Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trichomonas vaginalis | conserved hypothetical protein | 0.1054 | 0.5 | 0.5 |
Leishmania major | arginase | 0.1054 | 0.5 | 0.5 |
Schistosoma mansoni | arginase | 0.1054 | 0.5 | 0.5 |
Echinococcus granulosus | arginase 2 mitochondrial | 0.1054 | 0.5 | 0.5 |
Trichomonas vaginalis | Arginase, putative | 0.1054 | 0.5 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.1054 | 0.5 | 0.5 |
Echinococcus multilocularis | arginase 2, mitochondrial | 0.1054 | 0.5 | 0.5 |
Echinococcus multilocularis | 0.1054 | 0.5 | 0.5 | |
Entamoeba histolytica | Arginase, putative | 0.1054 | 0.5 | 0.5 |
Plasmodium vivax | arginase, putative | 0.1054 | 0.5 | 0.5 |
Plasmodium falciparum | arginase | 0.1054 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
MIC (functional) | > 250 uM | Antitubercular activity against Mycobacterium tuberculosis ATCC 27294 by Alamar blue assay | ChEMBL. | 20932608 |
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.