Evidence map›Paper›PMID 32662237›Full record

ArticlePharmacology research & perspectives2020

A simple open source bioinformatic methodology for initial exploration of GPCR ligands' agonistic/antagonistic properties.

Athanasios A Panagiotopoulos, Christina Papachristofi, Konstantina Kalyvianaki, Panagiotis Malamos, Panayiotis A Theodoropoulos, George Notas, Theodora Calogeropoulou, Elias Castanas, Marilena Kampa

Open access · goldAbstract read
In one paragraph

Article in Pharmacology research & perspectives, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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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 2 institutions in 1 country.

Athanasios A PanagiotopoulosLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Christina PapachristofiLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Konstantina KalyvianakiLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Panagiotis MalamosLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Panayiotis A TheodoropoulosLaboratory of Biochemistry, School of Medicine, University of Crete, Heraklion, Greece.
George NotasLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Theodora CalogeropoulouInstitute of Chemical Biology, National Hellenic Research Foundation, Athens, Greece.
Elias CastanasLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.
Marilena KampaLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.ORCID 0000-0002-6324-9570
University of Crete · GRNational Hellenic Research Foundation · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug development is an arduous procedure, necessitating testing the interaction of a large number of potential candidates with potential interacting (macro)molecules. Therefore, any method which could provide an initial screening of potential candidate drugs might be of interest for the acceleration of the procedure, by highlighting interesting compounds, prior to in vitro and in vivo validation. In this line, we present a method which may identify potential hits, with agonistic and/or antagonistic properties on GPCR receptors, integrating the knowledge on signaling events triggered by receptor activation (GPCRs binding to G

Indexed as

Computational BiologyCrystallographyDrug DevelopmentGuanosine DiphosphateGuanosine TriphosphateHumansLigandsMolecular Docking SimulationReceptors, G-Protein-CoupledSignal TransductionGuanosine DiphosphateGuanosine TriphosphateLigandsReceptors, G-Protein-Coupledagonistantagonistbiological activity predictiondockingGPCRin silicoOXER1

Identifiers

PMID32662237
PMCPMC7358596
OpenAlexW3042958168

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.