Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Dopamine transporter | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | a disintegrin and metalloproteinase with | 0.0119 | 0.3104 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0284 | 1 | 1 |
Onchocerca volvulus | 0.0109 | 0.2727 | 1 | |
Brugia malayi | Sodium:neurotransmitter symporter family protein | 0.0109 | 0.2727 | 0.139 |
Loa Loa (eye worm) | hypothetical protein | 0.009 | 0.1897 | 0.1897 |
Echinococcus multilocularis | serotonin transporter | 0.0109 | 0.2727 | 0.7568 |
Brugia malayi | angiogenesis inhibito | 0.0087 | 0.179 | 0.0281 |
Loa Loa (eye worm) | hypothetical protein | 0.0109 | 0.2727 | 0.2727 |
Loa Loa (eye worm) | serotonin transporter b | 0.0109 | 0.2727 | 0.2727 |
Echinococcus multilocularis | a disintegrin and metalloproteinase with | 0.0119 | 0.3104 | 1 |
Treponema pallidum | sodium- and chloride- dependent transporter | 0.0109 | 0.2727 | 0.5 |
Schistosoma mansoni | sodium/chloride dependent transporter | 0.0109 | 0.2727 | 0.7568 |
Schistosoma mansoni | ADAMTS5 peptidase (M12 family) | 0.0119 | 0.3104 | 1 |
Schistosoma mansoni | norepinephrine/norepinephrine transporter | 0.0109 | 0.2727 | 0.7568 |
Echinococcus granulosus | serotonin transporter | 0.0109 | 0.2727 | 0.7568 |
Loa Loa (eye worm) | hypothetical protein | 0.0081 | 0.1553 | 0.1553 |
Brugia malayi | ADAMTS-like protease | 0.0087 | 0.179 | 0.0281 |
Loa Loa (eye worm) | hypothetical protein | 0.0109 | 0.2727 | 0.2727 |
Loa Loa (eye worm) | norepinephrine transporter | 0.0109 | 0.2727 | 0.2727 |
Loa Loa (eye worm) | hypothetical protein | 0.0109 | 0.2727 | 0.2727 |
Loa Loa (eye worm) | solute carrier family 6 member 4 | 0.0109 | 0.2727 | 0.2727 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 1.4 nM | Inhibition of [3H]-dopamine uptake at the dopamine transporter in rat striatal tissue | ChEMBL. | 8960553 |
IC50 (functional) | = 1.4 nM | Inhibition of [3H]-dopamine uptake at the dopamine transporter in rat striatal tissue | ChEMBL. | 8960553 |
IC50 (binding) | = 2.5 nM | Ability to displace [3H]-WIN-35,428 from dopamine transporter in rat caudate putamen tissue | ChEMBL. | 12213055 |
IC50 (binding) | = 2.5 nM | Inhibition of [3H]-WIN- 35,428 binding to the dopamine transporter in rat brain | ChEMBL. | 8960553 |
IC50 (binding) | = 2.5 nM | Ability to displace [3H]-WIN-35,428 from dopamine transporter in rat caudate putamen tissue | ChEMBL. | 12213055 |
IC50 (binding) | = 2.5 nM | Inhibition of [3H]-WIN- 35,428 binding to the dopamine transporter in rat brain | ChEMBL. | 8960553 |
Uptake/Binding ratio (functional) | = 0.6 | The ratio of uptake/binding at Dopamine transporter | ChEMBL. | 8960553 |
Uptake/Binding ratio (functional) | = 0.6 | The ratio of uptake/binding at Dopamine transporter | ChEMBL. | 8960553 |
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.
2 literature references were collected for this gene.