Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0698 | 0.5 | 0.5 |
Mycobacterium tuberculosis | Conserved protein | 0.0698 | 0.5 | 0.5 |
Schistosoma mansoni | sphingoid long chain base kinase | 0.0698 | 0.5 | 0.5 |
Echinococcus multilocularis | sphingosine kinase 1 | 0.0698 | 0.5 | 0.5 |
Mycobacterium ulcerans | hypothetical protein | 0.0698 | 0.5 | 0.5 |
Entamoeba histolytica | hypothetical protein, conserved | 0.0698 | 0.5 | 0.5 |
Schistosoma mansoni | sphingosine kinase A B | 0.0698 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Log 1/C (binding) | = 6.7 | Inhibition of [3H]-dopamine uptake in HEK293 cells expressing recombinant Dopamine transporter | ChEMBL. | 11931612 |
Log 1/C (binding) | = 6.7 | Inhibition of [3H]-dopamine uptake in HEK293 cells expressing recombinant Dopamine transporter | ChEMBL. | 11931612 |
pKD (binding) | = 6.72 | Inhibition of [125I]-RTI-55 binding to human SERT in clonal cells | ChEMBL. | 11931612 |
pKD (binding) | = 8.41 | Inhibition of radioligand [125I]-RTI-55 binding to human Dopamine transporter in clonal cells | ChEMBL. | 11931612 |
pKD (binding) | = 6.72 | Inhibition of [125I]-RTI-55 binding to human SERT in clonal cells | ChEMBL. | 11931612 |
pKD (binding) | = 8.41 | Inhibition of radioligand [125I]-RTI-55 binding to human Dopamine transporter in clonal cells | ChEMBL. | 11931612 |
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.