Evidence map›Paper›PMID 41236800›Full record

ArticleChemistry & biodiversity2026

Integrative Network Pharmacology and Glucose Uptake Studies Identify Potential Phytochemicals From Syzygium cumini as Promising Antidiabetic Agents.

Sucindran Soundaryalakshmi, Muthu Kumar Thirunavukkarasu, Mani Vasanthi

Abstract read
In one paragraph

Article in Chemistry & biodiversity, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Sucindran SoundaryalakshmiDepartment of Biotechnology, Kamaraj College of Engineering and Technology, Madurai, India.
Muthu Kumar ThirunavukkarasuSchool of Sciences and Humanities, SR University, Warangal, India.
Mani VasanthiDepartment of Biotechnology, Kamaraj College of Engineering and Technology, Madurai, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetes mellitus (DM) is a multifaceted metabolic illness with significant detrimental effects during the conventional treatment approach. Therefore, this study aims to explore novel therapeutic targets and potential phytoconstituents using an edge-weighted network pharmacology approach. The bioactive compounds from Syzygium cumini were selected based on the literature evidence. Potential gene targets corresponding to these phytoconstituents were identified using gene-disease association, enrichment calculations, and KEGG pathway mapping analysis. These results reveal that PTPN1 is closely associated with the disease progression of DM. Binding interactions between phytochemicals and the candidate gene (PTPN1) were determined using molecular docking combined with molecular dynamics simulation and MM/PBSA calculations. Notably, chrysanthemin derived from S. cumini exhibited substantial inhibitory action in glucose uptake assays using L6 cell lines, PTP1B inhibition, and enzyme kinetics analyses. These findings suggest that this compound might be a promising candidate for PTPN1 inhibition, warranting further extensive research for its potential therapeutic application in DM.

Indexed as

GlucoseHypoglycemic AgentsNetwork PharmacologyPhytochemicalsSyzygiumAnimalsCell LineDose-Response Relationship, DrugHumansMolecular Docking SimulationMolecular StructureProtein Tyrosine Phosphatase, Non-Receptor Type 1RatsGlucoseHypoglycemic AgentsPhytochemicalsProtein Tyrosine Phosphatase, Non-Receptor Type 1PTPN1 protein, humanglucose uptake assaymolecular dynamicsnetwork pharmacologyPTPN1Type II diabetes mellitus

Identifiers

PMID41236800
PMCPMC13419909

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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.