Evidence map›Paper›PMID 39598746›Full record

ArticleMolecules (Basel, Switzerland)2024

Derivatives of Amodiaquine as Potent Human Cholinesterases Inhibitors: Implication for Treatment of Alzheimer's Disease.

Ana Matošević, Dejan M Opsenica, Marija Bartolić, Nikola Maraković, Andriana Stoilković, Katarina Komatović, Antonio Zandona, Suzana Žunec, Anita Bosak

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Molecular docking andJournal of Taibah University Medical Sciences · 2025
    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

9 authors.

Ana MatoševićInstitute for Medical Research and Occupational Health, Ksaverska Cesta 2, 10001 Zagreb, Croatia.ORCID 0009-0002-4459-7622
Dejan M OpsenicaInstitute of Chemistry Technology and Metallurgy, University of Belgrade, Njegoševa 12, 11000 Beograd, Serbia.ORCID 0000-0002-5948-0702
Marija BartolićInstitute for Medical Research and Occupational Health, Ksaverska Cesta 2, 10001 Zagreb, Croatia.ORCID 0009-0009-1713-8915
Nikola MarakovićInstitute for Medical Research and Occupational Health, Ksaverska Cesta 2, 10001 Zagreb, Croatia.ORCID 0000-0002-1709-6390
Andriana StoilkovićInstitute of Chemistry Technology and Metallurgy, University of Belgrade, Njegoševa 12, 11000 Beograd, Serbia.
Katarina KomatovićFaculty of Chemistry, University of Belgrade, Studentski trg 12-16, 11158 Belgrade, Serbia.ORCID 0000-0003-4858-0668
Antonio ZandonaInstitute for Medical Research and Occupational Health, Ksaverska Cesta 2, 10001 Zagreb, Croatia.ORCID 0000-0002-3937-3520
Suzana ŽunecInstitute for Medical Research and Occupational Health, Ksaverska Cesta 2, 10001 Zagreb, Croatia.ORCID 0000-0002-7710-8250
Anita BosakInstitute for Medical Research and Occupational Health, Ksaverska Cesta 2, 10001 Zagreb, Croatia.ORCID 0000-0003-0164-4994

Funding

Croatian Science Foundation IP-2020-02-9343MESTD of the Republic of Serbia 451-03-66/2024-03/200026 and 451-03-66/2024-03/200168Special Research Program COVID-19 7547552
6 · The paper itself

Abstract

As some previously reported studies have proven that amodiaquine, in addition to its primary antimalarial activity, also has potential for new applications such as the inhibition of cholinesterases, in our study we focused on the evaluation of the influence of different substituents in the aminoquinoline part of the amodiaquine structure on the inhibition of human acetylcholinesterase and butyrylcholinesterase to investigate the possibility for their use as drugs for the treatment of AD. We synthesized a series of amodiaquine derivatives bearing H-, F-, CF

Indexed as

AcetylcholinesteraseAlzheimer DiseaseAmodiaquineButyrylcholinesteraseCholinesterase InhibitorsAntioxidantsBlood-Brain BarrierHumansMolecular StructureStructure-Activity RelationshipAcetylcholinesteraseAmodiaquineAntioxidantsButyrylcholinesteraseCholinesterase Inhibitors4-aminoquinoline derivativesacetylcholinesterasebutyrylcholinesterasechelationcytotoxicity

Identifiers

PMID39598746
PMCPMC11596630

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.