Evidence map›Paper›PMID 33915212›Full record

ArticleInternational journal of biological macromolecules2021

Heparin: A simplistic repurposing to prevent SARS-CoV-2 transmission in light of its in-vitro nanomolar efficacy.

Yash Gupta, Dawid Maciorowski, Samantha E Zak, Chandrashekhar V Kulkarni, Andrew S Herbert, Ravi Durvasula, Jawed Fareed, John M Dye, Prakasha Kempaiah

Open access · greenAbstract read
In one paragraph

Article in International journal of biological macromolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  16. The Spike Mutants Website: A Worldwide Used Resource against SARS-CoV-2.International journal of molecular sciences · 2022
    Article
  17. Article
  18. Is heparan sulfate a target for inhibition of RNA virus infection?American journal of physiology. Cell physiology · 2022
    Review
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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

9 authors at 6 institutions in 2 countries.

Yash GuptaInfectious Diseases, Mayo Clinic, Jacksonville, FL, USA.
Dawid MaciorowskiLoyola University Chicago, Chicago, IL, USA.
Samantha E ZakUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA; The Geneva Foundation, 917 Pacific Avenue, Tacoma, WA, USA.
Chandrashekhar V KulkarniSchool of Natural Sciences, University of Central Lancashire, Preston, UK.
Andrew S HerbertUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.
Ravi DurvasulaInfectious Diseases, Mayo Clinic, Jacksonville, FL, USA.
Jawed FareedDepartment of Molecular Pharmacology & Neuroscience, Loyola University Chicago, Chicago, IL, USA.
John M DyeUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA; The Geneva Foundation, 917 Pacific Avenue, Tacoma, WA, USA.
Prakasha KempaiahInfectious Diseases, Mayo Clinic, Jacksonville, FL, USA. Electronic address: Kempaiah.Prakasha@mayo.edu.
Loyola University Chicago · USMayo Clinic in Florida · USUnited States Army Medical Research Institute of Infectious Diseases · USThe Geneva Foundation · USUniversity of Central Lancashire · GBWinnMed · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The world is currently facing a novel coronavirus (SARS-CoV-2) pandemic. The greatest threat that is disrupting the normal functioning of society is the exceptionally high species independent transmission. Drug repurposing is understood to be the best strategy to immediately deploy well-characterized agents against new pathogens. Several repurposable drugs are already in evaluation for determining suitability to treat COVID-19. One such promising compound includes heparin, which is widely used in reducing thrombotic events associated with COVID-19 induced pathology. As part of identifying target-specific antiviral compounds among FDA and world-approved libraries using high-throughput virtual screening (HTVS), we previously evaluated top hits for anti-SARS-CoV-2 activity. Here, we report results of highly efficacious viral entry blocking properties of heparin (IC

Indexed as

Drug RepositioningCOVID-19COVID-19 Drug TreatmentHeparinHumansSARS-CoV-2Spike Glycoprotein, CoronavirusHeparinSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2AnticoagulantCOVID-19HeparinLipid-based formulationsSARS-CoV2Spike proteinSulfated polysaccharideTopical deliveryTransmission-blocking

Identifiers

PMID33915212
PMCPMC8074525
OpenAlexW3159506049

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.