Evidence map›Paper›PMID 40572510›Full record

ReviewMolecules (Basel, Switzerland)2025

Structural Aspects of Arylpiperazines as Aminergic GPCR Ligands.

Agata Bartyzel, Beata Cristóvão, Agnieszka A Kaczor

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Agata BartyzelDepartment of General and Coordination Chemistry and Crystallography, Institute of Chemical Sciences, Faculty of Chemistry, Maria Curie-Sklodowska University in Lublin, Maria Curie-Sklodowska Sq. 2, 20-031 Lublin, Poland.ORCID 0000-0003-3765-6997
Beata CristóvãoDepartment of General and Coordination Chemistry and Crystallography, Institute of Chemical Sciences, Faculty of Chemistry, Maria Curie-Sklodowska University in Lublin, Maria Curie-Sklodowska Sq. 2, 20-031 Lublin, Poland.ORCID 0000-0001-5080-2413
Agnieszka A KaczorDepartment of Synthesis and Chemical Technology of Pharmaceutical Substances with Computer Modeling Laboratory, Faculty of Pharmacy, Medical University of Lublin, 4A Chodźki St., 20-093 Lublin, Poland.ORCID 0000-0001-8679-9623

Funding

Medical University of Lublin DS33
6 · The paper itself

Abstract

Arylpiperazines are considered a "privileged scaffold" in medical chemistry due to their versatility and modular structure, enabling modifications towards diverse molecular targets with desired potency, selectivity, and pharmacokinetic properties. In particular, arylpiperazines are aminergic G protein-coupled receptor (GPCR) ligands and neurotransmitter transporter inhibitors, making this group of compounds attractive in central nervous system (CNS) drug discovery for treating schizophrenia, depression, sleep disorders, and Parkinson's disease (PD). Furthermore, arylpiperazines may possess anticancer properties and can modulate some molecular targets involved in this disease. This review focuses on the structural aspects of arylpiperazines as aminergic GPCR ligands. The review centers on biologically active arylpiperazines with known X-ray structures, providing a detailed discussion of the conformations in the solid state. Next, their interactions with the aminergic GPCRs, based on experimental and molecular modelling studies, are addressed, making this review a comprehensive resource for medicinal and structural chemists working on arylpiperazines.

Indexed as

PiperazinesReceptors, G-Protein-CoupledAnimalsHumansLigandsModels, MolecularMolecular StructureStructure-Activity RelationshipLigandsPiperazinesReceptors, G-Protein-CoupledarylpiperazinesCNS disordersGPCRsmolecular modelingpharmacophore modelsstructure–activity relationshipX-ray structure

Identifiers

PMID40572510
PMCPMC12195839

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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.