Two new polymethoxyflavones with fully substituted A-ring from the peels of <i>Citrus reticulata</i> “dahongpao”

Phytochemical investigation of the peels of <i>Citrus reticulata</i> "Dahongpao" resulted in the isolation and characterization of six polymethoxyflavones. Their structures were elucidated as 5,6,7,3'-tetrahydroxy-8,4'-dimethoxyflavone (<b>1</b>), 5,6,7-trihydroxy-8,3',4'-trimethoxyflavone (<b>2</b>), 5,7,8-trihydroxy-6,3',4'-trimethoxyflavone (<b>3</b>), 5,8-dihydroxy -6,7,3',4'-tetramethoxyflavone (<b>4</b>), 5,6,7,8-tetrahydroxy-3',4'-dimethoxyflavone (<b>5</b>), and nobiletin (<b>6</b>) by analysis of their spectroscopic data. They feature a characteristic fully substituted A-ring and a 3',4'-disubstituted B-ring, analogous to nobiletin. Among them, compounds <b>1</b> and <b>2</b> are new compounds. Full assignment of NMR data for compounds <b>3</b> and <b>5</b> is presented here for the first time. Furthermore, the discrepancies in the previously reported NMR spectroscopic data of compound <b>4</b> are discussed.

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Journal
Journal of Asian Natural Products Research
Published
2025-10-08
DOI
https://doi.org/10.1080/10286020.2025.2567403
Primary Topic
Bioactive Compounds in Plants
Type
article
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article

Two new polymethoxyflavones with fully substituted A-ring from the peels of Citrus reticulata “dahongpao”

Bin Xiao, Y. H. Liu, Haoyuan Zheng, Juan Li et al.
Journal of Asian Natural Products Research
Bioactive Compounds in Plants
article

Two new polymethoxyflavones with fully substituted A-ring from the peels of Citrus reticulata “dahongpao”

Bin Xiao, Y. H. Liu, Haoyuan Zheng, Juan Li, Ding Liu, Chunlei Zhang, Qiang Zhan
article en

Abstract

Phytochemical investigation of the peels of <i>Citrus reticulata</i> "Dahongpao" resulted in the isolation and characterization of six polymethoxyflavones. Their structures were elucidated as 5,6,7,3'-tetrahydroxy-8,4'-dimethoxyflavone (<b>1</b>), 5,6,7-trihydroxy-8,3',4'-trimethoxyflavone (<b>2</b>), 5,7,8-trihydroxy-6,3',4'-trimethoxyflavone (<b>3</b>), 5,8-dihydroxy -6,7,3',4'-tetramethoxyflavone (<b>4</b>), 5,6,7,8-tetrahydroxy-3',4'-dimethoxyflavone (<b>5</b>), and nobiletin (<b>6</b>) by analysis of their spectroscopic data. They feature a characteristic fully substituted A-ring and a 3',4'-disubstituted B-ring, analogous to nobiletin. Among them, compounds <b>1</b> and <b>2</b> are new compounds. Full assignment of NMR data for compounds <b>3</b> and <b>5</b> is presented here for the first time. Furthermore, the discrepancies in the previously reported NMR spectroscopic data of compound <b>4</b> are discussed.

Journal of Asian Natural Products Research
Pingdingshan University (CN), Guangxi Normal University (CN), Jiangning District of Nanjing Chinese Medicine Hospital (CN), Bio-Medical Science (South Korea) (KR)
Openalex Percentile: Top 79%
Bioactive Compounds in Plants
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Two new polymethoxyflavones with fully substituted A-ring from the peels of <i>Citrus reticulata</i> “dahongpao” — Bin Xiao, Y. H. Liu, et al. · Journal of Asian Natural Products Research (2025) | TGRS Research Map | TGRS