Evidence map›Paper›PMID 40176969›Full record

ArticleRSC chemical biology2025

3'-

Jonathan P Dolan, Tessa Keenan, Aisling Ní Cheallaigh, Martin A Fascione, Gavin J Miller

Abstract read
In one paragraph

Article in RSC chemical biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. AnOrganic letters · 2026
    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

5 authors.

Jonathan P DolanSchool of Chemical & Physical Sciences and Centre for Glycoscience, Keele University Keele Staffordshire ST5 5BG UK j.dolan@keele.ac.uk g.j.miller@keele.ac.uk.ORCID https://orcid.org/0000-0002-7009-2225
Tessa KeenanDepartment of Chemistry, University of York York YO10 5DD UK.ORCID https://orcid.org/0000-0003-2466-6918
Aisling Ní CheallaighSchool of Chemical & Physical Sciences and Centre for Glycoscience, Keele University Keele Staffordshire ST5 5BG UK j.dolan@keele.ac.uk g.j.miller@keele.ac.uk.ORCID https://orcid.org/0000-0003-2666-5089
Martin A FascioneDepartment of Chemistry, University of York York YO10 5DD UK.ORCID https://orcid.org/0000-0002-0066-4419
Gavin J MillerSchool of Chemical & Physical Sciences and Centre for Glycoscience, Keele University Keele Staffordshire ST5 5BG UK j.dolan@keele.ac.uk g.j.miller@keele.ac.uk.ORCID https://orcid.org/0000-0001-6533-3306

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nucleoside analogue therapeutics have a proven capability within drug discovery as antiviral and antineoplastic agents. However, their efficacy can be limited by poor cellular uptake, off target toxicity and low bioavailability. Glycosylation of pharmaceutical agents/natural products represents a strategically simple method to modulate pharmacological profiles. Herein, we explore biocatalytic glycosylation of nucleoside analogues. The activity of the nucleoside-specific 3'-

Identifiers

PMID40176969
PMCPMC11959488

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.