A new hydroxybutanamide derivative from <i>Saussurea involucrata</i> with anti-PD activity on H <sub>2</sub> O <sub>2</sub> insult sH-SY5Y cells

A new hydroxybutanamide derivative, involucramide (<b>1</b>), was obtained from the traditional Chinese medicinal herb <i>Saussurea involucrata.</i> Five other isolates were characterised as betulinic acid (<b>2</b>), costunolide (<b>3</b>), dihydrocostunolide (<b>4</b>), isodihydrocostunolide (<b>5</b>), and dehydrocostus lactone (<b>6</b>). The structure of <b>1</b> was established through extensive data analyses encompassing its NMR, IR, UV, and HRESIMS data. All isolates were evaluated for the anti-PD activity on H<sub>2</sub>O<sub>2</sub>-insulted SH-SY5Y cells. Amongst them, compound <b>1</b> exhibited the potential activity with the EC<sub>50</sub> value of 6.84 <i>µ</i>M. Furthermore, at the concentration of 20 <i>µ</i>M, <b>1</b> attenuated the intracellular ROS accumulation, elevated the glutathione (GSH) levels, and reversed the downregulated mRNA expression of HO-1 and NQO1 in H<sub>2</sub>O<sub>2</sub>-injured SH-SY5Y cells.

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Journal
Natural Product Research
Published
2026-02-23
DOI
https://doi.org/10.1080/14786419.2026.2636164
Primary Topic
Natural product bioactivities and synthesis
Type
article
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article

A new hydroxybutanamide derivative from Saussurea involucrata with anti-PD activity on H 2 O 2 insult sH-SY5Y cells

Chenlu Lv, Yantao Shi, Abdulla Yusuf, Linzhen Hu et al.
Natural Product Research
Natural product bioactivities and synthesis
article

A new hydroxybutanamide derivative from Saussurea involucrata with anti-PD activity on H 2 O 2 insult sH-SY5Y cells

Chenlu Lv, Yantao Shi, Abdulla Yusuf, Linzhen Hu, Rongrong Dai, Yuben Qiao, Qi Huang, Jie Shi
article en

Abstract

A new hydroxybutanamide derivative, involucramide (<b>1</b>), was obtained from the traditional Chinese medicinal herb <i>Saussurea involucrata.</i> Five other isolates were characterised as betulinic acid (<b>2</b>), costunolide (<b>3</b>), dihydrocostunolide (<b>4</b>), isodihydrocostunolide (<b>5</b>), and dehydrocostus lactone (<b>6</b>). The structure of <b>1</b> was established through extensive data analyses encompassing its NMR, IR, UV, and HRESIMS data. All isolates were evaluated for the anti-PD activity on H<sub>2</sub>O<sub>2</sub>-insulted SH-SY5Y cells. Amongst them, compound <b>1</b> exhibited the potential activity with the EC<sub>50</sub> value of 6.84 <i>µ</i>M. Furthermore, at the concentration of 20 <i>µ</i>M, <b>1</b> attenuated the intracellular ROS accumulation, elevated the glutathione (GSH) levels, and reversed the downregulated mRNA expression of HO-1 and NQO1 in H<sub>2</sub>O<sub>2</sub>-injured SH-SY5Y cells.

Natural Product Research
Chinese Academy of Sciences (CN), Tianjin Economic-Technological Development Area (CN), Tianjin Institute of Industrial Biotechnology (CN), Kashi University (CN), Huazhong University of Science and Technology (CN), Southern Medical University (CN), Hubei University (CN)
Openalex Percentile: Top 44%
Natural product bioactivities and synthesis
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