Evidence map›Paper›PMID 15226499›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2004

Small molecules targeting severe acute respiratory syndrome human coronavirus.

Chung-Yi Wu, Jia-Tsrong Jan, Shiou-Hwa Ma, Chih-Jung Kuo, Hsueh-Fen Juan, Yih-Shyun E Cheng, Hsien-Hua Hsu, Hsuan-Cheng Huang, Douglass Wu, Ashraf Brik and 6 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04372628 (Trial of Early Therapies During Non-hospitalized Outpatient Window), which is not on this map. Cited by 289 papers.

0numbers the graph read from it
0cells of the map it votes in
289citing papers in PubMed
14.0field-weighted citation impact, top 1% 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.

NCT04372628 phase2completednot on this mapstarted 2020, after this paper: background citation

Trial of Early Therapies During Non-hospitalized Outpatient Window (TREAT NOW) for COVID-19

TypeinterventionalSponsorVanderbilt University Medical CenterRan2020 to 2022Enrolled452ConditionsCOVID-19ArmsLopinavir/Ritonavir 400 mg/100 mg, Placebo
3 · Its place in the literature

Who cites it

289 citing papers in PubMed, 532 citations in OpenAlex.

  1. Trial
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  3. Article
  4. Review
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  6. Article
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  8. Article
  9. The immune response to SARS-CoV-2 in people with HIV.Cellular & molecular immunology · 2024
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Identification ofMicrobiology spectrum · 2023
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

229 more citing papers are in PubMed but not listed here.

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

16 authors at 6 institutions in 1 country.

Chung-Yi WuGenomics Research Center and Institute of Biological Chemistry, Academia Sinica, Taipei 115, Taiwan.
Jia-Tsrong Jan
Shiou-Hwa Ma
Chih-Jung Kuo
Hsueh-Fen Juan
Yih-Shyun E Cheng
Hsien-Hua Hsu
Hsuan-Cheng Huang
Douglass Wu
Ashraf Brik
Fu-Sen Liang
Rai-Shung Liu
Jim-Min Fang
Shui-Tein Chen
Po-Huang Liang
Chi-Huey Wong
Institute of Biological Chemistry, Academia Sinica · TWNational Defense Medical Center · TWNational Taipei University of Technology · TWNational Taiwan University · TWNational Tsing Hua University · TWNational Defense University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome (SARS) is an infectious disease caused by a novel human coronavirus. Currently, no effective antiviral agents exist against this type of virus. A cell-based assay, with SARS virus and Vero E6 cells, was developed to screen existing drugs, natural products, and synthetic compounds to identify effective anti-SARS agents. Of >10,000 agents tested, approximately 50 compounds were found active at 10 microM; among these compounds, two are existing drugs (Reserpine 13 and Aescin 5) and several are in clinical development. These 50 active compounds were tested again, and compounds 2-6, 10, and 13 showed active at 3 microM. The 50% inhibitory concentrations for the inhibition of viral replication (EC(50)) and host growth (CC(50)) were then measured and the selectivity index (SI = CC(50)/EC(50)) was determined. The EC(50), based on ELISA, and SI for Reserpine, Aescim, and Valinomycin are 3.4 microM (SI = 7.3), 6.0 microM (SI = 2.5), and 0.85 microM (SI = 80), respectively. Additional studies were carried out to further understand the mode of action of some active compounds, including ELISA, Western blot analysis, immunofluorescence and flow cytometry assays, and inhibition against the 3CL protease and viral entry. Of particular interest are the two anti-HIV agents, one as an entry blocker and the other as a 3CL protease inhibitor (K(i) = 0.6 microM).

Indexed as

AnimalsAntiviral AgentsBlotting, WesternChlorocebus aethiopsCoronavirus 3C ProteasesCysteine EndopeptidasesEndopeptidasesEnzyme-Linked Immunosorbent AssayFlow CytometryFluorescent Antibody TechniqueSevere acute respiratory syndrome-related coronavirusVero CellsViral ProteinsVirus ReplicationAntiviral AgentsCoronavirus 3C ProteasesCysteine EndopeptidasesEndopeptidasesViral Proteins

Identifiers

PMID15226499
PMCPMC454157
OpenAlexW2061777515

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.