SKU: F011  / 
    CAS Number: 42835-25-6

    Flumequine

    $85.79 - $477.91

    Flumequine is a broad-spectrum, first-generation fluoroquinolone commonly used in veterinary research for enteric infections. It was patented in 1973 by Riker Labs. Flumequine is freely soluble in alkaline solutions and alcohol but is insoluble in water.

    Mechanism of Action Fluoroquinolone antibiotics target bacterial DNA gyrase, a bacterial Topoisomerase II inhibitor, an enzyme which reduces DNA strain during replication. Because DNA gyrase is required during DNA replication, subsequent DNA synthesis and ultimately cell division is inhibited.
    Spectrum Flumequine targets primarily Gram-negative bacteria, especially those which cause enteric infections in animals (infections of the intestinal tract)..
    Impurity Profile Impurity A| (RS)-5-methyl-1-oxo-6,7-dihydro-1H,5H-benzo[i,j]quinolizine-2-carboxylic acid (defluoroflumequine)||||
    Impurity B| ethyl (RS)-9-fluoro-5-methyl-1-oxo-6,7-dihydro-1H,5H-benzo[i,j]quinolizine-2-carboxylate (flumequine ethyl ester)||||
    Microbiology Applications Flumequine is commonly used in clinical in vitromicrobiological antimicrobial susceptibility tests (panels, discs, and MIC strips) against Gram negative microbial isolates. Medical microbiologists use AST results to recommend antibiotic treatment options.  Representative MIC values include:
    • Escherichia coli 0.12 µg/mL – 0.5 µg/mL
    • For a representative list of Flumequine MIC values, click here.
    Eukaryotic Cell Culture Applications

    Although quinolones are highly toxic to mammalian cells in culture, its mechanism of cytotoxic action is not known. Quinolone-induced DNA damage was first reported in 1986 (Hussy et al, 1986).

    Solubility DMSO: Soluble
    Water: Insoluble
    Note: Soluble in alkaline solutions.
    References

    Hussy P, Maass G, Tümmler B, Grosse F, Schomburg U (1986)  Effect of 4-quinolones and novobiocin on calf thymus DNA polymerase alpha primase complex, topoisomerases I and II, and growth of mammalian lymphoblasts. Antimicrob. Agents Chemother. 29(6):1073-1078  PMID 3015015

    O’Neil MJ (ed) (2013)  The Merck Index- An encyclopedia of chemicals, drugs, and biologicals. Royal Soc. Of Chemistry. Cambridge, UK. P. 759

    Wolfson, JS and Hooper DC (1985) The fluoroquinolones: Structures, mechanisms of action and resistance, and spectra of activity in vitro. Antimicrob. Agents Chemother. 28(4):581-586

    MIC Aeromonas hydrophila| 0.06 - >16 || Aeromonas salmonicida subsp. salmonicida| 0.015 - 0.25 || Aspergillus niger| 30.3|| Escherichia coli| 0.12 - 0.5 || Fusarium solani| 40.4|| Lactobacillus reuteri| 4000|| Mycoplasma gallisepticum| 2.5 - 10 || Mycoplasma hyopneumoniae| 0.25 - >16 || Mycoplasma synoviae | 5 - 50|| Pseudomonas aeruginosa| >128|| Rhizopus solani| 43.9||