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This paper introduces HEDGEHOG, a comprehensive six-stage filtration benchmark designed to rigorously evaluate generative molecular models used in drug discovery. By applying this benchmark to 23 molecular generators, the authors reveal that a mere 0.65% of the 230,000 generated compounds pass all stages, highlighting the inadequacy of existing evaluation metrics that fail to ensure medicinal plausibility. The findings underscore the need for more robust evaluation frameworks to prevent false positives and optimize computational resource usage in drug candidate identification.
Only 0.65% of drug candidates generated by popular models are actually viable when subjected to rigorous, multi-faceted evaluation.
Generative molecular models can support early drug discovery by proposing new candidate compounds de novo. In practice, useful candidates must balance target-relevant activity, synthetic accessibility, physicochemical properties, and other multiparameter design constraints. However, metrics commonly used to evaluate molecular generators only weakly reflect whether the generated compounds are medicinally plausible and suitable for downstream computation. This can produce false positives in model evaluation, incorrect assumptions, and inefficient use of computational resources. We introduce HEDGEHOG, a unified six-stage filtration benchmark that is inspired by industrial hit identification workflows: (i) preprocessing; (ii) physicochemical descriptor screening; (iii) structural alerts and graph-sanity checks; (iv) synthesis feasibility; (v) docking and binding affinity estimation; and (vi) three-dimensional pose and interaction checks. We evaluate 23 molecular generators across three model classes under a standardized protocol. Across 230,000 generated molecules, only 0.65% of initial molecules survive all stages. Our results expose a central limitation of current molecular generators: molecules that appear acceptable under isolated criteria rarely satisfy medicinal chemistry, synthesis, docking, and 3D pose filters simultaneously.