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依诺沙星:丝状大肠杆菌细胞的强效诱导剂(一则笔记)

Enoxacin: a potent inducer of filamentous Escherichia coli cells (a note).

作者信息

Uri J V, Actor P

出版信息

Acta Microbiol Hung. 1985;32(2):197-200.

PMID:3933273
Abstract

Enoxacin (CI-919; AT-2266), a new naphthyridine derivative was found to induce morphologic changes at very low concentrations in Escherichia coli but not in Staphylococcus aureus and Pseudomonas aeruginosa cells. The development of the long filamentous forms observed with nalidixic acid is most probably a consequence of inhibition of DNA synthesis. The phenomenon may, however, not be the sole mechanism of the broad-spectrum antimicrobial activity of enoxacin.

摘要

依诺沙星(CI - 919;AT - 2266),一种新型萘啶衍生物,被发现能在极低浓度下诱导大肠杆菌发生形态变化,但对金黄色葡萄球菌和铜绿假单胞菌细胞无此作用。萘啶酸所观察到的长丝状形态的形成很可能是DNA合成受到抑制的结果。然而,这种现象可能并非依诺沙星广谱抗菌活性的唯一机制。

相似文献

1
Enoxacin: a potent inducer of filamentous Escherichia coli cells (a note).依诺沙星:丝状大肠杆菌细胞的强效诱导剂(一则笔记)
Acta Microbiol Hung. 1985;32(2):197-200.
2
[Enoxacin and ciprofloxacin: in vitro effect on Enterobacteriaceae, Pseudomonas aeruginosa and Staphylococcus aureus].[依诺沙星和环丙沙星:对肠杆菌科细菌、铜绿假单胞菌和金黄色葡萄球菌的体外作用]
Med Clin (Barc). 1986 Jan 11;86(1):1-3.
3
In vitro activity of enoxacin compared with norfloxacin and amikacin.依诺沙星与诺氟沙星及阿米卡星的体外活性比较。
Eur J Clin Microbiol. 1985 Feb;4(1):55-8. doi: 10.1007/BF02148662.
4
In-vitro activity of enoxacin (CL-919), a new quinoline derivative, compared with that of other antimicrobial agents.新喹啉衍生物依诺沙星(CL-919)的体外活性与其他抗菌剂的比较。
J Antimicrob Chemother. 1984 Mar;13(3):237-44. doi: 10.1093/jac/13.3.237.
5
Laboratory evaluation of enoxacin: comparison with norfloxacin and nalidixic acid.依诺沙星的实验室评估:与诺氟沙星和萘啶酸的比较。
J Antimicrob Chemother. 1985 Jan;15(1):45-52. doi: 10.1093/jac/15.1.45.
6
Pyridonecarboxylic acids as antibacterial agents. 2. Synthesis and structure-activity relationships of 1,6,7-trisubstituted 1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acids, including enoxacin, a new antibacterial agent.吡啶酮羧酸类抗菌剂。2. 1,6,7-三取代的1,4-二氢-4-氧代-1,8-萘啶-3-羧酸包括新型抗菌剂依诺沙星的合成及其构效关系
J Med Chem. 1984 Mar;27(3):292-301. doi: 10.1021/jm00369a011.
7
[In vitro antimicrobial activity of CI-919 against gram-negative bacilli and Staphylococcus aureus isolated from various pathologies].CI-919对从各种病理情况中分离出的革兰氏阴性杆菌和金黄色葡萄球菌的体外抗菌活性
Rev Med Chil. 1985 Feb;113(2):94-102.
8
In vitro activity of enoxacin, a quinolone carboxylic acid, compared with those of norfloxacin, new beta-lactams, aminoglycosides, and trimethoprim.喹诺酮羧酸依诺沙星的体外活性与诺氟沙星、新型β-内酰胺类、氨基糖苷类及甲氧苄啶的体外活性比较。
Antimicrob Agents Chemother. 1983 Nov;24(5):754-63. doi: 10.1128/AAC.24.5.754.
9
In-vitro antimicrobial activity of enoxacin in combination with eight other antibiotics against Pseudomonas aeruginosa, Enterobacteriaceae and Staphylococcus aureus.依诺沙星与其他八种抗生素联合对铜绿假单胞菌、肠杆菌科细菌及金黄色葡萄球菌的体外抗菌活性。
J Antimicrob Chemother. 1987 Jan;19(1):45-8. doi: 10.1093/jac/19.1.45.
10
Pyridonecarboxylic acids as antibacterial agents. 9. Synthesis and antibacterial activity of 1-substituted 6-fluoro-1,4-dihydro-4-oxo-7-(4-pyridyl)-1,8-naphthyridine-3- carboxylic acids.吡啶酮羧酸类抗菌剂。9. 1-取代的6-氟-1,4-二氢-4-氧代-7-(4-吡啶基)-1,8-萘啶-3-羧酸的合成与抗菌活性
J Med Chem. 1987 Sep;30(9):1622-6. doi: 10.1021/jm00392a017.