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This research introduces QALPA, a generative framework that integrates E(3)-equivariant diffusion models with active learning and efficient quantum-mechanical methods to navigate the vast chemical space of flexible molecules. By coupling AI-driven generation with physics-based evaluation, the approach effectively populates sparse regions of property landscapes defined by dispersion energy and electronic gaps, offering a scalable pathway for molecular discovery. The method demonstrates improved transferability across diverse compound sizes, addressing key limitations in current 3D generative models for complex drug-like structures.
QALPA: Property-guided diffusion modeling for efficient exploration of chemical spaces of flexible molecules
arXiv:2609.16527v1 Announce Type: cross Abstract: Exploring the chemical space of flexible molecules remains challenging because the vast number of possible compounds and conformations, together with the increasing cost and limited generalization of 3D generative models for larger and more complex molecules, restrict access to unexplored chemistry. Here, we introduce QALPA ("Quantum-Aware Learning for Property-space Augmentation"), a property-guided generative framework that combines an E(3)-equivariant diffusion model with active learning and efficient quantum-mechanical (QM) methods to iteratively explore targeted QM property manifolds. By coupling generation with physics-based evaluation, QALPA improves molecular sampling and model reliability in sparsely populated regions of chemical space. Our results show that training on complementary QM datasets spanning both small (QM7-X) and large (Aquamarine) drug-like compounds enables accurate molecular generation across a broad size range, improving transferability beyond the training distribution for complex property manifolds involving both extensive and intensive properties. As a proof of concept, QALPA coupled with the machine learning-augmented tight-binding method EquiDTB efficiently augments alloQM, a QM dataset introduced in this work, comprising 6,253 conformers of allosteric drug molecules, by populating sparse regions of the property landscape defined by the many-body dispersion energy and HOMO-LUMO energy gap. These results demonstrate that the integration of generative AI with efficient ML/QM methods offers a practical pathway toward augmenting sparse QM datasets and sustainably expanding the exploration of chemical space for molecular discovery.
Abstract:Exploring the chemical space of flexible molecules remains challenging because the vast number of possible compounds and conformations, together with the increasing cost and limited generalization of 3D generative models for larger and more complex molecules, restrict access to unexplored chemistry. Here, we introduce QALPA ("Quantum-Aware Learning for Property-space Augmentation"), a property-guided generative framework that combines an E(3)-equivariant diffusion model with active learning and efficient quantum-mechanical (QM) methods to iteratively explore targeted QM property manifolds. By coupling generation with physics-based evaluation, QALPA improves molecular sampling and model reliability in sparsely populated regions of chemical space. Our results show that training on complementary QM datasets spanning both small (QM7-X) and large (Aquamarine) drug-like compounds enables accurate molecular generation across a broad size range, improving transferability beyond the training distribution for complex property manifolds involving both extensive and intensive properties. As a proof of concept, QALPA coupled with the machine learning-augmented tight-binding method EquiDTB efficiently augments alloQM, a QM dataset introduced in this work, comprising 6,253 conformers of allosteric drug molecules, by populating sparse regions of the property landscape defined by the many-body dispersion energy and HOMO-LUMO energy gap. These results demonstrate that the integration of generative AI with efficient ML/QM methods offers a practical pathway toward augmenting sparse QM datasets and sustainably expanding the exploration of chemical space for molecular discovery.
Chemical Physics (physics.chem-ph); Artificial Intelligence (cs.AI)
J.2; I.2.1; I.6.5
arXiv:2609.16527 [physics.chem-ph]
(or arXiv:2609.16527v1 [physics.chem-ph] for this version)
https://doi.org/10.48550/arXiv.2609.16527 Focus to learn more arXiv-issued DOI via DataCite (pending registration)
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Full text under the publisher's open licence · 320 words
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