• 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

天然呋喃香豆素白当归脑衍生的香豆素-1,2,3-三唑杂合体的设计、合成与抗菌活性

Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin.

机构信息

Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Lavrentyev Ave. 9, 630090 Novosibirsk, Russia.

Department of Microbiology, Immunology and Virology, Novosibirsk State Medical University, Krasny Prospect 52, 630091 Novosibirsk, Russia.

出版信息

Molecules. 2019 Jun 5;24(11):2126. doi: 10.3390/molecules24112126.

DOI:10.3390/molecules24112126
PMID:31195697
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6600338/
Abstract

Synthesis of 1,2,3-triazole-substituted coumarins and also 1,2,3-triazolyl or 1,2,3-triazolylalk-1-inyl-linked coumarin-2,3-furocoumarin hybrids was performed by employing the cross-coupling and copper catalyzed azide-alkyne cycloaddition reaction approaches. The synthesized compounds were evaluated for their in vitro antibacterial activity against , , and bacterial strains. Coumarin-benzoic acid hybrids , and 3-((4-acetylamino-3-(methoxycarbonyl)phenyl)ethynyl)coumarin () showed promising activity against . strains, and the 1,2,3-triazolyloct-1-inyl linked coumarin-2,3-furocoumarin hybrid was endowed with high selectivity against and species. The in vitro antibacterial activity of , , and can potentially be compared with that of a number of modern antibiotic drugs used in the clinic, suggesting promising prospects for further research. A detailed study of the molecular interactions with the targeted protein MurB was performed using docking simulations and the obtained results are quite promising.

摘要

通过交叉偶联和铜催化叠氮-炔环加成反应方法,合成了 1,2,3-三唑取代香豆素以及 1,2,3-三唑基或 1,2,3-三唑基炔-1-基连接的香豆素-2,3-呋喃香豆素杂合体。合成的化合物被评估了它们对 、 、 和 细菌菌株的体外抗菌活性。香豆素-苯甲酸杂合体 、 和 3-((4-乙酰氨基-3-(甲氧基羰基)苯基)乙炔基)香豆素()对 表现出有希望的活性。菌株,而 1,2,3-三唑基辛-1-基连接的香豆素-2,3-呋喃香豆素杂合体对 和 种具有高选择性。和 的体外抗菌活性可能与临床上使用的许多现代抗生素药物相当,这表明进一步研究具有广阔的前景。使用对接模拟对与靶蛋白 MurB 的分子相互作用进行了详细研究,得到的结果非常有前途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/b5f1417cf7e6/molecules-24-02126-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/7929b29ce312/molecules-24-02126-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/88eeb6d67328/molecules-24-02126-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/d26307eda648/molecules-24-02126-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/1e9d4783a197/molecules-24-02126-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/c5c452ddff6d/molecules-24-02126-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/5747234dadef/molecules-24-02126-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/b5f1417cf7e6/molecules-24-02126-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/7929b29ce312/molecules-24-02126-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/88eeb6d67328/molecules-24-02126-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/d26307eda648/molecules-24-02126-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/1e9d4783a197/molecules-24-02126-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/c5c452ddff6d/molecules-24-02126-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/5747234dadef/molecules-24-02126-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188d/6600338/b5f1417cf7e6/molecules-24-02126-g003a.jpg

