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April 26, 2026Chemistry & Biodiversity0 citations

Four New Dibenzo‐α‐pyrones From Helicosporium sexuale LZ15

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LZLijuan ZhangXMXiaoyan MaMHMeiyan Han

Key Points

  • The aim is to isolate and characterize new dibenzo-α-pyrone derivatives from Helicosporium sexuale.
  • Isolated four new dibenzo-α-pyrone derivatives and five known analogues from fermented rolled-oat culture.
  • Structures determined using 1D/2D NMR, HRESIMS, and x-ray crystallography.
  • Conducted in vitro cytotoxicity assays on various cancer cell lines.
  • Compound 5 showed moderate cytotoxicity toward HeLa cells.
  • Compound 6 displayed moderate activity against HepG2 and HeLa cells.
  • Compound 8 moderately inhibited A549 cells and weakly inhibited HeLa cells.

Abstract

Four new dibenzo-α-pyrone derivatives-helicolide A (1) and helicohydrins B-D (2-4)-along with five known analogues (5-9) were isolated from the fermented rolled-oat culture of Helicosporium sexuale LZ15. Their structures were determined by comprehensive spectroscopic analysis (1D/2D NMR, HRESIMS) and further confirmed by x-ray crystallography, NOE correlations, and ECD calculations. Structurally, helicolide A (1) is an isocoumarin derivative bearing carboxyl and acetyl groups, while Helicohydrins B-D (2-4) are polyhydroxylated fused isocoumarins. In vitro cytotoxicity assays revealed that compound 5 showed moderate cytotoxicity toward HeLa cells; compound 6 displayed moderate activity against HepG2 and HeLa; compound 7 exhibited weak cytotoxicity toward A2780 and A549; and compound 8 moderately inhibited A549 and weakly inhibited HeLa cells.

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Cite This Study

Zhang et al. (2026) studied this question.

synapsesocial.com/papers/69edad4b4a46254e215b4ef4https://doi.org/10.1002/cbdv.71229
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