Evidence map›Paper›PMID 40376715›Full record

ArticleFuture medicinal chemistry2025

Benzothiazole derivatives as inhibitors of chikungunya virus replicative cycle.

Shiraz Feferbaum-Leite, Natasha Marques Cassani, Uriel Enrique Aquino Ruiz, Renieidy Flávia Clemente Dias, Danilo Nascimento Farago, Marco Guevara-Vega, Nilson Nicolau-Junior, Robinson Sabino-Silva, Celso de Oliveira Rezende Júnior, Ana Carolina Gomes Jardim

Abstract read
In one paragraph

Article in Future medicinal chemistry, 2025. 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. Review
  2. 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.

Shiraz Feferbaum-LeiteLaboratory of Antiviral Research (LAPAV), Institute of Biomedical Science (ICBIM), Federal University of Uberlândia (UFU), Uberlândia, Minas Gerais, Brazil.
Natasha Marques CassaniLaboratory of Antiviral Research (LAPAV), Institute of Biomedical Science (ICBIM), Federal University of Uberlândia (UFU), Uberlândia, Minas Gerais, Brazil.
Uriel Enrique Aquino RuizLaboratory of Antiviral Research (LAPAV), Institute of Biomedical Science (ICBIM), Federal University of Uberlândia (UFU), Uberlândia, Minas Gerais, Brazil.
Renieidy Flávia Clemente DiasDrug Candidate Synthesis Laboratory (LaSFar), Institute of Chemistry, Federal University of Uberlândia (UFU), Uberlândia, Minas Gerais, Brazil.
Danilo Nascimento FaragoDrug Candidate Synthesis Laboratory (LaSFar), Institute of Chemistry, Federal University of Uberlândia (UFU), Uberlândia, Minas Gerais, Brazil.
Marco Guevara-VegaInnovation Center in Salivary Diagnostic and Nanobiotechnology, Department of Physiology, Institute of Biomedical Sciences, Federal University of Uberlandia, Uberlandia, Minas Gerais, Brazil.
Nilson Nicolau-JuniorInstitute of Biotechnology, Federal University of Uberlândia (UFU), Uberlândia, Minas Gerais, Brazil.
Robinson Sabino-SilvaInnovation Center in Salivary Diagnostic and Nanobiotechnology, Department of Physiology, Institute of Biomedical Sciences, Federal University of Uberlandia, Uberlandia, Minas Gerais, Brazil.
Celso de Oliveira Rezende JúniorDrug Candidate Synthesis Laboratory (LaSFar), Institute of Chemistry, Federal University of Uberlândia (UFU), Uberlândia, Minas Gerais, Brazil.
Ana Carolina Gomes JardimLaboratory of Antiviral Research (LAPAV), Institute of Biomedical Science (ICBIM), Federal University of Uberlândia (UFU), Uberlândia, Minas Gerais, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsChikungunya virus (CHIKV) is the agent of chikungunya fever (CHIKF), a reemerging disease prevalent in tropical regions. With no licensed treatments available, identifying effective antiviral compounds is critical. This study evaluates the antiviral potential of 20 synthetic sulfonamide derivatives against CHIKV. METHODOLOGY: We tested 13 heteroaromatic derivatives containing thiazole, benzimidazole, and benzothiazole (BTA) moieties, along with seven sulfonamides bearing ester and carboxylic acid groups. CHIKV-

resultsBTA derivatives 6, 9, 11, and 13 demonstrated potent CHIKV inhibition, with EC

conclusionsThese findings highlight BTA derivatives as promising CHIKV inhibitors. Compound 9's ability to interfere at multiple stages of infection suggests its potential for therapeutic development against CHIKF.

Indexed as

Antiviral AgentsBenzothiazolesChikungunya virusVirus ReplicationAnimalsChikungunya FeverChlorocebus aethiopsHumansMicrobial Sensitivity TestsMolecular Docking SimulationMolecular StructureStructure-Activity RelationshipVero CellsAntiviral AgentsbenzothiazoleBenzothiazolesbenzimidazolebenzothiazolecarboxylic acidChikungunya virussulfonamidethiazole

Identifiers

PMID40376715
PMCPMC12143675

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.