Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | sphingosine kinase 1 | 0.2118 | 0.5 | 0.5 |
Schistosoma mansoni | sphingoid long chain base kinase | 0.2118 | 0.5 | 0.5 |
Mycobacterium tuberculosis | Conserved protein | 0.2118 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.2118 | 0.5 | 0.5 |
Schistosoma mansoni | sphingosine kinase A B | 0.2118 | 0.5 | 0.5 |
Entamoeba histolytica | hypothetical protein, conserved | 0.2118 | 0.5 | 0.5 |
Mycobacterium ulcerans | hypothetical protein | 0.2118 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
GI50 (functional) | = 0.11 uM | Cytotoxicity against human DU145 cells by SRB method | ChEMBL. | 23867604 |
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.