Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | small conductance calcium activated potassium | 0.0528 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0528 | 1 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0528 | 1 | 1 |
Schistosoma mansoni | calcium-activated potassium channel | 0.0528 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | > 20 ug ml-1 | In vitro cytotoxicity against CCRF-CEM cells | ChEMBL. | 9083492 |
Inhibition (functional) | = 5 % | In vivo antitumor activity against subaxillary implanted 6C3HED lymphosarcoma implanted in C3H mice at a dose of 300 mg/kg administered perorally twice daily for a period of 8 days. | ChEMBL. | 9083492 |
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.