Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium ulcerans | hypothetical protein | 0.0514 | 0.5 | 0.5 |
Entamoeba histolytica | hypothetical protein, conserved | 0.0514 | 0.5 | 0.5 |
Schistosoma mansoni | sphingosine kinase A B | 0.0514 | 0.5 | 0.5 |
Schistosoma mansoni | sphingoid long chain base kinase | 0.0514 | 0.5 | 0.5 |
Echinococcus multilocularis | sphingosine kinase 1 | 0.0514 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0514 | 0.5 | 0.5 |
Mycobacterium tuberculosis | Conserved protein | 0.0514 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (binding) | = 9 % | Displacement of [3H]SCH23390 from human cloned dopamine D2 long receptor at 100 uM | ChEMBL. | 18164618 |
Activity (binding) | = 9 % | Displacement of [3H]SCH23390 from human cloned dopamine D2 long receptor at 100 uM | ChEMBL. | 18164618 |
Activity (binding) | = 21 % | Displacement of [3H]spiperone from human cloned dopamine D3 receptor at 100 uM | ChEMBL. | 18164618 |
Activity (binding) | = 21 % | Displacement of [3H]spiperone from human cloned dopamine D3 receptor at 100 uM | ChEMBL. | 18164618 |
Activity (binding) | = 44 % | Displacement of [3H]spiperone from human cloned dopamine D4 receptor at 100 uM | ChEMBL. | 18164618 |
Activity (binding) | = 44 % | Displacement of [3H]spiperone from human cloned dopamine D4 receptor at 100 uM | ChEMBL. | 18164618 |
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.