SynLaD: Latent Diffusion for Generating Synthesizable Molecules Conditioned on 3D Pharmacophore Profiles
- URL: http://arxiv.org/abs/2607.01105v1
- Date: Wed, 01 Jul 2026 15:57:19 GMT
- Title: SynLaD: Latent Diffusion for Generating Synthesizable Molecules Conditioned on 3D Pharmacophore Profiles
- Abstract summary: We present SynLaD, a latent diffusion framework for small-molecule generation.<n>Current models optimize one objective at the expense of the other, creating a bottleneck for discovering high-scoring and synthesizable molecules.<n>Across analogue generation tasks for bioactive synthesis, SynLaD outperforms existing baselines in synthesizable and diverse hit generation.
- Score: 6.375842344102895
- License: http://creativecommons.org/licenses/by/4.0/
- Abstract: We present SynLaD, a latent diffusion framework for small-molecule generation that unifies ligand-based drug design objectives (what to make) with synthetic accessibility (how to make it). Current models typically optimize one objective at the expense of the other, creating a bottleneck for discovering high-scoring and synthesizable molecules. SynLaD combines reaction-constrained generation with pharmacophore-conditioned 3D design by learning a latent space that decodes to both 3D structures and synthesis pathways. An encoder maps molecules to a latent representation used by two decoder heads: (i) a geometric head that reconstructs atom types and coordinates and (ii) an autoregressive synthesis head that outputs synthetic routes in a serialized, reaction-based notation. A diffusion transformer generates novel latents in the learned space, conditioned on pharmacophore profiles. Across analogue generation tasks for bioactive ligands, SynLaD outperforms existing baselines in synthesizable and diverse hit generation, demonstrating that a single model can produce shape-aligned molecules with feasible synthesis plans.
Related papers
- JEDEL: Zero-Shot DNA-Encoded Library Design for Early-Stage Drug Discovery [14.67301218726682]
We present JEDEL, a framework for generating DNA-ready synthesis-ready libraries (DELs) directly from three-dimensional pharmacophore representations of active instructions.<n> JEDEL is the first model to map pharmacophore interaction patterns to actionable, scalable synthesis instructions.
arXiv Detail & Related papers (2026-06-21T19:27:28Z) - Rethinking Molecule Synthesizability with Chain-of-Reaction [47.744071119775676]
We introduce ReaSyn, a generative framework for synthesizable projection.<n>We propose a novel perspective that views synthetic pathways akin to reasoning paths in large language models (LLMs)<n>With the CoR notation, ReaSyn can get dense supervision in every reaction step to explicitly learn chemical reaction rules.
arXiv Detail & Related papers (2025-09-19T15:29:57Z) - SynCoGen: Synthesizable 3D Molecule Generation via Joint Reaction and Coordinate Modeling [29.856853267388924]
We present SynCoGen, a framework that combines masked graph diffusion and flow matching for synthesizable 3D molecule generation.<n>To train the model, we curated SynSpace, a dataset containing over 600K-aware building block graphs and 3.3M conformers.
arXiv Detail & Related papers (2025-07-16T00:36:35Z) - Autonomous nanoparticle synthesis by design [32.63291717930695]
We introduce an autonomous approach explicitly targeting synthesis of atomic-scale structures.<n>Our method autonomously designs synthesis protocols by matching real time experimental total scattering (TS) and pair distribution function (PDF) data.<n>We demonstrate this capability at a synchrotron, successfully synthesising two structurally distinct gold NPs.
arXiv Detail & Related papers (2025-05-19T13:19:30Z) - Towards Unified and Lossless Latent Space for 3D Molecular Latent Diffusion Modeling [90.23688195918432]
3D molecule generation is crucial for drug discovery and material science.<n>Existing approaches typically maintain separate latent spaces for invariant and equivariant modalities.<n>We propose textbfUAE-3D, a multi-modal VAE that compresses 3D molecules into latent sequences from a unified latent space.
arXiv Detail & Related papers (2025-03-19T08:56:13Z) - SynthFormer: Equivariant Pharmacophore-based Generation of Synthesizable Molecules for Ligand-Based Drug Design [19.578382119811238]
We introduce SynthFormer, a novel machine learning model that generates fully synthesizable molecules, structured as synthetic trees, by introducing both 3D information and pharmacophores as input.<n>It is a first-of-its-kind approach that could provide capabilities for designing active molecules based on pharmacophores.
arXiv Detail & Related papers (2024-10-03T17:38:46Z) - DecompDiff: Diffusion Models with Decomposed Priors for Structure-Based Drug Design [62.68420322996345]
Existing structured-based drug design methods treat all ligand atoms equally.
We propose a new diffusion model, DecompDiff, with decomposed priors over arms and scaffold.
Our approach achieves state-of-the-art performance in generating high-affinity molecules.
arXiv Detail & Related papers (2024-02-26T05:21:21Z) - Generative Novel View Synthesis with 3D-Aware Diffusion Models [96.78397108732233]
We present a diffusion-based model for 3D-aware generative novel view synthesis from as few as a single input image.
Our method makes use of existing 2D diffusion backbones but, crucially, incorporates geometry priors in the form of a 3D feature volume.
In addition to generating novel views, our method has the ability to autoregressively synthesize 3D-consistent sequences.
arXiv Detail & Related papers (2023-04-05T17:15:47Z) - A Deep Learning Generative Model Approach for Image Synthesis of Plant
Leaves [62.997667081978825]
We generate via advanced Deep Learning (DL) techniques artificial leaf images in an automatized way.
We aim to dispose of a source of training samples for AI applications for modern crop management.
arXiv Detail & Related papers (2021-11-05T10:53:35Z) - Amortized Tree Generation for Bottom-up Synthesis Planning and
Synthesizable Molecular Design [2.17167311150369]
We report an amortized approach to generate synthetic pathways as a Markov decision process conditioned on a target molecular embedding.
This approach allows us to conduct synthesis planning in a bottom-up manner and design synthesizable molecules by decoding from optimized conditional codes.
arXiv Detail & Related papers (2021-10-12T22:43:25Z) - RetroXpert: Decompose Retrosynthesis Prediction like a Chemist [60.463900712314754]
We devise a novel template-free algorithm for automatic retrosynthetic expansion.
Our method disassembles retrosynthesis into two steps.
While outperforming the state-of-the-art baselines, our model also provides chemically reasonable interpretation.
arXiv Detail & Related papers (2020-11-04T04:35:34Z) - Learning To Navigate The Synthetically Accessible Chemical Space Using
Reinforcement Learning [75.95376096628135]
We propose a novel forward synthesis framework powered by reinforcement learning (RL) for de novo drug design.
In this setup, the agent learns to navigate through the immense synthetically accessible chemical space.
We describe how the end-to-end training in this study represents an important paradigm in radically expanding the synthesizable chemical space.
arXiv Detail & Related papers (2020-04-26T21:40:03Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.