Phenolic Acids Derivatives from <i>Meehania Fargesii</i> with Anti‐inflammation Effects

Utilizing systematic plant chemistry separation techniques, two previously unreported phenolic acids (1-2) and eighteen (3-20) phenolic acids were isolated from 70 % ethanol extract of Meehania fargesii var. radicans (Vaniot) C.Y.Wu. The structures of the unreported compounds were determined using spectroscopic methods, including 1D and 2D NMR, ECD, and HR-ESI-MS. The activity of all isolated phenolic acids was evaluated for their ability to inhibit nitric oxide (NO) production in RAW264.7 cells activated by lipopolysaccharide (LPS). Among the isolated compounds, compounds 1 and 19 exhibited significant inhibitory activity against NO production in RAW264.7 cells, with higher concentrations being more active than the indomethacin, without displaying cytotoxicity. This study provides a basis for the application and development of M. fargesii and the discovery of natural anti-inflammatory drugs.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2024-09-12
DOI
https://doi.org/10.1002/cbdv.202401414
Citations
3
Primary Topic
Phytochemistry and Biological Activities
Type
article
Field-Weighted Citation Impact
1.80

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article

Phenolic Acids Derivatives from Meehania Fargesii with Anti‐inflammation Effects

Mingyi Shen, Jun Zeng, Xingpeng Liu, Jia‐Liang Zhu et al.
3 citations
Chemistry & Biodiversity
Phytochemistry and Biological Activities
1.80
article

Phenolic Acids Derivatives from Meehania Fargesii with Anti‐inflammation Effects

Mingyi Shen, Jun Zeng, Xingpeng Liu, Jia‐Liang Zhu, Meng Da-li, Mingming Qiao, Hanchuan Wang
article en
3 citations

Abstract

Utilizing systematic plant chemistry separation techniques, two previously unreported phenolic acids (1-2) and eighteen (3-20) phenolic acids were isolated from 70 % ethanol extract of Meehania fargesii var. radicans (Vaniot) C.Y.Wu. The structures of the unreported compounds were determined using spectroscopic methods, including 1D and 2D NMR, ECD, and HR-ESI-MS. The activity of all isolated phenolic acids was evaluated for their ability to inhibit nitric oxide (NO) production in RAW264.7 cells activated by lipopolysaccharide (LPS). Among the isolated compounds, compounds 1 and 19 exhibited significant inhibitory activity against NO production in RAW264.7 cells, with higher concentrations being more active than the indomethacin, without displaying cytotoxicity. This study provides a basis for the application and development of M. fargesii and the discovery of natural anti-inflammatory drugs.

Chemistry & BiodiversityVol. 22(1)
Shenyang Pharmaceutical University (CN), National Institutes for Food and Drug Control (CN), ZheJiang Institute For Food and Drug Control (CN)
National Natural Science Foundation of China, Department of Education of Liaoning Province
Clean water and sanitation
Openalex Percentile: Top 13%
Phytochemistry and Biological Activities
1.80
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