Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | sodium channel, voltage-gated, type IX, alpha subunit | Starlite/ChEMBL | References |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 885 nM | Blockade of human Nav1.7 by FRET assay | ChEMBL. | 17588748 |
IC50 (binding) | = 885 nM | Blockade of human Nav1.7 by FRET assay | ChEMBL. | 17588748 |
Inhibition (binding) | = 79 % | Displacement of [35S]-MK0499 from human ERG receptor expressed in HEK293 cells at 10 uM | ChEMBL. | 17588748 |
Inhibition (binding) | = 79 % | Displacement of [35S]-MK0499 from human ERG receptor expressed in HEK293 cells at 10 uM | ChEMBL. | 17588748 |
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.