Evidence map›Paper›PMID 38069364›Full record

ArticleInternational journal of molecular sciences2023

Repurposing Study of 4-Acyl-1-phenylaminocarbonyl-2-substituted-piperazine Derivatives as Potential Anticancer Agents-In Vitro Evaluation against Breast Cancer Cells.

Emilio Guillén-Mancina, María Del Rosario García-Lozano, Estefanía Burgos-Morón, Sarah Mazzotta, Pablo Martínez-Aguado, José Manuel Calderón-Montaño, José Manuel Vega-Pérez, Miguel López-Lázaro, Fernando Iglesias-Guerra, Margarita Vega-Holm

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 40% 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, 3 citations in OpenAlex.

  1. Article
  2. Piperazine derivatives as anticancer agents: a medicinal chemistry review of structure, mechanism, and clinical translation.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
    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

10 authors at 4 institutions in 2 countries.

Emilio Guillén-MancinaDepartment of Pharmacology, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.
María Del Rosario García-LozanoDepartment of Organic and Medicinal Chemistry, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.ORCID 0000-0002-6255-4960
Estefanía Burgos-MorónDepartment of Pharmacology, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.ORCID 0000-0002-6231-190X
Sarah MazzottaDepartment of Organic and Medicinal Chemistry, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.ORCID 0000-0003-0029-7003
Pablo Martínez-AguadoDepartment of Organic and Medicinal Chemistry, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.
José Manuel Calderón-MontañoDepartment of Pharmacology, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.ORCID 0000-0001-6845-797X
José Manuel Vega-PérezDepartment of Organic and Medicinal Chemistry, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.
Miguel López-LázaroDepartment of Pharmacology, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.ORCID 0000-0003-2794-1647
Fernando Iglesias-GuerraDepartment of Organic and Medicinal Chemistry, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.
Margarita Vega-HolmDepartment of Organic and Medicinal Chemistry, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.ORCID 0000-0003-2197-2004
Universidad de Sevilla · ESHospital Universitario Virgen Macarena · ESInstituto de Biomedicina de Sevilla · ESUniversity of Milan · IT

Funding

Instituto de Salud Carlos III PI19/00589, PI19/01404, PI16/01842, PI17/00535 and GLD19/00100Junta de Andalucía 2017/CTS-657 and 2019/CTS-657Ministerio de Ciencia, Innovación y Universidades PID2019-104767RB-I00Universidad de Sevilla VIPPIT-2019-I.5, VIPPIT-2020-I.5, VIIPPIT-2023-I.3
6 · The paper itself

Abstract

Breast cancer is the most common type of cancer in women. Although current treatments can increase patient survival, they are rarely curative when the disease is advanced (metastasis). Therefore, there is an urgent need to develop new cytotoxic drugs with a high selectivity toward cancer cells. Since repurposing approved drugs for cancer therapy has been a successful strategy in recent years, in this study, we screened a library of antiviral piperazine-derived compounds as anticancer agents. The compounds included a piperazine ring and aryl urea functions, which are privileged structures present in several anti-breast cancer drugs. The selective cytotoxic activity of a set of thirty-four 4-acyl-2-substituted piperazine urea derivatives against MCF7 breast cancer cells and MCF 10A normal breast cells was determined. Compounds

Indexed as

Antineoplastic AgentsBreast NeoplasmsCarcinoma, Non-Small-Cell LungLung NeoplasmsCell ProliferationDrug RepositioningDrug Screening Assays, AntitumorFemaleHumansMCF-7 CellsMolecular StructurePiperazineStructure-Activity RelationshipUreaAntineoplastic AgentsPiperazineUreaaryl ureabreast cancercellular viabilitypiperazineselective cytotoxic activity

Identifiers

PMID38069364
PMCPMC10706865
OpenAlexW4389223642

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.