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Learning Joint 2D & 3D Diffusion Models for Complete Molecule Generation

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arxiv 2305.12347 v2 pith:7GAEV7BQ submitted 2023-05-21 q-bio.BM cs.LG

classification q-bio.BMcs.LG
keywords modeldiffusiongenerationmoleculesdatagraphjodojoint
verification ladder T0 review T1 audit T2 compute T3 formal
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Designing new molecules is essential for drug discovery and material science. Recently, deep generative models that aim to model molecule distribution have made promising progress in narrowing down the chemical research space and generating high-fidelity molecules. However, current generative models only focus on modeling either 2D bonding graphs or 3D geometries, which are two complementary descriptors for molecules. The lack of ability to jointly model both limits the improvement of generation quality and further downstream applications. In this paper, we propose a new joint 2D and 3D diffusion model (JODO) that generates complete molecules with atom types, formal charges, bond information, and 3D coordinates. To capture the correlation between molecular graphs and geometries in the diffusion process, we develop a Diffusion Graph Transformer to parameterize the data prediction model that recovers the original data from noisy data. The Diffusion Graph Transformer interacts node and edge representations based on our relational attention mechanism, while simultaneously propagating and updating scalar features and geometric vectors. Our model can also be extended for inverse molecular design targeting single or multiple quantum properties. In our comprehensive evaluation pipeline for unconditional joint generation, the results of the experiment show that JODO remarkably outperforms the baselines on the QM9 and GEOM-Drugs datasets. Furthermore, our model excels in few-step fast sampling, as well as in inverse molecule design and molecular graph generation. Our code is provided in https://github.com/GRAPH-0/JODO.

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Forward citations

Cited by 5 Pith papers

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

  1. TFG-Flow: Training-free Guidance in Multimodal Generative Flow

    cs.LG 2025-01 conditional novelty 7.0 of 10

    TFG-Flow guides multimodal flow models at inference time by weighted Monte Carlo sampling for discrete atom types and gradient ascent for continuous coordinates, improving targeted molecular generation without extra training.

  2. S1-Omni: A Unified Multimodal Reasoning Model for Scientific Understanding, Prediction, and Generation

    cs.AI 2026-07 conditional novelty 6.0 of 10

    A single 32B multimodal model with task-specific decoders handles roughly 200 scientific tasks across molecules, materials, proteins, spectra, and images, and outperforms general LLMs on most of 66 evaluated tasks.

  3. Learning Disentangled Equivariant Representation for Explicitly Controllable 3D Molecule Generation

    cs.LG 2024-12 conditional novelty 6.0 of 10

    An E(3)-equivariant Wasserstein autoencoder with disentangled property and structure latents for controllable 3D molecule generation.

  4. Exploring Discrete Flow Matching for 3D De Novo Molecule Generation

    cs.LG 2024-11 conditional novelty 6.0 of 10

    FlowMol-CTMC, using discrete-state continuous-time Markov chain flows, generates 3D molecules with higher stability and validity than prior 3D generation models while using far fewer parameters.

  5. Predictive Feature Caching for Training-free Acceleration of Molecular Geometry Generation

    cs.LG 2025-10 conditional novelty 4.0 of 10

    Predictive feature caching, borrowed from image diffusion, speeds up molecular flow-matching generation by 2-3x at near-matched quality by forecasting hidden features instead of recomputing them.

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