Evidence map›Paper›PMID 37118368›Full record

ArticleFolia microbiologica2023

Synthesis and antimicrobial activity of molecular hybrids based on eugenol and chloramphenicol pharmacophores.

Lucas M Oliveira, Fallon S Siqueira, Michelle T Silva, José V C Machado, Cleydson F Cordeiro, Lívia F Diniz, Marli M A Campos, Lucas L Franco, Thiago B Souza, Jamie A Hawkes and 1 more

Abstract read
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In one paragraph

Article in Folia microbiologica, 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
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

11 authors.

Lucas M OliveiraFaculdade de Ciências Farmacêuticas, Universidade Federal de Alfenas, Rua Gabriel Monteiro da Silva, 700, D-208E, Alfenas, MG, Brazil.ORCID http://orcid.org/0000-0002-7373-1686
Fallon S SiqueiraDepartamento de Análises Clínicas e Toxicológicas, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil.ORCID http://orcid.org/0000-0003-4454-0255
Michelle T SilvaFaculdade de Ciências Farmacêuticas, Universidade Federal de Alfenas, Rua Gabriel Monteiro da Silva, 700, D-208E, Alfenas, MG, Brazil.ORCID http://orcid.org/0000-0002-6793-0806
José V C MachadoFaculdade de Ciências Farmacêuticas, Universidade Federal de Alfenas, Rua Gabriel Monteiro da Silva, 700, D-208E, Alfenas, MG, Brazil.ORCID http://orcid.org/0000-0003-1503-1507
Cleydson F CordeiroFaculdade de Ciências Farmacêuticas, Universidade Federal de Alfenas, Rua Gabriel Monteiro da Silva, 700, D-208E, Alfenas, MG, Brazil.ORCID http://orcid.org/0000-0002-7564-1756
Lívia F DinizInstituto de Ciências Biomédicas, Universidade Federal de Alfenas, Alfenas, MG, 37130-001, Brazil.ORCID http://orcid.org/0000-0001-9398-6478
Marli M A CamposDepartamento de Análises Clínicas e Toxicológicas, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil.ORCID http://orcid.org/0000-0002-8717-0576
Lucas L FrancoFaculdade de Ciências Farmacêuticas, Universidade Federal de Alfenas, Rua Gabriel Monteiro da Silva, 700, D-208E, Alfenas, MG, Brazil.ORCID http://orcid.org/0000-0002-5196-9845
Thiago B SouzaEscola de Farmácia, Universidade Federal de Ouro Preto, Ouro Preto, MG, 35400-000, Brazil.ORCID http://orcid.org/0000-0003-3627-6407
Jamie A HawkesFaculdade de Ciências Farmacêuticas, Universidade Federal de Alfenas, Rua Gabriel Monteiro da Silva, 700, D-208E, Alfenas, MG, Brazil.ORCID http://orcid.org/0000-0003-3343-1854
Diogo T CarvalhoFaculdade de Ciências Farmacêuticas, Universidade Federal de Alfenas, Rua Gabriel Monteiro da Silva, 700, D-208E, Alfenas, MG, Brazil. diogo.carvalho@unifal-mg.edu.br.ORCID http://orcid.org/0000-0002-6362-2822

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior finance code 001'Fundação de Amparo à Pesquisa do Estado de Minas Gerais APQ-00686-18
6 · The paper itself

Abstract

In the constant search for new pharmacological compounds, molecular hybridisation is a well-known technique whereby two or more known pharmacophoric subunits are combined to create a new "hybrid" compound. This hybrid is expected to maintain the characteristics of the original compounds whilst demonstrating improvements to their pharmacological action. Accordingly, we report here a series of molecular hybrid compounds based upon eugenol and chloramphenicol pharmacophores. The hybrid compounds were screened for their in vitro antimicrobial potential against Gram-negative and Gram-positive bacteria and also rapidly growing mycobacteria (RGM). The results highlight that the antimicrobial profiles of the hybrid compounds improve in a very clear fashion when moving through the series. The most prominent results were found when comparing the activity of the hybrid compounds against some of the multidrug-resistant clinical isolates of Pseudomonas aeruginosa, methicillin-resistant clinical isolates of Staphylococcus aureus (MRSA) and clinical isolates of rapidly growing mycobacteria.

Indexed as

Anti-Infective AgentsMethicillin-Resistant Staphylococcus aureusAnti-Bacterial AgentsChloramphenicolEugenolMicrobial Sensitivity TestsPharmacophoreStaphylococcus aureusAnti-Bacterial AgentsAnti-Infective AgentsChloramphenicolEugenolAntimicrobialChloramphenicolEugenolHybridisationRapidly growing mycobacteria

Identifiers

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.