Pretrained molecular language models are increasingly used as molecular encoders for learning structure-property relationships. However, their practical suitability for molecular discovery within and beyond their pretraining domain remains unclear. Herein, we systematically benchmark four molecular language models across six virtual molecular libraries spanning drug discovery, organic materials, and catalysis. Native molecular language model embeddings show substantial variation in discovery performance across libraries, whereas molecular fingerprints provide a consistently strong and robust baseline. Consistent with a potential domain-representation mismatch, we show that explicit domain adaptation substantially improves representation performance. Fine-tuning molecular language model encoders on structures from the target virtual library consistently improves sample efficiency, with several adapted encoders emerging as the top-performing representations across the benchmark tasks. These results show that molecular representation quality depends strongly on the target domain and that explicit adaptation can improve the practical utility of molecular foundation models. More broadly, our findings establish domain-adapted molecular representations as a promising strategy for sample-efficient adaptive decision making in virtual screening and self-driving laboratories.
This work introduces \textbf{MolEmb}, a lightweight framework that adapts MLLMs by aligning molecular profiles with textual descriptions in a shared embedding space using a bidirectional contrastive objective, and finds that context-aware molecular embedding is primarily a data property of the supervision.
Xinjian Zhao, Xiangru Jian, Yaoyao Xu et al.· 0 citations
It is shown that enhancing an LLMs capabilities for robust prediction of small molecule geometries still retains nearly all of its pre-trained language abilities by randomly mixing in small quantities of natural language prompt-response pairs into the fine-tuning.
Joe Cavanagh, Jonathan Arnold, G. Alteri et al.· 0 citations
This work proposes pretraining on low-noise, calculable molecular descriptors via supervised learning to obtain rich, highly transferable molecular representations and demonstrates this strategy with CheMeleon, a O(10M) parameter foundation model that enables directed message-passing neural networks to finally exceed the performance of classical methods in the low-data regime.
Jackson W. Burns, Akshat Shirish Zalte, C. Abreu et al.· Journal of Chemical Informat...· 0 citations
FragBERTa is introduced, a molecular fragment-aware transformer-based representation language model pretrained using masked language modeling on Sequential Attachment-based Fragment Embedding (SAFE) representations, suggesting that fragment-based string representations offer advantages over atom-level representations for scaffold-sensitive and interaction-driven tasks.
MolLingua, a token-centric, dual-modal framework designed for native molecular understanding, uses a dual-branch Residual Vector Quantization engine to discretize heterogeneous, high-dimensional spatial 2D and 3D features into compact code sequences rather than relying solely on continuous projections.
Haoyang Liu, Xikang Feng, Fei Guo et al.· IEEE journal of biomedical a...· 0 citations
The factors underlying performance differences across matcher architectures are clarified and motivate future research and benchmark designs that better disentangle architectural choices from model-level factors while explicitly evaluating distribution shift and cross-dataset transferability.
Zeyu Zhang, Xue Li, Iacer Calixto et al.· 0 citations
A new machine-learning framework aims to improve the success rate of computational protein design while moving away from results that reproduce sequences found in nature.