Evidence map›Paper›PMID 38893570›Full record

ArticleMolecules (Basel, Switzerland)2024

Design, Synthesis, and Cytotoxic Assessment of New Haloperidol Analogues as Potential Anticancer Compounds Targeting Sigma Receptors.

Daniele Zampieri, Maurizio Romano, Sara Fortuna, Emanuele Amata, Maria Dichiara, Giuseppe Cosentino, Agostino Marrazzo, Maria Grazia Mamolo

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. Review
  2. 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

8 authors.

Daniele ZampieriDepartment of Chemical and Pharmaceutical Sciences, University of Trieste, Via Giorgieri 1, 34127 Trieste, Italy.ORCID 0000-0002-1397-7334
Maurizio RomanoDepartment of Life Sciences, University of Trieste, Via Valerio 28, 34127 Trieste, Italy.ORCID 0000-0002-4820-2897
Sara FortunaCresset-New Cambridge House, Bassingbourn Road, Litlington, Cambridge SG8 0SS, UK.
Emanuele AmataDepartment of Drug and Health Sciences, University of Catania, Viale Doria 6, 95125 Catania, Italy.ORCID 0000-0002-4750-3479
Maria DichiaraDepartment of Drug and Health Sciences, University of Catania, Viale Doria 6, 95125 Catania, Italy.ORCID 0000-0001-6380-7176
Giuseppe CosentinoDepartment of Drug and Health Sciences, University of Catania, Viale Doria 6, 95125 Catania, Italy.ORCID 0009-0004-6185-5747
Agostino MarrazzoDepartment of Drug and Health Sciences, University of Catania, Viale Doria 6, 95125 Catania, Italy.ORCID 0000-0002-8728-8857
Maria Grazia MamoloDepartment of Chemical and Pharmaceutical Sciences, University of Trieste, Via Giorgieri 1, 34127 Trieste, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sigma receptors (SRs), including SR1 and SR2 subtypes, have attracted increasing interest in recent years due to their involvement in a wide range of activities, including the modulation of opioid analgesia, neuroprotection, and potential anticancer activity. In this context, haloperidol (HAL), a commonly used antipsychotic drug, also possesses SR activity and cytotoxic effects. Herein, we describe the identification of novel SR ligands, obtained by a chemical hybridization approach. There wereendowed with pan-affinity for both SR subtypes and evaluated their potential anticancer activity against SH-SY5Y and HUH-7 cancer cell lines. Through a chemical hybridization approach, we identified novel compounds (

Indexed as

Antineoplastic AgentsDrug DesignHaloperidolReceptors, sigmaCell Line, TumorCell ProliferationCell SurvivalDrug Screening Assays, AntitumorHumansLigandsMolecular StructureStructure-Activity RelationshipAntineoplastic AgentsHaloperidolLigandsReceptors, sigmaaffinityanticancerdockingselectivitysigma 1 receptorsigma 2 receptor

Identifiers

PMID38893570
PMCPMC11173765

What OpenQuestion holds

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LicenceCC BY
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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.