New <i>α</i> ‐Glucosidase Inhibitors from Vietnamese <i>Garcinia schomburgkiana</i> Fruits

The chemical investigation of the fruits of Garcinia schomburgkiana growing in Vietnam led to the isolation of a new anofinic acid derivative, 5-hydroxy-8-methoxyanofinic acid (1), a new xanthone, xanthoschome C (2), and a known synthetic phenolic analog, 4-(2-hydroxybenzyl)-2-(4-hydroxybenzyl) phenol (3), along with seven known xanthones (4-10). The structures of all isolated compounds were determined using spectroscopic techniques (nuclear magnetic resonance and mass spectrometry), in conjunction with a comparison to existing literature data. All isolated compounds were assessed for their α-glucosidase inhibitory activity and showed significant inhibition, with half-maximal inhibitory concentration (IC<sub>50</sub>) values ranging from 12.1 to 65.7 µM, surpassing the potency of the positive control, acarbose (IC<sub>50</sub> 179 ± 6.02 µM). Among them, compound 8 exhibited the strongest inhibitory activity, with an IC<sub>50</sub> value of 12.1 ± 0.44 µM.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2025-01-27
DOI
https://doi.org/10.1002/cbdv.202403406
Citations
1
Primary Topic
Natural Compound Pharmacology Studies
Type
article
Field-Weighted Citation Impact
1.75
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article

New α ‐Glucosidase Inhibitors from Vietnamese Garcinia schomburgkiana Fruits

T. M. Lien, Jirapast Sichaem, Quyen H. N. Tran, Huong Nguyen et al.
1 citations
Chemistry & Biodiversity
Natural Compound Pharmacology Studies
1.75
article

New α ‐Glucosidase Inhibitors from Vietnamese Garcinia schomburgkiana Fruits

T. M. Lien, Jirapast Sichaem, Quyen H. N. Tran, Huong Nguyen, Thùy Linh Nguyễn
article en
1 citations

Abstract

The chemical investigation of the fruits of Garcinia schomburgkiana growing in Vietnam led to the isolation of a new anofinic acid derivative, 5-hydroxy-8-methoxyanofinic acid (1), a new xanthone, xanthoschome C (2), and a known synthetic phenolic analog, 4-(2-hydroxybenzyl)-2-(4-hydroxybenzyl) phenol (3), along with seven known xanthones (4-10). The structures of all isolated compounds were determined using spectroscopic techniques (nuclear magnetic resonance and mass spectrometry), in conjunction with a comparison to existing literature data. All isolated compounds were assessed for their α-glucosidase inhibitory activity and showed significant inhibition, with half-maximal inhibitory concentration (IC<sub>50</sub>) values ranging from 12.1 to 65.7 µM, surpassing the potency of the positive control, acarbose (IC<sub>50</sub> 179 ± 6.02 µM). Among them, compound 8 exhibited the strongest inhibitory activity, with an IC<sub>50</sub> value of 12.1 ± 0.44 µM.

Chemistry & BiodiversityVol. 22(6)
Thammasat University (TH), Ho Chi Minh City Open University (VN), Lampang Rajabhat University (TH), Ho Chi Minh City University of Technology (VN), Saigon University (VN)
Openalex Percentile: Top 18%
Natural Compound Pharmacology Studies
1.75
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