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新氟喹诺酮类抗菌药—Sitafloxacin的体外抗菌活性

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出处 《华西医学》 CAS 2001年第1期122-124,共3页 West China Medical Journal
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参考文献10

  • 1Kitamura A,Hoshino K,Kimura Y,et al.Contribution of the C-8 substituent of DU6859a, a new potent fluoroquinolone, to its activity against DNA Gyrase mutants of pseudomonas aeruginosa[].Antimicrobial Agents and Chemotherapy.1995
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  • 3Sato K,Hoshino K,Tanaka M,et al.Antimirobial activity of DU-6859a, a new potent fluoroquinolone, against clinical isolates[].Antimicrobial Agents and Chemotherapy.1992
  • 4Nakane T,Iyobe S,Sato K,et al.In vitro antibacterial activity of DU-6859a, a new fluroquinolone[].Antimicrobial Agents and Chemotherapy.1995
  • 5Akasaka T,Kurosaka S,Uchida Y,et al.Antibacterial activities and inhibitory effects of Sitafloxacin (DU-6859a) and its optical isomers against type topoisomerases[].Antimicrobial Agents and Chemotherapy.1998
  • 6Tanaka M,Onodera Y,Uchida Y,et al.Inhibitory activities of quinolones against DNA Gyrase and Topoisomerase Ⅳpurified from staphylococcus aureur[].Antimicrobial Agents and Chemotherapy.1997
  • 7Wang T,Tanaka M,Sato K.Detection of grlA and gyrA mutations in 334 staphylococcus aureus strains[].Antimicrobial Agents and Chemotherapy.1998
  • 8Masshall SA,Jones RN,Murray PR,et al.In-vitro comparison of DU-6859a, a novel fluoroquinolone, with other quinolones and oral cephalosporins tested against 5086 recent clinical isolates[].Journal of Antimicrobial Chemotherapy.1993
  • 9Deguchi T,Yasuda M,Nakano M,et al.Antimicrobial activity of a new fluoroquinolone DU-6859a, against quinolone-resistant clinical isolates of Neisseria gonorrhoeae with genetic alterations in the gyrA subunit of DNA gyrase and the parC subunit of topoisomeraseⅣ[].Journal of Antimicrobial Chemotherapy.1997
  • 10Visalli MA,Jacobs MR,Appelbaum PC.MIC and time-kill study of activities of DU-6859a,Ciprofloxacin, Levofloxacin, Sparfloxacin, Cefotaxime, Imipenem, and Vancomycin against nine penicllin-susceptical and Resistant pneumcocci[].Antimicrobial Agents and Chemotherapy.1996

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