Rufloxacin

Chemical compound
  • J01MA10 (WHO)
Legal statusLegal status
  • In general: ℞ (Prescription only)
Identifiers
  • 9-Fluoro-10-(4-methylpiperazin-1-yl)-7-oxo-2,3-dihydro-7H-[1,4]thiazino[2,3,4-ij]quinoline-6-carboxylic acid
CAS Number
  • 101363-10-4 checkY 106017-08-7
PubChem CID
  • 58258
ChemSpider
  • 52489 ☒N
UNII
  • Y521XM2900
ChEMBL
  • ChEMBL295619 ☒N
CompTox Dashboard (EPA)
  • DTXSID6048412 Edit this at Wikidata
Chemical and physical dataFormulaC17H18FN3O3SMolar mass363.41 g·mol−13D model (JSmol)
  • Interactive image
  • CN1CCN(CC1)C2=C(C=C3C4=C2SCCN4C=C(C3=O)C(=O)O)F
InChI
  • InChI=1S/C17H18FN3O3S/c1-19-2-4-20(5-3-19)14-12(18)8-10-13-16(14)25-7-6-21(13)9-11(15(10)22)17(23)24/h8-9H,2-7H2,1H3,(H,23,24) ☒N
  • Key:NJCJBUHJQLFDSW-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Rufloxacin is a quinolone antibiotic.[1] It is sold under the brand names, Ruflox, Monos, Qari, Tebraxin, Uroflox, Uroclar.

See also

  • Quinolones

References

  1. ^ Rafalsky V, Andreeva I, Rjabkova E (July 2006). "Quinolones for uncomplicated acute cystitis in women". The Cochrane Database of Systematic Reviews. 3 (3): CD003597. doi:10.1002/14651858.CD003597.pub2. PMC 7003573. PMID 16856014.
  • 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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