Undescribed dihydro- <i>β</i> -agarofuran sesquiterpenoids from the roots of <i>Tripterygium wilfordii</i>

Two undescribed dihydro-<i>β</i>-agarofuran sesquiterpene polyesters, named tripterysines H (<b>1</b>) and I (<b>2</b>), were obtained from <i>Tripterygium wilfordii</i> roots, alongside five reported analogues (<b>3-7</b>). The chemical structures of two undescribed compounds were unambiguously assigned by comprehensive analysis of their NMR data in combination with HRESIMS results, and the absolute configurations of them were established <i>via</i> electronic circular dichroism (ECD) calculations. In addition, compounds <b>1</b> and <b>3</b> demonstrated potent cytotoxicity against SK-MEL-2 and HCC1806 cell lines (IC<sub>50</sub> 4.59-8.14 <i>μ</i>M), with potency comparable to the positive control.

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Publication Details

Journal
Natural Product Research
Published
2026-01-19
DOI
https://doi.org/10.1080/14786419.2026.2619413
Primary Topic
Natural Compounds in Disease Treatment
Type
article
Field-Weighted Citation Impact
0.00
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article

Undescribed dihydro- β -agarofuran sesquiterpenoids from the roots of Tripterygium wilfordii

Ya-Lin Hu, Jing-Yi Huang, Wen-Jie Chen, Yi-Ping Xie et al.
Natural Product Research
Natural Compounds in Disease Treatment
article

Undescribed dihydro- β -agarofuran sesquiterpenoids from the roots of Tripterygium wilfordii

Ya-Lin Hu, Jing-Yi Huang, Wen-Jie Chen, Yi-Ping Xie, Chong Wang, Jia-Li Huang
article en

Abstract

Two undescribed dihydro-<i>β</i>-agarofuran sesquiterpene polyesters, named tripterysines H (<b>1</b>) and I (<b>2</b>), were obtained from <i>Tripterygium wilfordii</i> roots, alongside five reported analogues (<b>3-7</b>). The chemical structures of two undescribed compounds were unambiguously assigned by comprehensive analysis of their NMR data in combination with HRESIMS results, and the absolute configurations of them were established <i>via</i> electronic circular dichroism (ECD) calculations. In addition, compounds <b>1</b> and <b>3</b> demonstrated potent cytotoxicity against SK-MEL-2 and HCC1806 cell lines (IC<sub>50</sub> 4.59-8.14 <i>μ</i>M), with potency comparable to the positive control.

Natural Product Research
Hunan University of Science and Engineering (CN)
Openalex Percentile: Top 82%
Natural Compounds in Disease Treatment
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