Date published: 2025-12-1

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Garenoxacin (CAS 194804-75-6)

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Alternate Names:
1-Cyclopropyl-8-(difluoromethoxy)-7-[(1R)-2,3-dihydro-1-methyl-1H-isoindol-5-yl]-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid
Application:
Garenoxacin is an antibacterial agent and a Topo II inhibitor
CAS Number:
194804-75-6
Molecular Weight:
426.41
Molecular Formula:
C23H20F2N2O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Garenoxacin, a synthetic fluoroquinolone antibiotic, has garnered attention in scientific research for its potent antibacterial activity and unique mechanism of action. This chemical inhibits bacterial DNA gyrase and topoisomerase IV enzymes, critical for DNA replication and repair in bacteria. By binding to these enzymes, garenoxacin disrupts the DNA supercoiling process, leading to the inhibition of bacterial growth and proliferation. Research has focused on exploring the efficacy of garenoxacin against a broad spectrum of bacterial pathogens, including both Gram-positive and Gram-negative species. Additionally, investigations into the pharmacokinetics and pharmacodynamics of garenoxacin have provided valuable insights into its absorption, distribution, metabolism, and excretion in various biological systems. Furthermore, research efforts have aimed to explain the structure-activity relationship of garenoxacin derivatives to optimize its antibacterial potency and minimize the development of antibiotic resistance. Beyond its antibacterial properties, recent studies have also explored the potential of garenoxacin as a scaffold for the development of novel antimicrobial agents targeting bacterial infections, highlighting its significance in combating antibiotic-resistant pathogens and advancing strategies in infectious disease research.


Garenoxacin (CAS 194804-75-6) References

  1. Comparative articular toxicity of garenoxacin, a novel quinolone antimicrobial agent, in juvenile beagle dogs.  |  Nagai, A., et al. 2002. J Toxicol Sci. 27: 219-28. PMID: 12238145
  2. Efficacy of garenoxacin in treatment of experimental endocarditis due to Staphylococcus aureus or viridans group streptococci.  |  Entenza, JM., et al. 2004. Antimicrob Agents Chemother. 48: 86-92. PMID: 14693523
  3. Activity of garenoxacin, an investigational des-F(6)-quinolone, tested against pathogens from community-acquired respiratory tract infections, including those with elevated or resistant-level fluoroquinolone MIC values.  |  Jones, RN., et al. 2007. Diagn Microbiol Infect Dis. 58: 9-17. PMID: 17408903
  4. Garenoxacin activity against isolates form patients hospitalized with community-acquired pneumonia and multidrug-resistant Streptococcus pneumoniae.  |  Jones, RN., et al. 2007. Diagn Microbiol Infect Dis. 58: 1-7. PMID: 17408904
  5. Inhibitory activity of garenoxacin against DNA gyrase of Mycoplasma pneumoniae.  |  Nakatani, M., et al. 2012. J Antimicrob Chemother. 67: 1850-2. PMID: 22532464
  6. Comparison of garenoxacin with levofloxacin as antimicrobial prophylaxis in acute myeloid leukemia.  |  Uni, M., et al. 2015. Jpn J Clin Oncol. 45: 745-8. PMID: 25989991
  7. Pharmacokinetic study of garenoxacin in severe renal failure patients.  |  Yamagishi, Y., et al. 2015. Jpn J Antibiot. 68: 141-50. PMID: 26349115
  8. Comparison of levofloxacin and garenoxacin for antibacterial prophylaxis during neutropenia.  |  Yamasaki, R., et al. 2017. Int J Hematol. 105: 835-840. PMID: 28168415
  9. Proposed Pharmacokinetic-Pharmacodynamic Breakpoint of Garenoxacin and Other Quinolones.  |  Yamagishi, Y., et al. 2017. Jpn J Infect Dis. 70: 616-620. PMID: 28890509
  10. The clinical efficacy of garenoxacin for male non-gonococcal urethritis.  |  Yamada, H., et al. 2020. J Infect Chemother. 26: 353-357. PMID: 31757739

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Garenoxacin, 25 mg

sc-490878
25 mg
$380.00