Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | hypothetical protein | 0.0161 | 1 | 1 |
Schistosoma mansoni | calcium-activated potassium channel | 0.0161 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0161 | 1 | 1 |
Echinococcus multilocularis | small conductance calcium activated potassium | 0.0161 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
MIC (functional) | = 0.8 ug ml-1 | Antifungal activity against Candida albicans was determined in vitro | ChEMBL. | 3302258 |
MIC (functional) | = 0.8 ug ml-1 | Antifungal activity against Candida albicans was determined in vitro | ChEMBL. | 3302258 |
MIC (functional) | = 1.6 ug ml-1 | Antifungal activity against Trichophyton asteroides was determined in vitro | ChEMBL. | 3302258 |
MIC (functional) | = 6.3 ug ml-1 | Antifungal activity against Aspergillus fumigatus was determined in vitro | ChEMBL. | 3302258 |
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.