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 |
---|---|---|---|---|
Activity (functional) | = 14 % | Percent GR-mediated repression of NFkB activity in TNF-alpha stimulated A549 (K9) cells relative to 1 uM dexamethasone at 10 uM | ChEMBL. | 15380227 |
Activity (functional) | = 14 % | Percent GR-mediated repression of NFkB activity in TNF-alpha stimulated A549 (K9) cells relative to 1 uM dexamethasone at 10 uM | ChEMBL. | 15380227 |
Activity (functional) | = 40 % | Percent activity relative to DEX (1 uM) in CV-1 cell transactivation assay at 10 uM | ChEMBL. | 15380227 |
Activity (functional) | = 40 % | Percent activity relative to DEX (1 uM) in CV-1 cell transactivation assay at 10 uM | ChEMBL. | 15380227 |
IC50 (binding) | > 2000 nM | Binding affinity for recombinant human glucocorticoid receptor | ChEMBL. | 15380227 |
IC50 (binding) | > 2000 nM | Binding affinity for recombinant human glucocorticoid receptor | ChEMBL. | 15380227 |
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.