Evidence map›Paper›PMID 42310894›Full record

ArticleJournal of the science of food and agriculture2026

Bio-guided fractionation of (9Z )-5,8,11-trihydroxyoctadec-9-enoic acid from Abelmoschus sagittifolius root as a potent α-glucosidase inhibitor: An integrated in vitro and in silico study.

Nguyen Phuong Mai, Nguyen Van Quan, Nguyen Dang Duc, Tran Dang Xuan

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Article in Journal of the science of food and agriculture, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Nguyen Phuong MaiTransdisciplinary Science and Engineering Program, Graduate School of Advanced Science and Engineering, Hiroshima University, Higashihiroshima, Japan.ORCID https://orcid.org/0000-0001-8508-1388
Nguyen Van QuanDepartment of Pharmacy, Thai Nguyen University of Medicine and Pharmacy, Thái Nguyên, Vietnam.
Nguyen Dang DucBach Mai Hospital, Hanoi, Vietnam.
Tran Dang XuanTransdisciplinary Science and Engineering Program, Graduate School of Advanced Science and Engineering, Hiroshima University, Higashihiroshima, Japan.ORCID https://orcid.org/0000-0001-7103-5698

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAbelmoschus sagittifolius stands out as a valuable medicinal source for developing functional food targeting type 2 diabetes. This study investigated the α-glucosidase inhibitory potential of an active fraction obtained from A. sagittifolius roots (ASR), enriched in (9Z)-5,8,11-trihydroxyoctadec-9-enoic acid (OA), using both enzyme kinetics and molecular docking analyses. The effect of simulated digestion and in silico acute oral toxicity was also evaluated.

resultsThe bioactive fraction, with OA as major component, exhibited strong α-glucosidase inhibitory activity [half-inhibitory concentration (IC

conclusionThis study provides the first investigation into the potential of an OA enriched fraction and its inhibitory mechanism, highlighting OA as a promising bioactive compound for the development of functional foods or nutraceuticals aimed at managing type 2 diabetes. However, further studies, including enzyme-based validation, toxicity evaluation, bioavailability assessment and clinical investigation, are required to comprehensively confirm the efficacy and safety of OA as a potent α-glucosidase inhibitor. © 2026 The Author(s). Journal of the Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Indexed as

Glycoside Hydrolase InhibitorsPlant Extractsalpha-GlucosidasesAnimalsComputer SimulationDiabetes Mellitus, Type 2HumansKineticsMolecular Docking SimulationPlant Rootsalpha-GlucosidasesGlycoside Hydrolase InhibitorsPlant ExtractsAbelmoschus sagittifoliusdigestionin silico toxicitymixed inhibitorα‐glucosidase

Identifiers

PMID42310894
PMCPMC13543704

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.