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In silico discovery of α-glucosidase inhibitors from Mitragyna speciosa for antidiabetic therapy

Mat Rasid, Siti Norain and Khatib, Alfi and Nando, Dendi Noventri and Ahmad Mizher, Hussam Abdeljabar and Mohd Nasir, Mohd Hamzah and Arzmi, Mohd Hafiz (2025) In silico discovery of α-glucosidase inhibitors from Mitragyna speciosa for antidiabetic therapy. In: 1st International Biomedical Conference 2025, 3-4 Sep 2025, Kuantan, Malaysia.

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Abstract

INTRODUCTION: Mitragyna speciosa (kratom) is a medicinal plant known for its richness in phytochemicals with potential antidiabetic activity. α-glucosidase is an enzyme that plays a key role in carbohydrate hydrolysis. The inhibition of α-glucosidase activity represents a validated therapeutic approach to manage postprandial hyperglycaemia in type 2 diabetes. This study investigates the potential of M. speciosa leaf extract as an α-glucosidase inhibitor. OBJECTIVE(S): To identify bioactive compounds in M. speciosa ethanolic leaf extract that inhibit α-glucosidase and to evaluate their interaction with the enzyme through in silico molecular docking. MATERIALS & METHODS: Phytochemical profiling of the 95% ethanolic extract of M. speciosa leaf was performed using LC-MS QTOF. In vitro α-glucosidase inhibition assay was conducted to determine the IC₅₀ value of the extract. Selected compounds were subjected to molecular docking analysis using AutoDock software against α-glucosidase enzyme (PDB ID: 3A4A), and key binding interactions were analysed. RESULTS: A total of 16 putative bioactive compounds were identified from the extract. The extract exhibited α-glucosidase inhibitory activity with an IC₅₀ of 21.64 µg/mL. In the molecular docking analysis, Rhyncophylline showed strong binding to α-glucosidase (ΔG = -8.8 kcal/mol), comparable to standard inhibitors. Its interaction with ASP352, a known catalytic residue, suggests that Rhyncophylline may act as a potential α-glucosidase inhibitor. CONCLUSION: The ethanolic leaf extract of M. speciosa exhibits α-glucosidase inhibitory activity. Rhyncophylline, identified via in silico docking, is a promising lead compound for future antidiabetic drug development.

Item Type: Proceeding Paper (Poster)
Uncontrolled Keywords: Mitragyna speciosa, α-Glucosidase, Molecular Docking, Rhyncophylline
Subjects: R Medicine > R Medicine (General)
R Medicine > RM Therapeutics. Pharmacology
Kulliyyahs/Centres/Divisions/Institutes (Can select more than one option. Press CONTROL button): Kulliyyah of Dentistry
Kulliyyah of Dentistry > Department of Fundamental Dental and Medical Sciences
Kulliyyah of Pharmacy
Kulliyyah of Pharmacy > Department of Basic Medical Sciences
Kulliyyah of Pharmacy > Department of Pharmaceutical Chemistry
Kulliyyah of Science
Kulliyyah of Science > Department of Biotechnology
Kulliyyah of Medicine
Kulliyyah of Medicine > Department of Basic Medical
Depositing User: Dr. Siti Norain Mat Rasid
Date Deposited: 16 Dec 2025 15:06
Last Modified: 16 Dec 2025 15:06
Queue Number: 2025-12-Q989
URI: http://irep.iium.edu.my/id/eprint/125079

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