Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) | Starlite/ChEMBL | References |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 15 nM | Inhibition of [3H]-dexamethasone binding to human glucocorticoid receptor | ChEMBL. | 15261265 |
IC50 (binding) | = 15 nM | Inhibition of [3H]-dexamethasone binding to human glucocorticoid receptor | ChEMBL. | 15261265 |
IC50 (functional) | = 760 nM | Inhibition of dexamethasone-induced glucocorticoid receptor mediated alkaline phosphatase activity | ChEMBL. | 15261265 |
IC50 (functional) | = 760 nM | Inhibition of dexamethasone-induced glucocorticoid receptor mediated alkaline phosphatase activity | ChEMBL. | 15261265 |
IC50 (functional) | > 30 uM | Inhibition of dexamethasone-induced glucocorticoid receptor mediated tyrosine aminotransferase in rat hepatocytes | ChEMBL. | 15261265 |
IC50 (functional) | > 30 uM | Inhibition of dexamethasone-induced glucocorticoid receptor mediated tyrosine aminotransferase in rat hepatocytes | ChEMBL. | 15261265 |
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.