相似文献

1
Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin.天然呋喃香豆素白当归脑衍生的香豆素-1,2,3-三唑杂合体的设计、合成与抗菌活性
Molecules. 2019 Jun 5;24(11):2126. doi: 10.3390/molecules24112126.
2
Synthesis, in vitro anticancer and antibacterial activities and in silico studies of new 4-substituted 1,2,3-triazole-coumarin hybrids.新型 4-取代 1,2,3-三唑-香豆素杂合体的合成、体外抗癌和抗菌活性及计算机研究。
Eur J Med Chem. 2016 Nov 29;124:794-808. doi: 10.1016/j.ejmech.2016.08.062. Epub 2016 Aug 31.
3
Synthesis, in vivo Anticoagulant Evaluation and Molecular Docking Studies of Bicoumarins Obtained from Furocoumarin Peucedanin.从呋喃香豆素前胡素中获得的双香豆素的合成、体内抗凝评估及分子对接研究
Med Chem. 2016;12(7):674-683. doi: 10.2174/1573406412666160129105115.
4
Click-chemistry-inspired synthesis of new series of 1,2,3-triazole fused chromene with glucose triazole conjugates: Antibacterial activity assessment with molecular docking evaluation.点击化学启发的新型 1,2,3-三唑并色烯与葡萄糖三唑缀合物系列的合成:结合分子对接评价的抗菌活性评估。
Carbohydr Res. 2024 Sep;543:109222. doi: 10.1016/j.carres.2024.109222. Epub 2024 Jul 30.
5
Synthesis of 1H-1,2,3-triazole linked aryl(arylamidomethyl) - dihydrofurocoumarin hybrids and analysis of their cytotoxicity.1H-1,2,3-三唑连接的芳基(芳酰胺甲基)-二氢呋喃并香豆素杂合体的合成及其细胞毒性分析。
Eur J Med Chem. 2015 Jul 15;100:119-28. doi: 10.1016/j.ejmech.2015.05.016. Epub 2015 May 12.
6
1H-1,2,3-Triazolyl-substituted 1,3,4-oxadiazole derivatives containing structural features of ibuprofen/naproxen: Their synthesis and antibacterial evaluation.含布洛芬/萘普生结构特征的1H-1,2,3-三唑基取代的1,3,4-恶二唑衍生物:其合成与抗菌评价
Bioorg Med Chem Lett. 2016 Nov 1;26(21):5212-5217. doi: 10.1016/j.bmcl.2016.09.059. Epub 2016 Sep 25.
7
Synthesis, characterization and antibacterial activity of some triazole Mannich bases carrying diphenylsulfone moieties.一些带有二苯砜基团的三唑曼尼希碱的合成、表征及抗菌活性
Eur J Med Chem. 2009 Jul;44(7):3083-9. doi: 10.1016/j.ejmech.2008.07.003. Epub 2008 Jul 12.
8
Oxazolone-1,2,3-Triazole Hybrids: Design, Synthesis and Antimicrobial Evaluation.噁唑烷-1,2,3-三唑杂合体的设计、合成与抗菌评价。
Curr Top Med Chem. 2018;18(17):1506-1513. doi: 10.2174/1568026618666180913110456.
9
Synthesis, molecular docking, and evaluation of antibacterial activity of 1,2,4-triazole-norfloxacin hybrids.合成、分子对接及 1,2,4-三唑-诺氟沙星杂合体的抗菌活性评价。
Bioorg Chem. 2021 Oct;115:105270. doi: 10.1016/j.bioorg.2021.105270. Epub 2021 Aug 17.
10
Design, Synthesis and Antibacterial Evaluation of Compounds Based on New Benzoxepine-oxime-1,2,3-triazole Hybrid.基于新型苯并[B]氧杂环庚烯-肟-1,2,3-三唑杂合的设计、合成与抗菌评价。
Mini Rev Med Chem. 2018;18(9):803-809. doi: 10.2174/1389557517666170717123741.

引用本文的文献

1
Mitigating Antimicrobial Resistance through Strategic Design of Multimodal Antibacterial Agents Based on 1,2,3-Triazole with Click Chemistry.基于点击化学的1,2,3-三唑多模态抗菌剂的策略性设计以减轻抗菌药物耐药性
ACS Bio Med Chem Au. 2025 Mar 17;5(4):486-504. doi: 10.1021/acsbiomedchemau.4c00132. eCollection 2025 Aug 20.
2
Computational Investigation of Montelukast and Its Structural Derivatives for Binding Affinity to Dopaminergic and Serotonergic Receptors: Insights from a Comprehensive Molecular Simulation.孟鲁司特及其结构衍生物与多巴胺能和5-羟色胺能受体结合亲和力的计算研究:综合分子模拟的见解
Pharmaceuticals (Basel). 2025 Apr 10;18(4):559. doi: 10.3390/ph18040559.
3

