Evidence map›Paper›PMID 29565562›Full record

ReviewACS infectious diseases2019

Chemical Approaches to Inhibiting the Hepatitis B Virus Ribonuclease H.

John E Tavis, Grigoris Zoidis, Marvin J Meyers, Ryan P Murelli

Open access · greenAbstract readReview
In one paragraph

Review in ACS infectious diseases, 2019. 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
3.4field-weighted citation impact, top 7% 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, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Novel Pyrazino[1,2-Viruses · 2024
    Article
  5. Molecules (Basel, Switzerland) · 2024
    Article
  6. Review
  7. Viral Nucleases.Viruses · 2023
    Article
  8. The progress of molecules and strategies for the treatment of HBV infection.Frontiers in cellular and infection microbiology · 2023
    Review
  9. Article
  10. Article
  11. Recent Advances in Hepatitis B Treatment.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  12. Article
  13. Moving Fast Toward Hepatitis B Virus Elimination.Advances in experimental medicine and biology · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. Article
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

4 authors at 4 institutions in 2 countries.

John E TavisDepartment of Molecular Microbiology and Immunology and Saint Louis University Liver Center, School of Medicine , Saint Louis University , 1100 S. Grand Blvd. , Saint Louis , Missouri 63104 , United States.ORCID 0000-0002-8711-4240
Grigoris ZoidisDepartment of Pharmaceutical Chemistry, School of Health Sciences, Faculty of Pharmacy , National and Kapodistrian University of Athens , Panepistimiopolis-Zografou, Athens , GR-15771 , Greece.
Marvin J MeyersDepartment of Chemistry , Saint Louis University , Monsanto Hall 125, 3501 Laclede Avenue , St. Louis , Missouri 63103 , United States.
Ryan P MurelliDepartment of Chemistry , Brooklyn College, The City University of New York , Brooklyn , New York 11210 , United States.ORCID 0000-0002-4247-3936
Monsanto (United States) · USNational and Kapodistrian University of Athens · GRSaint Louis University · USThe Graduate Center, CUNY · US

Funding

Optimization of alpha-hydroxytropolones as novel inhibitors of the HBV RNaseHR01AI122669 · NIAID · SAINT LOUIS UNIVERSITY · PI TAVIS, JOHN E · 2016 to 2020
$2.2M
Defining approaches for improving HID and HPD compounds as HBV RNaseH antagonistsR21AI124672 · NIAID · SAINT LOUIS UNIVERSITY · PI MEYERS, MARVIN J, TAVIS, JOHN E · 2017 to 2018
$417k
NIAID NIH HHS R01 AI122669NIAID NIH HHS R21 AI124672
6 · The paper itself

Abstract

Hepatitis B virus (HBV) chronically infects >250 million people and kills nearly a million annually, and current antivirals cannot clear the infection or adequately suppress disease. The virus replicates by reverse transcription, and the dominant antiviral drugs are nucleos(t)ide analogs that target the viral reverse transcriptase. We are developing antivirals targeting the other essential viral enzymatic activity, the ribonuclease H (RNaseH). HBV RNaseH inhibitors with efficacies in the low micromolar to nanomolar range against viral replication in culture have been identified in the α-hydroxytropolone and hydroxyimide chemotypes. Here, we review the promise of RNaseH inhibitors, their current structure-activity relationships, and challenges to optimizing the inhibitors into leads for clinical assessment.

Indexed as

Antiviral AgentsEnzyme InhibitorsHepatitis B virusRibonuclease HStructure-Activity RelationshipVirus ReplicationAntiviral AgentsEnzyme InhibitorsRibonuclease H

Identifiers

PMID29565562
PMCPMC7202671
OpenAlexW2793638189

What OpenQuestion holds

Textmetadata
LicenceTDM
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.