Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | serotonin transporter | 0.0556 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0556 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0556 | 1 | 1 |
Echinococcus granulosus | nicotinic acetylcholine receptor subunit alpha 8 | 0.0526 | 0.916 | 0.916 |
Echinococcus granulosus | nicotinic acetylcholine receptor a11 subunit | 0.0526 | 0.916 | 0.916 |
Schistosoma mansoni | sodium/chloride dependent transporter | 0.0556 | 1 | 1 |
Echinococcus multilocularis | nicotinic acetylcholine receptor a11 subunit | 0.0526 | 0.916 | 0.916 |
Echinococcus multilocularis | serotonin transporter | 0.0556 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0526 | 0.916 | 0.916 |
Echinococcus multilocularis | nicotinic acetylcholine receptor subunit alpha 8 | 0.0526 | 0.916 | 0.916 |
Loa Loa (eye worm) | serotonin transporter b | 0.0556 | 1 | 1 |
Echinococcus multilocularis | nicotinic acetylcholine receptor alpha subunit | 0.0526 | 0.916 | 0.916 |
Loa Loa (eye worm) | norepinephrine transporter | 0.0556 | 1 | 1 |
Loa Loa (eye worm) | nicotinic acetylcholine receptor alpha subunit | 0.0526 | 0.916 | 0.916 |
Echinococcus granulosus | nicotinic acetylcholine receptor alpha subunit | 0.0526 | 0.916 | 0.916 |
Treponema pallidum | sodium- and chloride- dependent transporter | 0.0556 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0556 | 1 | 1 |
Onchocerca volvulus | 0.0556 | 1 | 1 | |
Loa Loa (eye worm) | solute carrier family 6 member 4 | 0.0556 | 1 | 1 |
Brugia malayi | nicotinic acetylcholine receptor alpha subunit, putative | 0.0526 | 0.916 | 0.916 |
Onchocerca volvulus | Putative nachr subunit | 0.0526 | 0.916 | 0.916 |
Schistosoma mansoni | norepinephrine/norepinephrine transporter | 0.0556 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 16 ug ml-1 | Inhibition of rat liver aminopeptidase B using 0.2 mM L-leucine-beta-naphthylamide by colorimetry | ChEMBL. | 850237 |
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.