Automating drug discovery | Nature Reviews Drug Discovery
The Time and Place for Nature in Drug Discovery | JACS Au
Exploring protein hotspots by optimized fragment pharmacophores | Nature Communications
Late-stage C–H functionalization offers new opportunities in drug discovery | Nature Reviews Chemistry
Designing hydrogels for controlled drug delivery | Nature Reviews Materials
A combined high-throughput and high-content platform for unified on-chip synthesis, characterization and biological screening | Nature Communications
Counting on natural products for drug design | Nature Chemistry
A machine learning-based chemoproteomic approach to identify drug targets and binding sites in complex proteomes | Nature Communications
New strategy for drug discovery by large-scale association analysis of molecular networks of different species | Scientific Reports
Evaluating drug targets through human loss-of-function genetic variation | Nature
MuSyC is a consensus framework that unifies multi-drug synergy metrics for combinatorial drug discovery | Nature Communications
Advances in covalent drug discovery | Nature Reviews Drug Discovery
Avidity in antibody effector functions and biotherapeutic drug design | Nature Reviews Drug Discovery
A unified drug–target interaction prediction framework based on knowledge graph and recommendation system | Nature Communications
Network-based approach to prediction and population-based validation of in silico drug repurposing | Nature Communications
DNA-encoded chemistry: enabling the deeper sampling of chemical space | Nature Reviews Drug Discovery
A rational blueprint for the design of chemically-controlled protein switches | Nature Communications
Strategies and challenges for the next generation of antibody–drug conjugates | Nature Reviews Drug Discovery
Modulating biomolecular condensates: a novel approach to drug discovery | Nature Reviews Drug Discovery
The expanding role for small molecules in immuno-oncology | Nature Reviews Drug Discovery
Immune targets for therapeutic development in depression: towards precision medicine | Nature Reviews Drug Discovery
Improving Drug Candidates by Design: A Focus on Physicochemical Properties As a Means of Improving Compound Disposition and Safety | Chemical Research in Toxicology
