Evidence map›Paper›PMID 33066278›Full record

ArticleMolecules (Basel, Switzerland)2020

High-Throughput Screening for Inhibitors of the SARS-CoV-2 Protease Using a FRET-Biosensor.

Alistair S Brown, David F Ackerley, Mark J Calcott

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 11% 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.

NCT04483973 phase2completednot on this mapstarted 2021, after this paper: background citation

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose Escalation Study to Evaluate the Safety and Efficacy of SPI-1005 in Severe COVID-19 Patients

TypeinterventionalSponsorSound Pharmaceuticals, IncorporatedRan2021 to 2023Enrolled25ConditionsCovid19, Coronavirus, Coronavirus Infection, Corona Virus InfectionArmsEbselen, Placebo
NCT04484025 phase2enrolling by invitationnot on this mapstarted 2021, after this paper: background citation

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose Escalation Study to Evaluate the Safety and Efficacy of SPI-1005 in Moderate COVID-19 Patients

TypeinterventionalSponsorSound Pharmaceuticals, IncorporatedRan2021 to 2023Enrolled60ConditionsCovid19, Corona Virus Infection, Coronavirus, Coronavirus InfectionArmsEbselen, Placebo
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. A Novel Fluorescence Polarization Binding Assay for the Main Protease (MACS pharmacology & translational science · 2025
    Article
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  6. Acta pharmaceutica Sinica. B · 2024
    Review
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  16. Imaging Techniques: Essential Tools for the Study of SARS-CoV-2 Infection.Frontiers in cellular and infection microbiology · 2022
    Review
  17. A genetically encoded BRET-based SARS-CoV-2 MCommunications chemistry · 2022
    Article
  18. A Bioluminescent 3CLViruses · 2021
    Article
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Alistair S BrownSchool of Biological Sciences, Victoria University of Wellington, Wellington 6012, New Zealand.ORCID 0000-0001-5314-1999
David F AckerleySchool of Biological Sciences, Victoria University of Wellington, Wellington 6012, New Zealand.ORCID 0000-0002-6188-9902
Mark J CalcottSchool of Biological Sciences, Victoria University of Wellington, Wellington 6012, New Zealand.
Victoria University of Wellington · NZ

Funding

Health Research Council of New Zealand 18-532Royal Society of New Zealand 18-VUW-082
6 · The paper itself

Abstract

The global SARS-CoV-2 pandemic started late 2019 and currently continues unabated. The lag-time for developing vaccines means it is of paramount importance to be able to quickly develop and repurpose therapeutic drugs. Protein-based biosensors allow screening to be performed using routine molecular laboratory equipment without a need for expensive chemical reagents. Here we present a biosensor for the 3-chymotrypsin-like cysteine protease from SARS-CoV-2, comprising a FRET-capable pair of fluorescent proteins held in proximity by a protease cleavable linker. We demonstrate the utility of this biosensor for inhibitor discovery by screening 1280 compounds from the Library of Pharmaceutically Active Compounds collection. The screening identified 65 inhibitors, with the 20 most active exhibiting sub-micromolar inhibition of 3CL

Indexed as

BetacoronavirusBiosensing TechniquesCoronavirus 3C ProteasesCoronavirus InfectionsCOVID-19Cysteine EndopeptidasesFluorescence Resonance Energy TransferHigh-Throughput Screening AssaysHumansPandemicsPneumonia, ViralProtease InhibitorsSARS-CoV-2Viral Nonstructural ProteinsCoronavirus 3C ProteasesCysteine EndopeptidasesProtease InhibitorsViral Nonstructural Proteins3CLProapomorphineaporphineCOVID-19cysteine proteaseebselenSARS-CoV-2

Identifiers

PMID33066278
PMCPMC7587356
OpenAlexW3092572185

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.