Evidence map›Paper›PMID 41981068›Full record

ArticleScientific reports2026

Computational and preliminary screening of anti-caries active compounds of Caesalpinia sappan.

Yongliang Jia, Dongdong Zhang, Hongxing Lu, Yanhong Li, Yuehu Wang

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Article in Scientific reports, 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

What it found

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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

5 authors.

Yongliang JiaDepartment of Preventive Dentistry, The Affiliated Stomatology Hospital, Kunming Medical University, Kunming, 650106, China.
Dongdong ZhangDepartment of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, China.
Hongxing LuDepartment of Preventive Dentistry, The Affiliated Stomatology Hospital, Kunming Medical University, Kunming, 650106, China.
Yanhong LiDepartment of Preventive Dentistry, The Affiliated Stomatology Hospital, Kunming Medical University, Kunming, 650106, China. yanhongli_kmu@126.com.
Yuehu WangKey Laboratory of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, China. wangyuehu@mail.kib.ac.cn.

Funding

National Natural Science Foundation of China 82160179
6 · The paper itself

Abstract

Dental caries is a significant global oral health problem, primarily caused by Streptococcus mutans (S. mutans). Although previous studies have indicated that Caesalpinia sappan (CS) exhibits anti-caries properties, its specific anti-caries active compounds remain largely unidentified. This study aimed to identify the potential anti-caries components of CS through an integrated strategy involving bioassay-guided isolation targeting S. mutans, UPLC-MS/MS, network pharmacology, molecular docking, and molecular dynamics simulation. Bioassay-guided isolation led to the identification of 33 compounds in fraction 5 from CS, among which brazilin showed the highest content and effectively inhibited biofilm formation and acid production by S. mutans. Network pharmacology analysis predicted 11 active ingredients in CS, including brazilin, targeting 7 potential targets related to dental caries: AKT1, EGFR, BCL2, PTGS2, MMP9, ERBB2, and HSP90AA1, as well as two pathways-nitrogen metabolism and calcium signaling. Molecular docking revealed strong binding affinities of brazilin to PTGS2, EGFR, MMP9, GtfC, GtfD, and GbpC. Further, molecular dynamics simulation revealed strong stability between brazilin and PTGS2, GtfC. Together, these findings not only clarify the anti-caries chemical constituents of CS and their potential mechanisms of action, but also provide new insights into the bioactive components and mechanisms of natural plant-derived medicines for the prevention and treatment of dental caries.

Indexed as

Anti-Bacterial AgentsCaesalpiniaDental CariesPlant ExtractsStreptococcus mutansBenzopyransBiofilmsHumansMolecular Docking SimulationMolecular Dynamics SimulationNetwork PharmacologyTandem Mass SpectrometryAnti-Bacterial AgentsBenzopyransbrazilinPlant ExtractsCaesalpinia sappanDental cariesMolecular dockingNetwork pharmacologyStreptococcus mutans

Identifiers

PMID41981068
PMCPMC13237023

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