Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | uridine phosphorylase | 0.1181 | 0.5 | 0.5 |
Loa Loa (eye worm) | uridine phosphorylase | 0.1181 | 0.5 | 0.5 |
Echinococcus multilocularis | uridine phosphorylase 1 | 0.1181 | 0.5 | 0.5 |
Echinococcus granulosus | uridine phosphorylase 1 | 0.1181 | 0.5 | 0.5 |
Mycobacterium leprae | probable uridine phosphorylase | 0.1181 | 0.5 | 0.5 |
Schistosoma mansoni | uridine phosphorylase | 0.1181 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Calcium release (functional) | 0 | Ability of compound to release intracellular calcium from Fluo-4 loaded 3T3 cells; + = Release | ChEMBL. | 15454234 |
GI50 (functional) | = 13 uM | Inhibition of human lung cancer cell line (A549) growth by 50% in sulforhodamineB assay | ChEMBL. | 15454234 |
GI50 (functional) | = 13 uM | Inhibition of human lung cancer cell line (A549) growth by 50% in sulforhodamineB assay | ChEMBL. | 15454234 |
Inhibition (binding) | 0 | Inhibition of human recombinant PRL-3 up to 50 uM | ChEMBL. | 16530413 |
Ratio (functional) | = 1.17 | Ratio of intensity of phosphorylation of phosphorylated eIF2a to the intensity of the total eIF2a was determined | ChEMBL. | 15454234 |
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.