Danofloxacin

Chemical compound
  • QJ01MA92 (WHO)
Identifiers
  • 1-Cyclopropyl-6-fluoro-7-[(1S,4S)-3-methyl-3,6-diazabicyclo[2.2.1]heptan-6-yl]-4-oxoquinoline-3-carboxylic acid
CAS Number
  • 112398-08-0 checkY
PubChem CID
  • 71335
ChemSpider
  • 64439 ☒N
UNII
  • 24CU1YS91D
ChEMBL
  • ChEMBL157548 ☒N
CompTox Dashboard (EPA)
  • DTXSID0046432 Edit this at Wikidata
ECHA InfoCard100.166.385 Edit this at WikidataChemical and physical dataFormulaC19H20FN3O3Molar mass357.385 g·mol−13D model (JSmol)
  • Interactive image
  • O=C(O)\C4=C\N(c3cc(N1C[C@H]2N(C)C[C@@H]1C2)c(F)cc3C4=O)C5CC5
InChI
  • InChI=1S/C19H20FN3O3/c1-21-7-12-4-11(21)8-22(12)17-6-16-13(5-15(17)20)18(24)14(19(25)26)9-23(16)10-2-3-10/h5-6,9-12H,2-4,7-8H2,1H3,(H,25,26)/t11-,12-/m0/s1 ☒N
  • Key:QMLVECGLEOSESV-RYUDHWBXSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Danofloxacin is a fluoroquinolone antibiotic used in veterinary medicine.[1]

References

  1. ^ Lees P, Shojaee Aliabadi F (April 2002). "Rational dosing of antimicrobial drugs: animals versus humans". International Journal of Antimicrobial Agents. 19 (4): 269–84. doi:10.1016/s0924-8579(02)00025-0. PMID 11978498.
  • v
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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
Nitrofuran derivatives
RNA synthesis
Rifamycins/
RNA polymerase
Lipiarmycins
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