Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Serotonin transporter | Starlite/ChEMBL | References |
Rattus norvegicus | Dopamine transporter | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | norepinephrine transporter | 0.0182 | 0.5 | 0.5 |
Echinococcus granulosus | serotonin transporter | 0.0182 | 0.5 | 0.5 |
Echinococcus multilocularis | serotonin transporter | 0.0182 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0182 | 0.5 | 0.5 |
Loa Loa (eye worm) | serotonin transporter b | 0.0182 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0182 | 0.5 | 0.5 |
Loa Loa (eye worm) | solute carrier family 6 member 4 | 0.0182 | 0.5 | 0.5 |
Schistosoma mansoni | sodium/chloride dependent transporter | 0.0182 | 0.5 | 0.5 |
Schistosoma mansoni | norepinephrine/norepinephrine transporter | 0.0182 | 0.5 | 0.5 |
Treponema pallidum | sodium- and chloride- dependent transporter | 0.0182 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0182 | 0.5 | 0.5 |
Onchocerca volvulus | 0.0182 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 72 nM | Binding affinity at the dopamine transporter using [125I]-RTI-55 in rat caudate membranes. | ChEMBL. | 9057857 |
IC50 (binding) | = 72 nM | Binding affinity at the dopamine transporter using [125I]-RTI-55 in rat caudate membranes. | ChEMBL. | 9057857 |
IC50 (functional) | = 111 nM | Reuptake inhibition at the dopamine transporter labeled with radioligand [3H]-dopamine on synaptosomes obtained from rat caudate. | ChEMBL. | 9057857 |
IC50 (functional) | = 111 nM | Reuptake inhibition at the dopamine transporter labeled with radioligand [3H]-dopamine on synaptosomes obtained from rat caudate. | ChEMBL. | 9057857 |
IC50 (binding) | = 1160 nM | Binding affinity at the serotonin transporter using [125I]-RTI-55 in rat caudate membranes. | ChEMBL. | 9057857 |
IC50 (binding) | = 1160 nM | Binding affinity at the serotonin transporter using [125I]-RTI-55 in rat caudate membranes. | ChEMBL. | 9057857 |
IC50 (functional) | = 3040 nM | Reuptake inhibition at the dopamine transporter labeled with radioligand [3H]-5-HT on synaptosomes obtained from whole rat brain minus cerebellum. | ChEMBL. | 9057857 |
IC50 (functional) | = 3040 nM | Reuptake inhibition at the dopamine transporter labeled with radioligand [3H]-5-HT on synaptosomes obtained from whole rat brain minus cerebellum. | ChEMBL. | 9057857 |
Ratio (functional) | = 1.5 | Ratio of reuptake inhibition on DA with respect to binding affinity of DA | ChEMBL. | 9057857 |
Ratio (functional) | = 1.5 | Ratio of reuptake inhibition on DA with respect to binding affinity of DA | ChEMBL. | 9057857 |
Ratio (binding) | = 16 | Ratio of binding affinity on SERT with respect to DA | ChEMBL. | 9057857 |
Ratio (functional) | = 27 | Ratio of reuptake inhibition of 5-HT with respect to DA | ChEMBL. | 9057857 |
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.