# Computational Analysis of Balanites aegyptiaca Phytochemicals as Inhibitors of Human Pancreatic α‐Amylase

**Authors:** Surendra Kumar Gautam, Rakesh Kumar Paul, Smita Jain, Iqrar Ahmad, Ammar A. Razzak Mahmood, Harun Patel, Penke Vijaya Babu, Muhammad Wahajuddin, Kaisar Raza

PMC · DOI: 10.1002/cbdv.202503133 · 2026-02-12

## TL;DR

This study uses computational methods to identify compounds in Balanites aegyptiaca that may inhibit α-amylase, a target for diabetes treatment.

## Contribution

The study identifies two phytochemicals from Balanites aegyptiaca with strong inhibitory potential against α-amylase through in silico and network pharmacology approaches.

## Key findings

- Balanitesin and SN0224203 showed the highest docking scores and binding free energy as α-amylase inhibitors.
- SN0224203 was found to be associated with genes and pathways related to Type II diabetes mellitus.
- Molecular dynamics simulations confirmed the stability of SN0224203 binding to α-amylase.

## Abstract

Balanites aegyptiaca (BA) is a plant of paramount potential for the management of diabetes mellitus. The study investigates in silico studies of natural library compounds including that from BA with the assistance of network pharmacology. Balanitesin (compound 1) exhibited the highest docking score and binding free energy (∆G) values of −14.406 and −125.47 kcal/mol, respectively, and SN0224203 (compound 9) exhibited the docking score of −13.019 kcal/mol and binding free energy of −128.41 kcal/mol. These were found to be the most potential α‐amylase inhibitor out of the phytoconstituents of BA, whereas the standard compound exhibited the docking score of −12.500 kcal/mol and ∆G value of −81.275 kcal/mol. The network pharmacology results also showed that SN0224203 might act as an α‐amylase inhibitor, it was found to be associated with various genes like GCK, VDCC, PIK3, and mTOR and Type II diabetes mellitus pathway. The MDS results showed that the binding of SN0224203 with α‐amylase was more stable as vivid from 50 to 300 ns simulation. Genes. Our results suggest that the compounds of BA were found to be potent against α‐amylase. The findings are promising and suggest further in‐vitro and in‐vivo validation studies of the potent compounds from BA for better diabetes management.

## Linked entities

- **Genes:** GCK (glucokinase) [NCBI Gene 2645], PIK3CG (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma) [NCBI Gene 5294], MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475]
- **Diseases:** Type II diabetes mellitus (MONDO:0005148)
- **Species:** Balanites aegyptiaca (taxon 886265)

## Full-text entities

- **Genes:** PIK3CG (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma) [NCBI Gene 5294] {aka IMD97, PI3CG, PI3K, PI3Kgamma, PIK3, p110gamma}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, AMY2A (amylase alpha 2A) [NCBI Gene 279] {aka AMY2, PA}, GCK (glucokinase) [NCBI Gene 2645] {aka FGQTL3, GK, GLK, HHF3, HK4, HKIV}
- **Diseases:** diabetes (MESH:D003920), Type II diabetes mellitus (MESH:D003924)
- **Chemicals:** Balanitesin (MESH:C113524), SN0224203 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Lacticaseibacillus casei (species) [taxon 1582]

## Figures

21 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12895220/full.md

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Source: https://tomesphere.com/paper/PMC12895220