Evidence map›Paper›PMID 28645623›Full record

ArticleAntiviral research2017

Identification of a coumarin-based antihistamine-like small molecule as an anti-filoviral entry inhibitor.

Han Cheng, Adam Schafer, Veronica Soloveva, Dima Gharaibeh, Tara Kenny, Cary Retterer, Rouzbeh Zamani, Sina Bavari, Norton P Peet, Lijun Rong

Open access · greenAbstract read
In one paragraph

Article in Antiviral research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Pseudotyped Viruses for Marburgvirus and Ebolavirus.Advances in experimental medicine and biology · 2023
    Article
  4. Article
  5. Ebola Virus Entry Inhibitors.Advances in experimental medicine and biology · 2022
    Article
  6. Review
  7. Observational
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. 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

10 authors at 2 institutions in 1 country.

Han ChengDepartment of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, Chicago, IL, 60612, USA. Electronic address: hancheng@uic.edu.
Adam SchaferDepartment of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, Chicago, IL, 60612, USA.
Veronica SolovevaUS Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, 21702, USA.
Dima GharaibehUS Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, 21702, USA.
Tara KennyUS Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, 21702, USA.
Cary RettererUS Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, 21702, USA.
Rouzbeh ZamaniUS Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, 21702, USA.
Sina BavariUS Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, 21702, USA.
Norton P PeetChicago BioSolutions, Inc., 2242 West Harrison Suite 201, Chicago, IL, 60612, USA.
Lijun RongDepartment of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, Chicago, IL, 60612, USA. Electronic address: lijun@uic.edu.
United States Army Medical Research Institute of Infectious Diseases · USUniversity of Illinois Chicago · US

Funding

Screening and development of anti-Ebola entry inhibitorsU01AI077767 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RONG, LIJUN · 2009 to 2010
$2.1M
NIAID NIH HHS U01 AI077767
6 · The paper itself

Abstract

Filoviruses, consisting of Ebola virus, Marburg virus and Cuevavirus, cause severe hemorrhagic fevers in humans with high mortality rates up to 90%. Currently, there is no approved vaccine or therapy available for the prevention and treatment of filovirus infection in humans. The recent 2013-2015 West African Ebola epidemic underscores the urgency to develop antiviral therapeutics against these infectious diseases. Our previous study showed that GPCR antagonists, particularly histamine receptor antagonists (antihistamines) inhibit Ebola and Marburg virus entry. In this study, we screened a library of 1220 small molecules with predicted antihistamine activity, identified multiple compounds with potent inhibitory activity against entry of both Ebola and Marburg viruses in human cancer cell lines, and confirmed their anti-Ebola activity in human primary cells. These small molecules target a late-stage of Ebola virus entry. Further structure-activity relationship studies around one compound (cp19) reveal the importance of the coumarin fused ring structure, especially the hydrophobic substituents at positions 3 and/or 4, for its antiviral activity, and this identified scaffold represents a favorable starting point for the rapid development of anti-filovirus therapeutic agents.

Indexed as

AnimalsAntiviral AgentsCell LineCell Line, TumorCoumarinsDrug DiscoveryEbolavirusHemorrhagic Fever, EbolaHigh-Throughput Screening AssaysHistamine AntagonistsHumansHydrophobic and Hydrophilic InteractionsMarburgvirusMarburg Virus DiseaseSmall Molecule LibrariesStructure-Activity RelationshipAntiviral AgentscoumarinCoumarinsHistamine AntagonistsSmall Molecule LibrariesAntihistamineAntiviralEbolaHistamine receptor antagonistMarburg

Identifiers

PMID28645623
PMCPMC5666694
OpenAlexW2647136810

What OpenQuestion holds

Textmetadata
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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.