Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | acetylcholinesterase | 0.0969 | 0.5 | 0.5 |
Echinococcus granulosus | acetylcholinesterase | 0.0969 | 0.5 | 0.5 |
Echinococcus multilocularis | acetylcholinesterase | 0.0969 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0969 | 0.5 | 0.5 |
Echinococcus granulosus | carboxylesterase 5A | 0.0969 | 0.5 | 0.5 |
Loa Loa (eye worm) | carboxylesterase | 0.0969 | 0.5 | 0.5 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0969 | 0.5 | 0.5 |
Echinococcus multilocularis | carboxylesterase 5A | 0.0969 | 0.5 | 0.5 |
Loa Loa (eye worm) | acetylcholinesterase 1 | 0.0969 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0969 | 0.5 | 0.5 |
Echinococcus granulosus | acetylcholinesterase | 0.0969 | 0.5 | 0.5 |
Brugia malayi | Carboxylesterase family protein | 0.0969 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Inhibitory response (functional) | = 96 % | Antiinflammatory activity in rats by using reverse passive Arthus reaction (RPAR) assay at dose level of 50 mg/Kg by peroral administration | ChEMBL. | 6606708 |
Relative potency (functional) | = 0.15 | The relative potency of the compound was evaluated by considering the potency of indomethacin as 1 | ChEMBL. | 6606708 |
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.