Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 0.49 nM | Inhibitory activity of the compound against GHRH-stimulated GH release from monolayercultures of rat pituitary cells | ChEMBL. | 12617894 |
IC50 (functional) | > 1000 nM | Cytotoxic activity of the compound against human neuroblastoma IMR32 cells which over-express somatostatin receptors | ChEMBL. | 12617894 |
T1/2 (ADMET) | 0 hr | Half-life of the compound in phosphate buffer; na is not available | ChEMBL. | 12617894 |
T1/2 (ADMET) | 0 hr | Half-life of the compound in rat serum; na is not available | ChEMBL. | 12617894 |
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.