Dihydroagarofuran sesquiterpene derivatives from the roots of <i>Tripterygium wilfordii</i>

Two new (<b>1-2</b>) and five known (<b>3-7</b>) dihydro-<i>β</i>-agarofuran derivatives were isolated from the roots of <i>Tripterygium wilfordii</i>. The structures of new compounds were elucidated by spectroscopic techniques, such as UV, IR, HRESIMS and NMR. And the structure of compound <b>1</b> was confirmed by X-ray crystallographic. Cytotoxic activity assays against four human tumor cell lines (SK-MEL-2, HCC1806, HUH-7, PANC-1) were assessed for compounds <b>1-7</b>. Compound <b>2</b> exhibited pronounced cytotoxicity against SK-MEL-2 cells with an IC<sub>50</sub> value of 9.18 μM. Additionally, compound <b>5</b> showed significant cytotoxic effects on SK-MEL-2 and HCC1806 cells with IC<sub>50</sub> values of 4.59 μM and 8.14 μM, respectively.

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Publication Details

Journal
Journal of Asian Natural Products Research
Published
2025-11-12
DOI
https://doi.org/10.1080/10286020.2025.2579867
Primary Topic
Natural Compounds in Disease Treatment
Type
article
Field-Weighted Citation Impact
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article

Dihydroagarofuran sesquiterpene derivatives from the roots of Tripterygium wilfordii

Ping-Ting Hong, Chong Wang, Ya-Lin Hu, Yuting Lei et al.
Journal of Asian Natural Products Research
Natural Compounds in Disease Treatment
article

Dihydroagarofuran sesquiterpene derivatives from the roots of Tripterygium wilfordii

Ping-Ting Hong, Chong Wang, Ya-Lin Hu, Yuting Lei, Jiali Huang, Wen Li, Zhijie Li, Wen‐Jie Chen, Zhen Li
article en

Abstract

Two new (<b>1-2</b>) and five known (<b>3-7</b>) dihydro-<i>β</i>-agarofuran derivatives were isolated from the roots of <i>Tripterygium wilfordii</i>. The structures of new compounds were elucidated by spectroscopic techniques, such as UV, IR, HRESIMS and NMR. And the structure of compound <b>1</b> was confirmed by X-ray crystallographic. Cytotoxic activity assays against four human tumor cell lines (SK-MEL-2, HCC1806, HUH-7, PANC-1) were assessed for compounds <b>1-7</b>. Compound <b>2</b> exhibited pronounced cytotoxicity against SK-MEL-2 cells with an IC<sub>50</sub> value of 9.18 μM. Additionally, compound <b>5</b> showed significant cytotoxic effects on SK-MEL-2 and HCC1806 cells with IC<sub>50</sub> values of 4.59 μM and 8.14 μM, respectively.

Journal of Asian Natural Products Research
Hunan University of Traditional Chinese Medicine (CN), Hunan University of Science and Engineering (CN), Zhejiang Hisun Pharmaceutical (China) (CN)
Openalex Percentile: Top 49%
Natural Compounds in Disease Treatment
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