Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 1.2 uM | Concentration of the compound required to reduce 50% growth of L1210 cells in 48 hr | ChEMBL. | 2002470 |
K app (binding) | = 290000000 M-1 | DNA affinity constant of the compound to poly[d(A-T)] | ChEMBL. | 2002470 |
K app (binding) | = 820000000 M-1 | DNA affinity constant of the compound to poly[d(G-C)] | ChEMBL. | 2002470 |
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.