Evidence map›Paper›PMID 38877863›Full record

ArticleCurrent medicinal chemistry2025

Determination of Inhibitory Effect of PKM2 Enzyme and Antitumoral Activity of Novel Coumarin-naphthoquinone Hybrids.

Amanda de Andrade Borges, Gabriel Ouverney, Afonso Thales Sousa Arruda, Amanda Vieira Ribeiro, Ruan Carlos Busquet Ribeiro, Acacio Silva de Souza, Anna Carolina Carvalho da Fonseca, Lucas Nicolau de Queiroz, Elan Cardozo Paes de Almeida, Bruno Pontes and 6 more

Abstract read
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Article in Current medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

16 authors.

Amanda de Andrade BorgesDepartamento de Química Orgânica, Instituto de Química, Universidade Federal Fluminense, CEP, Niterói, 24020-141, RJ, Brazil.
Gabriel OuverneyPrograma de Pós-graduação em Ciências Aplicadas a Produtos para Saúde, Faculdade de Farmácia, Universidade Federal Fluminense, CEP, Niterói, 24020-141, RJ, Brazil.
Afonso Thales Sousa ArrudaDepartamento de Ciência Básica, Universidade Federal Fluminense, Campus Universitário de Nova Friburgo, CEP, Nova Friburgo, 28625-650, RJ, Brazil.
Amanda Vieira RibeiroDepartamento de Ciência Básica, Universidade Federal Fluminense, Campus Universitário de Nova Friburgo, CEP, Nova Friburgo, 28625-650, RJ, Brazil.
Ruan Carlos Busquet RibeiroDepartamento de Química Orgânica, Instituto de Química, Universidade Federal Fluminense, CEP, Niterói, 24020-141, RJ, Brazil.
Acacio Silva de SouzaDepartamento de Tecnologia Farmacêutica, Faculdade de Farmácia, Universidade Federal Fluminense, CEP, Niterói, 24020-141, RJ, Brazil.
Anna Carolina Carvalho da FonsecaPrograma de Pós-graduação em Odontologia, Instituto de Saúde de Nova Friburgo, Universidade Federal Fluminense, CEP, Nova Friburgo, 28625-650, RJ, Brazil.
Lucas Nicolau de QueirozPrograma de Pós-graduação em Ciências Aplicadas a Produtos para Saúde, Faculdade de Farmácia, Universidade Federal Fluminense, CEP, Niterói, 24020-141, RJ, Brazil.
Elan Cardozo Paes de AlmeidaDepartamento de Ciência Básica, Universidade Federal Fluminense, Campus Universitário de Nova Friburgo, CEP, Nova Friburgo, 28625-650, RJ, Brazil.
Bruno PontesInstituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, CEP, Rio de Janeiro, 21941-902, RJ, Brazil.
Vitor Won-Held RabeloInstituto de Biodiversidade e Sustentabilidade, Universidade Federal do Rio de Janeiro, CEP , Macaé, 27965-045, RJ, Brazil.
Vitor FerreiraDepartamento de Tecnologia Farmacêutica, Faculdade de Farmácia, Universidade Federal Fluminense, CEP, Niterói, 24020-141, RJ, Brazil.
Paula Alvarez AbreuInstituto de Biodiversidade e Sustentabilidade, Universidade Federal do Rio de Janeiro, CEP , Macaé, 27965-045, RJ, Brazil.
Fernando de Carvalho da SilvaDepartamento de Química Orgânica, Instituto de Química, Universidade Federal Fluminense, CEP, Niterói, 24020-141, RJ, Brazil.ORCID 0000-0002-2042-3778
Luana da Silva Magalhaes ForeziDepartamento de Química Orgânica, Instituto de Química, Universidade Federal Fluminense, CEP, Niterói, 24020-141, RJ, Brazil.ORCID 0000-0002-7657-4268
Bruno Kaufmann RobbsDepartamento de Ciência Básica, Universidade Federal Fluminense, Campus Universitário de Nova Friburgo, CEP, Nova Friburgo, 28625-650, RJ, Brazil.

Funding

CNPq, Conselho Nacional de Desenvolvimento Científico e Tecnológico 1A 301873/2019-4, 301873/2019-4Coordination for the Improvement of Higher Education Personnel - Brazil (CAPES) 001FAPERJ, Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/010.101106/2018, E-26/202, 787/2019, E-26/10.002250/2019, E-26/210.085/2022, E-26/010.001318/2019, E-26/211.343/2021, E-26/210.068/2021, E-26/203.191/2017-JCNE, E-26 /202.800/2017-CNE, E-26/010.101106/2018, E-26/200 .870/2021-CNE, E-26/201.369/2021-JCNE, E-26/010/ 001687/2015, E-26/202.787/2019, E-26/210.514/2019, E-26/10.002250/2019, E-26/211.343/2021, E-26/210. 085/2022, E-26/210.068/2021
6 · The paper itself

Abstract

backgroundOral squamous cell carcinoma (OSCC) represents the primary form of oral cancer, posing a significant global health threat. The existing chemotherapy options are accompanied by notable side effects impacting patient treatment adherence. Consequently, the exploration and development of novel substances with enhanced anticancer effects and fewer side effects have become pivotal in the realms of biological and chemical science.

objectiveThis work presents the pioneering examples of naphthoquinone-coumarin hybrids as a new category of highly effective cytotoxic substances targeting oral squamous cell carcinoma (OSCC).

methodsGiven the significance of both naphthoquinones and coumarins as essential pharmacophores/ privileged structures in the quest for anticancer compounds, this study focused on the synthesis and evaluation of novel naphthoquinones/coumarin hybrids against oral squamous cell carcinoma.

resultsBy several

conclusionWe assert that compound 6e shows promise as a potential lead for a novel chemotherapeutic drug targeting OSCC, with potential applicability to other cancer types.

Indexed as

Antineoplastic AgentsCarrier ProteinsCoumarinsEnzyme InhibitorsMembrane ProteinsNaphthoquinonesThyroid HormonesAnimalsApoptosisCell Line, TumorCell ProliferationDose-Response Relationship, DrugDrug Screening Assays, AntitumorHumansMiceMolecular StructureAntineoplastic AgentsCarrier ProteinscoumarinCoumarinsEnzyme InhibitorsMembrane ProteinsNaphthoquinonesThyroid Hormone-Binding ProteinsThyroid Hormoneschemotherapycoumarinnaphthoquinoneoral cancer.Oral squamous cell carcinomapyruvate kinase M2

Identifiers

What OpenQuestion holds

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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.