本文引用的文献

1
Comprehensive review on the anti-bacterial activity of 1,2,3-triazole hybrids.1,2,3-三唑杂合物的抗菌活性的综合评价
Eur J Med Chem. 2019 Apr 15;168:357-372. doi: 10.1016/j.ejmech.2019.02.055. Epub 2019 Feb 22.
2
On the relationship of anthranilic derivatives structure and the FXR (Farnesoid X receptor) agonist activity.关于邻氨基苯甲酸衍生物结构与 FXR(法尼醇 X 受体)激动剂活性的关系。
J Biomol Struct Dyn. 2018 Dec;36(16):4378-4391. doi: 10.1080/07391102.2017.1417161. Epub 2018 Jan 10.
3
Coumarin derivatives: an updated patent review (2015-2016).
Antibacterial Activity for Synthesized Coumarin Derivatives and a Coumarin Component of Lime Peel ().
合成香豆素衍生物及酸橙皮中一种香豆素成分的抗菌活性。
Bioengineering (Basel). 2024 Jul 24;11(8):752. doi: 10.3390/bioengineering11080752.
4
A Pharmacological Update of Triazole Derivative: A Review.三唑衍生物的药理学更新:综述。
Curr Top Med Chem. 2024;24(23):2033-2049. doi: 10.2174/0115680266308359240708094001.
5
The impact of continuous cultivation of Ganoderma lucidum on soil nutrients, enzyme activity, and fruiting body metabolites.灵芝连续栽培对土壤养分、酶活性和子实体代谢物的影响。
Sci Rep. 2024 May 2;14(1):10097. doi: 10.1038/s41598-024-60750-y.
6
In-silico identification and exploration of small molecule coumarin-1,2,3-triazole hybrids as potential EGFR inhibitors for targeting lung cancer.计算机模拟鉴定和探索小分子香豆素-1,2,3-三唑杂化物作为靶向肺癌的潜在表皮生长因子受体(EGFR)抑制剂
Mol Divers. 2024 Dec;28(6):4301-4324. doi: 10.1007/s11030-024-10817-9. Epub 2024 Mar 12.
7
Anti-Tuberculosis Mur Inhibitors: Structural Insights and the Way Ahead for Development of Novel Agents.抗结核分枝杆菌抑制剂:结构见解与新型药物开发的未来方向
Pharmaceuticals (Basel). 2023 Mar 1;16(3):377. doi: 10.3390/ph16030377.
8
Effects of Coumarin on Rhizosphere Microbiome and Metabolome of .香豆素对[具体植物名称]根际微生物组和代谢组的影响
Plants (Basel). 2023 Mar 1;12(5):1096. doi: 10.3390/plants12051096.
9
Synthesis and biological evaluation of new 3-substituted coumarin derivatives as selective inhibitors of human carbonic anhydrase IX and XII.新型 3-取代香豆素衍生物的合成及作为人碳酸酐酶 IX 和 XII 的选择性抑制剂的生物评价。
J Enzyme Inhib Med Chem. 2023 Dec;38(1):2185760. doi: 10.1080/14756366.2023.2185760.
10
Coumarin Triazoles as Potential Antimicrobial Agents.香豆素三唑类作为潜在的抗菌剂。
Antibiotics (Basel). 2023 Jan 12;12(1):160. doi: 10.3390/antibiotics12010160.
香豆素衍生物:最新专利综述(2015 - 2016年)
Expert Opin Ther Pat. 2017 Nov;27(11):1201-1226. doi: 10.1080/13543776.2017.1360284. Epub 2017 Aug 14.
4
Rapid Access to Oxazine Fused Furocoumarins and in vivo and in silico Studies of theirs Biological Activity.快速获取噁嗪稠合呋喃香豆素及其生物活性的体内和计算机模拟研究
Med Chem. 2017;13(7):625-632. doi: 10.2174/1573406413666170601114527.
5
Macromolecular agents with antimicrobial potentialities: A drive to combat antimicrobial resistance.具有抗菌潜力的高分子药物:应对抗菌药物耐药性的推动力。
Int J Biol Macromol. 2017 Oct;103:554-574. doi: 10.1016/j.ijbiomac.2017.05.071. Epub 2017 May 19.
6
Medicinal attributes of 1,2,3-triazoles: Current developments.1,2,3-三唑的药用特性:当前进展
Bioorg Chem. 2017 Apr;71:30-54. doi: 10.1016/j.bioorg.2017.01.010. Epub 2017 Jan 18.
7
Synthesis, characterization and molecular docking studies of substituted 4-coumarinylpyrano[2,3-c]pyrazole derivatives as potent antibacterial and anti-inflammatory agents.取代的4-香豆素基吡喃并[2,3-c]吡唑衍生物作为强效抗菌和抗炎剂的合成、表征及分子对接研究
Eur J Med Chem. 2017 Jan 5;125:101-116. doi: 10.1016/j.ejmech.2016.09.021. Epub 2016 Sep 13.
8
Design and synthesis of antimicrobial, anticoagulant, and anticholinesterase hybrid molecules from 4-methylumbelliferone.基于4-甲基伞形酮的抗菌、抗凝和抗胆碱酯酶杂合分子的设计与合成
J Enzyme Inhib Med Chem. 2016 Dec;31(6):1566-75. doi: 10.3109/14756366.2016.1158171. Epub 2016 Apr 1.
9
Synthesis, in vivo Anticoagulant Evaluation and Molecular Docking Studies of Bicoumarins Obtained from Furocoumarin Peucedanin.从呋喃香豆素前胡素中获得的双香豆素的合成、体内抗凝评估及分子对接研究
Med Chem. 2016;12(7):674-683. doi: 10.2174/1573406412666160129105115.
10
OPLS3: A Force Field Providing Broad Coverage of Drug-like Small Molecules and Proteins.OPLS3:一种提供广泛覆盖药物样小分子和蛋白质的力场。
J Chem Theory Comput. 2016 Jan 12;12(1):281-96. doi: 10.1021/acs.jctc.5b00864. Epub 2015 Dec 1.