Evidence map›Paper›PMID 35534355›Full record

ReviewTrends in pharmacological sciences2022

Thapsigargin: key to new host-directed coronavirus antivirals?

Mohammed Samer Shaban, Christin Mayr-Buro, Johanna Meier-Soelch, Benadict Vincent Albert, M Lienhard Schmitz, John Ziebuhr, Michael Kracht

Open access · bronzeAbstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.0field-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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Membrane-Targeting Antivirals.International journal of molecular sciences · 2025
    Review
  7. Review
  8. Article
  9. Review
  10. The Role of Cyclodextrins in COVID-19 Therapy-A Literature Review.International journal of molecular sciences · 2023
    Review
  11. Review
  12. Article
  13. Article
  14. 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.

Mohammed Samer ShabanRudolf Buchheim Institute of Pharmacology, Justus Liebig University, Giessen, Germany.
Christin Mayr-BuroRudolf Buchheim Institute of Pharmacology, Justus Liebig University, Giessen, Germany.
Johanna Meier-SoelchRudolf Buchheim Institute of Pharmacology, Justus Liebig University, Giessen, Germany.
Benadict Vincent AlbertRudolf Buchheim Institute of Pharmacology, Justus Liebig University, Giessen, Germany.
M Lienhard SchmitzInstitute of Biochemistry, Justus Liebig University, Giessen, Germany; German Center for Lung Research (DZL) and Universities of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany.
John ZiebuhrInstitute of Medical Virology, Justus Liebig University, Giessen, Germany; German Center for Infection Research (DZIF), partner site Giessen-Marburg-Langen, Giessen, Germany.
Michael KrachtRudolf Buchheim Institute of Pharmacology, Justus Liebig University, Giessen, Germany; German Center for Lung Research (DZL) and Universities of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany. Electronic address: michael.kracht@pharma.med.uni-giessen.de.
Justus-Liebig-Universität Gießen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the great success of vaccines that protect against RNA virus infections, and the development and clinical use of a limited number of RNA virus-specific drugs, there is still an urgent need for new classes of antiviral drugs against circulating or emerging RNA viruses. To date, it has proved difficult to efficiently suppress RNA virus replication by targeting host cell functions, and there are no approved drugs of this type. This opinion article discusses the recent discovery of a pronounced and sustained antiviral activity of the plant-derived natural compound thapsigargin against enveloped RNA viruses such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), Middle East respiratory syndrome coronavirus (MERS-CoV), and influenza A virus. Based on its mechanisms of action, thapsigargin represents a new prototype of compounds with multimodal host-directed antiviral activity.

Indexed as

COVID-19 Drug TreatmentMiddle East Respiratory Syndrome CoronavirusAntiviral AgentsHumansSARS-CoV-2ThapsigarginAntiviral AgentsThapsigargincoronavirusCOVID-19ERADER membraneshost-directed antiviralsproteomethapsigargin

Identifiers

PMID35534355
PMCPMC9013669
OpenAlexW4223985753

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.