Isolation, Identification, and α-Glucosidase Inhibitory Activity of the Chemical Composition of Daphne genkwa

Abstract: Phytochemical investigation of Daphne genkwa led to the isolation and identification of one previously undescribed indole alkaloid (1) and twenty-three known compounds. The isolated compounds were categorized as follows: three alkaloids (1–3), eight yuanhuacin derivatives (4–11), seven lignans (12–18), five flavonoids (19–23), and one monoterpene (24). The structure of the new indole alkaloid (1) was elucidated through comprehensive spectroscopic analysis, including UV, HRESIMS, and 1D/2D NMR techniques. All isolated compounds were evaluated for their α- glucosidase inhibitory activity. Among them, compounds 11, 20, and 23 exhibited moderate inhibitory effects, with IC50 values of 13.39, 16.64, and 18.04 μM, respectively. These findings suggest that certain constituents of D. genkwa might hold potential as α-glucosidase inhibitors, warranting further investigation into their therapeutic applications.

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Publication Details

Journal
Letters in Organic Chemistry
Published
2026-01-02
DOI
https://doi.org/10.2174/0115701786405154251119043658
Primary Topic
Bioactive Natural Diterpenoids Research
Type
article
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article

Isolation, Identification, and α-Glucosidase Inhibitory Activity of the Chemical Composition of Daphne genkwa

Heng‐Shan Wang, Hai-Ying Luo, Mei-Shan Li, Jia-Zi Luo et al.
Letters in Organic Chemistry
Bioactive Natural Diterpenoids Research
article

Isolation, Identification, and α-Glucosidase Inhibitory Activity of the Chemical Composition of Daphne genkwa

Heng‐Shan Wang, Hai-Ying Luo, Mei-Shan Li, Jia-Zi Luo, Gang Wei, Xi-Xi Song, Zi-Shuo Song
article en

Abstract

Abstract: Phytochemical investigation of Daphne genkwa led to the isolation and identification of one previously undescribed indole alkaloid (1) and twenty-three known compounds. The isolated compounds were categorized as follows: three alkaloids (1–3), eight yuanhuacin derivatives (4–11), seven lignans (12–18), five flavonoids (19–23), and one monoterpene (24). The structure of the new indole alkaloid (1) was elucidated through comprehensive spectroscopic analysis, including UV, HRESIMS, and 1D/2D NMR techniques. All isolated compounds were evaluated for their α- glucosidase inhibitory activity. Among them, compounds 11, 20, and 23 exhibited moderate inhibitory effects, with IC50 values of 13.39, 16.64, and 18.04 μM, respectively. These findings suggest that certain constituents of D. genkwa might hold potential as α-glucosidase inhibitors, warranting further investigation into their therapeutic applications.

Letters in Organic ChemistryVol. 23
Guangxi Normal University (CN), Affiliated Hospital of Youjiang Medical University for Nationalities (CN)
Openalex Percentile: Top 97%
Bioactive Natural Diterpenoids Research
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