Evidence map›Paper›PMID 27572397›Full record

ArticleAntimicrobial agents and chemotherapy2016

N-Desmethylclozapine, Fluoxetine, and Salmeterol Inhibit Postentry Stages of the Dengue Virus Life Cycle.

Guruprasad R Medigeshi, Rinki Kumar, Ekta Dhamija, Tanvi Agrawal, Meenakshi Kar

Open access · hybridAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

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  12. Discovery of HIV entry inhibitors via a hybrid CXCR4 and CCR5 receptor pharmacophore-based virtual screening approach.European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences · 2020
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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

5 authors at 2 institutions in 1 country.

Guruprasad R MedigeshiVaccine and Infectious Disease Research Center, Translational Health Science and Technology Institute, Haryana, India gmedigeshi@thsti.res.in.ORCID 0000-0001-5333-9743
Rinki KumarVaccine and Infectious Disease Research Center, Translational Health Science and Technology Institute, Haryana, India.
Ekta DhamijaVaccine and Infectious Disease Research Center, Translational Health Science and Technology Institute, Haryana, India.
Tanvi AgrawalVaccine and Infectious Disease Research Center, Translational Health Science and Technology Institute, Haryana, India.
Meenakshi KarVaccine and Infectious Disease Research Center, Translational Health Science and Technology Institute, Haryana, India.
Translational Health Science and Technology Institute · INJamia Hamdard · IN

Funding

DBT-Wellcome Trust India Alliance IA/S(I)/14/1/501291
6 · The paper itself

Abstract

Around 10,000 people die each year due to severe dengue disease, and two-thirds of the world population lives in a region where dengue disease is endemic. There has been remarkable progress in dengue virus vaccine development; however, there are no licensed antivirals for dengue disease, and none appear to be in clinical trials. We took the approach of repositioning approved drugs for anti-dengue virus activity by screening a library of pharmacologically active compounds. We identified N-desmethylclozapine, fluoxetine hydrochloride, and salmeterol xinafoate as dengue virus inhibitors based on reductions in the numbers of infected cells and viral titers. Dengue virus RNA levels were diminished in inhibitor-treated cells, and this effect was specific to dengue virus, as other flaviviruses, such as Japanese encephalitis virus and West Nile virus, or other RNA viruses, such as respiratory syncytial virus and rotavirus, were not affected by these inhibitors. All three inhibitors specifically inhibited dengue virus replication with 50% inhibitory concentrations (IC

Indexed as

A549 CellsAnimalsAntipsychotic AgentsAntiviral AgentsBronchodilator AgentsCell LineCell Line, TumorClozapineCricetinaeDengue VirusDrug RepositioningEpithelial CellsFluoxetineHepatocytesHumansInhibitory Concentration 50Antipsychotic AgentsAntiviral AgentsBronchodilator AgentsClozapineFluoxetinenorclozapineRNA, ViralSalmeterol Xinafoate

Identifiers

PMID27572397
PMCPMC5075077
OpenAlexW2510847522

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.