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Geometric Latent Diffusion Models for 3D Molecule Generation

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arxiv 2305.01140 v1 pith:YQ5VFXLK submitted 2023-05-02 cs.LG q-bio.QM

classification cs.LGq-bio.QM
keywords latentgeoldmmodelsdiffusiongenerationmoleculedemonstrategeometric
verification ladder T0 review T1 audit T2 compute T3 formal
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Generative models, especially diffusion models (DMs), have achieved promising results for generating feature-rich geometries and advancing foundational science problems such as molecule design. Inspired by the recent huge success of Stable (latent) Diffusion models, we propose a novel and principled method for 3D molecule generation named Geometric Latent Diffusion Models (GeoLDM). GeoLDM is the first latent DM model for the molecular geometry domain, composed of autoencoders encoding structures into continuous latent codes and DMs operating in the latent space. Our key innovation is that for modeling the 3D molecular geometries, we capture its critical roto-translational equivariance constraints by building a point-structured latent space with both invariant scalars and equivariant tensors. Extensive experiments demonstrate that GeoLDM can consistently achieve better performance on multiple molecule generation benchmarks, with up to 7\% improvement for the valid percentage of large biomolecules. Results also demonstrate GeoLDM's higher capacity for controllable generation thanks to the latent modeling. Code is provided at \url{https://github.com/MinkaiXu/GeoLDM}.

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Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. Applications of Modular Co-Design for De Novo 3D Molecule Generation

    cs.LG 2025-05 conditional novelty 6.0 of 10

    A new transformer architecture with joint continuous and discrete denoising improves 3D molecule generation and moves generated structures closer to low-energy physical minima.

  2. TABASCO: A Fast, Simplified Model for Molecular Generation with Improved Physical Quality

    cs.LG 2025-07 conditional novelty 5.0 of 10

    TABASCO achieves 0.92 PoseBusters validity on GEOM-Drugs with a 59M-parameter non-equivariant transformer, no bond modeling, and post-hoc RDKit bond recovery, while sampling about 10x faster than SemlaFlow.

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