Two new polyacetylenes from the roots of <i>Atractylodes macrocephala</i>

Two new polyacetylenes, (5<i>Z</i>,12<i>E</i>)-14-hydroxytetradeca-5,12-dien-8,10-diyn-1-yl 3-methylbut-2-enoate (<b>1</b>) and 5<i>S</i>, 1'<i>R</i>-(6<i>E</i>,12<i>E</i>)-1-hydroxytetradeca-6,12-dien-8,10-diyn-5-yl 2-methylbutanoate (<b>2</b>), together with two known ones, (2<i>E</i>,8<i>E</i>)-12-<i>β</i>-methylbutyryltetradeca-2,8-diene-4,6-diyne-1,14-diol (<b>3</b>), and (<i>E</i>)-5-[5-(but-3-en-1-yn-1-yl)thiophen-2-yl]pent-2-en-4-yn-1-yl acetate (<b>4</b>) were isolated from the ethyl acetate extract of the roots of <i>Atractylodes macrocephala</i> by various chromatographic methods, such as normal phase silica gel column, MPLC, and semi-preparative HPLC. Their structures were identified by kinds of spectroscopic methods including 1D NMR, 2D NMR, IR, UV, HR-ESI-MS, and ECD. Compound <b>1</b> exhibited cytotoxic activities in HepG2 and Huh7 cells with IC<sub>50</sub> values of 20.50 ± 2.07 and 19.99 ± 1.35 μM, respectively.

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Publication Details

Journal
Natural Product Research
Published
2025-01-09
DOI
https://doi.org/10.1080/14786419.2025.2450218
Citations
1
Primary Topic
Natural product bioactivities and synthesis
Type
article
Field-Weighted Citation Impact
0.81

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article

Two new polyacetylenes from the roots of Atractylodes macrocephala

Hui Liu, Zhihua Liao, Jiajia Liu, Fancheng Meng et al.
1 citations
Natural Product Research
Natural product bioactivities and synthesis
0.81
article

Two new polyacetylenes from the roots of Atractylodes macrocephala

Hui Liu, Zhihua Liao, Jiajia Liu, Fancheng Meng, Guowei Wang, Gang-Gang Zhou, Min Chen, J. Wang
article en
1 citations

Abstract

Two new polyacetylenes, (5<i>Z</i>,12<i>E</i>)-14-hydroxytetradeca-5,12-dien-8,10-diyn-1-yl 3-methylbut-2-enoate (<b>1</b>) and 5<i>S</i>, 1'<i>R</i>-(6<i>E</i>,12<i>E</i>)-1-hydroxytetradeca-6,12-dien-8,10-diyn-5-yl 2-methylbutanoate (<b>2</b>), together with two known ones, (2<i>E</i>,8<i>E</i>)-12-<i>β</i>-methylbutyryltetradeca-2,8-diene-4,6-diyne-1,14-diol (<b>3</b>), and (<i>E</i>)-5-[5-(but-3-en-1-yn-1-yl)thiophen-2-yl]pent-2-en-4-yn-1-yl acetate (<b>4</b>) were isolated from the ethyl acetate extract of the roots of <i>Atractylodes macrocephala</i> by various chromatographic methods, such as normal phase silica gel column, MPLC, and semi-preparative HPLC. Their structures were identified by kinds of spectroscopic methods including 1D NMR, 2D NMR, IR, UV, HR-ESI-MS, and ECD. Compound <b>1</b> exhibited cytotoxic activities in HepG2 and Huh7 cells with IC<sub>50</sub> values of 20.50 ± 2.07 and 19.99 ± 1.35 μM, respectively.

Natural Product Research
Southwest University (CN), Foshan University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 32%
Natural product bioactivities and synthesis
0.81
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