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SPADE: Faster Drug Discovery by Learning from Sparse Data

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Drug discovery seeks molecules (ligands) that bind strongly and selectively to a target protein. However, fewer than 5% of candidate ligands pass the bar for even the early stages of drug discovery. Furthermore, we want methods that work for novel proteins for which we have no prior data. Starting from scratch, we have to iteratively select and test candidate ligands such that we find enough ligands of the desired quality in as few tests as possible. Our proposed algorithm, named SPADE, introduces a novel approach to ligand selection that requires only 40 tests on average to find 10 high-quality ligands. In one-vs-one comparisons, SPADE outperforms deep learning and Bayesian optimization methods on more proteins, achieving median improvements of 7%-32% in sample efficiency. SPADE is also 10x faster than its closest competitor at scoring candidate drugs. Dataset and code is available at https://anonymous.4open.science/r/SPADE_Fast_Drug_Discovery_by_Learning_from_Sparse_Data-F028/README.md

Rahul Nandakumar, Ben Fauber, Deepayan Chakrabarti• 2026

Related benchmarks

TaskDatasetResultRank
Virtual Screening100 Proteins--
45
Protein hit discoveryChEMBL Proteins
Win % (Avg Top-10, PIC 7.0)95
20
Ligand discovery100 Proteins Average Top-10 endpoint
MLT Score (PIC 7.0)17
11
Ligand discovery100 Proteins Min Top-3 endpoint
MLT (Target PIC 7.0)12
11
Ligand scoring1,000,000 ligands
Inference Time (s)4
4
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