Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trypanosoma cruzi | developmentally regulated phosphoprotein, putative | 0.0531 | 1 | 1 |
Echinococcus granulosus | Pyruvate dehydrogenase lipoamide kinase | 0.0531 | 1 | 0.5 |
Trypanosoma brucei | developmentally regulated phosphoprotein | 0.0531 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0531 | 1 | 0.5 |
Echinococcus multilocularis | Pyruvate dehydrogenase (lipoamide) kinase | 0.0531 | 1 | 0.5 |
Echinococcus multilocularis | Pyruvate dehydrogenase (lipoamide) kinase | 0.0531 | 1 | 0.5 |
Schistosoma mansoni | pyruvate dehydrogenase | 0.0531 | 1 | 1 |
Leishmania major | developmentally regulated phosphoprotein-like protein | 0.0531 | 1 | 1 |
Toxoplasma gondii | ATPase/histidine kinase/DNA gyrase B/HSP90 domain-containing protein | 0.0215 | 0.0855 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Delta TC (functional) | = 8 % | Acute in vivo activity of the compound was measured by the total plasma cholesterol concentration levels(TC) at dose 50 mg/kg | ChEMBL. | 8632431 |
Delta TC (functional) | = 8 % | Acute in vivo activity of the compound was measured by the total plasma cholesterol concentration levels(TC) at dose 50 mg/kg | ChEMBL. | 8632431 |
IC50 (binding) | = 52 uM | In vitro inhibitory activity against acyl coenzyme A:cholesterol acyltransferase 1 in microsomes of rat liver | ChEMBL. | 8632431 |
IC50 (binding) | = 52 uM | In vitro inhibitory activity against acyl coenzyme A:cholesterol acyltransferase 1 in microsomes of rat liver | ChEMBL. | 8632431 |
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.