A new cyclohexenone and two new phenanthrones from <i>Elatostema tenuicaudatum</i>

A new cyclohexenone, 5<i>S</i>-(3,4-dihydroxyphenethyl)cyclohex-2-en-1-one (<b>1</b>), along with two new phenanthrones, (4a<i>S</i>,10a<i>S</i>)- 1,9,10,10a -tetrahydro-4a,6,7-trihydroxy-4(4a<i>H</i>)-phenanthrone (<b>2</b>) and (4a<i>S</i>,10a<i>S</i>)-4a-hydroxy-7-methoxy-1,9,10,10a-tetrahydro-4(4a<i>H</i>)-phenanthrone 6-O-<i>β</i>-D-glucopyranoside (<b>3</b>) were isolated from the whole plant of <i>Elatostema tenuicaudatum.</i> The structures were determined by spectroscopic methods including 1D, 2D NMR and HR-ESI-MS. The absolute configurations of compounds <b>1-3</b> were determined by their experimental and calculated ECD spectral data. The isolates were evaluated for inhibitory activity on nitric oxide (NO) production in lipopolysaccharide (LPS)-activated RAW 264.7 macrophage cells, and compound <b>2</b> showed the strongest activity with an IC<sub>50</sub> value of 9.5 ± 1.2 μM.

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Publication Details

Journal
Journal of Asian Natural Products Research
Published
2025-10-28
DOI
https://doi.org/10.1080/10286020.2025.2577883
Primary Topic
Biological and pharmacological studies of plants
Type
article
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article

A new cyclohexenone and two new phenanthrones from Elatostema tenuicaudatum

Le Quoc Thang, Nguyễn Thành Tâm, Nguyen Hoang, Đào Đức Thiện
Journal of Asian Natural Products Research
Biological and pharmacological studies of plants
article

A new cyclohexenone and two new phenanthrones from Elatostema tenuicaudatum

Le Quoc Thang, Nguyễn Thành Tâm, Nguyen Hoang, Đào Đức Thiện
article en

Abstract

A new cyclohexenone, 5<i>S</i>-(3,4-dihydroxyphenethyl)cyclohex-2-en-1-one (<b>1</b>), along with two new phenanthrones, (4a<i>S</i>,10a<i>S</i>)- 1,9,10,10a -tetrahydro-4a,6,7-trihydroxy-4(4a<i>H</i>)-phenanthrone (<b>2</b>) and (4a<i>S</i>,10a<i>S</i>)-4a-hydroxy-7-methoxy-1,9,10,10a-tetrahydro-4(4a<i>H</i>)-phenanthrone 6-O-<i>β</i>-D-glucopyranoside (<b>3</b>) were isolated from the whole plant of <i>Elatostema tenuicaudatum.</i> The structures were determined by spectroscopic methods including 1D, 2D NMR and HR-ESI-MS. The absolute configurations of compounds <b>1-3</b> were determined by their experimental and calculated ECD spectral data. The isolates were evaluated for inhibitory activity on nitric oxide (NO) production in lipopolysaccharide (LPS)-activated RAW 264.7 macrophage cells, and compound <b>2</b> showed the strongest activity with an IC<sub>50</sub> value of 9.5 ± 1.2 μM.

Journal of Asian Natural Products Research
University of Education, Winneba (GH), University of Khanh Hoa (VN), Hue University (VN), Vietnam Academy of Science and Technology (VN)
Openalex Percentile: Top 65%
Biological and pharmacological studies of plants
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