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抗菌药物研发:正确行事。

Antibacterial drug discovery: doing it right.

作者信息

Gengenbacher Martin, Dick Thomas

机构信息

Tuberculosis Research Laboratory, Department of Microbiology, Yong Loo Lin School of Medicine, National University Health System, National University of Singapore, Singapore 117545, Republic of Singapore.

Antibacterial Drug Discovery Laboratory, Department of Microbiology, Yong Loo Lin School of Medicine, National University Health System, National University of Singapore, Singapore 117545, Republic of Singapore.

出版信息

Chem Biol. 2015 Jan 22;22(1):5-6. doi: 10.1016/j.chembiol.2014.12.005.

DOI:10.1016/j.chembiol.2014.12.005
PMID:25615950
Abstract

Antibacterial drug discovery needs to develop new strategies to identify attractive hit-target couples for more effective lead finding and optimization. In this issue of Chemistry & Biology, Park and coworkers describe a novel target-based whole cell combination screening approach resulting in the identification of new inhibitors of biotin biosynthesis in Mycobacterium tuberculosis.

摘要

抗菌药物研发需要制定新策略,以识别有吸引力的命中靶点组合,从而更有效地发现和优化先导化合物。在本期《化学生物学》中,帕克及其同事描述了一种基于靶点的新型全细胞组合筛选方法,该方法鉴定出了结核分枝杆菌生物素生物合成的新抑制剂。

相似文献

1
Antibacterial drug discovery: doing it right.抗菌药物研发:正确行事。
Chem Biol. 2015 Jan 22;22(1):5-6. doi: 10.1016/j.chembiol.2014.12.005.
2
Biotin biosynthesis in Mycobacterium tuberculosis: physiology, biochemistry and molecular intervention.结核分枝杆菌生物素生物合成:生理学、生物化学和分子干预。
Protein Cell. 2011 Sep;2(9):691-5. doi: 10.1007/s13238-011-1100-8.
3
Computationally Guided Identification of Novel Mycobacterium tuberculosis GlmU Inhibitory Leads, Their Optimization, and in Vitro Validation.基于计算引导的新型结核分枝杆菌GlmU抑制剂先导化合物的鉴定、优化及体外验证
ACS Comb Sci. 2016 Feb 8;18(2):100-16. doi: 10.1021/acscombsci.5b00019. Epub 2016 Jan 28.
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Next-generation antimicrobials: from chemical biology to first-in-class drugs.下一代抗菌药物:从化学生物学到一流药物
Arch Pharm Res. 2015 Sep;38(9):1702-17. doi: 10.1007/s12272-015-0645-0. Epub 2015 Aug 11.
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Identification of a novel class of small compounds with anti-tuberculosis activity by in silico structure-based drug screening.通过基于结构的计算机辅助药物筛选鉴定一类具有抗结核活性的新型小分子化合物。
J Antibiot (Tokyo). 2017 Nov;70(11):1057-1064. doi: 10.1038/ja.2017.106. Epub 2017 Sep 27.
6
Engineering another class of anti-tubercular lead: Hit to lead optimization of an intriguing class of gyrase ATPase inhibitors.工程另一类抗结核先导化合物:拓扑异构酶 ATP 酶抑制剂这一有趣类别中的命中到先导优化。
Eur J Med Chem. 2016 Oct 21;122:216-231. doi: 10.1016/j.ejmech.2016.06.042. Epub 2016 Jun 24.
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In silico analyses for the discovery of tuberculosis drug targets.用于发现结核病药物靶点的计算机模拟分析。
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Discovery of antibacterial biotin carboxylase inhibitors by virtual screening and fragment-based approaches.通过虚拟筛选和基于片段的方法发现抗菌生物素羧化酶抑制剂。
ACS Chem Biol. 2009 Jun 19;4(6):473-83. doi: 10.1021/cb9000102.
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Encoded library technology as a source of hits for the discovery and lead optimization of a potent and selective class of bactericidal direct inhibitors of Mycobacterium tuberculosis InhA.编码文库技术作为发现和优化强效和选择性杀菌直接抑制剂的新型结核分枝杆菌 InhA 的来源。
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Identification of new antibacterial targets in RNA polymerase of Mycobacterium tuberculosis by detecting positive selection sites.通过检测正选择位点鉴定结核分枝杆菌RNA聚合酶中的新抗菌靶点。
Comput Biol Chem. 2018 Apr;73:25-30. doi: 10.1016/j.compbiolchem.2017.11.002. Epub 2017 Nov 21.

引用本文的文献

1
Brief Overview of Approaches and Challenges in New Antibiotic Development: A Focus On Drug Repurposing.新型抗生素开发方法与挑战简述:以药物再利用为重点
Front Cell Infect Microbiol. 2021 May 17;11:684515. doi: 10.3389/fcimb.2021.684515. eCollection 2021.
2
in the Face of Host-Imposed Nutrient Limitation.在面临宿主施加的营养限制时。
Microbiol Spectr. 2017 Jun;5(3). doi: 10.1128/microbiolspec.TBTB2-0030-2016.
3
Synthesis and evaluation of functionalized benzoboroxoles as potential -tuberculosis agents.功能化苯并硼恶唑作为潜在抗结核药物的合成与评价
Tetrahedron. 2016 Jun 30;72(26):3795-3801. doi: 10.1016/j.tet.2016.03.038. Epub 2016 Mar 17.
4
Allocyclinones, hyperchlorinated angucyclinones from Actinoallomurus.别构环素,来自异壁放线菌属的高度氯化安古霉素类化合物。
J Antibiot (Tokyo). 2017 Jan;70(1):73-78. doi: 10.1038/ja.2016.62. Epub 2016 May 25.
5
Discovery and characterization of natural tropolones as inhibitors of the antibacterial target CapF from Staphylococcus aureus.天然托酚酮作为金黄色葡萄球菌抗菌靶点CapF抑制剂的发现与表征
Sci Rep. 2015 Oct 16;5:15337. doi: 10.1038/srep15337.