Evidence map›Paper›PMID 35182772›Full record

ArticleBioorganic & medicinal chemistry letters2022

Main protease mutants of SARS-CoV-2 variants remain susceptible to nirmatrelvir.

Sven Ullrich, Kasuni B Ekanayake, Gottfried Otting, Christoph Nitsche

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
19.6field-weighted citation impact, top 1% 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

102 citing papers in PubMed, 195 citations in OpenAlex.

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42 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Sven UllrichResearch School of Chemistry, Australian National University, Canberra, ACT, 2601, Australia.
Kasuni B EkanayakeResearch School of Chemistry, Australian National University, Canberra, ACT, 2601, Australia.
Gottfried OttingResearch School of Chemistry, Australian National University, Canberra, ACT, 2601, Australia.
Christoph NitscheResearch School of Chemistry, Australian National University, Canberra, ACT, 2601, Australia. Electronic address: christoph.nitsche@anu.edu.au.
Australian National University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The COVID-19 pandemic continues to be a public health threat. Multiple mutations in the spike protein of emerging variants of SARS-CoV-2 appear to impact on the effectiveness of available vaccines. Specific antiviral agents are keenly anticipated but their efficacy may also be compromised in emerging variants. One of the most attractive coronaviral drug targets is the main protease (M

Indexed as

COVID-19 Drug TreatmentSARS-CoV-2Antiviral AgentsHumansLactamsLeucineNitrilesPandemicsPeptide HydrolasesProlineProtease InhibitorsAntiviral AgentsLactamsLeucinenirmatrelvirNitrilesPeptide HydrolasesProlineProtease InhibitorsInhibitorsMain proteaseNirmatrelvirSARS-CoV-2Variants

Identifiers

PMID35182772
PMCPMC8856729
OpenAlexW4212949239

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.