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Pazufloxacin

Pazufloxacin

Catalog Number: orb1982128

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Catalog Numberorb1982128
CategorySmall Molecules
DescriptionPazufloxacin (T-3761) is a fluoroquinolone antibiotic used for antibacterial applications. This novel quinolone derivative exhibits robust and broad-spectrum antibacterial efficacy against systemic, pulmonary, and urinary tract infections in mice, effectively targeting both gram-positive and gram-negative bacteria, including quinolone-resistant strains such as Serratia marcescens and Pseudomonas aeruginosa. Compared to antibiotics like ofloxacin, ciprofloxacin, norfloxacin, and tosufloxacin, Pazufloxacin demonstrates comparable or superior efficacy across various infection models. While slightly less effective than tosufloxacin against certain gram-positive infections, it remains potent against methicillin-resistant Staphylococcus aureus. Its broad-spectrum activity is supported by minimum inhibitory concentrations (MICs) between 0.39 and 6.25 micrograms/ml for Staphylococcus aureus and Clostridium species, with minimum bactericidal concentrations (MBCs) close to the MICs. Additionally, its 50% inhibitory concentrations for DNA gyrases from E. coli and P. aeruginosa are 0.88 and 1.9 micrograms/ml respectively, highlighting its potent antibacterial mechanism of action.
MW318.3
CAS Number127045-41-4
FormulaC16H15FN2O4
SMILESC[C@H]1COc2c(c(F)cc3c2n1cc(C(O)=O)c3=O)C1(N)CC1
Storage-20°C
NoteFor research use only
Expiration Date12 months from date of receipt.
  • Pazufloxacin Mesylate [orb1226012]

    >98%(HPLC)

    163680-77-1

    414.4

    C16H15FN2O4·CH4O3S

    1 g, 500 mg, 25 mg, 50 mg, 100 mg, 200 mg
  • Pazufloxacin Mesylate [orb1307992]

    99.88%

    163680-77-1

    414.4

    C16H15FN2O4·CH4O3S

    100 mg, 50 mg, 1 ml x 10 mM (in DMSO), 500 mg, 1 g

For example, if the dosage of your experiment is 10mg/kg, the weight of each animal is 50g, and the volume of the dosing is 100μL, then the working solution concentration of your experiment is 5mg/mL. If the formula you used is 5% DMSO+ 30% PEG300+ 5% Tween 80 + 60% Saline/PBS/ddH2O, the preparation method is as follows:

Mother liquor preparation method: 5mg of drug dissolved in 100μL DMSO (mother liquor concentration is 50mg/mL). Preparation method of in vivo formulation: For 1mL of working solution preparation, take 50μL of DMSO mother liquor, add 300 μL of PEG300 to mix well and clarify, then add 50μL of Tween-80 to mix well and clarify, and finally add 600μL of Saline/PBS/ddH2O to mix well and clarify.

Note:
  1. For Reference Only. Please choose the appropriate dissolution protocol according to your experimental animal and administration method.
  2. We suggest that in cell experiments, the final concentration of DMSO is not more than 0.1%, in animal experiments, for healthy mice, the final concentration of DMSO is not more than 10%; For nude or frail mice, the final concentration of DMSO is not more than 2%.