Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Glutamate NMDA receptor | Starlite/ChEMBL | References |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 253 nM | Evaluated for their affinity at the PCP site for displacement of [3H]-TCP in rat brain homogenates | ChEMBL. | 8459395 |
IC50 (binding) | = 253 nM | Evaluated for their affinity at the PCP site for displacement of [3H]-TCP in rat brain homogenates | ChEMBL. | 8459395 |
logD (ADMET) | = 0.86 | Partition coefficient determined using standard shake flask method at pH 7.4. | ChEMBL. | 8459395 |
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.