Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | matrix metallopeptidase 7 M10 family | 0.0146 | 0.0439 | 0.5 |
Schistosoma mansoni | family A2 unassigned peptidase (A02 family) | 0.0227 | 0.1142 | 0.1142 |
Loa Loa (eye worm) | angiotensin-converting enzyme family protein | 0.0625 | 0.4584 | 1 |
Wolbachia endosymbiont of Brugia malayi | extracellular metallopeptidase | 0.0697 | 0.5212 | 0.5 |
Brugia malayi | Angiotensin-converting enzyme family protein | 0.0625 | 0.4584 | 1 |
Echinococcus multilocularis | matrix metallopeptidase 7 (M10 family) | 0.0146 | 0.0439 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
EC50 (functional) | = 17.3 uM | In vitro contraction of rabbit aorta strips. | ChEMBL. | 7837222 |
IC50 (functional) | > 30 uM | In vitro inhibition of potassium-induced contractions in rabbit aorta strips. | ChEMBL. | 7837222 |
Kd (binding) | > 50 uM | Displacement of [3H]-nitrendipine from dihydropyridine receptor of guinea pig myocardial membranes | ChEMBL. | 7837222 |
Kd (binding) | > 50 uM | Displacement of [3H]-nitrendipine from dihydropyridine receptor of guinea pig myocardial membranes | ChEMBL. | 7837222 |
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.