Evidence map›Paper›PMID 31646247›Full record

ArticleACS omega2019

Discovery of New Inhibitors of Hepatitis C Virus NS3/4A Protease and Its D168A Mutant.

Ittipat Meewan, Xingquan Zhang, Suchismita Roy, Carlo Ballatore, Anthony J O'Donoghue, Robert T Schooley, Ruben Abagyan

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Article
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  7. Article
  8. Article
  9. Article
  10. Article
  11. Discovery of PLACS omega · 2023
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Viral Hepatitis - The Road Traveled and the Journey Remaining.Hepatic medicine : evidence and research · 2022
    Review
  18. Review
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

7 authors at 1 institution in 1 country.

Ittipat MeewanSkaggs School of Pharmacy and Pharmaceutical Sciences, Department of Chemistry and Biochemistry, and School of Medicine, University of California San Diego, La Jolla, California 92093, United States.
Xingquan ZhangSkaggs School of Pharmacy and Pharmaceutical Sciences, Department of Chemistry and Biochemistry, and School of Medicine, University of California San Diego, La Jolla, California 92093, United States.
Suchismita RoySkaggs School of Pharmacy and Pharmaceutical Sciences, Department of Chemistry and Biochemistry, and School of Medicine, University of California San Diego, La Jolla, California 92093, United States.
Carlo BallatoreSkaggs School of Pharmacy and Pharmaceutical Sciences, Department of Chemistry and Biochemistry, and School of Medicine, University of California San Diego, La Jolla, California 92093, United States.
Anthony J O'DonoghueSkaggs School of Pharmacy and Pharmaceutical Sciences, Department of Chemistry and Biochemistry, and School of Medicine, University of California San Diego, La Jolla, California 92093, United States.
Robert T SchooleySkaggs School of Pharmacy and Pharmaceutical Sciences, Department of Chemistry and Biochemistry, and School of Medicine, University of California San Diego, La Jolla, California 92093, United States.
Ruben AbagyanSkaggs School of Pharmacy and Pharmaceutical Sciences, Department of Chemistry and Biochemistry, and School of Medicine, University of California San Diego, La Jolla, California 92093, United States.
University of California San Diego · US

Funding

Macromolecular DockingR01GM071872 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ABAGYAN, RUBEN · 2004 to 2017
$4.2M
Addressing biomedical challenges with computational mechanics and big dataR35GM131881 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ABAGYAN, RUBEN · 2019 to 2023
$1.9M
NIGMS NIH HHS R01 GM071872NIGMS NIH HHS R35 GM131881
6 · The paper itself

Abstract

Hepatitis C virus (HCV) is a human pathogen with high morbidity. The HCV NS3/4A protease is essential for viral replication and is one of the top three drug targets. Several drugs targeting the protease have been developed, but drug-resistant mutant strains emerged. Here, we screened a library and synthesized a novel class of small molecules based on a tryptophan derivative scaffold identified as HCV NS3/4A protease inhibitors that are active against both wild type and mutant form of the protease. Only the compounds with predicted binding poses not affected by the most frequent mutations in the active site were selected for experimental validation. The antiviral activities were evaluated by replicon and enzymatic assays. Twenty-two compounds were found to inhibit HCV with EC

Identifiers

PMID31646247
PMCPMC6796237
OpenAlexW2978923004

What OpenQuestion holds

Textmetadata
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.