Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | acetylcholinesterase 1 | 0.0288 | 0.5 | 0.5 |
Echinococcus multilocularis | acetylcholinesterase | 0.0288 | 0.5 | 0.5 |
Echinococcus granulosus | acetylcholinesterase | 0.0288 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0288 | 0.5 | 0.5 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0288 | 0.5 | 0.5 |
Echinococcus multilocularis | carboxylesterase 5A | 0.0288 | 0.5 | 0.5 |
Brugia malayi | Carboxylesterase family protein | 0.0288 | 0.5 | 0.5 |
Echinococcus granulosus | acetylcholinesterase | 0.0288 | 0.5 | 0.5 |
Loa Loa (eye worm) | carboxylesterase | 0.0288 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0288 | 0.5 | 0.5 |
Echinococcus granulosus | carboxylesterase 5A | 0.0288 | 0.5 | 0.5 |
Echinococcus multilocularis | acetylcholinesterase | 0.0288 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | 0 mM | In vitro inhibitory concentration against hydroxyl radical (-OH); (na : not active) | ChEMBL. | 15896960 |
IC50 (functional) | = 3.7 mM | In vitro inhibitory concentration against peroxynitrite(ONOO-): using pyrogallol red bleaching assay | ChEMBL. | 15896960 |
IC50 (functional) | = 22 mM | In vitro inhibitory concentration against NO (nitrous oxide) | ChEMBL. | 15896960 |
IC50 (functional) | = 23 mM | In vitro inhibitory concentration against lipid peroxidation(LPO) | ChEMBL. | 15896960 |
IC50 (functional) | = 2940 mM | In vitro inhibitory concentration against Total peroxyl radical-trapping antioxidant parameter(TRAP) | ChEMBL. | 15896960 |
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.