Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
ED50 (functional) | = 0.06 mM | Compound evaluated in vitro for the dose required to kill 50% of chinese hamster cells measured by colony formation after exposure for 2 hours to radiation | ChEMBL. | 4020837 |
PC | = 3.7 | Compound evaluated for the partition coefficient (PC) | ChEMBL. | 4020837 |
Ratio (functional) | = 1.7 | Evaluated for sensitizer enhancement ratio determined by dividing the D0 value from the control radiation survival curve by the K0 value from the radiation survival curve in the presence of the compound at a concentration of 0.025 mM. | ChEMBL. | 4020837 |
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.