Evidence map›Paper›PMID 40729356›Full record

ArticleJournal of chemical information and modeling2025

Transfer Learning for Heterocycle Retrosynthesis.

Ewa Wieczorek, Joshua W Sin, Sara Tanovic, Matthew T O Holland, Liam Wilbraham, Victor Sebastián-Pérez, Anthony Bradley, Dominik Miketa, Paul E Brennan, Fernanda Duarte

Abstract read
In one paragraph

Article in Journal of chemical information and modeling, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

10 authors.

Ewa WieczorekChemistry Research Laboratory, 12 Mansfield Road, Oxford OX1 3TA, U.K.
Joshua W SinChemistry Research Laboratory, 12 Mansfield Road, Oxford OX1 3TA, U.K.
Sara TanovicChemistry Research Laboratory, 12 Mansfield Road, Oxford OX1 3TA, U.K.
Matthew T O HollandChemistry Research Laboratory, 12 Mansfield Road, Oxford OX1 3TA, U.K.ORCID 0000-0003-2322-4384
Liam WilbrahamExscientia plc, The Schrödinger Building Oxford Science Park, Oxford OX4 4GE, U.K.
Victor Sebastián-PérezExscientia plc, The Schrödinger Building Oxford Science Park, Oxford OX4 4GE, U.K.
Anthony BradleyExscientia plc, The Schrödinger Building Oxford Science Park, Oxford OX4 4GE, U.K.
Dominik MiketaExscientia plc, The Schrödinger Building Oxford Science Park, Oxford OX4 4GE, U.K.
Paul E BrennanAlzheimer's Research UK Oxford Drug Discovery Institute, Centre for Artificial Intelligence in Precision Medicine, Centre for Medicines Discovery, Nuffield Department of Medicine, University of Oxford, Oxford OX3 7FZ, U.K.
Fernanda DuarteChemistry Research Laboratory, 12 Mansfield Road, Oxford OX1 3TA, U.K.ORCID 0000-0002-6062-8209

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heterocycles are important scaffolds in medicinal chemistry that can be used to modulate the binding mode as well as the pharmacokinetic properties of drugs. The importance of heterocycles has been exemplified by the publication of numerous data sets containing heterocyclic rings and their properties. However, those data sets lack synthetic routes toward the published heterocycles. Consequently, novel and uncommon heterocycles are not easily synthetically accessible. While retrosynthetic prediction models could usually be used to assist synthetic chemists, their performance is poor for heterocycle formation reactions due to low data availability. In this work, we compare the use of four different transfer learning methods to overcome the low data availability problem and improve the performance of retrosynthesis prediction models for ring-breaking disconnections. The mixed fine-tuned model achieves top-1 accuracy of 36.5%, and, moreover, 62.1% of its predictions are chemically valid and ring-breaking. Furthermore, we demonstrate the applicability of the mixed fine-tuned model in drug discovery by recreating synthetic routes toward two drug-like targets published in 2023. Finally, we introduce a method for further fine-tuning the model as new reaction data becomes available.

Indexed as

Heterocyclic CompoundsMachine LearningDrug DiscoveryHeterocyclic Compounds

Identifiers

PMID40729356
PMCPMC12344764

What OpenQuestion holds

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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.