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新型氟化4-喹诺酮衍生物PD 127,391的体外活性比较

Comparative in vitro activity of PD 127,391, a new fluorinated 4-quinolone derivative.

作者信息

Norrby S R, Jonsson M

机构信息

Department of Infectious Diseases, University of Umeå, Sweden.

出版信息

Antimicrob Agents Chemother. 1988 Aug;32(8):1278-81. doi: 10.1128/AAC.32.8.1278.

DOI:10.1128/AAC.32.8.1278
PMID:3142352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC172394/
Abstract

PD 127,391, a newly developed 4-quinolone chemically similar to ciprofloxacin, was studied in vitro by using agar and broth dilution and two inoculum sizes. PD 127,391 was found to be highly active against gram-negative aerobes, including Pseudomonas aeruginosa and other Pseudomonas spp. Its activity against gram-positive aerobes was better than that of ciprofloxacin.

摘要

PD 127,391是一种新开发的与环丙沙星化学结构相似的4-喹诺酮类药物,采用琼脂稀释法、肉汤稀释法以及两种接种量在体外进行了研究。结果发现,PD 127,391对包括铜绿假单胞菌和其他假单胞菌属在内的革兰氏阴性需氧菌具有高度活性。它对革兰氏阳性需氧菌的活性优于环丙沙星。

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Comparative in vitro activity of PD 127,391, a new fluorinated 4-quinolone derivative.新型氟化4-喹诺酮衍生物PD 127,391的体外活性比较
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本文引用的文献

1
Antibacterial activity of imipenem: the first thienamycin antibiotic.亚胺培南的抗菌活性:首个硫霉素类抗生素。
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Review of in vitro activity of third-generation cephalosporins and other newer beta-lactam antibiotics against clinically important bacteria.第三代头孢菌素及其他新型β-内酰胺类抗生素对临床重要细菌的体外活性综述
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The comparative in-vitro activity of eight newer quinolones and nalidixic acid.八种新型喹诺酮类药物与萘啶酸的体外活性比较
J Antimicrob Chemother. 1986 Nov;18 Suppl D:1-20. doi: 10.1093/jac/18.supplement_d.1.
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Quinolone antibacterial agents. Synthesis and structure-activity relationships of 8-substituted quinoline-3-carboxylic acids and 1,8-naphthyridine-3-carboxylic acids.喹诺酮类抗菌剂。8-取代喹啉-3-羧酸和1,8-萘啶-3-羧酸的合成及构效关系
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