Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Inhibition (binding) | = 28 % | Inhibition of BACE1 (unknown origin) at 10 uM by FRET assay | ChEMBL. | 18162398 |
Inhibition (binding) | = 28 % | Inhibition of BACE1 (unknown origin) at 10 uM by FRET assay | ChEMBL. | 18162398 |
Ratio IC50 (binding) | < 2 | Selectivity for BACE1 (unknown origin) over BACE2 (unknown origin) | ChEMBL. | 18162398 |
Ratio IC50 (binding) | > 50 | Selectivity for BACE1 (unknown origin) over cathepsin D (unknown origin) | ChEMBL. | 18162398 |
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.