Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | endothelin receptor type B | Starlite/ChEMBL | References |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Ki (binding) | = 19.8 nM | Inhibition of [125I]-ET-1 (ETA assay) binding to human cloned Endothelin A receptor in CHO cells | ChEMBL. | 10447946 |
Ki (binding) | = 19.8 nM | Inhibition of [125I]-ET-1 (ETA assay) binding to human cloned Endothelin A receptor in CHO cells | ChEMBL. | 10447946 |
Ki (binding) | = 94.1 nM | Inhibition of [125I]-ET-3 (ETB assay) binding to human cloned Endothelin B receptor in CHO cells | ChEMBL. | 10447946 |
Ki (binding) | = 94.1 nM | Inhibition of [125I]-ET-3 (ETB assay) binding to human cloned Endothelin B receptor in CHO cells | ChEMBL. | 10447946 |
Ratio (binding) | = 4.7 | Selectivity for Endothelin A receptor compared to Endothelin B receptor. | ChEMBL. | 10447946 |
Ratio (binding) | = 4.7 | Selectivity for Endothelin A receptor compared to Endothelin B receptor. | ChEMBL. | 10447946 |
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.