Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | calcium-activated potassium channel | 0.3686 | 1 | 1 |
Schistosoma mansoni | hypothetical protein | 0.3686 | 1 | 1 |
Echinococcus multilocularis | small conductance calcium activated potassium | 0.3686 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.3686 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Inhibition (binding) | Inhibition of MMP-9 activity in human HT1080 cells by gelatin zymography | ChEMBL. | 25907368 | |
Inhibition (binding) | Inhibition of MMP-2 activity in human HT1080 cells by gelatin zymography | ChEMBL. | 25907368 | |
Inhibition (functional) | = 0 % | Antituberculosis activity against Mycobacterium tuberculosis at a concentration of 12.5 ug/mL | ChEMBL. | 11514148 |
Inhibition (functional) | = 0 % | Antituberculosis activity against Mycobacterium tuberculosis at a concentration of 12.5 ug/mL | ChEMBL. | 11514148 |
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.
2 literature references were collected for this gene.