Sophflarines F–K: matrine-based alkaloids with a rare aromatic system from Sophora flavescens and their anti-inflammatory and synergistic antibacterial effects
{"title":"Sophflarines F–K: matrine-based alkaloids with a rare aromatic system from Sophora flavescens and their anti-inflammatory and synergistic antibacterial effects","authors":"Ding Luo, Le-Yan Wang, Xiang-Feng Zhao, Xiao-Lin Huang, Yang-Yi Hu, Qiong-Yun Jing, Yan-Jun Chen, He Tian, Si-Yan Chen, Yu-Yan Wang, Xian-Hui Huang, Zhen-Ling Zeng, Xiao-Ping Liao","doi":"10.1007/s13659-026-00595-2","DOIUrl":null,"url":null,"abstract":"<div><p>Six new matrine-based alkaloids, sophflarines F–K <b>(1–6)</b>, featuring a rare aromatic system, were obtained from the water-soluble alkaloid fractions of <i>Sophora flavescens</i> by UV-guided separation. Their structures were elucidated by the interpretation of spectroscopic analyses, quantum chemical calculation, and X-ray diffraction data. Compounds <b>1</b> and <b>2</b> represent highly modified 15,16-<i>seco</i>-17-<i>nor</i>-matrine derivatives incorporating a rare 4,5-dihydro-3<i>H</i>-pyrrolo[2,3,4-ij]quinolizine moiety, while compound <b>5</b> possesses an unusual 6/6/6–5 tetracyclic skeleton. A copper sulfate-induced zebrafish assay revealed that compounds <b>1</b>, <b>4</b>, and <b>5</b> exhibited moderate anti-inflammatory activity at non-toxic concentrations. Checkerboard assays demonstrated that compounds <b>5</b> and <b>6</b> potentiated colistin activity against <i>Escherichia coli</i> ATCC25922 and BW25113-<i>mcr</i>-1, reducing colistin MIC values by 16- and 32-fold, respectively. These findings expand the structural diversity of aromatic matrine-type alkaloids and highlight their potential as anti-inflammatory agents and antibacterial adjuvants.</p><h3>Graphical Abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture><span>The alternative text for this image may have been generated using AI.</span></div></div></figure></div></div>","PeriodicalId":718,"journal":{"name":"Natural Products and Bioprospecting","volume":"16 1","pages":""},"PeriodicalIF":4.9000,"publicationDate":"2026-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13076842/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Products and Bioprospecting","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s13659-026-00595-2","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
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Abstract
Six new matrine-based alkaloids, sophflarines F–K (1–6), featuring a rare aromatic system, were obtained from the water-soluble alkaloid fractions of Sophora flavescens by UV-guided separation. Their structures were elucidated by the interpretation of spectroscopic analyses, quantum chemical calculation, and X-ray diffraction data. Compounds 1 and 2 represent highly modified 15,16-seco-17-nor-matrine derivatives incorporating a rare 4,5-dihydro-3H-pyrrolo[2,3,4-ij]quinolizine moiety, while compound 5 possesses an unusual 6/6/6–5 tetracyclic skeleton. A copper sulfate-induced zebrafish assay revealed that compounds 1, 4, and 5 exhibited moderate anti-inflammatory activity at non-toxic concentrations. Checkerboard assays demonstrated that compounds 5 and 6 potentiated colistin activity against Escherichia coli ATCC25922 and BW25113-mcr-1, reducing colistin MIC values by 16- and 32-fold, respectively. These findings expand the structural diversity of aromatic matrine-type alkaloids and highlight their potential as anti-inflammatory agents and antibacterial adjuvants.
Graphical Abstract
The alternative text for this image may have been generated using AI.
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