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tosufloxacin

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  • Inhibitors & Agonists
    7
    TargetMol | Inhibitors_Agonists
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    TargetMol | Natural_Products
Tosufloxacin
tosufloxacin tosilate, Ozex, 7-(3-Aminopyrrolidin-1-yl)-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid
T9319108138-46-1
Tosufloxacin (Ozex) is a quinolone antimicrobial agent and potent inhibitor of the metabolism of theophylline.
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TargetMol | Inhibitor Sale
Tosufloxacin tosylate hydrate
Tosufloxacin p-Toluenesulfonate Hydrate, T-3262 Tosylate Hydrate, A-61827 tosylate hydrate
T80461400591-39-0
Tosufloxacin tosylate hydrate (A-61827 tosylate hydrate) is a fluoroquinolone antibacterial agent that is used to treat susceptible infections.
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Tosufloxacin tosylate
Tosufloxacin,T-3262,T3262,T 3262
T26368115964-29-9
Tosufloxacin is a fluoroquinolone antibiotic used to treat susceptible infections.
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7-10 days
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Tosufloxacin tosilate
T3522107097-79-0
Tosufloxacin tosilate is a fluoroquinolone antibiotic.
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Tosufloxacin hydrochloride
A-61827 hydrochloride, T-3262 hydrochloride
T8835104051-69-6
Tosufloxacin hydrochloride is a fluoroquinolone antibacterial agent used to treat bacterial infections.Tosufloxacin hydrochloride is also a bacterial Topo (DNA gyrase, topoisomerase)) inhibitor.
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A 71497
A71497,A-71497
T26436134762-03-1
A 71497 is the 3-formyl derivative of the antibiotic tosufloxacin.
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Pazufloxacin
T75296127045-41-4
Pazufloxacin (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.
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3-6 months
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