The moderate cytotoxic of isoeleutherol reported, a naphthalene-derived compound, from Eleutherine bulbosa bulbs collected in Simalungun, North Sumatra. The isolated compound, identified as (3S)-4-hydroxy-5-methoxy-3-methyl-3H-benzof2 benzofuran-1-one, was characterised through FTIR, NMR and EIMS analyses, confirming its structural integrity and molecular formula C14H12O4. Methanolic extraction of the bulb yielded the highest isoeleutherol concentration (17.35 ± 1.72 ppm), indicating that the bulb serves as the primary storage tissue. The cytotoxic evaluation revealed moderate antiproliferative activity against HeLa, A549 and MCF-7 cancer cell lines, with IC50 values of 27.63 ± 2.52, 32.68 ± 1.60 and 50.13 ± 1.49 μM, respectively, showing the highest sensitivity in HeLa cells. The observed activity is attributed to the naphthoquinone-type framework. These findings provide scientific validation of E. bulbosa's ethnomedicinal use and establish isoeleutherol as a potential lead compound for traditional herb medicine development.
Kurniawan et al. (2026) studied this question.