The undescribed alkaloids from <i>Jacobaea cannabifolia</i> (less.) E. Wiebe and their anti-inflammatory activities

From the whole herb of <i>Jacobaea cannabifolia</i> (Less.) E. Wiebe, one new alkaloid named cannabliold E (<b>1</b>), one new natural alkaloid derivative named methyl 4-(2-oxo-1-pyrrolidinyl) benzene acetate (<b>2</b>) along with seven known alkaloids (<b>3-9</b>) were successfully isolated. The structures of the newly identified compounds were elucidated using NMR spectroscopy and HR-ESI-MS. The absolute configurations of compound <b>1</b> were assigned through electronic circular dichroism (ECD) analysis. Identification of the known compounds was achieved by comparing their 1D NMR data with literature references. All isolated compounds were assessed for anti-inflammatory activity against LPS-induced RAW 264.7 cells; results indicated that compounds <b>6</b> and <b>8</b> exhibited significant anti-inflammatory effects with IC<sub>50</sub> values below 1.59 ± 0.18 μM.

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Publication Details

Journal
Natural Product Research
Published
2025-05-14
DOI
https://doi.org/10.1080/14786419.2025.2502145
Primary Topic
Chromatography in Natural Products
Type
article
Field-Weighted Citation Impact
0.00

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article

The undescribed alkaloids from Jacobaea cannabifolia (less.) E. Wiebe and their anti-inflammatory activities

Zhichao Hao, Bing‐You Yang, Qingshan Chen, Jianzhe Li et al.
Natural Product Research
Chromatography in Natural Products
article

The undescribed alkaloids from Jacobaea cannabifolia (less.) E. Wiebe and their anti-inflammatory activities

Zhichao Hao, Bing‐You Yang, Qingshan Chen, Jianzhe Li, Xinyue Wu, Yan Liu, Lili Zhang, Yu Bi, Wei Guan, Dalin Li, Hai‐Xue Kuang, Juan Pan
article en

Abstract

From the whole herb of <i>Jacobaea cannabifolia</i> (Less.) E. Wiebe, one new alkaloid named cannabliold E (<b>1</b>), one new natural alkaloid derivative named methyl 4-(2-oxo-1-pyrrolidinyl) benzene acetate (<b>2</b>) along with seven known alkaloids (<b>3-9</b>) were successfully isolated. The structures of the newly identified compounds were elucidated using NMR spectroscopy and HR-ESI-MS. The absolute configurations of compound <b>1</b> were assigned through electronic circular dichroism (ECD) analysis. Identification of the known compounds was achieved by comparing their 1D NMR data with literature references. All isolated compounds were assessed for anti-inflammatory activity against LPS-induced RAW 264.7 cells; results indicated that compounds <b>6</b> and <b>8</b> exhibited significant anti-inflammatory effects with IC<sub>50</sub> values below 1.59 ± 0.18 μM.

Natural Product Research
Northeast Agricultural University (CN), Heilongjiang University of Chinese Medicine (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 89%
Chromatography in Natural Products
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