Evidence map›Paper›PMID 40104788›Full record

ArticleACS medicinal chemistry letters2025

Enhanced Cytotoxicity of [10]-Gingerol-Coumarin-Triazole Hybrid as a Theranostic Agent for Triple Negative Breast Cancer.

Arthur Deponte Zutião, Bianca Cruz Pachane, Paulo Sérgio Gonçalves Nunes, Herika Danielle Almeida Vidal, Heloisa Sobreiro Selistre-de-Araujo, Arlene Gonçalves Corrêa, Marcia Regina Cominetti, Angelina Maria Fuzer

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Arthur Deponte ZutiãoDepartment of Gerontology, Universidade Federal de São Carlos - UFSCar, São Carlos, São Paulo 13565-905, Brazil.ORCID https://orcid.org/0009-0005-8844-8866
Bianca Cruz PachaneBiochemistry and Molecular Biology Laboratory, Department of Physiological Sciences, Universidade Federal de São Carlos - UFSCar, São Carlos, São Paulo 13565-905, Brazil.ORCID https://orcid.org/0000-0002-7302-4498
Paulo Sérgio Gonçalves NunesDepartment of Chemistry, Universidade Federal de São Carlos - UFSCar, São Carlos, São Paulo 13565-905, Brazil.
Herika Danielle Almeida VidalDepartment of Chemistry, Universidade Federal de São Carlos - UFSCar, São Carlos, São Paulo 13565-905, Brazil.
Heloisa Sobreiro Selistre-de-AraujoBiochemistry and Molecular Biology Laboratory, Department of Physiological Sciences, Universidade Federal de São Carlos - UFSCar, São Carlos, São Paulo 13565-905, Brazil.
Arlene Gonçalves CorrêaDepartment of Chemistry, Universidade Federal de São Carlos - UFSCar, São Carlos, São Paulo 13565-905, Brazil.ORCID https://orcid.org/0000-0003-4247-2228
Marcia Regina CominettiDepartment of Gerontology, Universidade Federal de São Carlos - UFSCar, São Carlos, São Paulo 13565-905, Brazil.ORCID https://orcid.org/0000-0001-6385-7392
Angelina Maria FuzerDepartment of Gerontology, Universidade Federal de São Carlos - UFSCar, São Carlos, São Paulo 13565-905, Brazil.ORCID https://orcid.org/0000-0003-0673-8287

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A leading cause of death worldwide, breast cancer is the second most prevalent cancer in women. Triple-negative breast cancer is an aggressive subtype that lacks targeted therapies and requires novel therapeutic approaches in clinical practice to improve the overall survival. Theranostic agents that integrate diagnostic and therapeutic capabilities in a single entity are promising strategies for personalized cancer management. Hybrid compounds combining biologically relevant moieties with different modes of action can enhance cytotoxicity and improve pharmacological properties. We focus on a hybrid containing coumarin, triazole, and [10]-gingerol, a compound with known antimetastatic potential in TNBC. The LSPN281 hybrid exhibited superior cytotoxic activity in a TNBC cell line

Identifiers

PMID40104788
PMCPMC11912263

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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.