Guided Isolation of Isopentenyl Flavonoids from <i>Daphne giraldii</i> Based on the Combination of GNPS and SMART

Six flavonoids (1-6), including 3 previously undescribed compounds (1-3), were isolated from the dried roots and stem skins of Daphne giraldii Nitsche. The strategy of LC-tandem mass spectrometry-based Global Natural Products Social Molecular Networking (GNPS) molecular network technology and NMR-based Small Molecule Accurate Recognition Technology (SMART) technology facilitated the precise separation of isopentenyl flavonoids in D. giraldii. The structures were determined through comprehensive spectroscopic analysis. Furthermore, all compounds were evaluated for their cytotoxic activity against Hep3B cells. Specifically, compounds 1 and 3 exhibited significant cytotoxicity with IC<sub>50</sub> values of 5.52 ± 0.57 and 2.53 ± 0.49 μM, respectively, compared to the positive control sorafenib (IC<sub>50</sub> = 7.08 ± 0.23 μM).

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Publication Details

Journal
Chemical and Pharmaceutical Bulletin
Published
2025-03-06
DOI
https://doi.org/10.1248/cpb.c24-00462
Citations
2
Primary Topic
Phytochemistry and Biological Activities
Type
article
Field-Weighted Citation Impact
3.50
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article

Guided Isolation of Isopentenyl Flavonoids from Daphne giraldii Based on the Combination of GNPS and SMART

Xiao‐Xiao Huang, Shuang Qiu, Bo-Yuan Zhao, Shao‐Jiang Song et al.
2 citations
Chemical and Pharmaceutical Bulletin
Phytochemistry and Biological Activities
3.50
article

Guided Isolation of Isopentenyl Flavonoids from Daphne giraldii Based on the Combination of GNPS and SMART

Xiao‐Xiao Huang, Shuang Qiu, Bo-Yuan Zhao, Shao‐Jiang Song, Guo‐Dong Yao, Ben-Song Xin
article en
2 citations

Abstract

Six flavonoids (1-6), including 3 previously undescribed compounds (1-3), were isolated from the dried roots and stem skins of Daphne giraldii Nitsche. The strategy of LC-tandem mass spectrometry-based Global Natural Products Social Molecular Networking (GNPS) molecular network technology and NMR-based Small Molecule Accurate Recognition Technology (SMART) technology facilitated the precise separation of isopentenyl flavonoids in D. giraldii. The structures were determined through comprehensive spectroscopic analysis. Furthermore, all compounds were evaluated for their cytotoxic activity against Hep3B cells. Specifically, compounds 1 and 3 exhibited significant cytotoxicity with IC<sub>50</sub> values of 5.52 ± 0.57 and 2.53 ± 0.49 μM, respectively, compared to the positive control sorafenib (IC<sub>50</sub> = 7.08 ± 0.23 μM).

Chemical and Pharmaceutical BulletinVol. 73(3)
Shenyang Pharmaceutical University (CN), Yantai University (CN)
Responsible consumption and production
Openalex Percentile: Top 9%
Phytochemistry and Biological Activities
3.50
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