Polyhydroxyalkanes from <i>Pachysandra terminalis</i> Sieb. et Zucc

Four polyhydroxyalkanes were isolated from the CH<sub>2</sub>Cl<sub>2</sub> part of <i>Pachysandra terminalis</i>, including two new ones, (2<i>S</i>,3<i>E</i>)-3-isopropylpent-3-ene-1,2,5-triol (<b>1</b>) and (4<i>R</i>,2<i>E</i>)-4,5-dihydroxy-2,3-dimethylpent-2-enoic acid (<b>2</b>); as well as one new natural product, 3-methylbut-3-ene-1,2-diol (<b>3</b>) and one known compound, 4-methyl-3-methylenepentane-1,2-diol (<b>4</b>). The structures were determined by physicochemical properties and spectroscopic methods including 1D, 2D NMR, IR, HR-ESI-MS, and ECD data. The cytotoxic activity of compounds against the human cancer lines A549, H460, and HepG2 cell lines of the isolated compounds was evaluated by the CCK8 method. However, compounds did not show significant activity.

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Publication Details

Journal
Natural Product Research
Published
2024-12-16
DOI
https://doi.org/10.1080/14786419.2024.2441497
Citations
2
Primary Topic
Cholinesterase and Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.90

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article

Polyhydroxyalkanes from Pachysandra terminalis Sieb. et Zucc

Xiaomei Song, Chenwang Liu, Wu Yao, Dongdong Zhang et al.
2 citations
Natural Product Research
Cholinesterase and Neurodegenerative Diseases
0.90
article

Polyhydroxyalkanes from Pachysandra terminalis Sieb. et Zucc

Xiaomei Song, Chenwang Liu, Wu Yao, Dongdong Zhang, Wei Wang, Yuze Li, Yuying Zhang, Chuanming Gong, Yu Sun
article en
2 citations

Abstract

Four polyhydroxyalkanes were isolated from the CH<sub>2</sub>Cl<sub>2</sub> part of <i>Pachysandra terminalis</i>, including two new ones, (2<i>S</i>,3<i>E</i>)-3-isopropylpent-3-ene-1,2,5-triol (<b>1</b>) and (4<i>R</i>,2<i>E</i>)-4,5-dihydroxy-2,3-dimethylpent-2-enoic acid (<b>2</b>); as well as one new natural product, 3-methylbut-3-ene-1,2-diol (<b>3</b>) and one known compound, 4-methyl-3-methylenepentane-1,2-diol (<b>4</b>). The structures were determined by physicochemical properties and spectroscopic methods including 1D, 2D NMR, IR, HR-ESI-MS, and ECD data. The cytotoxic activity of compounds against the human cancer lines A549, H460, and HepG2 cell lines of the isolated compounds was evaluated by the CCK8 method. However, compounds did not show significant activity.

Natural Product ResearchVol. 40(7)
Shaanxi University of Chinese Medicine (CN)
National Natural Science Foundation of China, State Administration of Traditional Chinese Medicine of the People's Republic of China
Openalex Percentile: Top 22%
Cholinesterase and Neurodegenerative Diseases
0.90
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