A new chromone from the roots of <i>Stellera chamaejasme</i> L.

A new chromone (<b>1</b>), together with three known compounds (<b>2-4</b>), was isolated from the roots of <i>Stellera chamaejasme</i> L. The structure of compound <b>1</b> was elucidated by comprehensive spectroscopic analyses, including 1D and 2D NMR (HSQC, COSY, HMBC) and HR-ESI-MS. The absolute configuration was further determined by comparison of the experimental and time-dependent density functional theory (TDDFT)-calculated electronic circular dichroism (ECD) spectra. And all compounds (<b>1-4</b>) exhibited weak cytotoxicity against HL-60 and HeLa cell lines.

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Publication Details

Journal
Natural Product Research
Published
2026-01-14
DOI
https://doi.org/10.1080/14786419.2026.2615748
Primary Topic
Bioactive Natural Diterpenoids Research
Type
article
Field-Weighted Citation Impact
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article

A new chromone from the roots of Stellera chamaejasme L.

Hong-Qian Pan, Bai Jing-jie, Zhi-Chao Feng, Qiong Liu et al.
Natural Product Research
Bioactive Natural Diterpenoids Research
article

A new chromone from the roots of Stellera chamaejasme L.

Hong-Qian Pan, Bai Jing-jie, Zhi-Chao Feng, Qiong Liu, Chengshan Yuan, Duo-Xiu Li
article en

Abstract

A new chromone (<b>1</b>), together with three known compounds (<b>2-4</b>), was isolated from the roots of <i>Stellera chamaejasme</i> L. The structure of compound <b>1</b> was elucidated by comprehensive spectroscopic analyses, including 1D and 2D NMR (HSQC, COSY, HMBC) and HR-ESI-MS. The absolute configuration was further determined by comparison of the experimental and time-dependent density functional theory (TDDFT)-calculated electronic circular dichroism (ECD) spectra. And all compounds (<b>1-4</b>) exhibited weak cytotoxicity against HL-60 and HeLa cell lines.

Natural Product Research
State Key Laboratory of Chemical Engineering (CN), Lanzhou University (CN)
Openalex Percentile: Top 88%
Bioactive Natural Diterpenoids Research
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