<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> Graphical Abstract <p></p>

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Sophflarines F–K: matrine-based alkaloids with a rare aromatic system from Sophora flavescens and their anti-inflammatory and synergistic antibacterial effects

  • 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

摘要

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