Structure-Based Optimization of 10-DEBC Derivatives as Potent and Selective Pim-1 Kinase Inhibitors
Impact of Electronic Polarizability on Protein-Functional Group Interactions
Identification and characterization of fragment binding sites for allosteric ligand design using the site identification by ligand competitive saturation hotspots approach (SILCS-Hotspots)
Exploring protein‐protein interactions using the site‐identification by ligand competitive saturation methodology
Pharmacophore Modeling Using Site-Identification by Ligand Competitive Saturation (SILCS) with Multiple Probe Molecules
Second harmonic generation detection of Ras conformational changes and discovery of a small molecule binder
Optimization and Evaluation of Site-Identification by Ligand Competitive Saturation (SILCS) as a Tool for Target-Based Ligand Optimization
SILCS-MC validation highlights Full text