Machine learning is transforming drug discovery, with generative models (GMs) gaining attention for their ability to design molecules with specific properties. However, GMs often struggle with target engagement, synthetic accessibility, or generalization. To address these, we developed a GM workflow integrating a variational autoencoder with two nested active learning cycles. These iteratively refine their predictions using chemoinformatics and molecular modeling predictors. We tested our workflow on two systems, CDK2 and KRAS, successfully generating diverse, drug-like molecules with high predicted affinity and synthesis accessibility. Notably, we generated novel scaffolds distinct from those known for each target. For CDK2, we synthetized 9 molecules yielding 8 with in vitro activity, including one with nanomolar potency. For KRAS, in silico methods validated by CDK2 assays identified 4 molecules with potential activity. These findings showcase our GM workflow's ability to explore novel chemical spaces tailored for specific targets, thereby opening new avenues in drug discovery.
Building similarity graph...
Analyzing shared references across papers
Loading...
Isaac Filella-Mercè
Alexis Molina
Lucía Díaz
Communications Chemistry
Universitat de Barcelona
Institució Catalana de Recerca i Estudis Avançats
Universitat Politècnica de Catalunya
Building similarity graph...
Analyzing shared references across papers
Loading...
Filella-Mercè et al. (Fri,) studied this question.
www.synapsesocial.com/papers/68c1bd3b54b1d3bfb60ee5f4 — DOI: https://doi.org/10.1038/s42004-025-01635-7