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BiochemistryJournal of Chemical Information and Modeling
Peer-reviewed journal article

FragDockRL: A Reinforcement Learning Method for Fragment-Based Ligand Design via Building Block Assembly and Tethered Docking

Seung Hwan HongiD, Hyunsoo Kim, Sejin KimiD, Soosung KangiD

Abstract

Efficient exploration of combinatorial chemical space under synthetic constraints remains a central challenge in computational molecular design. Here, we present FragDock, a molecular design framework that combines building block (BB)-based virtual synthesis with tethered docking guided by a predefined core structure. FragDock defines a structured search space by assembling molecules from synthetically accessible BBs through known chemical reactions and evaluating candidates using tethered docking with a restrained core binding pose. Within this framework, we introduce FragDockRL, a reinforcement learning-based search method that uses docking-score-based rewards and a modified Deep Q-Network (DQN) to guide stepwise molecular growth. We evaluated FragDockRL on three protein targets, CSF1R, FA10, and VEGFR2, using training-cycle analysis and benchmark comparisons with One-Step Reaction, Random Search, Beam Search, and Monte Carlo Tree Search. FragDockRL progressively enriched molecules with favorable docking scores during learning and generated more cutoff-passing unique molecules than Random Search across all three targets, supporting the benefit of learning-guided prioritization. However, the best-performing search strategy was target-dependent: One-Step Reaction, FragDockRL, and Beam Search each showed advantages in different cases. Representative molecular case studies showed that selected compounds retained reference-like binding poses while introducing structural variation in peripheral regions. The reaction schemes used commercially available BBs and well-established medicinal chemistry transformations, supporting the synthetic plausibility of the selected compounds. Overall, FragDock provides a flexible framework for synthetically constrained, structure-guided molecular exploration, and FragDockRL offers a learning-guided search mode for productive candidate prioritization under limited generation budgets.

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