacin sesquihydrate′s significance in advancing our understanding of antimicrobial pharmacology and combating infectious diseases.


Gatifloxacin sesquihydrate (CAS 180200-66-2) References

  1. Effects of sub-minimum inhibitory concentrations of gatifloxacin on the inhibition of Staphylococcus aureus and Escherichia coli adherence.  |  Braga, PC. and Dal Sasso, M. 2002. Arzneimittelforschung. 52: 109-12. PMID: 11878198
  2. Determination of gatifloxacin in human serum and urine by high-performance liquid chromatography with ultraviolet detection.  |  Overholser, BR., et al. 2003. J Chromatogr B Analyt Technol Biomed Life Sci. 798: 167-73. PMID: 14630373
  3. Spectrophotometric determination of gatifloxacin in pure form and in pharmaceutical formulation.  |  Amin, AS., et al. 2007. Spectrochim Acta A Mol Biomol Spectrosc. 67: 1306-12. PMID: 17113819
  4. Radiation sterilization of fluoroquinolones in solid state: investigation of effect of gamma radiation and electron beam.  |  Singh, BK., et al. 2010. Appl Radiat Isot. 68: 1627-35. PMID: 20444612
  5. Ocular insert for sustained delivery of gatifloxacin sesquihydrate: Preparation and evaluations.  |  Khurana, G., et al. 2012. Int J Pharm Investig. 2: 70-7. PMID: 23119235
  6. Identification of anti-inflammatory and other biological activities of 3-carboxamide, 3-carbohydrazide and ester derivatives of gatifloxacin.  |  Sultana, N., et al. 2013. Chem Cent J. 7: 6. PMID: 23316796
  7. Simultaneous quantification of gatifloxacin, moxifloxacin, and besifloxacin concentrations in cornea and aqueous humor by LC-QTOF/MS after topical ocular dosing.  |  Domingos, LC., et al. 2017. J Pharmacol Toxicol Methods. 83: 87-93. PMID: 27670369

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Gatifloxacin sesquihydrate, 1 g

sc-353614
1 g
$185.00

Gatifloxacin sesquihydrate, 5 g

sc-353614A
5 g
$510.00