Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Serotonin transporter | Starlite/ChEMBL | References |
Rattus norvegicus | Dopamine transporter | Starlite/ChEMBL | References |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 2.2 nM | Tested for the ability to displace [125I]- RTI-55 binding in rat striatal membrane against dopamine transporter | ChEMBL. | 11958976 |
IC50 (binding) | = 2.2 nM | Tested for the ability to displace [125I]- RTI-55 binding in rat striatal membrane against dopamine transporter | ChEMBL. | 11958976 |
Ki (binding) | = 2.44 nM | Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporter | ChEMBL. | 11958976 |
Ki (binding) | = 2.44 nM | Tested for the ability to displace [3H]- paroxetine binding in rat frontal cortex membrane against Serotonin transporter | ChEMBL. | 11958976 |
Ratio (binding) | = 0.9 | Ratio of serotonin transporter potency to that of dopamine transporter potency | ChEMBL. | 11958976 |
Ratio (binding) | = 0.9 | Ratio of serotonin transporter potency to that of dopamine transporter potency | ChEMBL. | 11958976 |
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.