Evidence map›Paper›PMID 40723805›Full record

ArticleBiomolecules2025

Discovery of Dietary Plant Flavonols as Novel Potent Inhibitors Targeting DYRK1A Kinase.

Jin Jin, Qihong Zhou, Bin Guo, Zongchao Jia

Abstract read
In one paragraph

Article in Biomolecules, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Jin JinDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, ON KL7 3N6, Canada.
Qihong ZhouKey Laboratory of Phytochemical R&D of Hunan Province, Key Laboratory of Chemical Biology, and Traditional Chinese Medicine Research (Ministry of Education of China), Hunan Normal University, Changsha 410081, China.
Bin GuoKey Laboratory of Phytochemical R&D of Hunan Province, Key Laboratory of Chemical Biology, and Traditional Chinese Medicine Research (Ministry of Education of China), Hunan Normal University, Changsha 410081, China.
Zongchao JiaDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, ON KL7 3N6, Canada.ORCID 0000-0002-9322-9394

Funding

Natural Sciences and Engineering Research Council RGPIN-2024-05181
6 · The paper itself

Abstract

DYRK1A kinase is a critical regulator in cellular signaling pathways and a promising therapeutic target for neurodegenerative diseases, diabetes and cancers. Despite its significance, the development of potent, selective and safe inhibitors remains a significant challenge. Several natural flavonoids have been reported to inhibit DYRK1A by binding in the ATP-binding pocket, exhibiting antidiabetic properties. However, a systematic screening of these structural derivatives remains lacking. In this study, we aimed to expand the pool of flavonoid-based DYRK1A inhibitor candidates for drug development against DYRK1A through targeted screening and structure-based analysis. A focused library of 13 flavonoid derivatives was screened to identify novel DYRK1A inhibitors, revealing eight new flavonol inhibitors with IC

Indexed as

FlavonolsProtein Kinase InhibitorsProtein Serine-Threonine KinasesProtein-Tyrosine KinasesDrug DiscoveryDyrk KinasesFlavonoidsHumansMolecular Docking SimulationStructure-Activity RelationshipDyrk KinasesfisetinFlavonoidsFlavonolsProtein Kinase InhibitorsProtein Serine-Threonine KinasesProtein-Tyrosine KinasesDYRK1Aflavonoidsmolecular dockingprotein kinase inhibitorsstructure-activity relationship

Identifiers

PMID40723805
PMCPMC12292390

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Registered trials

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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.