Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Toxoplasma gondii | LsmAD domain-containing protein | 0.0025 | 0.0225 | 0.5 |
Plasmodium falciparum | ataxin-2 like protein, putative | 0.0025 | 0.0225 | 0.5 |
Trypanosoma cruzi | malonyl-CoA decarboxylase, mitochondrial precursor, putative | 0.0159 | 0.368 | 1 |
Brugia malayi | hypothetical protein | 0.0025 | 0.0225 | 0.0225 |
Leishmania major | malonyl-coa decarboxylase-like protein | 0.0159 | 0.368 | 1 |
Wolbachia endosymbiont of Brugia malayi | malonyl-CoA decarboxylase | 0.0405 | 1 | 0.5 |
Trypanosoma brucei | malonyl-CoA decarboxylase, mitochondrial precursor, putative | 0.0159 | 0.368 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0405 | 1 | 1 |
Plasmodium vivax | ataxin-2 like protein, putative | 0.0025 | 0.0225 | 0.5 |
Trypanosoma cruzi | malonyl-CoA decarboxylase, mitochondrial precursor, putative | 0.0159 | 0.368 | 1 |
Plasmodium falciparum | ataxin-2 like protein, putative | 0.0025 | 0.0225 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (functional) | = 7 % | Negative chronotropic activity in guinea pig right atrium at 100 uM | ChEMBL. | 16913709 |
Activity (functional) | = 10 % | Vasorelaxant activity assessed as inhibition of calcium-induced contraction of potassium ion-depolarized guinea pig aortic strips at 100 uM | ChEMBL. | 16913709 |
Activity (functional) | = 52 % | Negative inotropic activity in guinea pig left atrium at 100 uM | ChEMBL. | 16913709 |
EC50 (functional) | = 6.13 uM | Negative inotropic activity in guinea pig left atrium | ChEMBL. | 16913709 |
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.