Aug 2026· Molecular Informatics· Vol 45· 0 citations· 110 references
Medicine
Abstract
Deep neural network (DNN)‐based in silico models show great promise in predicting the properties and bioactivities of novel compounds, including small molecules. Among traditional approaches, structure‐based drug design (SBDD) remains a fundamental approach for drug discovery using molecular docking, scoring functions, and molecular dynamics simulations. However, these approaches are often constrained by limited flexibility, resolution, and generalizability. Geometric deep learning (GDL) offers a transformative alternative by enabling models to learn directly from non‐Euclidean molecular representations, such as graphs, point clouds, and meshes, capturing critical 3D spatial relationships inherent to protein–ligand interactions. This review highlights the theoretical underpinnings and practical applications of GDL in small‐molecule drug discovery, focusing on tasks including binding affinity prediction, virtual screening, de novo molecule generation, pose prediction, ADMET profiling, and protein flexibility modeling. We explore key GDL architectures, graph neural networks, SE(3)‐equivariant networks, 3D convolutional neural networks, point cloud models, and geometric transformers, and assess their performance across various drug discovery benchmarks. The integration of geometry‐aware AI models with experimental and computational workflows was also highlighted for its potential to streamline hit‐to‐lead optimization and advance rational drug design. Despite remarkable progress, the field faces challenges including limited high‐quality 3D structural datasets, protein flexibility representation, and the interpretability of deep models. Addressing these issues through hybrid modeling approaches, multi‐resolution learning, and self‐supervised training could further elevate GDL's impact. Ultimately, GDL stands at the frontier of AI‐enhanced pharmaceutical innovation, offering unprecedented precision, efficiency, and insight in the pursuit of next‐generation therapeutics.
A decision-oriented taxonomy and a benchmark-driven evaluation playbook that specifies minimum standards for splits, metrics, baselines, and ablations to isolate the topological contribution are presented.
Beatriz Suay-García, Antonio Falcó· Briefings in Bioinformatics· 0 citations
This chapter explores the systematic deep learning pipeline for virtual screening, covering data acquisition, molecular representation learning, model architectures, training strategies, and uncertainty estimation, and discusses advanced model optimization techniques, including curriculum learning, transfer learning, and adversarial training, which enhance predictive accuracy and robustness.
Fatima Noor, Muhammad Tahir Ul Qamar· Methods in molecular biology· 0 citations
This review elucidates the paradigm shift in drug discovery from serendipitous exploration to rational, structure-driven polypharmacological molecular engineering, thereby providing a clear, structured guide for navigating the complexities of next-generation therapeutics.
Tianming Han, Zhijie Pan, Wenchi Ge et al.· 0 citations
A state-aware functional classifier (SAFC) is developed that integrates molecular dynamics derived receptor ensembles, ensemble docking and protein ligand interaction graphs that provides dynamics-aware functional activity rankings for generated molecules that were partly complementary to docking, drug-likeness and synthetic accessibility scores.
H. Kumar, Zhengxiao Yang, Yankai Yu et al.· bioRxiv· 0 citations
Drug discovery and development is time-consuming and resource-intensive, motivating computational approaches such as diffusion models for de novo drug design. Many such models follow the structure-based drug design (SBDD) paradigm, generating molecules to fit a target binding pocket. However, existing diffusion-based SBDD methods typically couple pocket and ligand representation learning, model interactions only at the atom level, and prioritize binding affinity over other developability properties. Here, we introduce conDitar-dev, a conditional diffusion-based SBDD framework for generating ligands with strong binding affinities and favorable ADMET properties. It consists of three modules: msPRL, a pretrained multi-scale pocket representation learning module; conDitar, a pocket-conditioned diffusion model guided by msPRL representations; and paOPT, a generation-time method for optimizing ligand developability. On a newly curated benchmark of human disease targets, conDitar outperforms state-of-the-art SBDD baselines, achieving an average binding score of -8.85 kcal/mol. Across five ADMET properties, conDitar-dev improves performance by up to 73% over conDitar. To further validate the abilities of conDitar-dev to generate developable molecules, we have applied it to two validated druggable targets: programmed death-ligand 1 (PD-L1) and colony-stimulating factor 1 receptor (CSF1R) proteins. Top-ranked generatively designed molecules and their analogs have been experimentally synthesized and biologically tested. Two molecules generated directly by conDitar-dev for PD-L1 exhibited SPR-derived $K_D$ values of 3.49 and 3.75 $\mu$M, respectively. Hit expansion based on conDitar-dev-designed molecules identified selective CSF1R inhibitors with IC$_{50}$ values as low as 200 nM, while also uncovering opportunities for drug repositioning.
Ruoxi Gao, Jiangweizhi Peng, Ziqi Chen et al.· 0 citations
A new baseline method is developed 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.
Matthias Blaschke, Daniel Kienzle, Zsuzsanna Koczor-Benda et al.· arXiv.org· 0 citations