Beyond Drug Discovery: The Nanotechnology Molecular Optimization (NMO) Benchmark
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Abstract (arXiv)
Generative molecular design is shaped by simple proxy benchmarks for drug-like properties and models pretrained on large pharmaceutical datasets. This combination yields strong benchmark metrics but limits transferability to domains structurally distinct from drug discovery. To overcome this limitation and drive discovery toward real, scientifically grounded targets, we introduce the Nanotechnology Molecular Optimization (NMO) Benchmark, which bridges machine learning (ML) and quantum materials science. NMO acts simultaneously as a rigorous testbed for the ML community and a discovery engine for nanotechnology research. The suite replaces proxy oracles with quantum simulations and introduces strict protocols that prioritize scientific utility over leaderboard-oriented overfitting. The physics-based NMO tasks impose hard structural constraints and rugged fitness landscapes, posing fundamentally new requirements on generative models. Notably, advanced molecular optimization methods underperform much simpler approaches on the NMO tasks. We develop a new baseline method identifying the critical components to solve the NMO tasks, including a novel representation for modeling structural constraints and a domain-agnostic pretraining strategy to eliminate pharmaceutical dataset bias. Our results surpass state-of-the-art physical properties and reveal previously unknown structural motifs, offering new insights for the nanotechnology community and demonstrating that ML can drive genuine scientific discovery.
Key facts. No citing papers in the map yet (data through 7 Oct 2026). Builds on 23 of its 101 references that are in the map. First posted on arXiv 29 Jun 2026.
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23 of 101 references.
References · 23
- 2017Attention Is All You Needcited by 59,932
- 2014Adam: A Method for Stochastic Optimizationcited by 36,960
- 2021RoFormer: Enhanced Transformer with Rotary Position Embeddingcited by 4,581
- 2014Learning Phrase Representations using RNN Encoder-Decoder for Statistical Machine Translationcited by 4,016
- 2021Flow Network based Generative Models for Non-Iterative Diverse Candidate Generationcited by 384
- 2017Molecular De Novo Design through Deep Reinforcement Learningcited by 264
- 2022Biological Sequence Design with GFlowNetscited by 172
- 2019Symmetry-adapted generation of 3d point sets for the targeted discovery of moleculescited by 171
- 2022Sample Efficiency Matters: A Benchmark for Practical Molecular Optimizationcited by 151
- 2022Evaluation Gaps in Machine Learning Practicecited by 48
- 2025GenMol: A Drug Discovery Generalist with Discrete Diffusioncited by 47
- 2023Gotta be SAFE: A New Framework for Molecular Designcited by 45
11 more
- 2024Genetic-guided GFlowNets for Sample Efficient Molecular Optimizationcited by 36
- 2022Group SELFIES: A Robust Fragment-Based Molecular String Representationcited by 32
- 2023Genetic algorithms are strong baselines for molecule generationcited by 31
- 2023Learning to Scale Logits for Temperature-Conditional GFlowNetscited by 26
- 2024Molecule Generation with Fragment Retrieval Augmentationcited by 22
- 2024QGFN: Controllable Greediness with Action Valuescited by 18
- 2022Tartarus: A Benchmarking Platform for Realistic And Practical Inverse Molecular Designcited by 16
- 2025Adaptive Divergence Regularized Policy Optimization for Fine-tuning Generative Modelscited by 6
- 2025FragFM: Hierarchical Framework for Efficient Molecule Generation via Fragment-Level Discrete Flow Matchingcited by 5
- 2025Refine Drugs, Don't Complete Them: Uniform-Source Discrete Flows for Fragment-Based Drug Discoverycited by 4
- 2025Relative Trajectory Balance is equivalent to Trust-PCLcited by 3
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