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5-表异霉素与其他氨基糖苷类药物的活性比较。

Activity of 5-episisomicin compared with that of other aminoglycosides.

作者信息

Fu K P, Neu H C

出版信息

Antimicrob Agents Chemother. 1978 Aug;14(2):194-200. doi: 10.1128/AAC.14.2.194.

Abstract

5-Episisomicin, a semisynthetic aminoglycoside, has been shown to inhibit many members of the Enterobacteriaceae, Pseudomonas aeruginosa, and Staphylococcus aureus. At a concentration of 3.1 mug/ml, more than 90% of Escherichia coli, Klebsiella pneumoniae, Enterobacter, Citrobacter, indole-positive Proteus, and Providencia were inhibited. 5-Episisomicin had activity against S. aureus, E. coli, Klebsiella, Enterobacter, and Citrobacter similar to gentamicin and netilmicin. It had activity similar to amikacin and netilmicin against many gentamicin-resistant bacteria. The activity of 5-episisomicin was greatest at an alkaline pH and in medium of low magnesium content. Synergy of 5-episisomicin and carbenicillin was found to occur most often against Pseudomonas.

摘要

5-表异丝氨酸霉素是一种半合成氨基糖苷类抗生素,已被证明能抑制许多肠杆菌科细菌、铜绿假单胞菌和金黄色葡萄球菌。在浓度为3.1微克/毫升时,超过90%的大肠杆菌、肺炎克雷伯菌、肠杆菌、柠檬酸杆菌、吲哚阳性变形杆菌和普罗威登斯菌受到抑制。5-表异丝氨酸霉素对金黄色葡萄球菌、大肠杆菌、克雷伯菌、肠杆菌和柠檬酸杆菌的活性与庆大霉素和奈替米星相似。它对许多耐庆大霉素的细菌的活性与阿米卡星和奈替米星相似。5-表异丝氨酸霉素在碱性pH值和低镁含量的培养基中活性最强。发现5-表异丝氨酸霉素和羧苄青霉素之间的协同作用最常出现在对抗铜绿假单胞菌时。

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1
Mechanisms of antibiotic resistance in bacteria.细菌中的抗生素耐药机制。
Annu Rev Biochem. 1973;42:471-506. doi: 10.1146/annurev.bi.42.070173.002351.
2
Mutamicins; biosynthetically created new sisomicin analogues.
J Antibiot (Tokyo). 1974 Dec;27(12):917-21. doi: 10.7164/antibiotics.27.917.
4
Tobramycin: an overview.
J Infect Dis. 1976 Aug;134 Suppl:S3-19. doi: 10.1093/infdis/134.supplement_1.s3.
7
Aminoglycoside-modifying enzymes.氨基糖苷类修饰酶
Methods Enzymol. 1975;43:611-28. doi: 10.1016/0076-6879(75)43124-x.

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