Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Onchocerca volvulus | 0.0017 | 0 | 0.5 | |
Loa Loa (eye worm) | hypothetical protein | 0.0124 | 1 | 1 |
Schistosoma mansoni | tgf-beta family | 0.0017 | 0 | 0.5 |
Onchocerca volvulus | 0.0017 | 0 | 0.5 | |
Brugia malayi | Transforming growth factor beta like domain containing protein | 0.0068 | 0.4739 | 0.4739 |
Schistosoma mansoni | tgf-beta family | 0.0017 | 0 | 0.5 |
Loa Loa (eye worm) | bone morphogenic protein 6 | 0.0068 | 0.4739 | 0.4739 |
Echinococcus multilocularis | anti dorsalizing morphogenetic protein 1a | 0.0068 | 0.4739 | 1 |
Echinococcus granulosus | anti dorsalizing morphogenetic protein 1a | 0.0068 | 0.4739 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Inhibition (binding) | = 22 % | In vitro inhibition of binding of [125I]-Bolton-Hunter SP to Tachykinin receptor 1 in human IM-9 cell line at a concentration of 10 nM | ChEMBL. | 11425527 |
Inhibition (binding) | = 22 % | In vitro inhibition of binding of [125I]-Bolton-Hunter SP to Tachykinin receptor 1 in human IM-9 cell line at a concentration of 10 nM | ChEMBL. | 11425527 |
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.