The CNS-MPO Library represents a subset of compounds from ChemBridge’s stock of more than 1.3 million lead-like and drug-like small molecule screening compounds representing a wide range of different chemotypes.
Hyperpolarization-Activated Cyclic Nucleotide-Gated (HCN) Channel Blocker library (657 compounds in total) was designed as a special screening library containing compounds with predicted HCN channels blocking activity and selectivity.
OTAVAchemicals offers a 5-HT1B Receptor Targeted Library (1,836 compounds in total) designed with the receptor-based virtual screening of pre-filtered compound library docked in orthosteric and extended pockets of the 5-HT1B ligand-binding site. This lib
We also offer a library of small molecular compounds, optimized for researchers focused on diseases of the central nervous system, 60100-molecules big, our CNS library was optimized to only include compounds with predicted high blood-brain barrier penetra
We offer Alzheimer's Disease Targeted Polypharmacology Library (631 compounds in total), which is a special screening library that contains compounds with predicted inhibitory activity against both AChE and BACE-1.
This library contains about 2,000 compounds with physicochemical properties preferable for BBB penetration and simultaneously suitable for oral administration.
ChemBridge has identified a subset of more than 3,000 macrocyclic compounds from its Macrocycle Library predicted to have a high probability of good blood-brain barrier penetration based on an MPO scoring approach.
GSK3 inhibitors might also have the potential for neurodegenerative disorders, such as Alzheimer's disease. Glycogen synthase kinase 3 (GSK3) inhibitor library contains 479 compounds.
It is patently obvious that CNS activity (and trans-cellular permeability in general) is a complex function of physical chemical properties of molecules such as size, lipophilicity, hydrogen-bonding potential, charge, and conformation.
Life Chemicals has designed its original Phosphodiesterase PDE10 Screening Library by combining different computational approaches to develop a unique method for in silico search of small-molecule screening compounds with potential PDE10 inhibitory activity.