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1
Mecillinam, a novel penicillanic acid derivative with unusual activity against gram-negative bacteria.美西林,一种新型青霉素酸衍生物,对革兰氏阴性菌具有独特活性。
Antimicrob Agents Chemother. 1976 May;9(5):793-9. doi: 10.1128/AAC.9.5.793.
2
Synergy of mecillinam, a beta-amidinopenicillanic acid derivative, combined with beta-lactam antibiotics.β-脒基青霉素酸衍生物美西林与β-内酰胺类抗生素的协同作用。
Antimicrob Agents Chemother. 1976 Sep;10(3):535-42. doi: 10.1128/AAC.10.3.535.
3
Mecillinam (FL 1060), a 6beta-amidinopenicillanic acid derivative: in vitro evaluation.美西林(FL 1060),一种6β-脒基青霉烷酸衍生物:体外评价
Antimicrob Agents Chemother. 1975 Sep;8(3):266-70. doi: 10.1128/AAC.8.3.266.
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Piperacillin, a new penicillin active against many bacteria resistant to other penicillins.哌拉西林,一种新型青霉素,对许多耐其他青霉素的细菌有活性。
Antimicrob Agents Chemother. 1978 Mar;13(3):358-67. doi: 10.1128/AAC.13.3.358.
5
In vitro activity of apalcillin compared with that of other new penicillins and anti-Pseudomonas cephalosporins.阿帕西林与其他新型青霉素及抗假单胞菌头孢菌素的体外活性比较。
Antimicrob Agents Chemother. 1982 Jun;21(6):906-11. doi: 10.1128/AAC.21.6.906.
6
Azlocillin and mezlocillin: new ureido penicillins.阿洛西林和美洛西林:新型脲基青霉素。
Antimicrob Agents Chemother. 1978 Jun;13(6):930-8. doi: 10.1128/AAC.13.6.930.
7
Laboratory studies on mecillinam: activity alone and combined with cephradine.美西林的实验室研究:单独及与头孢拉定联合使用时的活性
J Antimicrob Chemother. 1977 Jul;3 Suppl B:53-8. doi: 10.1093/jac/3.suppl_b.53.
8
In-vitro activity of the combinations of ampicillin with mecillinam or with beta-lactamase inhibitors against strains resistant to ampicillin.氨苄西林与美西林或β-内酰胺酶抑制剂联合使用对氨苄西林耐药菌株的体外活性。
J Antimicrob Chemother. 1985 Dec;16(6):719-25. doi: 10.1093/jac/16.6.719.
9
Semisynthetic penicillin 6-(D(--)-alpha-carboxy-3-thienylacetamido) penicillanic acid active against Pseudomonas in vitro.半合成青霉素6 -(D(-)-α-羧基-3-噻吩基乙酰胺基)青霉烷酸在体外对假单胞菌有活性。
Appl Microbiol. 1971 Jan;21(1):66-70. doi: 10.1128/am.21.1.66-70.1971.
10
Comparative in vitro antibacterial activity of seven semi-synthetic penicillins against aerobic gram-negative bacteria and enterococci.七种半合成青霉素对需氧革兰氏阴性菌和肠球菌的体外抗菌活性比较
Infection. 1982;10 Suppl 3:S249-56. doi: 10.1007/BF01640683.

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Resistance to Mecillinam and Nine Other Antibiotics for Oral Use in Isolated from Urine Specimens of Primary Care Patients in Germany, 2019/20.2019/20年从德国初级保健患者尿液样本中分离出的对美西林和其他九种口服抗生素的耐药性
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The Chemical Relationship Among Beta-Lactam Antibiotics and Potential Impacts on Reactivity and Decomposition.β-内酰胺类抗生素之间的化学关系及其对反应活性和分解的潜在影响。
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Penicillins. A current review of their clinical pharmacology and therapeutic use.青霉素。对其临床药理学和治疗用途的当前综述。
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8
Comparative in vitro antibacterial activity of seven semi-synthetic penicillins against aerobic gram-negative bacteria and enterococci.七种半合成青霉素对需氧革兰氏阴性菌和肠球菌的体外抗菌活性比较
Infection. 1982;10 Suppl 3:S249-56. doi: 10.1007/BF01640683.
9
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Antimicrob Agents Chemother. 1983 Jun;23(6):827-30. doi: 10.1128/AAC.23.6.827.
10
Pharmacokinetics of bacmecillinam and pivmecillinam in volunteers.巴美西林和匹美西林在志愿者体内的药代动力学。
Eur J Clin Pharmacol. 1982;23(3):249-52. doi: 10.1007/BF00547563.

