Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Onchocerca volvulus | Cirhin homolog | 0.0211 | 0 | 0.5 |
Echinococcus multilocularis | beta catenin | 0.0212 | 0.0031 | 0.5 |
Loa Loa (eye worm) | HMP-2 protein | 0.0212 | 0.0031 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0517 | 0.6851 | 1 |
Brugia malayi | Armadillo/beta-catenin-like repeat family protein | 0.0212 | 0.0031 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 74.91 uM | Inhibition of jack bean urease assessed as ammonia production after 30 mins by indophenol method | ChEMBL. | 24185379 |
IZ (functional) | = 3 mm | Antifungal activity against Saccharomyces cerevisiae after 24 to 48 hrs by agar well diffusion method | ChEMBL. | 24185379 |
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.