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硫霉素的体外对比研究。

A comparative in vitro study of thienamycin.

作者信息

Fainstein V, LeBlanc B, Weaver S, Bodey G P

出版信息

Infection. 1982 Jan;10(1):50-2. doi: 10.1007/BF01640839.

DOI:10.1007/BF01640839
PMID:7068233
Abstract

The in vitro activity of thienamycin was compared to that of other antibiotics against a large panel of bacteria obtained in blood cultures from cancer patients. This compound was the most active against gram-positive cocci and also proved to be extremely active against the gram-negative bacteria. It was also very active against multi-resistant gram-negative bacilli. Because of its broad spectrum of activity including Pseudomonas spp., thienamycin deserves clinical testing in the future.

摘要

将硫霉素的体外活性与其他抗生素针对从癌症患者血培养物中分离出的大量细菌的活性进行了比较。该化合物对革兰氏阳性球菌活性最强,对革兰氏阴性菌也极具活性。它对多重耐药革兰氏阴性杆菌也非常有效。由于其包括假单胞菌属在内的广泛活性谱,硫霉素值得在未来进行临床试验。

相似文献

1
A comparative in vitro study of thienamycin.硫霉素的体外对比研究。
Infection. 1982 Jan;10(1):50-2. doi: 10.1007/BF01640839.
2
In vitro activity of thienamycin.硫霉素的体外活性。
Antimicrob Agents Chemother. 1978 Sep;14(3):436-8. doi: 10.1128/AAC.14.3.436.
3
In vitro activity of thienamycin.硫霉素的体外活性。
Methods Find Exp Clin Pharmacol. 1981 Nov-Dec;3(6):387-90.
4
Activity of N-formimidoyl thienamycin and cephalosporins against isolates from nosocomially acquired bacteremia.N-甲酰亚胺硫霉素和头孢菌素对医院获得性菌血症分离株的活性。
Antimicrob Agents Chemother. 1982 Mar;21(3):509-12. doi: 10.1128/AAC.21.3.509.
5
N-formimidoyl thienamycin (MK0787): in vitro study.N-甲酰亚胺基硫霉素(MK0787):体外研究。
Antimicrob Agents Chemother. 1981 Jan;19(1):201-4. doi: 10.1128/AAC.19.1.201.
6
In vitro activity of N-formimidoyl thienamycin (MK0787).N-甲酰亚胺基硫霉素(MK0787)的体外活性
Antimicrob Agents Chemother. 1980 Oct;18(4):642-4. doi: 10.1128/AAC.18.4.642.
7
Thienamycin: new beta-lactam antibiotic with potent broad-spectrum activity.硫霉素:具有强大广谱活性的新型β-内酰胺抗生素。
Antimicrob Agents Chemother. 1979 Apr;15(4):518-21. doi: 10.1128/AAC.15.4.518.
8
[Effect of multiresistance on the minimal inhibitory concentration of N-formimidoyl thienamycin and 6 comparing substances against P. aeruginosa and 4 Enterobacteriaceae species].[多重耐药性对N-甲酰亚胺硫霉素及6种对照物质对铜绿假单胞菌和4种肠杆菌科细菌的最低抑菌浓度的影响]
Zentralbl Bakteriol Mikrobiol Hyg A Med Mikrobiol Infekt Parasitol. 1983 Feb;253(4):531-43.
9
Antibacterial activities of a new stabilized thienamycin, N-formimidoyl thienamycin, in comparison with other antibiotics.一种新型稳定化硫霉素(N-甲脒基硫霉素)与其他抗生素相比的抗菌活性。
Antimicrob Agents Chemother. 1980 Jun;17(6):912-7. doi: 10.1128/AAC.17.6.912.
10
The antibacterial activity of thienamycin against multiresistant bacteria-comparison with beta-lactamase stable compounds.硫霉素对多重耐药菌的抗菌活性——与β-内酰胺酶稳定化合物的比较
J Antimicrob Chemother. 1980 Sep;6(5):601-6. doi: 10.1093/jac/6.5.601.

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1
Carbapenems: past, present, and future.碳青霉烯类抗生素:过去、现在和未来。
Antimicrob Agents Chemother. 2011 Nov;55(11):4943-60. doi: 10.1128/AAC.00296-11. Epub 2011 Aug 22.

本文引用的文献

1
MK0787 (N-formimidoyl thienamycin): evaluation of in vitro and in vivo activities.MK0787(N-亚胺甲酰硫霉素):体内外活性评估
Antimicrob Agents Chemother. 1980 Jun;17(6):993-1000. doi: 10.1128/AAC.17.6.993.
2
In vitro activity of N-formimidoyl thienamycin in comparison with cefotaxime, moxalactam, and ceftazidime.与头孢噻肟、拉氧头孢和头孢他啶相比,N-甲酰亚胺硫霉素的体外活性。
Antimicrob Agents Chemother. 1981 Mar;19(3):402-6. doi: 10.1128/AAC.19.3.402.