• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

In vitro activity of A-16686, a new glycopeptide.

作者信息

Neu H C, Neu N M

出版信息

Chemotherapy. 1986;32(5):453-7. doi: 10.1159/000238450.

DOI:10.1159/000238450
PMID:3757587
Abstract

A-16686 is a novel glycopeptide antibiotic derived from Actinoplanes. A-16686 inhibited hemolytic streptococci groups A, B, C, F, and G at concentrations of less than or equal to 0.06 to 0.5 microgram/ml, with 90% inhibited by 0.5 microgram/ml, including erythromycin-resistant isolates. S. bovis, various viridans groups streptococci, S. mitis, S. mutans, and S. sanguis were inhibited by less than or equal to 1 microgram/ml, and MICs of S. faecalis and S. faecium were 0.5-2 micrograms/ml. Most staphylococci, including methicillin-resistant strains, were inhibited by 1 or 2 micrograms/ml. A-16686 was bactericidal with minimal difference between MIC and MBC for gram-positive species. A-16686 did not inhibit Enterobacteriaceae or Pseudomonas.

摘要

相似文献

1
In vitro activity of A-16686, a new glycopeptide.
Chemotherapy. 1986;32(5):453-7. doi: 10.1159/000238450.
2
A-16686, a new antibiotic from Actinoplanes. II. Biological properties.
J Antibiot (Tokyo). 1984 Apr;37(4):318-24. doi: 10.7164/antibiotics.37.318.
3
In vitro activities of two ketolides, HMR 3647 and HMR 3004, against gram-positive bacteria.两种酮内酯类药物HMR 3647和HMR 3004对革兰氏阳性菌的体外活性
Antimicrob Agents Chemother. 1999 Apr;43(4):930-6. doi: 10.1128/AAC.43.4.930.
4
In vitro activity of the new glycopeptide decaplanin.
Eur J Clin Microbiol Infect Dis. 1992 May;11(5):458-62. doi: 10.1007/BF01961864.
5
In vitro activity of LY146032 (daptomycin), a new peptolide.新型缩酚肽LY146032(达托霉素)的体外活性
Eur J Clin Microbiol. 1987 Feb;6(1):84-90. doi: 10.1007/BF02097208.
6
In vitro activities of two oxazolidinone antimicrobial agents, DuP 721 and DuP 105.两种恶唑烷酮类抗菌剂DuP 721和DuP 105的体外活性
Antimicrob Agents Chemother. 1988 Apr;32(4):580-3. doi: 10.1128/AAC.32.4.580.
7
In vitro evaluation of the new paulomycin antibiotic paldimycin.新型保洛霉素类抗生素帕地霉素的体外评价
Eur J Clin Microbiol. 1987 Jun;6(3):306-8. doi: 10.1007/BF02017620.
8
In vitro activity of LY146032 (daptomycin) against selected aerobic bacteria.LY146032(达托霉素)对特定需氧菌的体外活性。
Eur J Clin Microbiol. 1987 Feb;6(1):91-6. doi: 10.1007/BF02097209.
9
Comparative in vitro activity of the new glycopeptide SK&F 104662 against problematic gram-positive bacteria.新型糖肽SK&F 104662对难对付的革兰氏阳性菌的体外活性比较
Eur J Clin Microbiol Infect Dis. 1991 Sep;10(9):782-4. doi: 10.1007/BF01972511.
10
In vitro activity of decaplanin (M86-1410), a new glycopeptide antibiotic.新型糖肽类抗生素去甲普兰宁(M86-1410)的体外活性
Antimicrob Agents Chemother. 1992 Apr;36(4):873-5. doi: 10.1128/AAC.36.4.873.

引用本文的文献

1
Cyclic lipodepsipeptides: a new class of antibacterial agents in the battle against resistant bacteria.环状脂肽:对抗耐药菌的新型抗菌药物。
Future Med Chem. 2013 Jul;5(11):1311-30. doi: 10.4155/fmc.13.86.
2
Generation of ramoplanin-resistant Staphylococcus aureus.耐雷普霉素金黄色葡萄球菌的产生。
FEMS Microbiol Lett. 2010 Sep 1;310(2):104-11. doi: 10.1111/j.1574-6968.2010.02051.x. Epub 2010 Jul 2.
3
In vitro evaluation of ramoplanin (MDL 62198, A 16686).瑞莫拉宁(MDL 62198,A 16686)的体外评估
Eur J Clin Microbiol Infect Dis. 1988 Dec;7(6):819-21. doi: 10.1007/BF01975062.
4
In vitro activities of ramoplanin and four glycopeptide antibiotics against clinical isolates of Clostridium difficile.雷莫拉宁和四种糖肽类抗生素对艰难梭菌临床分离株的体外活性
Antimicrob Agents Chemother. 1991 Jan;35(1):195-7. doi: 10.1128/AAC.35.1.195.