Evidence map›Paper›PMID 41565685›Full record

ArticleScientific reports2026

Ligand-based machine learning models to classify active compounds for prostaglandin EP2 receptor.

Paul Dupuyds, Anita Rayar, Vaitea Opuu, Camille Lescanne, Shuhui Wang, Jean-Philippe Annereau, Philippe Nghe, Luis Briseño-Roa

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Paul DupuydsMedetia Pharmaceuticals, 24 Boulevard du Montparnasse, 75015, Paris, France.
Anita RayarMedetia Pharmaceuticals, 24 Boulevard du Montparnasse, 75015, Paris, France.
Vaitea OpuuLaboratory of Biophysics and Evolution, UMR CNRS-ESPCI 8231 Chimie Biologie Innovation, PSL Research University, ESPCI Paris, Paris, France.
Camille LescanneMedetia Pharmaceuticals, 24 Boulevard du Montparnasse, 75015, Paris, France.
Shuhui WangLaboratory of Biophysics and Evolution, UMR CNRS-ESPCI 8231 Chimie Biologie Innovation, PSL Research University, ESPCI Paris, Paris, France.
Jean-Philippe AnnereauMedetia Pharmaceuticals, 24 Boulevard du Montparnasse, 75015, Paris, France.
Philippe NgheLaboratory of Biophysics and Evolution, UMR CNRS-ESPCI 8231 Chimie Biologie Innovation, PSL Research University, ESPCI Paris, Paris, France.
Luis Briseño-RoaMedetia Pharmaceuticals, 24 Boulevard du Montparnasse, 75015, Paris, France. roa@cantab.net.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostaglandin receptors are pharmacologically validated targets with implications in several medical indications, including glaucoma, cardiac cyanotic disease, pulmonary hypertension, oncology, and various rare diseases. In this study, we developed a ligand-based machine learning (ML) model to classify chemical compounds as either active or inactive against the prostaglandin receptor EP2. From an initial set of 1,826 descriptors, 20 were selected to train random forest algorithms, yielding an area under the curve score (AUC) of > 0.8 for compound classification in the test set. Our resulting ML classifier showed an overall accuracy of 88.9% towards newly experimentally tested EP2 ligands. This adaptable and tractable workflow can be extended to other EP receptors and possibly other similar targets.

Indexed as

Machine LearningReceptors, Prostaglandin E, EP2 SubtypeClassification AlgorithmsDrug DiscoveryHumansLigandsPrediction AlgorithmsPredictive Learning ModelsQuantitative Structure-Activity RelationshipRandom ForestLigandsReceptors, Prostaglandin E, EP2 SubtypeChemo-informaticsDrug discoveryEP2Machine-learningProstaglandinsQSAR

Identifiers

PMID41565685
PMCPMC12828033

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Registered trials

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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.