Examines cytotoxic effects of new dibenzo-α-pyrone compounds on cancer cell lines, suggesting potential therapeutic applications.
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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Zhang et al. (2026) studied this question.
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