Generative Access to Make-on-Demand Chemical Space Enables Ultra-Large Virtual Screening
In the authors' words
Ultra-large-scale virtual screening (ULVS) increasingly relies on make-on-demand chemical spaces, but efficient access to these spaces remains challenging because their scale far exceeds what can be exhaustively enumerated and docked. Here, we present REAL-SWIT, a generative ULVS framework that learns Enamine REAL Space as a synthesizable molecular distribution and couples this generator with a target-specific scoring model to enable docking-guided exploration of REAL Space at the level of complete molecule. The generative model learned transferable features of the REAL Space distribution: approximately 96% of generated molecules were found in REAL Space, and a subset of generated molecules absent from the training release appeared in later expanded releases. In computational benchmarks, REAL-SWIT identified more molecules with favorable docking scores than representative fragment-based search strategies, including cooperative building-block combinations that fragment-level prioritization tended to miss. Experimental validation for ROCK1 yielded six biochemical inhibitors among 23 synthesized compounds, including RX-3 with an IC50 of 0.17 M. These results establish generative access to make-on-demand chemical space as a practical strategy for ULVS.
Appeared: Thursday, September 24. bioRxiv. Preprint, not yet peer-reviewed.