本文引用的文献

1
Cefamandole, a cephalosporin antibiotic with an unusually wide spectrum of activity.头孢孟多,一种具有异常广泛活性谱的头孢菌素抗生素。
Antimicrob Agents Chemother. 1974 Aug;6(2):177-82. doi: 10.1128/AAC.6.2.177.
2
Cefoxitin, a semisynthetic cephamycin antibiotic: antibacterial spectrum and resistance to hydrolysis by gram-negative beta-lactamases.头孢西丁,一种半合成头孢霉素抗生素:抗菌谱及对革兰氏阴性β-内酰胺酶水解的抗性。
Antimicrob Agents Chemother. 1974 Aug;6(2):170-6. doi: 10.1128/AAC.6.2.170.
3
A comparative study of eight distinct beta-lactamases synthesized by gram-negative bacteria.对革兰氏阴性菌合成的八种不同β-内酰胺酶的比较研究。
J Gen Microbiol. 1970 Apr;61(1):43-61. doi: 10.1099/00221287-61-1-43.
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Antibiotic resistance of salmonella in northeastern United States 1968-199.1968 - 199年美国东北部沙门氏菌的抗生素耐药性
N Y State J Med. 1971 Jun 1;71(11):1196-200.
5
Mechanism of action and development of resistance to a new amidino penicillin.一种新型脒基青霉素的作用机制及耐药性发展
J Bacteriol. 1974 Feb;117(2):578-87. doi: 10.1128/jb.117.2.578-587.1974.
6
FL-1060: a new penicillin with a unique mode of action.FL-1060:一种具有独特作用方式的新型青霉素。
Biochem Biophys Res Commun. 1973 Apr 16;51(4):863-8. doi: 10.1016/0006-291x(73)90006-5.
7
The effect of osmolality on the response of Escherichia coli and Proteus mirabilis to penicillins.渗透压摩尔浓度对大肠杆菌和奇异变形杆菌对青霉素反应的影响。
Br J Exp Pathol. 1972 Oct;53(5):457-64.
8
6 -amidinopenicillanic acids--a new group of antibiotics.6-脒基青霉烷酸——一类新型抗生素。
Nat New Biol. 1972 Apr 5;236(66):135-7. doi: 10.1038/newbio236135a0.
9
Light and electron microscopy of the early response of Escherichia coli to a 6beta-amidinopenicillanic acid (FL 1060).大肠杆菌对6β-脒基青霉烷酸(FL 1060)早期反应的光学显微镜和电子显微镜观察
Acta Pathol Microbiol Scand B Microbiol Immunol. 1973 Aug;81(4):393-407. doi: 10.1111/j.1699-0463.1973.tb02222.x.
10
FL 1060: a new beta-lactam antibiotic with novel properties.FL 1060:一种具有新型特性的新型β-内酰胺抗生素。
J Clin Pathol. 1973 Jan;26(1):1-6. doi: 10.1136/jcp.26.1.1.

美西林,一种新型青霉素酸衍生物,对革兰氏阴性菌具有独特活性。

Mecillinam, a novel penicillanic acid derivative with unusual activity against gram-negative bacteria.

作者信息

Neu H C

出版信息

Antimicrob Agents Chemother. 1976 May;9(5):793-9. doi: 10.1128/AAC.9.5.793.

DOI:10.1128/AAC.9.5.793
PMID:949176
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC429623/
Abstract

The in vitro activity of mecillinam, a 6 beta-amidinopenicillanic acid derivative, was investigated. Mecillinam is not active against most gram-positive coccal or bacilliary forms. Many members of the Enterobacteriaceae are inhibited, with 86% of Escherichia coli, 71% of Klebsiella, 62% of Enterobacter, 75% of Salmonella, 69% of Shigella, and 70% of Citrobacter inhibited by 6.3 mug/ml. Indole-positive Proteus and Serratia were generally resistant as are Pseudomonas strains. Although mecillinam is hydrolyzed by gram-negative beta-lactamases, the compound inhibits beta-lactamase-producing organisms, particularly E. coli. The conductivity of medium used to determine minimal inhibitory concentration and inoculum size produce markedly different values. In medium of high conductivity, 10 mS, mecillinam is inactive against many strains of bacteria. In all media there is a great difference between the minimal inhibitory and minimal bactericidal levels.

摘要

对6β-脒基青霉烷酸衍生物美西林的体外活性进行了研究。美西林对大多数革兰氏阳性球菌或杆菌形式无活性。许多肠杆菌科成员受到抑制,6.3微克/毫升可抑制86%的大肠杆菌、71%的克雷伯菌、62%的肠杆菌、75%的沙门氏菌、69%的志贺氏菌和70%的柠檬酸杆菌。吲哚阳性变形杆菌和沙雷氏菌通常耐药,假单胞菌菌株也是如此。虽然美西林可被革兰氏阴性β-内酰胺酶水解,但该化合物可抑制产β-内酰胺酶的生物体,尤其是大肠杆菌。用于确定最低抑菌浓度的培养基电导率和接种量会产生明显不同的值。在高电导率(10毫西门子)的培养基中,美西林对许多细菌菌株无活性。在所有培养基中,最低抑菌水平和最低杀菌水平之间存在很大差异。