Evidence map›Paper›PMID 28333153›Full record

ArticleScientific reports2017

A Novel Inhibitor IDPP Interferes with Entry and Egress of HCV by Targeting Glycoprotein E1 in a Genotype-Specific Manner.

Myungeun Lee, Jaewon Yang, Eunji Jo, Ji-Young Lee, Hee-Young Kim, Ralf Bartenschlager, Eui-Cheol Shin, Yong-Soo Bae, Marc P Windisch

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 24 citations in OpenAlex.

  1. RSC advances · 2022
    Article
  2. Article
  3. Article
  4. Discovery and development of safe-in-man broad-spectrum antiviral agents.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2020
    Review
  5. Article
  6. Article
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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

9 authors at 4 institutions in 2 countries.

Myungeun LeeDepartment of Applied Molecular Virology, Hepatitis Research Laboratory, Institut Pasteur Korea, 696, Seongnam-si, Gyeonggi-do, 463-400, Republic of Korea.
Jaewon YangDepartment of Applied Molecular Virology, Hepatitis Research Laboratory, Institut Pasteur Korea, 696, Seongnam-si, Gyeonggi-do, 463-400, Republic of Korea.
Eunji JoDepartment of Applied Molecular Virology, Hepatitis Research Laboratory, Institut Pasteur Korea, 696, Seongnam-si, Gyeonggi-do, 463-400, Republic of Korea.
Ji-Young LeeDepartment of Infectious Diseases, Molecular Virology, University Hospital Heidelberg, Heidelberg, Germany.
Hee-Young KimDepartment of Applied Molecular Virology, Hepatitis Research Laboratory, Institut Pasteur Korea, 696, Seongnam-si, Gyeonggi-do, 463-400, Republic of Korea.
Ralf BartenschlagerDepartment of Infectious Diseases, Molecular Virology, University Hospital Heidelberg, Heidelberg, Germany.
Eui-Cheol ShinLaboratory of Immunology and Infectious Diseases, Graduate School of Medical Science and engineering, KAIST, Daejeon, Republic of Korea.
Yong-Soo BaeDepartment of Biological Science, Sungkyunkwan University, Seobu-ro, Jangan-gu, Suwon-si, Gyeonggi-do, Republic of Korea.
Marc P WindischDepartment of Applied Molecular Virology, Hepatitis Research Laboratory, Institut Pasteur Korea, 696, Seongnam-si, Gyeonggi-do, 463-400, Republic of Korea.
Institut Pasteur Korea · KRGerman Center for Infection Research · DEKorea Advanced Institute of Science and Technology · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite recent advances in curing chronic hepatitis C (CHC), the high economic burden to therapy, viral drug resistance, difficult to treat hepatitis C virus (HCV) genotypes and patient groups are still of concern. To address this unmet medical needs, we devised strategies to identify novel viral interventions through target-free high-throughput screening of small molecules utilizing a phenotypic-based HCV infection assay. Thereby, a very potent (EC

Indexed as

Amino Acid SubstitutionAntiviral AgentsCarbamatesDrug CombinationsDrug DiscoveryDrug Resistance, ViralDrug SynergismGene ExpressionHepacivirusHepatocytesHigh-Throughput Screening AssaysHost-Pathogen InteractionsHumansImidazolesInterferon-alphaOligopeptidesAntiviral AgentsCarbamatesdaclatasvirDrug CombinationsE1 protein, Hepatitis C virusImidazolesInterferon-alphaOligopeptidesPyridinesPyrimidinesPyrrolidinesSofosbuvirtelaprevirValineViral Envelope Proteins

Identifiers

PMID28333153
PMCPMC5363083
OpenAlexW2599836722

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.