Evidence map›Paper›PMID 25793970›Full record

ArticlePloS one2015

Depsides: lichen metabolites active against hepatitis C virus.

Thi Huyen Vu, Anne-Cécile Le Lamer, Claudia Lalli, Joël Boustie, Michel Samson, Françoise Lohézic-Le Dévéhat, Jacques Le Seyec

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
6.8field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 46 citations in OpenAlex.

  1. Unassuming Lichens: Nature's Hidden Antimicrobial Warriors.International journal of molecular sciences · 2025
    Review
  2. Article
  3. Envelope Protein-Targeting Zika Virus Entry Inhibitors.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
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  10. Review
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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

7 authors at 4 institutions in 1 country.

Thi Huyen VuCNRS, UMR-6226, Institut des Sciences Chimiques de Rennes (ISCR), Rennes, France; Université de Rennes 1, Rennes, France.
Anne-Cécile Le LamerCNRS, UMR-6226, Institut des Sciences Chimiques de Rennes (ISCR), Rennes, France; Université de Rennes 1, Rennes, France; Université de Toulouse III, Toulouse, France.
Claudia LalliCNRS, UMR-6226, Institut des Sciences Chimiques de Rennes (ISCR), Rennes, France; Université de Rennes 1, Rennes, France.
Joël BoustieCNRS, UMR-6226, Institut des Sciences Chimiques de Rennes (ISCR), Rennes, France; Université de Rennes 1, Rennes, France.
Michel SamsonUniversité de Rennes 1, Rennes, France; INSERM, UMR-1085, Institut de Recherche Santé Environnement & Travail (IRSET), Rennes, France; Fédération de Recherche BioSit de Rennes, Rennes, France.
Françoise Lohézic-Le DévéhatCNRS, UMR-6226, Institut des Sciences Chimiques de Rennes (ISCR), Rennes, France; Université de Rennes 1, Rennes, France.
Jacques Le SeyecUniversité de Rennes 1, Rennes, France; INSERM, UMR-1085, Institut de Recherche Santé Environnement & Travail (IRSET), Rennes, France; Fédération de Recherche BioSit de Rennes, Rennes, France.
Université de Rennes · FRInstitut des Sciences Chimiques de Rennes · FRCentre National de la Recherche Scientifique · FRStructure Fédérative de Recherche en Biologie et Santé de Rennes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A thorough phytochemical study of Stereocaulon evolutum was conducted, for the isolation of structurally related atranorin derivatives. Indeed, pilot experiments suggested that atranorin (1), the main metabolite of this lichen, would interfere with the lifecycle of hepatitis C virus (HCV). Eight compounds, including one reported for the first time (2), were isolated and characterized. Two analogs (5, 6) were also synthesized, to enlarge the panel of atranorin-related structures. Most of these compounds were active against HCV, with a half-maximal inhibitory concentration of about 10 to 70 µM, with depsides more potent than monoaromatic phenols. The most effective inhibitors (1, 5 and 6) were then added at different steps of the HCV lifecycle. Interestingly, atranorin (1), bearing an aldehyde function at C-3, inhibited only viral entry, whereas the synthetic compounds 5 and 6, bearing a hydroxymethyl and a methyl function, respectively, at C-3 interfered with viral replication.

Indexed as

DepsidesHepacivirusHydroxybenzoatesLichensVirus ReplicationatranorinDepsidesHydroxybenzoates

Identifiers

PMID25793970
PMCPMC4368788
OpenAlexW1989139826

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.