Evidence map›Paper›PMID 40887592›Full record

ArticleJournal of cheminformatics2025

Evaluation of chirality descriptors derived from SMILES heteroencoders.

Natalia Baimacheva, Xinyue Gao, Joao Aires-de-Sousa

Abstract read
In one paragraph

Article in Journal of cheminformatics, 2025. 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
–field-weighted citation impact
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.

  1. 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

3 authors.

Natalia BaimachevaFaculty of Chemistry, University of Strasbourg, 4, Blaise Pascal Str., 67081, Strasbourg, France.
Xinyue GaoFaculty of Sciences, Université Paris Cité, 75013, Paris, France.
Joao Aires-de-SousaLAQV and REQUIMTE, Chemistry Department, NOVA School of Science and Technology, Universidade Nova de Lisboa, 2829-516, Caparica, Portugal. jas@fct.unl.pt.

Funding

European Union Erasmus Mundus Joint Masters ChEMoinformaticsplus project (Programme ERASMUS2027, ERASMUS-EDU-2021-PEX-EMJM-MOB, Project number 101050809)Fundação para a Ciência e a Tecnologia LA/P/0008/2020 DOI 10.54499/LA/P/0008/2020, UIDP/50006/2020 DOI 10.54499/UIDP/50006/2020, UIDB/50006/2020 DOI 10.54499/UIDB/50006/2020 and UID/50006/2023
6 · The paper itself

Abstract

Molecular representations of chirality, derived from latent space vectors (LSVs) of SMILES heteroencoders, were explored to train machine learning models to predict chiral properties, and were compared to conventional circular fingerprints. Latent space arithmetic was applied to enhance the representation of chirality, by calculating differences between the original descriptor of a molecule and the descriptor of its enantiomer, or the difference between the original descriptor and the descriptor obtained with the stereochemistry-depleted SMILES string. Machine learning was performed with the Random Forest algorithm applied to a dataset of 3858 molecules extracted from the literature (1929 pairs of enantiomers) to predict the elution order observed on the Chiralpak® AD-H column, as well as intrinsic structural chirality labels (R/S or canonical SMILES @/@@). The descriptors derived from the heteroencoders achieved an accuracy of up to 0.75 in the prediction of the elution order, and the fingerprints were superior (0.82). A better predictive ability was observed with the difference LSV descriptors than with the original descriptors.

Indexed as

Artificial intelligenceChiral HPLCChiralityNeural networkQuantitative structure-enantioselectivity relationshipsRandom forest

Identifiers

PMID40887592
PMCPMC12398957

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.