Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | calcium-activated potassium channel | 0.0094 | 0.4406 | 0.141 |
Loa Loa (eye worm) | acetylcholinesterase 1 | 0.0134 | 1 | 1 |
Echinococcus multilocularis | potassium large conductance calcium activated | 0.0094 | 0.4406 | 0.141 |
Echinococcus granulosus | carboxylesterase 5A | 0.0134 | 1 | 1 |
Echinococcus multilocularis | calcium activated potassium channel | 0.0094 | 0.4406 | 0.141 |
Loa Loa (eye worm) | carboxylesterase | 0.0134 | 1 | 1 |
Echinococcus granulosus | calcium activated potassium channel | 0.0094 | 0.4406 | 0.141 |
Echinococcus multilocularis | acetylcholinesterase | 0.0134 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0134 | 1 | 1 |
Echinococcus granulosus | acetylcholinesterase | 0.0134 | 1 | 1 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0134 | 1 | 1 |
Echinococcus multilocularis | acetylcholinesterase | 0.0134 | 1 | 1 |
Brugia malayi | Carboxylesterase family protein | 0.0134 | 1 | 1 |
Echinococcus granulosus | acetylcholinesterase | 0.0134 | 1 | 1 |
Echinococcus multilocularis | carboxylesterase 5A | 0.0134 | 1 | 1 |
Loa Loa (eye worm) | large conductance calcium-activated potassium channel alpha subunit ai | 0.0088 | 0.3487 | 0.3487 |
Echinococcus granulosus | potassium large conductance calcium activated | 0.0094 | 0.4406 | 0.141 |
Loa Loa (eye worm) | hypothetical protein | 0.0134 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Ca2+ elevation (functional) | 0 nM | Compound was evaluated in vitro for its effect on intracellular ca++ elevation was determined in comparison to the ATP at 10 uM on rat cardiomyocytes; Not active | ChEMBL. | 10411489 |
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.