Evidence map›Paper›PMID 41979032›Full record

ArticleJournal of chemical information and modeling2026

A Multimodal Sequence-to-Sequence Model for Automatic Assignment of ATC Codes in Drug Discovery and Repurposing.

Trinidad Crozes, Eugenia Ulzurrun, Juan A Páez, Nuria E Campillo, Axel J Soto, Ignacio Ponzoni

Abstract read
In one paragraph

Article in Journal of chemical information and modeling, 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Trinidad CrozesInstitute for Computer Science and Engineering, UNS-CONICET, 8000 Bahía Blanca, Argentina.
Eugenia UlzurrunCentro de Investigaciones Biológicas Margarita Salas (CIB Margarita Salas-CSIC), C/Ramiro de Maeztu, 9, 28040 Madrid, Spain.
Juan A PáezInstituto de Química Médica (IQM-CSIC), C/Juan de la Cierva, 3, 28006 Madrid, Spain.
Nuria E CampilloCentro de Investigaciones Biológicas Margarita Salas (CIB Margarita Salas-CSIC), C/Ramiro de Maeztu, 9, 28040 Madrid, Spain.ORCID 0000-0002-9948-2665
Axel J SotoInstitute for Computer Science and Engineering, UNS-CONICET, 8000 Bahía Blanca, Argentina.ORCID 0000-0002-9021-7566
Ignacio PonzoniInstitute for Computer Science and Engineering, UNS-CONICET, 8000 Bahía Blanca, Argentina.ORCID 0000-0002-6923-9592

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Anatomical Therapeutic Chemical (ATC) code is a drug classification system that indicates the therapeutic potential use of a compound. Predicting ATC codes for drugs using automatic approaches is key to guide clinical trials and for drug repurposing. However, such automatic assignment is challenging due to the hierarchical organization of the code in four levels, possible polypharmacological behavior, and the imbalance and scarcity of annotated data in relation to the large number of compounds and possible ATC codes a drug may have. In this work, we propose a novel multimodal generative approach for predicting ATC codes, which leverages molecular information using a sequence-to-sequence architecture. Our hypothesis explores the idea that describing the chemical structure of the input compounds using two different representations, i.e., modes, the SMILES code and its molecular descriptors, provides complementary information, hence improving the accuracy of the predictions. Furthermore, given the multilabel nature of generative sequence-based models, we also present an additional prediction method to determine when to stop generating ATC labels for each compound. We compared the performance of our proposed methods against several baselines, both for new drugs and in drug repurposing tasks. In all of these cases, the superior performance of our multimodal proposals is clearly demonstrated. The source code and different data sets used to train and evaluate the models are made publicly available.

Indexed as

Drug DiscoveryDrug RepositioningAutomationPharmaceutical PreparationsPharmaceutical Preparations

Identifiers

PMID41979032
PMCPMC13126624

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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.