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Irloxacin

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Irloxacin Basic information

Product Name:
Irloxacin
Synonyms:
  • Irloxacin
  • pirfloxacin
  • 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1H-pyrrol-1-yl)-3-quinolinecarboxylic acid
  • 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1H-pyrrol-1-yl)quinoline-3-carboxylic acid
  • E-3432
  • Irloxacin USP/EP/BP
  • Inhibitor,acid pH,antibacterial agent,Bacterial,gram-positive,oral,Irloxacin,Pirfloxacin,gram-negative bacteria,inhibit
  • 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1H-pyrrol-1-yl)-
CAS:
91524-15-1
MF:
C16H13FN2O3
MW:
300.28
Mol File:
91524-15-1.mol
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Irloxacin Chemical Properties

Melting point:
252-255 °C(Solv: N,N-dimethylformamide (68-12-2))
Boiling point:
495.9±45.0 °C(Predicted)
Density 
1.36±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
DMSO:0.0(Max Conc. mg/mL);0.0(Max Conc. mM)
pka
-0.07±0.20(Predicted)
form 
Solid
color 
White to off-white
CAS DataBase Reference
91524-15-1
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Irloxacin Usage And Synthesis

Uses

Irloxacin (Pirfloxacin) is a quinolone antibacterial agent. Irloxacin shows greater activity with an acid pH. Irloxacin has a good in vitro antimicrobial spectrum against both gram-positive and gram-negative bacteria. Orally active[1].

Hazard

Low toxicity by ingestion.

References

[1] Casal M, et al. Preliminary study of the in vitro activity of irloxacin against mycobacteria. Chemotherapy. 1995;41(3):204-207. DOI:10.1159/000239345
[2] Guzmán A, et al. Acute and subchronic toxicity studies of the new quinolone antibacterial agent irloxacin in rodents. Arzneimittelforschung. 1999;49(5):448-456. DOI:10.1055/s-0031-1300441

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