Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (binding) | = 15 % | Inhibition of BCRP expressed in human HEK293 cells assessed as maximal mitoxantrone accumulation at 20 uM relative control | ChEMBL. | 17341062 |
Activity (binding) | = 15 % | Inhibition of BCRP expressed in human HEK293 cells assessed as maximal mitoxantrone accumulation at 20 uM relative control | ChEMBL. | 17341062 |
IC50 (functional) | = 48 ug ml-1 | Antifungal activity against MDR knockout Candida albicans DSY1024 after 24 hrs by XTT assay | ChEMBL. | 11277746 |
IC50 (functional) | > 200 ug ml-1 | Antifungal activity against wild type Candida albicans SC5314 after 24 hrs by XTT assay | ChEMBL. | 11277746 |
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.