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MoTIF-X advances molecular representation learning by using chemical motifs as shared anchors to integrate graphs, SMILES strings, and 3D conformations for improved drug discovery modeling. The framework demonstrates superior performance on ADMET endpoints and drug-target interactions while offering substructure-level interpretability through motif attribution. This work represents a significant step forward in machine learning applications for computational chemistry and pharmaceutical research.
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MoTIF-X: A Multimodal Tokenized Framework for Interpretable and Extensible Molecular Representation Learning

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arXiv:2609.37384v1 Announce Type: new Abstract: Molecular representation learning is central to computer-aided drug discovery. Molecular graphs, SMILES strings, and 3D conformations provide complementary structural information, yet many multimodal approaches encode these views independently and align them only at a later stage, limiting fine-grained cross-modal interaction and substructure-level interpretability. To address these limitations, we introduce MoTIF-X, a motif-centered framework that uses graph-grounded chemical motifs as shared anchors for multimodal integration and interpretation. Its first pretraining stage learns motif representations through hierarchical contrastive learning across atomic, motif, and molecular scales. The second stage contextualizes these representations with SMILES and torsion-angle tokens through multimodal masked token modeling. After pretraining on drug-like molecules with multiple conformers, MoTIF-X achieved the lowest mean absolute error on all nine OpenADMET ExpansionRx endpoints and the best overall performance among the evaluated methods. Significance analyses supported its advantage in the vast majority of endpoint-baseline comparisons after multiple-testing correction. Ablation studies supported the complementary contributions of motif-token contextualization, multimodal integration, and two-stage pretraining. Beyond molecular properties, the framework extended to drug-target interaction prediction, achieving the best average classification performance across the evaluated benchmarks and generalizing to an external drug-cold-start dataset without additional fine-tuning. Its motif-centered design also enabled substructure-level interpretation: higher motif attribution scores were associated with larger experimentally measured activity shifts. Together, these findings support MoTIF-X as a transferable and interpretable framework for molecular modeling.

Abstract:Molecular representation learning is central to computer-aided drug discovery. Molecular graphs, SMILES strings, and 3D conformations provide complementary structural information, yet many multimodal approaches encode these views independently and align them only at a later stage, limiting fine-grained cross-modal interaction and substructure-level interpretability. To address these limitations, we introduce MoTIF-X, a motif-centered framework that uses graph-grounded chemical motifs as shared anchors for multimodal integration and interpretation. Its first pretraining stage learns motif representations through hierarchical contrastive learning across atomic, motif, and molecular scales. The second stage contextualizes these representations with SMILES and torsion-angle tokens through multimodal masked token modeling. After pretraining on drug-like molecules with multiple conformers, MoTIF-X achieved the lowest mean absolute error on all nine OpenADMET ExpansionRx endpoints and the best overall performance among the evaluated methods. Significance analyses supported its advantage in the vast majority of endpoint-baseline comparisons after multiple-testing correction. Ablation studies supported the complementary contributions of motif-token contextualization, multimodal integration, and two-stage pretraining. Beyond molecular properties, the framework extended to drug-target interaction prediction, achieving the best average classification performance across the evaluated benchmarks and generalizing to an external drug-cold-start dataset without additional fine-tuning. Its motif-centered design also enabled substructure-level interpretation: higher motif attribution scores were associated with larger experimentally measured activity shifts. Together, these findings support MoTIF-X as a transferable and interpretable framework for molecular modeling.

5 figures. Supplementary material is available as an ancillary file. Code: this https URL

Machine Learning (cs.LG)

arXiv:2609.37384 [cs.LG]

(or arXiv:2609.37384v1 [cs.LG] for this version)

https://doi.org/10.48550/arXiv.2609.37384 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

supplementary_information.pdf

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