Evidence map›Paper›PMID 28009436›Full record

ArticleBritish journal of pharmacology2017

Pharmacological characterization of N-[(2S)-5-(6-fluoro-3-pyridinyl)-2, 3-dihydro-1H-inden-2-yl]-2-propanesulfonamide: a novel, clinical AMPA receptor positive allosteric modulator.

Simon E Ward, Paul Beswick, Novella Calcinaghi, Lee A Dawson, Jane Gartlon, Francesca Graziani, Declan N C Jones, Laurent Lacroix, M H Selina Mok, Beatrice Oliosi and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

14 authors at 4 institutions in 2 countries.

Simon E WardUniversity of Sussex, Brighton, UK.
Paul BeswickUniversity of Sussex, Brighton, UK.
Novella CalcinaghiNeurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline Medicines Research Centre, Verona, Italy.
Lee A DawsonNeurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline, Harlow, UK.
Jane GartlonNeurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline, Harlow, UK.
Francesca GrazianiNeurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline Medicines Research Centre, Verona, Italy.
Declan N C JonesNeurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline, Harlow, UK.
Laurent LacroixNeurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline, Harlow, UK.
M H Selina MokNeurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline, Harlow, UK.
Beatrice OliosiNeurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline Medicines Research Centre, Verona, Italy.
Joanne PardoeNeurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline, Harlow, UK.
Kathryn StarrNeurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline, Harlow, UK.
Marie L WoolleyNeurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline, Harlow, UK.
Mark H HarriesNeurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline, Harlow, UK.
GlaxoSmithKline (United Kingdom) · GBGlaxoSmithKline (Italy) · ITUniversity of Sussex · GBUniversity of Roehampton · GB

Funding

Wellcome Trust WT-103096/Z/13/Z
6 · The paper itself

Abstract

background and purposeAMPA receptor positive allosteric modulators represent a potential therapeutic strategy to improve cognition in people with schizophrenia. These studies collectively constitute the preclinical pharmacology data package used to build confidence in the pharmacology of this molecule and enable a clinical trial application. EXPERIMENTAL APPROACH: [N-[(2S)-5-(6-fluoro-3-pyridinyl)-2,3-dihydro 1H-inden-2-yl]-2-propanesulfonamide] (UoS12258) was profiled in a number of in vitro and in vivo studies to highlight its suitability as a novel therapeutic agent. KEY

resultsWe demonstrated that UoS12258 is a selective, positive allosteric modulator of the AMPA receptor. At rat native hetero-oligomeric AMPA receptors, UoS12258 displayed a minimum effective concentration of approximately 10 nM in vitro and enhanced AMPA receptor-mediated synaptic transmission at an estimated free brain concentration of approximately 15 nM in vivo. UoS12258 reversed a delay-induced deficit in novel object recognition in rats after both acute and sub-chronic dosing. Sub-chronic dosing reduced the minimum effective dose from 0.3 to 0.03 mg·kg CONCLUSION AND IMPLICATIONS: We conclude that UoS12258 is a potent and selective AMPA receptor modulator exhibiting cognition enhancing properties in several rat behavioural models superior to other molecules that have previously entered clinical evaluation.

Indexed as

Allosteric RegulationAnimalsAvoidance LearningBehavior, AnimalCognitionDose-Response Relationship, DrugElectroshockHumansIndenesMaleMaze LearningNootropic AgentsRatsRats, Sprague-DawleyRats, WistarReceptors, AMPAIndenesN-(5-(6-fluoro-3-pyridinyl)-2,3-dihydro-1H-inden-2-yl)-2-propanesulfonamideNootropic AgentsReceptors, AMPAScopolamineSulfonamides

Identifiers

PMID28009436
PMCPMC5301047
OpenAlexW2564472380

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.