• 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

抗生素研发进程中的新进展。

What's new in the antibiotic pipeline.

作者信息

Lee V J, Miller G H, Yagisawa M

机构信息

Microcide Pharmaceuticals Inc. 850 Maude Avenue, Mountain View, CA 94043, USA. mailto:

出版信息

Curr Opin Microbiol. 1999 Oct;2(5):475-82. doi: 10.1016/s1369-5274(99)00003-x.

DOI:10.1016/s1369-5274(99)00003-x
PMID:10508732
Abstract

Many advances have recently been made in the development of chemotherapeutic agents for bacterial infections. As a consequence of problematic antimicrobial-resistant bacteria, research is now directed towards narrow-spectrum agents rather than broad-spectrum agents. Further, orally active agents have always been desirable, but today's cost-saving environment, in line with a desire to minimize treatment costs, values reduced administration costs and keeping patients out of the hospital. There has been a recent increase in research into orally active antibacterial agents, such as carbapenems and cephalosporins, and non-glycopeptide natural products.

摘要

最近在用于细菌感染的化疗药物开发方面取得了许多进展。由于存在有问题的抗菌耐药细菌,现在的研究方向是窄谱药物而非广谱药物。此外,口服活性药物一直是人们所期望的,而在当今注重节约成本的环境下,出于将治疗成本降至最低的愿望,人们重视降低给药成本并让患者无需住院。最近对口服活性抗菌药物的研究有所增加,如碳青霉烯类和头孢菌素类,以及非糖肽类天然产物。

相似文献

1
What's new in the antibiotic pipeline.抗生素研发进程中的新进展。
Curr Opin Microbiol. 1999 Oct;2(5):475-82. doi: 10.1016/s1369-5274(99)00003-x.
2
What's new on the antimicrobial horizon?抗菌领域有哪些新进展?
Int J Antimicrob Agents. 2008 Dec;32 Suppl 4:S207-13. doi: 10.1016/S0924-8579(09)70004-4.
3
What's new and not so new on the antimicrobial horizon?抗菌领域有哪些新进展和并非全新的情况?
Clin Microbiol Infect. 2008 Dec;14 Suppl 6:19-29. doi: 10.1111/j.1469-0691.2008.02124.x.
4
[A choice of antibacterial chemotherapy for nosocomial infections caused by pathogens producing broad-spectrum beta-lactamases].
Antibiot Khimioter. 2001;46(12):3-7.
5
Fighting antibiotic resistance.对抗抗生素耐药性。
Science. 1994 Dec 2;266(5190):1462. doi: 10.1126/science.7985006.
6
Late stage antibacterial drugs in the clinical pipeline.临床研发阶段的晚期抗菌药物。
Curr Opin Microbiol. 2007 Oct;10(5):441-6. doi: 10.1016/j.mib.2007.08.007. Epub 2007 Oct 22.
7
Pathogens resistant to antimicrobial agents. Epidemiology, molecular mechanisms, and clinical management.对抗菌药物耐药的病原体。流行病学、分子机制及临床管理。
Infect Dis Clin North Am. 2000 Jun;14(2):293-319. doi: 10.1016/s0891-5520(05)70249-x.
8
New developments in carbapenems.碳青霉烯类药物的新进展。
Clin Microbiol Infect. 2008 Dec;14(12):1102-11. doi: 10.1111/j.1469-0691.2008.02101.x.
9
Interaction between antimicrobial consumption and selection of resistant bacterial strains.抗菌药物使用与耐药菌株选择之间的相互作用。
Scand J Infect Dis Suppl. 1990;70:18-24.
10
Mechanisms of bacterial resistance to antimicrobial agents.细菌对抗菌药物的耐药机制。
J Med Liban. 2000 Jul-Aug;48(4):186-98.

引用本文的文献

1
Structural and Functional analysis of Staphylococcus aureus NADP-dependent IDH and its comparison with Bacterial and Human NADPdependent IDH.金黄色葡萄球菌NADP依赖型异柠檬酸脱氢酶的结构与功能分析及其与细菌和人类NADP依赖型异柠檬酸脱氢酶的比较。
Bioinformation. 2014 Feb 19;10(2):81-6. doi: 10.6026/97320630010081. eCollection 2014.
2
Cloning, expression, purification and characterization of UMP kinase from Staphylococcus aureus.从金黄色葡萄球菌中克隆、表达、纯化和鉴定 UMP 激酶。
Protein J. 2012 Apr;31(4):345-52. doi: 10.1007/s10930-012-9410-0.
3
Structural basis for effectiveness of siderophore-conjugated monocarbams against clinically relevant strains of Pseudomonas aeruginosa.
铁载体偶联单碳青霉烯类化合物对临床相关铜绿假单胞菌的有效性的结构基础。
Proc Natl Acad Sci U S A. 2010 Dec 21;107(51):22002-7. doi: 10.1073/pnas.1013092107. Epub 2010 Dec 6.
4
Inhibition of class A beta-lactamases by carbapenems: crystallographic observation of two conformations of meropenem in SHV-1.碳青霉烯类对A类β-内酰胺酶的抑制作用:美罗培南在SHV-1中两种构象的晶体学观察
J Am Chem Soc. 2008 Sep 24;130(38):12656-62. doi: 10.1021/ja7111146. Epub 2008 Aug 30.
5
Structures of S. aureus thymidylate kinase reveal an atypical active site configuration and an intermediate conformational state upon substrate binding.金黄色葡萄球菌胸苷酸激酶的结构揭示了一个非典型的活性位点构型以及底物结合时的一种中间构象状态。
Protein Sci. 2006 Apr;15(4):774-84. doi: 10.1110/ps.052002406. Epub 2006 Mar 7.