Evidence map›Paper›PMID 21524502›Full record

ArticleEuropean journal of medicinal chemistry2011

Synthesis and inhibitory activity of sialic acid derivatives targeted at viral sialate-O-acetylesterases.

Mathew Stanley, Juliane Mayr, Wolfgang Huber, Reinhard Vlasak, Hansjörg Streicher

Open access · bronzeAbstract read
In one paragraph

Article in European journal of medicinal chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 91% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 2 countries.

Mathew StanleyDepartment of Chemistry and Biochemistry, University of Sussex, Brighton, BN1 9QG, UK.
Juliane Mayr
Wolfgang Huber
Reinhard Vlasak
Hansjörg Streicher
University of Salzburg · ATUniversity of Sussex · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of sialosides modified at the 4- and 9-hydroxy group were synthesised and tested for inhibition of the viral haemagglutinin-esterase activity from various Orthomyxoviruses and Coronaviruses. While no inhibition of the sialate-4-O-acetylesterases from mouse hepatitis virus strain S or sialodacryoadenitis virus was found, a 9-O-methyl derivative displayed inhibitory activity against recombinant sialate-9-O-acetylesterase from influenza C virus.

Indexed as

AcetylesteraseAnimalsAntiviral AgentsCoronavirusDrug DesignGammainfluenzavirusHemagglutinins, ViralMiceN-Acetylneuraminic AcidOrthomyxoviridaeRecombinant ProteinsStructure-Activity RelationshipSubstrate SpecificityTorovirusViral Fusion ProteinsViral ProteinsAcetylesteraseAntiviral Agentshemagglutinin esteraseHemagglutinins, ViralN-Acetylneuraminic AcidRecombinant Proteinssialate O-acetylesteraseViral Fusion ProteinsViral Proteins

Identifiers

PMID21524502
PMCPMC7111470
OpenAlexW2025975247

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.