Bonenncarpas A–K: Coumarin derivatives with anti-inflammatory activity from Boenninghausenia sessilicarpa

Eleven previously undescribed coumarin derivatives, bonenncarpas A-K (1-11), along with three known analogues (12-14), were isolated from the whole plant of Boenninghausenia sessilicarpa. The structures of these compounds were elucidated through comprehensive spectroscopic and spectrometric analyses. Their absolute configurations were determined by comparing experimental and calculated electronic circular dichroism data, as well as by X-ray crystallography. Notably, compound 1 features an open-ring coumarin structure with a five-membered lactone ring, while compounds 9-11 are characterized by a dihydrofuran ring at C-3 and C-4. All compounds were evaluated for their inhibitory effects on lipopolysaccharide-induced nitric oxide production in RAW 264.7 macrophage cells. At a concentration of 10 μM, compounds (-)-3, (+)-5, (+)-6, (+)-9, (-)-9, (+)-10, and (-)-10 exhibited inhibition of NO production, ranging from 25.5% to 95.0%.

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Publication Details

Journal
Phytochemistry
Published
2025-01-29
DOI
https://doi.org/10.1016/j.phytochem.2025.114415
Citations
2
Primary Topic
Phytochemistry and Biological Activities
Type
article
Field-Weighted Citation Impact
3.50
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article

Bonenncarpas A–K: Coumarin derivatives with anti-inflammatory activity from Boenninghausenia sessilicarpa

Jusheng Li, Zhengyu Cao, Chuchu Xi, Gang-Zhong Zhou et al.
2 citations
Phytochemistry
Phytochemistry and Biological Activities
3.50
article

Bonenncarpas A–K: Coumarin derivatives with anti-inflammatory activity from Boenninghausenia sessilicarpa

Jusheng Li, Zhengyu Cao, Chuchu Xi, Gang-Zhong Zhou, Qi-Jing Fan, Ruo-Xi Hu, Yan-Gang Cao, Chunlei Zhang
article en
2 citations

Abstract

Eleven previously undescribed coumarin derivatives, bonenncarpas A-K (1-11), along with three known analogues (12-14), were isolated from the whole plant of Boenninghausenia sessilicarpa. The structures of these compounds were elucidated through comprehensive spectroscopic and spectrometric analyses. Their absolute configurations were determined by comparing experimental and calculated electronic circular dichroism data, as well as by X-ray crystallography. Notably, compound 1 features an open-ring coumarin structure with a five-membered lactone ring, while compounds 9-11 are characterized by a dihydrofuran ring at C-3 and C-4. All compounds were evaluated for their inhibitory effects on lipopolysaccharide-induced nitric oxide production in RAW 264.7 macrophage cells. At a concentration of 10 μM, compounds (-)-3, (+)-5, (+)-6, (+)-9, (-)-9, (+)-10, and (-)-10 exhibited inhibition of NO production, ranging from 25.5% to 95.0%.

PhytochemistryVol. 234
China Pharmaceutical University (CN), Guangxi Normal University (CN), First Affiliated Hospital of Henan University (CN)
Openalex Percentile: Top 10%
Phytochemistry and Biological Activities
3.50
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