Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | sodium bile acid cotransporter | 1.2449 | 1 | 0.5 |
Echinococcus multilocularis | sodium bile acid cotransporter | 1.2449 | 1 | 0.5 |
Onchocerca volvulus | 1.2449 | 1 | 0.5 | |
Schistosoma mansoni | sodium-bile acid cotransporter related | 1.2449 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 1.2449 | 1 | 0.5 |
Echinococcus multilocularis | sodium bile acid cotransporter | 1.2449 | 1 | 0.5 |
Echinococcus multilocularis | sodium bile acid cotransporter | 1.2449 | 1 | 0.5 |
Echinococcus granulosus | sodium bile acid cotransporter | 1.2449 | 1 | 0.5 |
Echinococcus granulosus | sodium bile acid cotransporter | 1.2449 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (functional) | = 43.6 % | Antiinflammatory activity in mouse RAW264.7 cells assessed as accumulation of LPS-induced iNOS at 10 uM by immunoblot analysis | ChEMBL. | 20979397 |
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.