Design, synthesis and anti-plant-bacterial (Xoc, Xac, Psa) activity of coumarins derivatives containing amide and sulfonamide moieties.

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Song Bai, Miaohe Zhang, Rong Wu, Suran Wan, Lijun Chen, Shouying Tang, Xian Wei, Shuang Feng, Miao Li
{"title":"Design, synthesis and anti-plant-bacterial (Xoc, Xac, Psa) activity of coumarins derivatives containing amide and sulfonamide moieties.","authors":"Song Bai, Miaohe Zhang, Rong Wu, Suran Wan, Lijun Chen, Shouying Tang, Xian Wei, Shuang Feng, Miao Li","doi":"10.1186/s13065-025-01573-4","DOIUrl":null,"url":null,"abstract":"<p><p>In this study, coumarin derivatives containing amide and sulfanilamide moieties were designed and synthesized, and their antibacterial activities were systematically evaluated. Among the synthesised compounds, compound A7 exhibited good inhibitory activity against Psa, with an EC<sub>50</sub> value of 59.4 mg/L. Compound A2 presented the most potent antibacterial effect against Xoc, with an EC<sub>50</sub> value of 43.2 mg/L. Compound A3 showed notable efficacy against Xac, with an EC<sub>50</sub> value of 53.2 mg/L. Further mechanistic studies involving scanning electron microscopy (SEM) and extracellular conductivity (EC) measurements revealed that A2 induced morphological deformation and alterations in membrane permeability alterations in Xoc cells, suggesting a potential disruption of bacterial membrane integrity. Additionally, the structure-activity relationship (SAR) of these derivatives was elucidated using 3D-QSAR model, providing insights for further structural optimization. Furthermore, the chemical reactivity of potential bioactive compounds was evaluated using density functional theory (DFT).</p>","PeriodicalId":496,"journal":{"name":"BMC Chemistry","volume":"19 1","pages":"178"},"PeriodicalIF":4.3000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12220336/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1186/s13065-025-01573-4","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

In this study, coumarin derivatives containing amide and sulfanilamide moieties were designed and synthesized, and their antibacterial activities were systematically evaluated. Among the synthesised compounds, compound A7 exhibited good inhibitory activity against Psa, with an EC50 value of 59.4 mg/L. Compound A2 presented the most potent antibacterial effect against Xoc, with an EC50 value of 43.2 mg/L. Compound A3 showed notable efficacy against Xac, with an EC50 value of 53.2 mg/L. Further mechanistic studies involving scanning electron microscopy (SEM) and extracellular conductivity (EC) measurements revealed that A2 induced morphological deformation and alterations in membrane permeability alterations in Xoc cells, suggesting a potential disruption of bacterial membrane integrity. Additionally, the structure-activity relationship (SAR) of these derivatives was elucidated using 3D-QSAR model, providing insights for further structural optimization. Furthermore, the chemical reactivity of potential bioactive compounds was evaluated using density functional theory (DFT).

含酰胺类和磺胺类香豆素衍生物的设计、合成及其抗植物细菌(Xoc, Xac, Psa)活性。
本研究设计并合成了含有酰胺和磺胺基团的香豆素衍生物,并对其抗菌活性进行了系统评价。在所合成的化合物中,化合物A7对Psa具有良好的抑制活性,EC50值为59.4 mg/L。化合物A2对Xoc的抑菌效果最好,EC50值为43.2 mg/L。化合物A3对Xac有明显的抑制作用,EC50值为53.2 mg/L。进一步的机制研究包括扫描电子显微镜(SEM)和细胞外电导率(EC)测量显示,A2诱导Xoc细胞的形态变形和膜通透性改变,表明可能破坏细菌膜的完整性。此外,利用3D-QSAR模型阐明了这些衍生物的构效关系(SAR),为进一步的结构优化提供了见解。此外,利用密度泛函理论(DFT)评价了潜在生物活性化合物的化学反应性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
BMC Chemistry
BMC Chemistry Chemistry-General Chemistry
CiteScore
5.30
自引率
2.20%
发文量
92
审稿时长
27 weeks
期刊介绍: BMC Chemistry, formerly known as Chemistry Central Journal, is now part of the BMC series journals family. Chemistry Central Journal has served the chemistry community as a trusted open access resource for more than 10 years – and we are delighted to announce the next step on its journey. In January 2019 the journal has been renamed BMC Chemistry and now strengthens the BMC series footprint in the physical sciences by publishing quality articles and by pushing the boundaries of open chemistry.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信