Evidence map›Paper›PMID 33615181›Full record

ArticleACS pharmacology & translational science2021

Deciphering the Agonist Binding Mechanism to the Adenosine A1 Receptor.

Giuseppe Deganutti, Kerry Barkan, Barbara Preti, Michele Leuenberger, Mark Wall, Bruno G Frenguelli, Martin Lochner, Graham Ladds, Christopher A Reynolds

Open access · greenAbstract read
In one paragraph

Article in ACS pharmacology & translational science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

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  6. The full activation mechanism of the adenosine AProceedings of the National Academy of Sciences of the United States of America · 2022
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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 4 institutions in 3 countries.

Giuseppe DeganuttiCentre for Sport, Exercise and Life Sciences, Faculty of Health and Life Sciences, Coventry University, Alison Gingell Building, Coventry CV1 5FB, U.K.
Kerry BarkanDepartment of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge, CB2 1PD, U.K.
Barbara PretiInstitute of Biochemistry and Molecular Medicine, University of Bern, 3012 Bern, Switzerland.
Michele LeuenbergerInstitute of Biochemistry and Molecular Medicine, University of Bern, 3012 Bern, Switzerland.
Mark WallSchool of Life Sciences, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, U.K.
Bruno G FrenguelliSchool of Life Sciences, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, U.K.
Martin LochnerInstitute of Biochemistry and Molecular Medicine, University of Bern, 3012 Bern, Switzerland.
Graham LaddsDepartment of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge, CB2 1PD, U.K.
Christopher A ReynoldsCentre for Sport, Exercise and Life Sciences, Faculty of Health and Life Sciences, Coventry University, Alison Gingell Building, Coventry CV1 5FB, U.K.
University of Bern · CHCoventry University · GBUniversity of Cambridge · GBUniversity of Warwick · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite being among the most characterized G protein-coupled receptors (GPCRs), adenosine receptors (ARs) have always been a difficult target in drug design. To date, no agonist other than the natural effector and the diagnostic regadenoson has been approved for human use. Recently, the structure of the adenosine A1 receptor (A

Identifiers

PMID33615181
PMCPMC7887845
OpenAlexW3121668723

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.