Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | sodium bile acid cotransporter | 0.1873 | 1 | 0.5 |
Echinococcus granulosus | sodium bile acid cotransporter | 0.1873 | 1 | 0.5 |
Echinococcus multilocularis | sodium bile acid cotransporter | 0.1873 | 1 | 0.5 |
Echinococcus multilocularis | sodium bile acid cotransporter | 0.1873 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.1873 | 1 | 0.5 |
Onchocerca volvulus | 0.1873 | 1 | 0.5 | |
Schistosoma mansoni | sodium-bile acid cotransporter related | 0.1873 | 1 | 1 |
Echinococcus granulosus | sodium bile acid cotransporter | 0.1873 | 1 | 0.5 |
Echinococcus multilocularis | sodium bile acid cotransporter | 0.1873 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Drug uptake (binding) | = 158 uM | Induction of NADPH:quinone reductase activity in mouse Hepa-1c1c7 cells assessed as drug level required to double specific enzyme activity | ChEMBL. | 21050753 |
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.