Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | acetylcholinesterase | 0.3269 | 0.5 | 0.5 |
Echinococcus granulosus | acetylcholinesterase | 0.3269 | 0.5 | 0.5 |
Echinococcus multilocularis | acetylcholinesterase | 0.3269 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.3269 | 0.5 | 0.5 |
Echinococcus granulosus | carboxylesterase 5A | 0.3269 | 0.5 | 0.5 |
Loa Loa (eye worm) | carboxylesterase | 0.3269 | 0.5 | 0.5 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.3269 | 0.5 | 0.5 |
Echinococcus multilocularis | carboxylesterase 5A | 0.3269 | 0.5 | 0.5 |
Loa Loa (eye worm) | acetylcholinesterase 1 | 0.3269 | 0.5 | 0.5 |
Echinococcus granulosus | acetylcholinesterase | 0.3269 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.3269 | 0.5 | 0.5 |
Brugia malayi | Carboxylesterase family protein | 0.3269 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | Inhibition of aminopeptidase activity of human leukotriene A4 hydrolase by Dixon plot analysis | ChEMBL. | 21292493 | |
IC50 (binding) | > 100 uM | Inhibition of bovine lens cytosolic leucine aminopeptidase by Dixon plot analysis | ChEMBL. | 21292493 |
IC50 (binding) | = 310 uM | Inhibition of human aminopeptidase N by Dixon plot analysis | ChEMBL. | 21292493 |
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.