Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0206 | 1 | 1 |
Echinococcus multilocularis | hormone sensitive lipase | 0.0206 | 1 | 1 |
Brugia malayi | Carboxylesterase family protein | 0.0143 | 0 | 0.5 |
Brugia malayi | Carboxylesterase family protein | 0.0143 | 0 | 0.5 |
Schistosoma mansoni | hormone-sensitive lipase (S09 family) | 0.0206 | 1 | 1 |
Schistosoma mansoni | hormone-sensitive lipase (S09 family) | 0.0206 | 1 | 1 |
Schistosoma mansoni | hormone-sensitive lipase (S09 family) | 0.0206 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 21.7 uM | Inhibition of ovine COX1 assessed as PGF2alpha production by reduction of PGH2 with stannous chloride by enzyme immunoassay | ChEMBL. | 23914900 |
IC50 (binding) | = 25.5 uM | Inhibition of ovine COX2 assessed as PGF2alpha production by reduction of PGH2 with stannous chloride by enzyme immunoassay | ChEMBL. | 23914900 |
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.