C15H9D8FN4O3•HCl
货号:ajcx24430
CAS:N/A
分子式:C15H9D8FN4O3•HCl
分子量：364.8
溶解度:DMSO: warmed,Water: soluble
纯度：98%
存储：Store at -20°C
库存：现货

Background:

Enoxacin-d₈is intended for use as an internal standard for the quantification of enoxacin by GC- or LC-MS. Enoxacin is a fluoroquinolone antibiotic.^1,2,3,4It is active against clinical isolates of a variety of Gram-positive and Gram-negative bacteria, includingS. aureus,E. coli,K. pneumoniae,P. aeruginosa, andS. marcescens(MIC₅₀s = 1, 0.12, 0.25, 0.5, and 1 mg/L, respectively).¹Enoxacin inhibitsS. aureusDNA gyrase supercoiling activity and topoisomerase IV DNA decatenation (IC₅₀s = 126 and 26.5 µg/ml, respectively).²It increases survival in mouse models of systemicS. aureus,E. coli,K. pneumoniae,P. aeruginosa, andS. marcescensinfection with ED₅₀values of 15.1, 2.2, 4.1, 120.3, and 7.6 mg/kg, respectively.³Enoxacin (4 and 8 mg/kg per day) also reduces tumor growth in a 143B human osteosarcoma mouse xenograft model.⁴Formulations containing enoxacin have previously been used in the treatment of urinary tract infections and gonorrhea.

1.Clarke, A.M., Zemcov, S.J., and Campbell, M.E.In-vitro activity of pefloxacin compared to enoxacin, norfloxacin, gentamicin and new β-lactamsJ. Antimicrob. Chemother.15(1)39-44(1985) 2.Takei, M., Fukuda, H., Kishii, R., et al.Target preference of 15 quinolones against Staphylococcus aureus, based on antibacterial activities and target inhibitionAntimicrob. Agents Chemother.45(12)3544-3547(2001) 3.Ozaki, M., Matsuda, M., Tomii, Y., et al.In vivo evaluation of NM441, a new thiazeto-quinoline derivativeAntimicrob. Agents Chemother.35(12)2496-2499(1991) 4.Luo, X., Liu, X., Tao, Q., et al.Enoxacin inhibits proliferation and invasion of human osteosarcoma cells and reduces bone tumour volume in a murine xenograft modelOncol. Lett.20(2)1400-1408(2020)