Evidence map›Paper›PMID 30532192›Full record

ArticlePloS one2018

Novel broad spectrum virucidal molecules against enveloped viruses.

Valeria Cagno, Cristina Tintori, Andrea Civra, Roberta Cavalli, Marika Tiberi, Lorenzo Botta, Annalaura Brai, Giulio Poli, Caroline Tapparel, David Lembo and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 28 citations in OpenAlex.

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  10. Lipid-based therapies against SARS-CoV-2 infection.Reviews in medical virology · 2021
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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 3 countries.

Valeria CagnoLaboratory of Molecular Virology and Antiviral Research, Department of Clinical and Biological Sciences, University of Torino, Orbassano, Torino, Italy.
Cristina TintoriDepartment of Biotechnology, Chemistry and Pharmacy, University of Siena, Siena, Italy.
Andrea CivraLaboratory of Molecular Virology and Antiviral Research, Department of Clinical and Biological Sciences, University of Torino, Orbassano, Torino, Italy.
Roberta CavalliDepartment of Drug Science and Technology, University of Torino, Torino, Italy.
Marika TiberiDepartment of Biotechnology, Chemistry and Pharmacy, University of Siena, Siena, Italy.
Lorenzo BottaDepartment of Biotechnology, Chemistry and Pharmacy, University of Siena, Siena, Italy.
Annalaura BraiDepartment of Biotechnology, Chemistry and Pharmacy, University of Siena, Siena, Italy.
Giulio PoliDepartment of Biotechnology, Chemistry and Pharmacy, University of Siena, Siena, Italy.
Caroline TapparelDepartment of Molecular Microbiology, University of Geneva, Geneva, Switzerland.
David LemboLaboratory of Molecular Virology and Antiviral Research, Department of Clinical and Biological Sciences, University of Torino, Orbassano, Torino, Italy.
Maurizio BottaDepartment of Biotechnology, Chemistry and Pharmacy, University of Siena, Siena, Italy.ORCID 0000-0003-0456-6995
University of Siena · ITUniversity of Turin · ITUniversity of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viral infections are an important cause of death worldwide. Unfortunately, there is still a lack of antiviral drugs or vaccines for a large number of viruses, and this represents a remarkable challenge particularly for emerging and re-emerging viruses. For this reason, the identification of broad spectrum antiviral compounds provides a valuable opportunity for developing efficient antiviral therapies. Here we report on a class of rhodanine and thiobarbituric derivatives displaying a broad spectrum antiviral activity against seven different enveloped viruses including an HSV-2 acyclovir resistant strain with favorable selectivity indexes. Due to their selective action on enveloped viruses and to their lipid oxidation ability, we hypothesize a mechanism on the viral envelope that affects the fluidity of the lipid bilayer, thus compromising the efficiency of virus-cell fusion and preventing viral entry.

Indexed as

Antiviral AgentsHerpesvirus 2, HumanLipid BilayersRhodanineThiobarbituratesVirusesAntiviral AgentsLipid BilayersRhodanineThiobarbituratesthiobarbituric acid

Identifiers

PMID30532192
PMCPMC6285983
OpenAlexW2904030169

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.