Evidence map›Paper›PMID 32230915›Full record

ArticleMolecules (Basel, Switzerland)2020

Design, Synthesis and Characterization of a New Series of Fluorescent Metabotropic Glutamate Receptor Type 5 Negative Allosteric Modulators.

Víctor Fernández-Dueñas, Mingcheng Qian, Josep Argerich, Carolina Amaral, Martijn D P Risseeuw, Serge Van Calenbergh, Francisco Ciruela

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. 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
0.2field-weighted citation impact, top 55% 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, 3 citations in OpenAlex.

  1. The ADORA1 mutation linked to early-onset Parkinson's disease alters adenosine ABiomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2022
    Article
  2. 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

7 authors at 2 institutions in 2 countries.

Víctor Fernández-DueñasUnitat de Farmacologia, Departament de Patologia i Terapèutica Experimental, Facultat de Medicina i Ciències de la Salut, IDIBELL, Universitat de Barcelona, 08907 L'Hospitalet de Llobregat, Spain.
Mingcheng QianLaboratory for Medicinal Chemistry (FFW), Ghent University, Ottergemsesteenweg 460, B-9000 Ghent, Belgium.
Josep ArgerichUnitat de Farmacologia, Departament de Patologia i Terapèutica Experimental, Facultat de Medicina i Ciències de la Salut, IDIBELL, Universitat de Barcelona, 08907 L'Hospitalet de Llobregat, Spain.
Carolina AmaralUnitat de Farmacologia, Departament de Patologia i Terapèutica Experimental, Facultat de Medicina i Ciències de la Salut, IDIBELL, Universitat de Barcelona, 08907 L'Hospitalet de Llobregat, Spain.
Martijn D P RisseeuwLaboratory for Medicinal Chemistry (FFW), Ghent University, Ottergemsesteenweg 460, B-9000 Ghent, Belgium.
Serge Van CalenberghLaboratory for Medicinal Chemistry (FFW), Ghent University, Ottergemsesteenweg 460, B-9000 Ghent, Belgium.
Francisco CiruelaUnitat de Farmacologia, Departament de Patologia i Terapèutica Experimental, Facultat de Medicina i Ciències de la Salut, IDIBELL, Universitat de Barcelona, 08907 L'Hospitalet de Llobregat, Spain.
Institut d'Investigació Biomédica de Bellvitge · ESGhent University · BE

Funding

Catalan government 2017 SGR 1604Fonds Wetenschappelijk Onderzoek SBO-140028Fundació la Marató de TV3 Grant 20152031Ministerio de Ciencia, Innovación y Universidades SAF2017-87349-R
6 · The paper itself

Abstract

In recent years, new drug discovery approaches based on novel pharmacological concepts have emerged. Allosteric modulators, for example, target receptors at sites other than the orthosteric binding sites and can modulate agonist-mediated activation. Interestingly, allosteric regulation may allow a fine-tuned regulation of unbalanced neurotransmitter' systems, thus providing safe and effective treatments for a number of central nervous system diseases. The metabotropic glutamate type 5 receptor (mGlu

Indexed as

Allosteric RegulationAllosteric SiteBinding SitesBioluminescence Resonance Energy Transfer TechniquesBoron CompoundsCalciumDrug DiscoveryFluorescent DyesHEK293 CellsHumansLigandsPorphobilinogenProtein BindingReceptor, Metabotropic Glutamate 5Boron CompoundsCalciumdipyrrometheneFluorescent DyesGRM5 protein, humanLigandsPorphobilinogenReceptor, Metabotropic Glutamate 5allosterismfluorescent ligandsmGlu5RnanoBRET

Identifiers

PMID32230915
PMCPMC7180738
OpenAlexW3013489768

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.