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 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.
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.
This library contains about 2,000 compounds with physicochemical properties preferable for BBB penetration and simultaneously suitable for oral administration.
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
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.