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1
Activity of pirlimycin (U57930E) against strains of the Bacteroides fragilis group.吡利霉素(U57930E)对脆弱拟杆菌群菌株的活性。
Antimicrob Agents Chemother. 1982 Nov;22(5):893-4. doi: 10.1128/AAC.22.5.893.
2
In vitro activity of josamycin and rosamicin against Bacteroides fragilis compared with clindamycin, erythromycin, and metronidazole.与克林霉素、红霉素和甲硝唑相比,交沙霉素和蔷薇霉素对脆弱拟杆菌的体外活性。
Antimicrob Agents Chemother. 1976 Jul;10(1):188-90. doi: 10.1128/AAC.10.1.188.
3
Susceptibility of anaerobic bacteria to five antimicrobial agents and demonstration of resistance of Bacteroides fragilis to clindamycin.厌氧菌对五种抗菌剂的敏感性及脆弱拟杆菌对克林霉素耐药性的证明。
Methods Find Exp Clin Pharmacol. 1982;4(3):173-7.
4
[Activity of seven antimicrobial agents against "Bacteroides fragilis" (author's transl)].七种抗菌剂对脆弱拟杆菌的活性(作者译)
Ann Microbiol (Paris). 1980 Jan-Feb;131(1):39-44.
5
Characterization of bactericidal activity of clindamycin against Bacteroides fragilis via kill curve methods.通过杀菌曲线法表征克林霉素对脆弱拟杆菌的杀菌活性。
Antimicrob Agents Chemother. 1996 Aug;40(8):1941-4. doi: 10.1128/AAC.40.8.1941.
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Synthesis and antimicrobial activity of clindamycin analogues: pirlimycin, 1,2 a potent antibacterial agent.克林霉素类似物的合成与抗菌活性:吡利霉素,一种强效抗菌剂。
J Med Chem. 1984 Feb;27(2):216-23. doi: 10.1021/jm00368a020.
7
Bacteroides fragilis resistance to clindamycin in vitro.脆弱拟杆菌对克林霉素的体外耐药性。
Antimicrob Agents Chemother. 1982 Nov;22(5):771-4. doi: 10.1128/AAC.22.5.771.
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Bacteriostatic and bactericidal activities of various antibiotics against Bacteroides fragilis.多种抗生素对脆弱拟杆菌的抑菌和杀菌活性
Antimicrob Agents Chemother. 1973 Feb;3(2):152-6. doi: 10.1128/AAC.3.2.152.
9
Comparison of the bactericidal activity of clindamycin and metronidazole against cefoxitin-susceptible and cefoxitin-resistant isolates of the Bacteroides fragilis group.克林霉素和甲硝唑对脆弱拟杆菌群中对头孢西丁敏感及耐药菌株的杀菌活性比较。
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10
Bactericidal activity of ceftizoxime, cefotetan, and clindamycin against cefoxitin-resistant strains of the Bacteroides fragilis group.头孢唑肟、头孢替坦和克林霉素对脆弱拟杆菌群耐头孢西丁菌株的杀菌活性。
J Antimicrob Chemother. 1991 Nov;28(5):701-5. doi: 10.1093/jac/28.5.701.

本文引用的文献

1
Novel method for detection of beta-lactamases by using a chromogenic cephalosporin substrate.一种使用显色头孢菌素底物检测β-内酰胺酶的新方法。
Antimicrob Agents Chemother. 1972 Apr;1(4):283-8. doi: 10.1128/AAC.1.4.283.
2
Bacteroides fragilis resistant to the administration of clindamycin.脆弱拟杆菌对克林霉素给药耐药。
Am J Med. 1976 Mar;60(3):426-8. doi: 10.1016/0002-9343(76)90759-2.
3
Medium for use in antibiotic susceptibility testing of anaerobic bacteria.用于厌氧菌抗生素敏感性测试的培养基。
Antimicrob Agents Chemother. 1976 Dec;10(6):926-8. doi: 10.1128/AAC.10.6.926.
4
In vitro susceptibility studies with piromidic acid.吡咯米酸的体外药敏试验。
J Antimicrob Chemother. 1978 May;4(3):289-91. doi: 10.1093/jac/4.3.289.

吡利霉素(U57930E)对脆弱拟杆菌群菌株的活性。

Activity of pirlimycin (U57930E) against strains of the Bacteroides fragilis group.

作者信息

Garcia-Rodriguez J A, Garcia-Sanchez J E, Prieto J, Sanchez de S Lorenzo A

出版信息

Antimicrob Agents Chemother. 1982 Nov;22(5):893-4. doi: 10.1128/AAC.22.5.893.

DOI:10.1128/AAC.22.5.893
PMID:7181494
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC185677/
Abstract

The activities of pirlimycin (U57930E), lincomycin, clindamycin, erythromycin, josamycin, oleandomycin, and spiramycin were compared against strains of the Bacteroides fragilis group. Pirlimycin was the most active; the 90% minimal inhibitory concentration was 1 microgram/ml, and the activity range was 0.125 to 4 micrograms/ml. This drug was fourfold more active than any of the other drugs, including clindamycin. The minimal bactericidal concentration (range, 0.5 to 16 micrograms/ml) shows that pirlimycin behaves as a bacteriostatic antibiotic.

摘要

比较了吡利霉素(U57930E)、林可霉素、克林霉素、红霉素、交沙霉素、竹桃霉素和螺旋霉素对脆弱拟杆菌属菌株的活性。吡利霉素活性最强;90%最小抑菌浓度为1微克/毫升,活性范围为0.125至4微克/毫升。该药物的活性比包括克林霉素在内的其他任何药物都高四倍。最小杀菌浓度(范围为0.5至16微克/毫升)表明吡利霉素表现为一种抑菌性抗生素。