Evidence map›Paper›PMID 37110664›Full record

ArticleMolecules (Basel, Switzerland)2023

Cytotoxicity Profiles and Neuroprotective Properties of the Novel Ifenprodil Analogues as Sigma Ligands.

Daniele Zampieri, Antonella Calabretti, Maurizio Romano, Sara Fortuna, Simona Collina, Emanuele Amata, Maria Dichiara, Agostino Marrazzo, Maria Grazia Mamolo

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 38% of its field
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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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 at 4 institutions in 1 country.

Daniele ZampieriDepartment of Chemical and Pharmaceutical Sciences, University of Trieste, Via Giorgieri 1, 34127 Trieste, Italy.ORCID 0000-0002-1397-7334
Antonella CalabrettiDepartment of Chemical and Pharmaceutical Sciences, University of Trieste, Via Giorgieri 1, 34127 Trieste, Italy.
Maurizio RomanoDepartment of Life Sciences, University of Trieste, Via Valerio 28, 34127 Trieste, Italy.ORCID 0000-0002-4820-2897
Sara FortunaItalian Institute of Technology (IIT), Via E. Melen 83, 16152 Genova, Italy.
Simona CollinaDepartment of Drug Sciences, Medicinal Chemistry and Pharmaceutical Technology Section, University of Pavia, Viale Taramelli 6 and 12, 27100 Pavia, Italy.ORCID 0000-0002-2954-7558
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.
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.
University of Trieste · ITUniversity of Catania · ITItalian Institute of Technology · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurodegeneration is a slow and progressive loss of neuronal cells or their function in specific regions of the brain or in the peripheral system. Among several causes responsible for the most common neurodegenerative diseases (NDDs), cholinergic/dopaminergic pathways, but also some endogenous receptors, are often involved. In this context, sigma 1 receptor (S1R) modulators can be used as neuroprotective and antiamnesic agents. Herein, we describe the identification of novel S1R ligands endowed with antioxidant properties, potentially useful as neuroprotective agents. We also computationally assessed how the most promising compounds might interact with the S1R protein's binding sites. The in silico predicted ADME properties suggested that they could be able to cross the brain-blood-barrier (BBB), and to reach the targets. Finally, the observation that at least two novel ifenprodil analogues (

Indexed as

NeuroblastomaNeuroprotective AgentsReceptors, sigmaAntioxidantsHumansLigandsNeuroprotectionPiperidinesAntioxidantsifenprodilLigandsNeuroprotective AgentsPiperidinesReceptors, sigmaacetylcholinesteraseantioxidant propertiesdockingneuroprotective agentssigma 1 receptor

Identifiers

PMID37110664
PMCPMC10146949
OpenAlexW4365453058

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.