This analysis reveals molecular property predictions using Word2Vec and transformer embeddings in SMILES formats, suggesting efficient cheminformatics approaches.
This paper investigates the effectiveness of Word2Vec-based molecular representation learning on SMILES (Simplified Molecular Input Line Entry System) strings for a downstream prediction task related to the market approvability of chemical compounds. Here, market approvability is treated as a proxy classification label derived from approval status, where only the molecular structure is analyzed. We train character-level embeddings using Continuous Bag of Words (CBOW) and Skip-Gram with Negative Sampling architectures and apply the resulting embeddings in a downstream classification task using a multi-layer perceptron (MLP). To evaluate the utility of these lightweight embedding techniques, we conduct experiments on a curated SMILES dataset labeled by approval status under both imbalanced and SMOTE-balanced training conditions. In addition to our Word2Vec-based models, we include a ChemBERTa-based baseline using the pretrained ChemBERTa-77M model. Our findings show that while ChemBERTa achieves a higher performance, the Word2Vec-based models offer a favorable trade-off between accuracy and computational efficiency. This efficiency is especially relevant in large-scale compound screening, where rapid exploration of the chemical space can support early-stage cheminformatics workflows. These results suggest that traditional embedding models can serve as viable alternatives for scalable and interpretable cheminformatics pipelines, particularly in resource-constrained environments.
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Hashemian et al. (2025) studied this question.
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