Evidence map›Paper›PMID 41987312›Full record

ArticleJournal of cheminformatics2026

ANNalog: generation of MedChem-similar molecules.

Wei Dai, Jonathan D Tyzack, Arianna Fornili, Chris de Graaf, Noel M O'Boyle

Abstract read
In one paragraph

Article in Journal of cheminformatics, 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

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

5 authors.

Wei DaiSchool of Physical and Chemical Sciences, Queen Mary University of London, London, E1 4NS, UK. w.d.dai@qmul.ac.uk.
Jonathan D TyzackNxera Pharma, Steinmetz Building, Granta Park, Great Abington, Cambridge, CB21 6DG, UK.
Arianna ForniliSchool of Physical and Chemical Sciences, Queen Mary University of London, London, E1 4NS, UK.
Chris de GraafStructure Therapeutics, 601 Gateway Blvd, Suite 900, South San Francisco, CA, 94080, USA.
Noel M O'BoyleEMBL's European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SD, UK. oboyle@ebi.ac.uk.

Funding

Biotechnology and Biological Sciences Research Council BB/X511778/1
6 · The paper itself

Abstract

Generative deep learning models have demonstrated significant potential in designing drug-like molecules. However, medicinal chemistry typically requires generating analogues that combine structural similarity with scaffold hopping, which is the replacement of molecular scaffolds while retaining biological relevance. To address this, we introduce ANNalog, a transformer-based sequence-to-sequence generative model trained on pairs of molecules extracted from the same bioactivity assay in a paper as recorded in ChEMBL33. The dataset was constructed based on the idea that molecules tested within the same assay can be considered analogues in medicinal chemistry space. Paired molecules were encoded as Simplified Molecular Input Line Entry System strings, and Levenshtein distance-guided alignment was applied to maximise intrapair string similarity; this preprocessing step was found to markedly enhance model performance. ANNalog has the ability to produce structurally similar analogues involving minor modifications, such as substituent replacements, as well as the ability to perform scaffold hopping, generating structurally distinct yet chemically relevant analogues. Scaffold-hopping capability was validated using manually curated molecule pairs and further confirmed through a case study involving orexin-2 receptor antagonists from patent literature. When the generation process was constrained using ANNalog's prefix control feature, approximately 25% of the known scaffolds from the patent set were successfully recovered by the model, illustrating enhanced performance under user-guided conditions. Scientific Contribution: This study introduces ANNalog, a generative model trained using pairs of molecules synthesised and tested together within the same medicinal chemistry project. Unlike previous models trained on pairs of molecules selected according to similarity measures, ANNalog successfully generates not only structurally similar molecules but also diverse scaffold-hopping transformations that have precedent in the medicinal chemistry literature.

Indexed as

Generative modellingMolecular generationScaffold hopping

Identifiers

PMID41987312
PMCPMC13126752

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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.