Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Muscarinic acetylcholine receptor | Starlite/ChEMBL | References |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 63 nM | Binding affinity against muscarinic receptor in rat brain membranes using oxotremorine-M as ligand | ChEMBL. | 9873644 |
IC50 (binding) | = 63 nM | Binding affinity against muscarinic receptor in rat brain membranes using oxotremorine-M as ligand | ChEMBL. | 9873644 |
Max PI (functional) | = 12 % | Stimulation of phosphoinositide hydrolysis in BHK cells expressing human m1 receptor | ChEMBL. | 9873644 |
Max PI (functional) | = 12 % | Stimulation of phosphoinositide hydrolysis in BHK cells expressing human m1 receptor | ChEMBL. | 9873644 |
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.