Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | hypothetical protein | 0.0332 | 1 | 1 |
Giardia lamblia | NADPH oxidoreductase, putative | 0.009 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0166 | 0.3167 | 0.0935 |
Giardia lamblia | NADPH oxidoreductase, putative | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0332 | 1 | 1 |
Giardia lamblia | NADPH oxidoreductase, putative | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | NAD(P)H dehydrogenase, putative | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Schistosoma mansoni | calcium-activated potassium channel | 0.0332 | 1 | 1 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Echinococcus multilocularis | small conductance calcium activated potassium | 0.0332 | 1 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | NAD(P)H dehydrogenase, putative | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.009 | 0 | 0.5 |
Trichomonas vaginalis | NAD(P)H dehydrogenase, putative | 0.009 | 0 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
CC50 (functional) | = 172.15 uM | Cytotoxicity against human Jurkat cells | ChEMBL. | 17967539 |
CC50 (functional) | = 172.15 uM | Cytotoxicity against human Jurkat cells | ChEMBL. | 17967539 |
MIC (functional) | >= 163 uM | Antimicrobial activity against Bacillus subtilis | ChEMBL. | 17967539 |
MIC (functional) | >= 189 uM | Antimicrobial activity against Escherichia coli | ChEMBL. | 17967539 |
MIC (functional) | >= 189 uM | Antimicrobial activity against Escherichia coli | ChEMBL. | 17967539 |
MIC (functional) | >= 197 uM | Antimicrobial activity against Saccharomyces cerevisiae | ChEMBL. | 17967539 |
MIC (functional) | >= 197 uM | Antimicrobial activity against Saccharomyces cerevisiae | ChEMBL. | 17967539 |
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.