Evidence map›Paper›PMID 26843462›Full record

ArticleScientific reports2016

Inhibition of Chikungunya Virus Replication by 1-[(2-Methylbenzimidazol-1-yl) Methyl]-2-Oxo-Indolin-3-ylidene] Amino] Thiourea(MBZM-N-IBT).

Priyadarsee Mishra, Abhishek Kumar, Prabhudutta Mamidi, Sameer Kumar, Itishree Basantray, Tanuja Saswat, Indrani Das, Tapas Kumar Nayak, Subhasis Chattopadhyay, Bharat Bhusan Subudhi and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

46 citing papers in PubMed, 93 citations in OpenAlex.

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  16. Identification of sulphonamide-tetheredJournal of enzyme inhibition and medicinal chemistry · 2023
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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

11 authors at 3 institutions in 1 country.

Priyadarsee MishraSchool of Pharmaceutical Sciences, Siksha O Anusandhan University, Bhubaneswar, India.
Abhishek KumarInstitute of Life Sciences, Bhubaneswar, India.
Prabhudutta MamidiInstitute of Life Sciences, Bhubaneswar, India.
Sameer KumarInstitute of Life Sciences, Bhubaneswar, India.
Itishree BasantrayInstitute of Life Sciences, Bhubaneswar, India.
Tanuja SaswatInstitute of Life Sciences, Bhubaneswar, India.
Indrani DasInstitute of Life Sciences, Bhubaneswar, India.
Tapas Kumar NayakSchool of Biological Sciences, National Institute of Science Education &Research, Bhubaneswar, India.
Subhasis ChattopadhyaySchool of Biological Sciences, National Institute of Science Education &Research, Bhubaneswar, India.
Bharat Bhusan SubudhiSchool of Pharmaceutical Sciences, Siksha O Anusandhan University, Bhubaneswar, India.
Soma ChattopadhyayInstitute of Life Sciences, Bhubaneswar, India.
Institute of Life Sciences · INSiksha O Anusandhan University · INNational Institute of Science Education and Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chikungunya virus (CHIKV) infection is one of the most challenging human Arboviral infections with global significance and without any specific antiviral. In this investigation, 1-[(2-methylbenzimidazol-1-yl) methyl]-2-oxo-indolin-3-ylidene] amino] thiourea (MBZM-N-IBT) was synthesised as a molecular hybrid of 2-methyl benzimidazole and isatin-β-thiosemicarbazone and its anti-CHIKV property was evaluated. The release of infectious virus particles was calculated by plaque assay, expression profile of viral RNA was estimated by RT-PCR and viral protein profiles were assessed by Western blot and FACS analyses. The safety index of MBZM-N-IBT was found to be >21. The CHIKV infectious viral particle formation was abrogated around 76.02% by MBZM-N-IBT during infection in mammalian system and the viral RNA synthesis was reduced by 65.53% and 23.71% for nsP2 and E1 respectively. Surprisingly, the viral protein levels were reduced by 97% for both nsP2 and E2. In the time-of-addition experiment it abrogated viral infection at early as well as late phase of viral life cycle, which indicates about multiple mechanisms for its anti-CHIKV action. In silico analysis justified development of MBZM-N-IBT with good affinities for potential target proteins of CHIKV and related virus. With predictions of good drug-likeness property, it shows potential of a drug candidate which needs further experimental validation.

Indexed as

AnimalsAntiviral AgentsBenzimidazolesBinding SitesBlotting, WesternCell SurvivalChikungunya virusChlorocebus aethiopsFlow CytometryIsatinMolecular Docking SimulationProtein BindingProtein Structure, TertiaryReal-Time Polymerase Chain ReactionRNA, ViralThiourea1-((2-methylbenzimidazol-1-yl)methyl)-2-oxoindolin-3-ylidene)amino)thioureaAntiviral AgentsBenzimidazolesIsatinRNA, ViralThioureaViral Nonstructural Proteins

Identifiers

PMID26843462
PMCPMC4740769
OpenAlexW2404410565

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.