Evidence map›Paper›PMID 30513600›Full record

ArticleViruses2018

Identification of Diaryl-Quinoline Compounds as Entry Inhibitors of Ebola Virus.

Qinghua Cui, Han Cheng, Rui Xiong, Gang Zhang, Ruikun Du, Manu Anantpadma, Robert A Davey, Lijun Rong

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 33 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

8 authors at 4 institutions in 2 countries.

Qinghua CuiCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan 250355, China. user753951@163.com.
Han ChengDepartment of Microbiology and Immunology, College of Medicine, The University of Illinois at Chicago, Chicago, IL 60612, USA. hancheng@uic.edu.
Rui XiongDepartment of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, and UICentre, University of Illinois at Chicago, Chicago, IL 60612, USA. rxiong3@uic.edu.
Gang ZhangState Key Laboratory of Bioactive Substances and Function of Natural Medicine, Institute of Materia Medica, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100050, China. gzhang@imm.ac.cn.ORCID 0000-0003-0774-5710
Ruikun DuCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan 250355, China. ruikun7128@gmail.com.
Manu AnantpadmaDepartment of Virology and Immunology, Texas Biomedical Research Institute, San Antonio, TX 78227, USA. manantpadma@txbiomed.org.
Robert A DaveyDepartment of Virology and Immunology, Texas Biomedical Research Institute, San Antonio, TX 78227, USA. radavey@bu.edu.
Lijun RongDepartment of Microbiology and Immunology, College of Medicine, The University of Illinois at Chicago, Chicago, IL 60612, USA. lijun@uic.edu.
University of Illinois Chicago · USBoston University · USShandong University of Traditional Chinese Medicine · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ebola virus is the causative agent of Ebola virus disease in humans. The lethality of Ebola virus infection is about 50%, supporting the urgent need to develop anti-Ebola drugs. Glycoprotein (GP) is the only surface protein of the Ebola virus, which is functionally critical for the virus to attach and enter the host cells, and is a promising target for anti-Ebola virus drug development. In this study, using the recombinant HIV-1/Ebola pseudovirus platform we previously established, we evaluated a small molecule library containing various quinoline compounds for anti-Ebola virus entry inhibitors. Some of the quinoline compounds specifically inhibited the entry of the Ebola virus. Among them, compound SYL1712 was the most potent Ebola virus entry inhibitor with an IC

Indexed as

Dietary SupplementsAntiviral AgentsCell LineDrug Evaluation, PreclinicalEbolavirusHemorrhagic Fever, EbolaHigh-Throughput Screening AssaysHumansInhibitory Concentration 50Microbial Sensitivity TestsModels, MolecularMolecular ConformationMolecular StructureQuinolinesStructure-Activity RelationshipVirus InternalizationAntiviral AgentsQuinolinesassayEBOVentry inhibitorglycoproteinlead compoundquinoline

Identifiers

PMID30513600
PMCPMC6315506
OpenAlexW2902340288

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.