• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

氟罗沙星(Ro23 - 6240),一种新型氟化4 - 喹诺酮类药物,对癌症患者分离菌株的体外活性。

In vitro activity of fleroxacin (Ro23-6240), a new fluorinated 4-quinolone against isolates from cancer patients.

作者信息

Rolston K, Ho D H, LeBlanc B, Bodey G P

机构信息

Department of Medical Specialties, University of Texas System Cancer Center, M.D. Anderson Hospital and Tumor Institute, Houston.

出版信息

Chemotherapy. 1988;34(6):448-54. doi: 10.1159/000238607.

DOI:10.1159/000238607
PMID:3149568
Abstract

The in vitro activity of Fleroxacin (Ro23-6240; AM 833), a new fluorinated 4-quinolone, was compared to that of ciprofloxacin, enoxacin and A-56620, against 747 isolates from cancer patients. Fleroxacin inhibited more than 90% of Enterobacteriacea isolates at a concentration of less than or equal to 0.25 micrograms/ml. It was also extremely active against Aeromonas hydrophila and Haemophilus influenzae isolates with MIC90 values of 0.12 and 0.06 micrograms/ml, respectively. The MIC90 for Acinetobacter spp. was 1.0 micrograms/ml, for Pseudomonas aeruginosa and Pseudomonas fluorescens 4.0 micrograms/ml, and for other Pseudomonas spp., 8.0 micrograms/ml. Staphylococcus aureus isolates including methicillin-resistant strains were inhibited by less than or equal to 1.0 microgram/ml. The MIC90 for three different species of coagulase-negative Staphylococci was 1.0 microgram/ml. Streptococcal species required 8-16 micrograms/ml for inhibition. Fleroxacin was also active against group JK-diphtheroids and Bacillus cereus. The overall activity of fleroxacin was similar to that of enoxacin and less than that of A-56620 and ciprofloxacin.

摘要

将新型氟化4-喹诺酮类药物氟罗沙星(Ro23 - 6240;AM 833)的体外活性与环丙沙星、依诺沙星和A - 56620进行比较,以检测其对747株癌症患者分离菌株的活性。氟罗沙星在浓度小于或等于0.25微克/毫升时可抑制90%以上的肠杆菌科分离菌株。它对嗜水气单胞菌和流感嗜血杆菌分离菌株也具有极高活性,其MIC90值分别为0.12和0.06微克/毫升。不动杆菌属的MIC90为1.0微克/毫升,铜绿假单胞菌和荧光假单胞菌为4.0微克/毫升,其他假单胞菌属为8.0微克/毫升。包括耐甲氧西林菌株在内的金黄色葡萄球菌分离菌株在浓度小于或等于1.0微克/毫升时受到抑制。三种不同的凝固酶阴性葡萄球菌的MIC90为1.0微克/毫升。链球菌属菌株抑制浓度需要8 - 16微克/毫升。氟罗沙星对JK组类白喉杆菌和蜡样芽孢杆菌也有活性。氟罗沙星的总体活性与依诺沙星相似,低于A - 56620和环丙沙星。

相似文献

1
In vitro activity of fleroxacin (Ro23-6240), a new fluorinated 4-quinolone against isolates from cancer patients.氟罗沙星(Ro23 - 6240),一种新型氟化4 - 喹诺酮类药物,对癌症患者分离菌株的体外活性。
Chemotherapy. 1988;34(6):448-54. doi: 10.1159/000238607.
2
The comparative activity of fleroxacin, three other quinolones and eight unrelated antimicrobial agents.氟罗沙星、其他三种喹诺酮类药物及八种不相关抗菌药物的比较活性
Chemotherapy. 1992;38(5):308-18. doi: 10.1159/000239019.
3
In-vitro activity of fleroxacin compared with three other quinolones.氟罗沙星与其他三种喹诺酮类药物的体外活性比较。
J Antimicrob Chemother. 1988 Oct;22 Suppl D:19-23. doi: 10.1093/jac/22.supplement_d.19.
4
In vitro activity of sparfloxacin (CI-978; AT-4140) against clinical isolates from cancer patients.司帕沙星(CI-978;AT-4140)对癌症患者临床分离株的体外活性。
Antimicrob Agents Chemother. 1990 Nov;34(11):2263-6. doi: 10.1128/AAC.34.11.2263.
5
In vitro activities of sparfloxacin, tosufloxacin, ciprofloxacin, and fleroxacin.司帕沙星、妥舒沙星、环丙沙星和氟罗沙星的体外活性。
Antimicrob Agents Chemother. 1991 May;35(5):955-60. doi: 10.1128/AAC.35.5.955.
6
In vitro activity of CI-934 compared with ciprofloxacin, enoxacin, norfloxacin, and vancomycin.CI-934与环丙沙星、依诺沙星、诺氟沙星及万古霉素的体外活性比较。
Diagn Microbiol Infect Dis. 1987 Apr;6(4):301-6. doi: 10.1016/0732-8893(87)90179-9.
7
Antimicrobial activity evaluations of two new quinolones, PD127391 (CI-960 and AM-1091) and PD131628.两种新型喹诺酮类药物PD127391(CI - 960和AM - 1091)和PD131628的抗菌活性评估
Diagn Microbiol Infect Dis. 1991 Sep-Oct;14(5):389-401. doi: 10.1016/0732-8893(91)90066-o.
8
In vitro activity of PD127,391, a new quinolone against bacterial isolates from cancer patients.新型喹诺酮类药物PD127,391对癌症患者细菌分离株的体外活性
Chemotherapy. 1990;36(5):365-72. doi: 10.1159/000238789.
9
Antimicrobial activity of a new antipseudomonal dual-action drug, Ro 25-0534.
Diagn Microbiol Infect Dis. 1994 Jan;18(1):61-8. doi: 10.1016/0732-8893(94)90135-x.
10
In vitro antimicrobial activity of sparfloxacin (AT-4140, CI-978, PD 131501) compared with numerous other quinolone compounds.与众多其他喹诺酮类化合物相比,司帕沙星(AT - 4140、CI - 978、PD 131501)的体外抗菌活性。
Diagn Microbiol Infect Dis. 1991 Jul-Aug;14(4):319-30. doi: 10.1016/0732-8893(91)90023-9.

引用本文的文献

1
In vitro susceptibility of Xanthomonas (Pseudomonas) maltophilia to newer antimicrobial agents.嗜麦芽窄食单胞菌(假单胞菌)对新型抗菌药物的体外敏感性
Antimicrob Agents Chemother. 1990 Aug;34(8):1609-10. doi: 10.1128/AAC.34.8.1609.