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Ibafloxacin

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Chemical compound Pharmaceutical compound
Ibafloxacin
Clinical data
Trade namesIbaflin
AHFS/Drugs.comInternational Drug Names
ATCvet code
Legal status
Legal status
Identifiers
IUPAC name
  • 6,7-dihydro-5,8-dimethyl-9-fluoro-1-oxo-1H,5H-benzoquinolizine-2-carboxylic acid
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC15H14FNO3
Molar mass275.279 g·mol
3D model (JSmol)
SMILES
  • Fc2cc1C(=O)/C(C(=O)O)=C\N3c1c(c2C)CCC3C
InChI
  • InChI=1S/C15H14FNO3/c1-7-3-4-9-8(2)12(16)5-10-13(9)17(7)6-11(14(10)18)15(19)20/h5-7H,3-4H2,1-2H3,(H,19,20)
  • Key:DXKRGNXUIRKXNR-UHFFFAOYSA-N
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Ibafloxacin (INN) is a fluoroquinolone antibiotic drug formally approved for use in the European Union for veterinary medicine.

References

  1. Horspool LJ, van Laar P, van den Bos R, Mawhinney I (June 2004). "Treatment of canine pyoderma with ibafloxacin and marbofloxacin--fluoroquinolones with different pharmacokinetic profiles". Journal of Veterinary Pharmacology and Therapeutics. 27 (3): 147–53. doi:10.1111/j.1365-2885.2004.00561.x. PMID 15189300.
  2. "EUROPEAN PUBLIC ASSESSMENT REPORT (EPAR) IBAFLIN" (PDF). European Medicines Agency. 1 September 2007.
Antibacterials that inhibit nucleic acid (J01E, J01M)
Antifolates
(inhibit bacterial
purine metabolism,
thereby inhibiting
DNA and RNA
synthesis)
DHFR inhibitor
Sulfonamides
(DHPS inhibitor)
Short-acting
Intermediate-acting
Long-acting
Other/ungrouped
Combinations
Other DHPS inhibitors
Quinolones
(inhibit bacterial
topoisomerase
and/or DNA gyrase,
thereby inhibiting
DNA replication)
1st generation
Fluoroquinolones
2nd generation
3rd generation
4th generation
Veterinary
Newer non-fluorinated
Related (DG)
Anaerobic DNA
inhibitors
Nitroimidazole derivatives
RNA synthesis
Rifamycins/
RNA polymerase
Lipiarmycins


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