Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | voltage dependent calcium channel subunit | 1.0716 | 1 | 1 |
Schistosoma mansoni | dihydropyridine-sensitive l-type calcium channel | 0.4675 | 0.2941 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.2158 | 0 | 0.5 |
Schistosoma mansoni | serine-rich repeat protein | 0.2517 | 0.042 | 0.0693 |
Brugia malayi | Cache domain containing protein | 0.2158 | 0 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.2517 | 0.042 | 0.0693 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
EC50 (functional) | = 76.07 uM | Effective concentration required for the lysis of Trypanosoma cruzi trypomastigotes in blood stream after 24 hours of treatment | ChEMBL. | 15324878 |
IC50 (binding) | = 25.5 nM | Inhibition of Peptidyl-prolyl cis-trans isomerase Trypanosoma cruzi cyclophilin (CL Brener strain, p19) | ChEMBL. | 15324878 |
IC50 (functional) | = 33.75 uM | Compound was tested for the inhibition of Trypanosoma cruzi epimastigote growth after 72 hours of treatment | ChEMBL. | 15324878 |
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.