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MolE: a molecular foundation model for drug discovery

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arxiv 2211.02657 v1 pith:J6DAO7UG submitted 2022-11-03 q-bio.QM cs.LGq-bio.BM

classification q-bio.QMcs.LGq-bio.BM
keywords modelsmolemolecularpretrainingapproachchemicaldatadatasets
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Models that accurately predict properties based on chemical structure are valuable tools in drug discovery. However, for many properties, public and private training sets are typically small, and it is difficult for the models to generalize well outside of the training data. Recently, large language models have addressed this problem by using self-supervised pretraining on large unlabeled datasets, followed by fine-tuning on smaller, labeled datasets. In this paper, we report MolE, a molecular foundation model that adapts the DeBERTa architecture to be used on molecular graphs together with a two-step pretraining strategy. The first step of pretraining is a self-supervised approach focused on learning chemical structures, and the second step is a massive multi-task approach to learn biological information. We show that fine-tuning pretrained MolE achieves state-of-the-art results on 9 of the 22 ADMET tasks included in the Therapeutic Data Commons.

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Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. Breaking Bad Molecules: Are MLLMs Ready for Structure-Level Molecular Detoxification?

    cs.AI 2025-06 conditional novelty 7.0 of 10

    A new benchmark called ToxiMol evaluates how well 43 multimodal LLMs can edit toxic molecules into structurally similar, non-toxic, drug-like candidates; the best model succeeds on 43.3% of tasks.

  2. Quantum-Enhanced Multi-Task Learning with Learnable Weighting for Pharmacokinetic and Toxicity Prediction

    cs.LG 2025-09 conditional novelty 5.0 of 10

    Quantum descriptors plus a learnable data-scale loss weight let one multi-task model beat single-task Chemprop-RDKit on 12 of 13 ADMET classification tasks.

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