Anti‐Glioma Activity of Artejasminolide Isolated From <i>Artemisia argyi</i> Based on Bioactivity Evaluation and Network Pharmacology

Seven terpenoids were isolated from Artemisia argyi leaves, including one new triterpenoid featuring a unique terminal diagonal methoxy-substituted side chain and six known analogues. Their structures were confirmed by NMR and HR-ESI-MS spectral analyses, and the absolute stereochemistry of Compound 1 was elucidated via x-ray diffraction analysis. Bioassays revealed that 2 exhibited cytotoxicity against U251 glioma cells (IC<sub>50</sub> = 5.6 µM) and potently abrogated cell migration and invasion in a dose-proportional manner by suppressing PI3K/AKT/mTOR phosphorylation, as confirmed by Transwell and Western blot analyses. Bioinformatics analysis further suggested EGFR as a potential upstream target mediating these effects. These findings indicated A. argyi as a possible source of bioactive terpenoids with anti-glioma potential, providing a theoretical basis for further pharmacological studies.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2026-02-01
DOI
https://doi.org/10.1002/cbdv.202503722
Primary Topic
Sesquiterpenes and Asteraceae Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

Anti‐Glioma Activity of Artejasminolide Isolated From Artemisia argyi Based on Bioactivity Evaluation and Network Pharmacology

Zhe Ren, Tao Liu, Jiming Chen, Liju Zhang et al.
Chemistry & Biodiversity
Sesquiterpenes and Asteraceae Studies
article

Anti‐Glioma Activity of Artejasminolide Isolated From Artemisia argyi Based on Bioactivity Evaluation and Network Pharmacology

Zhe Ren, Tao Liu, Jiming Chen, Liju Zhang, Leyi Fu, Zitian Peng, Zhiling Yao
article en

Abstract

Seven terpenoids were isolated from Artemisia argyi leaves, including one new triterpenoid featuring a unique terminal diagonal methoxy-substituted side chain and six known analogues. Their structures were confirmed by NMR and HR-ESI-MS spectral analyses, and the absolute stereochemistry of Compound 1 was elucidated via x-ray diffraction analysis. Bioassays revealed that 2 exhibited cytotoxicity against U251 glioma cells (IC<sub>50</sub> = 5.6 µM) and potently abrogated cell migration and invasion in a dose-proportional manner by suppressing PI3K/AKT/mTOR phosphorylation, as confirmed by Transwell and Western blot analyses. Bioinformatics analysis further suggested EGFR as a potential upstream target mediating these effects. These findings indicated A. argyi as a possible source of bioactive terpenoids with anti-glioma potential, providing a theoretical basis for further pharmacological studies.

Chemistry & BiodiversityVol. 23(2)
Jinan University (CN), Guangdong Pharmaceutical University (CN), Shanghai Innovative Research Center of Traditional Chinese Medicine (CN), Key Laboratory of Guangdong Province (CN), First Affiliated Hospital of Jinan University (CN)
Openalex Percentile: Top 69%
Sesquiterpenes and Asteraceae Studies
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