Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | small conductance calcium activated potassium | 0.0362 | 0.2774 | 1 |
Echinococcus multilocularis | small conductance calcium activated potassium | 0.0362 | 0.2774 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0362 | 0.2774 | 1 |
Schistosoma mansoni | calcium-activated potassium channel | 0.0362 | 0.2774 | 0.2774 |
Schistosoma mansoni | hypothetical protein | 0.0362 | 0.2774 | 0.2774 |
Schistosoma mansoni | biogenic amine (5HT) receptor | 0.0269 | 0.0752 | 0.0752 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Inhibition (binding) | = 25.2 % | Inhibition of NorA in Staphylococcus aureus 1199B assessed as reduction in ethidium bromide efflux at 50 uM by fluorimetry after 5 mins | ChEMBL. | 21141825 |
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.