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Artemisiyneolides A-K, Guaiane Sesquiterpenoid-Heptatriyne Hybrids through C-C Linkages from Artemisia sieversiana with Antihepatoma Activity.

Aug 2026 · Journal of Organic Chemistry · Vol 91 32, pp. 11086-11094 · 0 citations · 19 references
Medicine

TL;DR

The investigation of antihepatoma activity suggested that compound 4 exhibited significant inhibition on HepG2, Huh7, and SK-Hep-1 cell lines, with IC50 values of 22.8 ± 1.8, 31.7 ± 1.4, and 26.3 ± 3.0 μM, respectively.

Abstract

Artemisiyneolides A-K (1-11), guaiane sesquiterpenoid-heptatriyne hybrids, were isolated from Artemisia sieversiana (Asteraceae). Their structures were elucidated using NMR, HRESIMS, ECD calculations, and X-ray diffraction analysis. Compounds 1-11 featured 5/5/7/5-fused ring frameworks bearing a 1,3,5-heptatriyne side chain by C-C linkages, which were biosynthetically generated by [4 + 2] Diels-Alder cycloadditions. The investigation of antihepatoma activity suggested that compound 4 exhibited significant inhibition on HepG2, Huh7, and SK-Hep-1 cell lines, with IC50 values of 22.8 ± 1.8, 31.7 ± 1.4, and 26.3 ± 3.0 μM, respectively.

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