Suppr超能文献

匹氨西林,一种具有广谱活性的新型半合成青霉素。

Pirbenicillin, a new semisynthetic penicillin with broad-spectrum activity.

作者信息

Bodey G P, Rodriguez V, Weaver S

出版信息

Antimicrob Agents Chemother. 1976 Apr;9(4):668-74. doi: 10.1128/AAC.9.4.668.

Abstract

Pirbenicillin is a new semisynthetic penicillin which inhibited 67% of isolates of Proteus aeruginosa tested in our laboratory, 93% of P. mirabilis, 31% of Enterobacter spp., 41% of Serratia spp., and 58% of Escherichia coli at a concentration of 6.25 mug/ml. Its activity appeared to be inoculum dependent and it was virtually inactive against 10(7) inocula of P. aeruginosa. It was more active than carbenicillin or ticarcillin, but less active than BL-P1654 against P. aeruginosa. Carbenicillin and ticarcillin appeared to be more active than pirbenicillin against Proteus spp., but pirbenicillin was active against some isolates of Klebsiella spp.

摘要

匹氨西林是一种新型半合成青霉素,在我们实验室中,其在浓度为6.25微克/毫升时,能抑制67%的铜绿假单胞菌分离株、93%的奇异变形杆菌、31%的肠杆菌属、41%的沙雷菌属以及58%的大肠杆菌。其活性似乎与接种量有关,对10⁷接种量的铜绿假单胞菌实际上无活性。它比羧苄西林或替卡西林更具活性,但对铜绿假单胞菌的活性比BL - P1654低。羧苄西林和替卡西林对变形杆菌属的活性似乎比匹氨西林更高,但匹氨西林对某些克雷伯菌属分离株有活性。

相似文献

1
Pirbenicillin, a new semisynthetic penicillin with broad-spectrum activity.
Antimicrob Agents Chemother. 1976 Apr;9(4):668-74. doi: 10.1128/AAC.9.4.668.
3
Comparative activity in vitro of ticarcillin, BL-P1654, and carbenicillin.
Antimicrob Agents Chemother. 1976 Aug;10(2):241-4. doi: 10.1128/AAC.10.2.241.
4
5
6
Laboratory studies with a new broad-spectrum penicillin, pirbenicillin.
Antimicrob Agents Chemother. 1976 Jun;9(6):975-82. doi: 10.1128/AAC.9.6.975.
7
In vitro activity of ticarcillin, carbenicillin and ampicillin against some gram-negative bacilli.
J Antibiot (Tokyo). 1975 Nov;28(11):912-9. doi: 10.7164/antibiotics.28.912.
8
In vitro studies of semisynthetic alpha-(substituted-ureido) penicillins.
Appl Microbiol. 1971 Apr;21(4):710-7. doi: 10.1128/am.21.4.710-717.1971.
10
Disparity between inhibitory and killing effects of BL-P1654.
Antimicrob Agents Chemother. 1975 Feb;7(2):215-8. doi: 10.1128/AAC.7.2.215.

引用本文的文献

2
CI-867, a new semisynthetic penicillin: in vitro studies.
Antimicrob Agents Chemother. 1980 Dec;18(6):939-43. doi: 10.1128/AAC.18.6.939.
3
Ticarcillin: a review of its pharmacological properties and therapeutic efficacy.
Drugs. 1980 Nov;20(5):325-52. doi: 10.2165/00003495-198020050-00001.
4
PC-904, a new semisynthetic penicillin.
Antimicrob Agents Chemother. 1978 Jan;13(1):14-8. doi: 10.1128/AAC.13.1.14.
5
7
Activity of azlocillin and mezlocillin against gram-negative organisms: comparison with other penicillins.
Antimicrob Agents Chemother. 1978 Apr;13(4):559-65. doi: 10.1128/AAC.13.4.559.
8
Azlocillin: in vitro studies of a new semisynthetic penicillin.
Antimicrob Agents Chemother. 1977 May;11(5):865-70. doi: 10.1128/AAC.11.5.865.

本文引用的文献

1
New semi-synthetic penicillin active against Pseudomonas pyocyanea.
Nature. 1967 Jul 1;215(5096):25-30. doi: 10.1038/215025a0.
3
In vitro studies of semisynthetic alpha-(substituted-ureido) penicillins.
Appl Microbiol. 1971 Apr;21(4):710-7. doi: 10.1128/am.21.4.710-717.1971.
4
Ticarcillin therapy of infections.
Antimicrob Agents Chemother. 1973 Oct;4(4):427-31. doi: 10.1128/AAC.4.4.427.
5
The hemostatic defect produced by carbenicillin.
N Engl J Med. 1974 Aug 8;291(6):265-70. doi: 10.1056/NEJM197408082910601.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验