Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | glycogen synthase kinase 3 beta | Starlite/ChEMBL | References |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 17.4 nM | Inhibition of human recombinant GSK3-beta expressed in baculovirus infected SF9 cells after 60 mins | ChEMBL. | 21295469 |
IC50 (binding) | = 800 nM | Inhibition of human GSK3-beta expressed in CHO AA8 cells co-expressing human tau protein after 2 hrs | ChEMBL. | 21295469 |
Inhibition (binding) | = 28 % | Inhibition of CLK1 at 10 uM | ChEMBL. | 21295469 |
Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.
1 literature reference was collected for this gene.