Identification of CNS compatible small molecules as glycogen synthase kinase-3β (GSK-3β) inhibitors through structure-based virtual screening

Alzheimer's Disease (AD) is one of the significant diseases of the aging population and affects Central Nervous System dominantly. Blood-brain-barrier permeation is a substantial complication in developing CNS drugs, and it is considered challenging with minimal success rates. Although Glycogen synthase kinase-3 beta (GSK-3 beta) is an attractive disease-modifying target for AD, there is no single GSK-3 beta inhibitor in clinical trials for AD. Here we performed structure-based virtual screening on the Chembridge CNS-Set library compounds. 10 hits were identified based on interaction, binding energy, dock score, and a potential ADME profile. These 10 chosen compounds were then investigated for in vitro kinase inhibitory activity against GSK-3 beta and other AD-related kinases. Among these, the molecule 7114202 showed 48% GSK-3 beta inhibition while showing selectivity over other AD-related kinases. Molecular dynamic simulations of apoenzyme, co-crystallized molecule, and 7114202 validated the Lys85, Val135, Leu188, Asp200 located in the active site of enzyme play a significant role in GSK-3 beta complex formation with inhibitors, and they are responsible for activity and selectivity. The in vitro studies also revealed a potent and selective Casein Kinase 1 epsilon (CK1 epsilon) inhibitor 7774767 with IC50 5.10 mu M. [GRAPHICS] .

Automated summary

Alzheimer's Disease is a significant disease affecting the aging population and is challenging to develop drugs due to blood-brain barrier permeation. This study performed virtual screening on a compound library and identified 10 potential compounds with favorable ADME profiles. In vitro studies revealed a compound with high GSK-3β inhibition and selectivity. Additionally, a potent and selective CK1ε inhibitor was discovered.