Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (functional) | 0 | Evaluated for the ovulation effects in the rat by administering the drug at the doses (250 ug); 5/5 | ChEMBL. | 10715147 |
Activity (functional) | 0 | Evaluated for the ovulation effects in the rat by administering the drug at the doses (1000 ug); 0/4 | ChEMBL. | 10715147 |
Ki (binding) | = 8.5 nM | Competitive radioligand binding assay, in human HEK-293 cells stably transfected with the rat Gonadotropin-releasing hormone receptor | ChEMBL. | 10715147 |
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.