Evidence map›Paper›PMID 41502758›Full record

ArticleACS omega2025

Electronic Structure and Redox of the Antidepressants Venlafaxine and Desvenlafaxine.

Jhon Kennedy Alves Pereira, Eufrásia de Sousa Pereira, Bárbara Júlia Gonçalves Dutra, Isaac Yves Lopes de Macêdo, Arthur Saldanha Guimarães, Bruno Junior Neves, Eric de Souza Gil, Freddy Fernandes Guimarães

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In one paragraph

Article in ACS omega, 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

8 authors.

Jhon Kennedy Alves PereiraLaboratory of Pharmaceutical and Environmental Analysis, Faculdade de Farmácia, Universidade Federal de Goiás, Goiânia 74605-170, Goiás, Brazil.
Eufrásia de Sousa PereiraLaboratory of Cheminformatics, Faculdade de Farmácia, Universidade Federal de Goiás, Goiânia 74605-170, Goiás, Brazil.
Bárbara Júlia Gonçalves DutraInstitute of Chemistry, Universidade Federal de Goiás, Goiânia 74605-170, Goiás, Brazil.
Isaac Yves Lopes de MacêdoLaboratory of Pharmaceutical and Environmental Analysis, Faculdade de Farmácia, Universidade Federal de Goiás, Goiânia 74605-170, Goiás, Brazil.
Arthur Saldanha GuimarãesLaboratory of Pharmaceutical and Environmental Analysis, Faculdade de Farmácia, Universidade Federal de Goiás, Goiânia 74605-170, Goiás, Brazil.
Bruno Junior NevesLaboratory of Cheminformatics, Faculdade de Farmácia, Universidade Federal de Goiás, Goiânia 74605-170, Goiás, Brazil.ORCID https://orcid.org/0000-0002-1309-8743
Eric de Souza GilLaboratory of Cheminformatics, Faculdade de Farmácia, Universidade Federal de Goiás, Goiânia 74605-170, Goiás, Brazil.
Freddy Fernandes GuimarãesInstitute of Chemistry, Universidade Federal de Goiás, Goiânia 74605-170, Goiás, Brazil.ORCID https://orcid.org/0000-0002-7859-7682

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Venlafaxine and its primary metabolite desvenlafaxine are antidepressants that block presynaptic reuptake of serotonin and norepinephrine in the brain. Electroanalytical and computational analyses were performed to evaluate the electrochemical characterization of these drugs through measurements using a carbon paste electrode alongside quantum calculations (DFT and TD-DFT) to support the electrochemical data and propose potential oxidation pathways. The results showed that both venlafaxine and desvenlafaxine exhibit different pH-dependent electrochemical behaviors, with desvenlafaxine showing higher anodic peak intensities at neutral pH, while venlafaxine peaks at alkaline pH. Computational insights from DFT calculations provided a deeper understanding of the molecular charge distribution, orbital profiles, and energetics of both drugs in neutral and protonated states. The Gibbs free energy variations in different medium environments revealed the critical role of the medium in modulating the thermodynamic stability. These findings presented here improve our understanding of the electrochemical and electronic properties of these antidepressants and may pave the way for the development of more effective therapeutic agents.

Identifiers

PMID41502758
PMCPMC12771420

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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.