Two new guaiane-type sesquiterpene glycosides from <i>Atractylodes Japonica</i> Koidz. ex Kitam

Two new guaiane-type sesquiterpene glycosides, atractylodes guaianoside I (<b>1</b>) and atractylodes guaianoside II (<b>2</b>), along with eleven known sesquiterpenes (<b>3</b>-<b>13</b>), were isolated from <i>Atractylodes Japonica</i> Koidz. ex Kitam. The structures of these two new compounds were elucidated by extensive spectroscopic analyses and mass spectrometric techniques. And their absolute configurations were confirmed by electronic circular dichroism (ECD) calculations. In addition, the isolated compounds were evaluated for their cytotoxic activities against three cancer cell lines HT-29, A-549, and MCF-7. Results showed that new compound <b>2</b> had inhibitory effects on three types of cancer cells, while new compound <b>1</b> only had inhibitory effects on HT-29 and MCF-7.

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Publication Details

Journal
Natural Product Research
Published
2024-10-11
DOI
https://doi.org/10.1080/14786419.2024.2413431
Citations
2
Primary Topic
Phytochemistry and Biological Activities
Type
article
Field-Weighted Citation Impact
1.20
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article

Two new guaiane-type sesquiterpene glycosides from Atractylodes Japonica Koidz. ex Kitam

Bing‐You Yang, Yan Liu, Jing Wang, Jie Sun et al.
2 citations
Natural Product Research
Phytochemistry and Biological Activities
1.20
article

Two new guaiane-type sesquiterpene glycosides from Atractylodes Japonica Koidz. ex Kitam

Bing‐You Yang, Yan Liu, Jing Wang, Jie Sun, Xiao-Juan Zhang, Zhao Sun, Zhen-Xing Fang, Yuanyuan Zhou
article en
2 citations

Abstract

Two new guaiane-type sesquiterpene glycosides, atractylodes guaianoside I (<b>1</b>) and atractylodes guaianoside II (<b>2</b>), along with eleven known sesquiterpenes (<b>3</b>-<b>13</b>), were isolated from <i>Atractylodes Japonica</i> Koidz. ex Kitam. The structures of these two new compounds were elucidated by extensive spectroscopic analyses and mass spectrometric techniques. And their absolute configurations were confirmed by electronic circular dichroism (ECD) calculations. In addition, the isolated compounds were evaluated for their cytotoxic activities against three cancer cell lines HT-29, A-549, and MCF-7. Results showed that new compound <b>2</b> had inhibitory effects on three types of cancer cells, while new compound <b>1</b> only had inhibitory effects on HT-29 and MCF-7.

Natural Product ResearchVol. 40(2)
Heilongjiang University of Chinese Medicine (CN), Heilongjiang Academy of Sciences (CN)
Life in Land
Openalex Percentile: Top 16%
Phytochemistry and Biological Activities
1.20
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Two new guaiane-type sesquiterpene glycosides from <i>Atractylodes Japonica</i> Koidz. ex Kitam — Bing‐You Yang, Yan Liu, et al. · Natural Product Research (2024) | TGRS Research Map | TGRS