Evidence map›Paper›PMID 33010635›Full record

ArticleEuropean journal of medicinal chemistry2021

Anti-tubercular profile of new selenium-menadione conjugates against Mycobacterium tuberculosis H37Rv (ATCC 27294) strain and multidrug-resistant clinical isolates.

Ruan C B Ribeiro, Daniel B de Marins, Iris Di Leo, Luana da Silva Gomes, Matheus G de Moraes, Bruno L Abbadi, Anne D Villela, Wellington F da Silva, Luiz Cláudio R P da Silva, Pablo Machado and 6 more

Abstract read
In one paragraph

Article in European journal of medicinal chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Role of Divalent Cations in Infections in Host-Pathogen Interaction.International journal of molecular sciences · 2024
    Review
  7. Following the Trace of Cyclodextrins on the Selenium and Tellurium Odyssey.International journal of molecular sciences · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. Menadione: a platform and a target to valuable compounds synthesis.Beilstein journal of organic chemistry · 2022
    Review
  12. 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

16 authors.

Ruan C B RibeiroUniversidade Federal Fluminense, Departamento de Química Orgânica, Instituto de Química, Campus Do Valonguinho, CEP 24020-150, Niterói, RJ, Brazil.
Daniel B de MarinsUniversidade Federal Fluminense, Departamento de Química Orgânica, Instituto de Química, Campus Do Valonguinho, CEP 24020-150, Niterói, RJ, Brazil.
Iris Di LeoUniversidade Federal Fluminense, Departamento de Química Orgânica, Instituto de Química, Campus Do Valonguinho, CEP 24020-150, Niterói, RJ, Brazil.
Luana da Silva GomesUniversidade Federal Fluminense, Departamento de Química Orgânica, Instituto de Química, Campus Do Valonguinho, CEP 24020-150, Niterói, RJ, Brazil.
Matheus G de MoraesUniversidade Federal Fluminense, Departamento de Química Orgânica, Instituto de Química, Campus Do Valonguinho, CEP 24020-150, Niterói, RJ, Brazil.
Bruno L AbbadiInstituto Nacional de Ciência e Tecnologia Em Tuberculose (INCT-TB), Centro de Pesquisas Em Biologia Molecular e Funcional, Pontifícia Universidade Católica Do Rio Grande Do Sul, PUCRS, Av. Ipiranga 6681 - Prédio 92A Tecnopuc, 90619-900, Porto Alegre, RS, Brazil.
Anne D VillelaInstituto Nacional de Ciência e Tecnologia Em Tuberculose (INCT-TB), Centro de Pesquisas Em Biologia Molecular e Funcional, Pontifícia Universidade Católica Do Rio Grande Do Sul, PUCRS, Av. Ipiranga 6681 - Prédio 92A Tecnopuc, 90619-900, Porto Alegre, RS, Brazil.
Wellington F da SilvaUniversidade Federal Do Rio de Janeiro, Faculdade de Farmácia, CEP 21941-902, Rio de Janeiro, RJ, Brazil.
Luiz Cláudio R P da SilvaUniversidade Federal Do Rio de Janeiro, Faculdade de Farmácia, CEP 21941-902, Rio de Janeiro, RJ, Brazil.
Pablo MachadoInstituto Nacional de Ciência e Tecnologia Em Tuberculose (INCT-TB), Centro de Pesquisas Em Biologia Molecular e Funcional, Pontifícia Universidade Católica Do Rio Grande Do Sul, PUCRS, Av. Ipiranga 6681 - Prédio 92A Tecnopuc, 90619-900, Porto Alegre, RS, Brazil.
Cristiano Valim BizarroInstituto Nacional de Ciência e Tecnologia Em Tuberculose (INCT-TB), Centro de Pesquisas Em Biologia Molecular e Funcional, Pontifícia Universidade Católica Do Rio Grande Do Sul, PUCRS, Av. Ipiranga 6681 - Prédio 92A Tecnopuc, 90619-900, Porto Alegre, RS, Brazil.
Luiz Augusto BassoInstituto Nacional de Ciência e Tecnologia Em Tuberculose (INCT-TB), Centro de Pesquisas Em Biologia Molecular e Funcional, Pontifícia Universidade Católica Do Rio Grande Do Sul, PUCRS, Av. Ipiranga 6681 - Prédio 92A Tecnopuc, 90619-900, Porto Alegre, RS, Brazil.
Marcela Cristina de MoraesUniversidade Federal Fluminense, Departamento de Química Orgânica, Instituto de Química, Campus Do Valonguinho, CEP 24020-150, Niterói, RJ, Brazil.
Vitor F FerreiraUniversidade Federal Fluminense, Faculdade de Farmácia, Departamento de Tecnologia Farmacêutica, CEP 24241-000, Niterói, RJ, Brazil.
Fernando de C da SilvaUniversidade Federal Fluminense, Departamento de Química Orgânica, Instituto de Química, Campus Do Valonguinho, CEP 24020-150, Niterói, RJ, Brazil.
Vanessa NascimentoUniversidade Federal Fluminense, Departamento de Química Orgânica, Instituto de Química, Campus Do Valonguinho, CEP 24020-150, Niterói, RJ, Brazil. Electronic address: nascimentovanessa@id.uff.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberculosis (TB) is one of the most fatal diseases and is responsible for the infection of millions of people around the world. Most recently, scientific frontiers have been engaged to develop new drugs that can overcome drug-resistant TB. Following this direction, using a designed scaffold based on the combination of two separate pharmacophoric groups, a series of menadione-derived selenoesters was developed with good yields. All products were evaluated for their in vitro activity against Mycobacterium tuberculosis H37Rv and attractive results were observed, especially for the compounds 8a, 8c and 8f (MICs 2.1, 8.0 and 8.1 μM, respectively). In addition, 8a, 8c and 8f demonstrated potent in vitro activity against multidrug-resistant clinical isolates (CDCT-16 and CDCT-27) with promising MIC values ranging from 0.8 to 3.1 μM. Importantly, compounds 8a and 8c were found to be non-toxic against the Vero cell line. The SI value of 8a (>23.8) was found to be comparable to that of isoniazid (>22.7), which suggests the possibility of carrying out advanced studies on this derivative. Therefore, these menadione-derived selenoesters obtained as hybrid compounds represent promising new anti-tubercular agents to overcome TB multidrug resistance.

Indexed as

AnimalsAntitubercular AgentsChlorocebus aethiopsHumansModels, MolecularMycobacterium tuberculosisSeleniumTuberculosisVero CellsVitamin K 3Antitubercular AgentsSeleniumVitamin K 3Antimycobacterial activityCytotoxicityDrug developmentMICMulti-drug-resistant tuberculosisMycobacterium tuberculosisNaphthoquinonesSelenoestersTuberculosis

Identifiers

PMID33010635
PMCPMC7510590

What OpenQuestion holds

Textmetadata
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.