Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 1.2 uM | In vitro inhibition of HIV-1 plaque formation | ChEMBL. | 2016713 |
IC50 (functional) | = 9 uM | In vitro inhibition of CEM-SS cell growth by 50 % | ChEMBL. | 2016713 |
Ratio (functional) | = 7.5 | Differential selectivity measured as the ratio of CEM-SS cell growth IC50 vs HIV plaque formation IC50. | ChEMBL. | 2016713 |
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.