Evidence map›Paper›PMID 33802584›Full record

ArticleMolecules (Basel, Switzerland)2021

Inhibitor Development against p7 Channel in Hepatitis C Virus.

Shukun Wei, Xiaoyou Hu, Lingyu Du, Linlin Zhao, Hongjuan Xue, Chaolun Liu, James J Chou, Jin Zhong, Yimin Tong, Shuqing Wang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

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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 5 institutions in 2 countries.

Shukun WeiState Key Laboratory of Molecular Biology, Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, 333 Haike Road, Shanghai 201203, China.
Xiaoyou HuUniversity of Chinese Academy of Sciences, Beijing 100049, China.
Lingyu DuState Key Laboratory of Molecular Biology, Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, 333 Haike Road, Shanghai 201203, China.
Linlin ZhaoState Key Laboratory of Molecular Biology, Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, 333 Haike Road, Shanghai 201203, China.
Hongjuan XueNational Facility for Protein Science in Shanghai, ZhangJiang Lab, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai 201210, China.
Chaolun LiuShanghaiTech University, Shanghai 201210, China.
James J ChouDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.
Jin ZhongUniversity of Chinese Academy of Sciences, Beijing 100049, China.
Yimin TongCAS Key Laboratory of Molecular Virology and Immunology, Institute Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai 200031, China.
Shuqing WangSchool of Pharmacy, Tianjin Medical University, Tianjin 300070, China.
Bo OuYangState Key Laboratory of Molecular Biology, Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, 333 Haike Road, Shanghai 201203, China.ORCID 0000-0002-2877-0635
Chinese Academy of Sciences · CNCenter for Excellence in Molecular Cell Science · CNHarvard University · USShanghaiTech University · CNTianjin Medical University · CN

Funding

National Natural Science Foundation of China 21772146
6 · The paper itself

Abstract

Hepatitis C Virus (HCV) is the key cause of chronic and severe liver diseases. The recent direct-acting antiviral agents have shown the clinical success on HCV-related diseases, but the rapid HCV mutations of the virus highlight the sustaining necessity to develop new drugs. p7, the viroporin protein from HCV, has been sought after as a potential anti-HCV drug target. Several classes of compounds, such as amantadine and rimantadine have been testified for p7 inhibition. However, the efficacies of these compounds are not high. Here, we screened some novel p7 inhibitors with amantadine scaffold for the inhibitor development. The dissociation constant (

Indexed as

Drug DevelopmentAntiviral AgentsCarcinoma, HepatocellularCell ProliferationHepacivirusHepatitis CHumansLiver NeoplasmsMolecular Docking SimulationTumor Cells, CulturedViral ProteinsViroporin ProteinsVirus ReplicationAntiviral Agentsp7 protein, Hepatitis C virusViral ProteinsViroporin ProteinsdockingHCV productionMD simulationp7 inhibitorsrational design

Identifiers

PMID33802584
PMCPMC7961618
OpenAlexW3134463457

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.