Evidence map›Paper›PMID 38877034›Full record

ArticleScientific reports2024

Synthesis of novel aryl-substituted 2-aminopyridine derivatives by the cascade reaction of 1,1-enediamines with vinamidinium salts to develop novel anti-Alzheimer agents.

Sama Loori, Hormoz Pourtaher, Abdolmohammad Mehranpour, Alireza Hasaninejad, Mohammadreza Eftekharian, Aida Iraji

Abstract read
In one paragraph

Article in Scientific reports, 2024. 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.

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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

6 authors.

Sama LooriDepartment of Chemistry, Faculty of Sciences, Persian Gulf University, Bushehr, 75169, Iran.
Hormoz PourtaherDepartment of Chemistry, Faculty of Sciences, Persian Gulf University, Bushehr, 75169, Iran.
Abdolmohammad MehranpourDepartment of Chemistry, Faculty of Sciences, Persian Gulf University, Bushehr, 75169, Iran. ammehranpour@hotmail.com.
Alireza HasaninejadDepartment of Chemistry, Faculty of Sciences, Persian Gulf University, Bushehr, 75169, Iran.
Mohammadreza EftekharianStudent Research Committee, Jahrom University of Medical Sciences, Jahrom, Iran.
Aida IrajiDepartment of Persian Medicine, School of Medicine, Research Center for Traditional Medicine and History of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran. iraji@sums.ac.ir.

Funding

Shiraz University of Medical Sciences IR.SUMS.REC.1402.013
6 · The paper itself

Abstract

Alzheimer's disease (AD), a severe neurodegenerative disorder, imposes socioeconomic burdens and necessitates innovative therapeutic strategies. Current therapeutic interventions are limited and underscore the need for novel inhibitors of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), enzymes implicated in the pathogenesis of AD. In this study, we report a novel synthetic strategy for the generation of 2-aminopyridine derivatives via a two-component reaction converging aryl vinamidinium salts with 1,1-enediamines (EDAMs) in a dimethyl sulfoxide (DMSO) solvent system, catalyzed by triethylamine (Et

Indexed as

AcetylcholinesteraseAlzheimer DiseaseAminopyridinesButyrylcholinesteraseCholinesterase InhibitorsMolecular Docking SimulationHumansIminesStructure-Activity RelationshipAcetylcholinesteraseAminopyridinesButyrylcholinesteraseCholinesterase InhibitorsImines1,1-EnediaminesAlzheimerAryl-substituted 2-aminopyridineAryl vinamidinium saltsMolecular dynamic simulation

Identifiers

PMID38877034
PMCPMC11178820

What OpenQuestion holds

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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.