Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Adrenergic receptor alpha-2 | Starlite/ChEMBL | References |
Rattus norvegicus | Serotonin 1a (5-HT1a) receptor | Starlite/ChEMBL | References |
Rattus norvegicus | Adrenergic receptor alpha-1 | Starlite/ChEMBL | References |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Ki (binding) | = 4.6 nM | Binding affinity against Alpha-1 adrenergic receptor by displacing [3H]-prazosin radioligand in rat cortex membrane. | ChEMBL. | 12166933 |
Ki (binding) | = 4.6 nM | Binding affinity against Alpha-1 adrenergic receptor by displacing [3H]-prazosin radioligand in rat cortex membrane. | ChEMBL. | 12166933 |
Ki (binding) | = 4.9 nM | Intrinsic activity for displacement of [3H]- prazosin from Alpha-1 adrenergic receptor of rat cerebral cortex membrane in the absence of 1 nM GTP | ChEMBL. | 12166933 |
Ki (binding) | = 4.9 nM | Intrinsic activity for displacement of [3H]- prazosin from Alpha-1 adrenergic receptor of rat cerebral cortex membrane in the absence of 1 nM GTP | ChEMBL. | 12166933 |
Ki (binding) | = 8.33 nM | Intrinsic activity for displacement of [3H]- prazosin from Alpha-1 adrenergic receptor of rat cerebral cortex membrane in the presence of 1 nM GTP | ChEMBL. | 12166933 |
Ki (binding) | = 8.33 nM | Intrinsic activity for displacement of [3H]- prazosin from Alpha-1 adrenergic receptor of rat cerebral cortex membrane in the presence of 1 nM GTP | ChEMBL. | 12166933 |
Ki (binding) | = 24.5 nM | Binding affinity against Alpha-2 adrenergic receptor by displacing [3H]-rauwolscine radioligand in rat cortex membrane | ChEMBL. | 12166933 |
Ki (binding) | = 24.5 nM | Binding affinity against Alpha-2 adrenergic receptor by displacing [3H]-rauwolscine radioligand in rat cortex membrane | ChEMBL. | 12166933 |
Ki (binding) | = 123 nM | Binding affinity against 5-hydroxytryptamine 1A receptor by displacing [3H]-8-OH-DPAT radioligand in rat cortex membrane | ChEMBL. | 12166933 |
Ki (binding) | = 123 nM | Binding affinity against 5-hydroxytryptamine 1A receptor by displacing [3H]-8-OH-DPAT radioligand in rat cortex membrane | ChEMBL. | 12166933 |
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.