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KI0703Ofloxacin50 mg$154

Chemical Characteristic

Product NameOfloxacin
SynonymsFloxin, Ocuflox
CAS No.82419-36-1
Molecular Weight 361.37
FormulaC18H20FN3O4
Chemical Name(+/-)-9-Fluoro-2, 3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid
SmilesO1CC(n2c3c1c(c(cc3c(=O)c(c2)C(=O)O)F)N1CCN(CC1)C)C
Chemical Structure

Biological activities

Ofloxacin is a synthetic chemotherapeutic antibiotic of the fluoroquinolone drug class. Ofloxacin is a racemic mixture, which consists of 50% levofloxacin (the biologically active component) and 50% of its??irror image or enantiomer dextrofloxacin. Ofloxacin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria. Ofloxacin inhibits DNA gyrase, a type II topoisomerase, and topoisomerase IV. The MICs of (+)-, (-)-, and (+)-ofloxacin for M. luteus ATCC 4698, as determined by the twofold broth dilution method with 105 CFU/mL, are 200, 0.78, and 1.56 µg/mL, respectively.[1] Ofloxacin inhibits the medium chain acyl-CoA synthetase in a mixed-type manner with Ki value of 38.2 µM.[2] In vitro, ofloxacin also inhibits migration of leukocytes with an IC50 of 0.63 µg/mL.[3] Ofloxacin inhibits all strains of Bacteroides fragilis at a concentration of 3.125 mg/L and the gram-positive anaerobes at 0.5 mg/L. In mice experimentally infected with various gram-positive and gram-negative bacteria, ofloxacin is more active than norfloxacin and pipemidic acid. With the gram-negative pathogens, orally administered ofloxacin is as active as gentamicin used parenterally.[4]

Protocols

In vivo: Ofloxacin is dissolved in saline.[4]

References

[1] Imamura M, et al. Inhibition of DNA gyrase by optically active ofloxacin. Antimicrob Agents Chemother. 1987, 31(2): 325-327.
[2] Kasuya F, et al. Inhibitory effect of quinolone antimicrobial and nonsteroidal anti-inflammatory drugs on a medium chain acyl-CoA synthetase. Biochem Pharmacol. 2001, 62(3): 363-367.
[3] Zhou Z, et al. Study on the effect of ofloxacin and tanshinone II A on human leukocyte chemotactic migration in vitro. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1997, 19(3): 232-235.
[4] Seibert G, et al. Comparison of the antibacterial in vitro and in vivo activity of ofloxacin (HOE 280 DL 8280) and nalidixic acid analogues. Eur J Clin Microbiol. 1983, 2(6): 548-553.

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