Evidence map›Paper›PMID 36443517›Full record

ArticleInflammopharmacology2023

Pharmacological evaluation of antinociceptive and anti-inflammatory activities of LQFM202: a new piperazine derivative.

Aline N Martins, Dionys de Souza Almeida, Iziara F Florentino, Lorrane K da Silva Moreira, Larissa C Turones, Daniel C Batista, Lucas S Machado, Boniek G Vaz, Luciano M Lião, Gerlon de Almeida Ribeiro Oliveira and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammopharmacology, 2023. 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
0.2field-weighted citation impact, top 48% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

15 authors at 2 institutions in 1 country.

Aline N MartinsInstitute of Biological Sciences, Department of Pharmacology, Federal University of Goiás, Campus Samambaia, Goiânia, GO, Brazil.
Dionys de Souza AlmeidaInstitute of Biological Sciences, Department of Pharmacology, Federal University of Goiás, Campus Samambaia, Goiânia, GO, Brazil.
Iziara F FlorentinoInstitute of Biological Sciences, Department of Pharmacology, Federal University of Goiás, Campus Samambaia, Goiânia, GO, Brazil.
Lorrane K da Silva MoreiraInstitute of Biological Sciences, Department of Pharmacology, Federal University of Goiás, Campus Samambaia, Goiânia, GO, Brazil.
Larissa C TuronesInstitute of Biological Sciences, Department of Pharmacology, Federal University of Goiás, Campus Samambaia, Goiânia, GO, Brazil.
Daniel C BatistaInstitute of Biological Sciences, Department of Pharmacology, Federal University of Goiás, Campus Samambaia, Goiânia, GO, Brazil.
Lucas S MachadoChemistry Institute, Federal University of Goiás, Campus Samambaia, Goiânia, GO, Brazil.
Boniek G VazChemistry Institute, Laboratory of Chromatography and Mass Spectrometry, Federal University of Goiás, Goiânia, GO, Brazil.
Luciano M LiãoChemistry Institute, Federal University of Goiás, Campus Samambaia, Goiânia, GO, Brazil.
Gerlon de Almeida Ribeiro OliveiraFaculty of Pharmacy, Laboratory of Medicinal Pharmaceutical Chemistry, Federal University of Goiás, Goiânia, GO, Brazil.
José Luís Rodrigues MartinsInstitute of Biological Sciences, Department of Pharmacology, Federal University of Goiás, Campus Samambaia, Goiânia, GO, Brazil.
James Oluwagbamigbe FajemiroyeInstitute of Biological Sciences, Department of Pharmacology, Federal University of Goiás, Campus Samambaia, Goiânia, GO, Brazil.
Ricardo MenegattiFaculty of Pharmacy, Laboratory of Medicinal Pharmaceutical Chemistry, Federal University of Goiás, Goiânia, GO, Brazil.
Elson A CostaInstitute of Biological Sciences, Department of Pharmacology, Federal University of Goiás, Campus Samambaia, Goiânia, GO, Brazil.
Daiany P B da SilvaInstitute of Biological Sciences, Department of Pharmacology, Federal University of Goiás, Campus Samambaia, Goiânia, GO, Brazil. daiany_priscilla_bueno@egresso.ufg.br.ORCID http://orcid.org/0000-0001-8003-7740
Universidade Federal de Goiás · BRInstituto Federal Goiano · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances have been made in the search for new multi-target modulators to control pain and inflammation. Therefore, compound 3,5-di-tert-butyl-4-hydroxyphenyl)(4-methylpiperazin-1-yl)methanone (LQFM202) was synthesised and evaluated. First, in vitro assays were performed for COX-1, COX-2, and 5-LOX enzymes. Subsequently, adult female Swiss albino mice treated orally with LQFM202 at doses of 25-200 mg/kg were subjected to acetic acid-induced writhing, formalin-induced pain, carrageenan-induced hyperalgesia, carrageenan- or zymosan-induced paw oedema, or pleurisy. LQFM202 inhibited COX-1, COX-2, and LOX-5 (IC

Indexed as

AnalgesicsPleurisyAnimalsAnti-Inflammatory AgentsCarrageenanCyclooxygenase 2EdemaFemaleInflammationMicePainPeroxidasePiperazinesPlant ExtractsZymosanAnalgesicsAnti-Inflammatory AgentsCarrageenanCyclooxygenase 2PeroxidasePiperazinesPlant ExtractsZymosanCOXCytokinesHyperalgesiaLOX

Identifiers

PMID36443517
OpenAlexW4310191215

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.