Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | solute carrier family 6 (neurotransmitter transporter), member 4 | Starlite/ChEMBL | References |
Rattus norvegicus | Serotonin transporter | Starlite/ChEMBL | References |
Homo sapiens | histamine receptor H3 | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | norepinephrine/norepinephrine transporter | 0.0146 | 0.5 | 0.5 |
Loa Loa (eye worm) | solute carrier family 6 member 4 | 0.0146 | 0.5 | 0.5 |
Schistosoma mansoni | sodium/chloride dependent transporter | 0.0146 | 0.5 | 0.5 |
Onchocerca volvulus | 0.0146 | 0.5 | 0.5 | |
Loa Loa (eye worm) | hypothetical protein | 0.0146 | 0.5 | 0.5 |
Treponema pallidum | sodium- and chloride- dependent transporter | 0.0146 | 0.5 | 0.5 |
Loa Loa (eye worm) | norepinephrine transporter | 0.0146 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0146 | 0.5 | 0.5 |
Loa Loa (eye worm) | serotonin transporter b | 0.0146 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0146 | 0.5 | 0.5 |
Echinococcus multilocularis | serotonin transporter | 0.0146 | 0.5 | 0.5 |
Echinococcus granulosus | serotonin transporter | 0.0146 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Kd (functional) | = 9.22 | Antagonist activity at human histamine H3 receptor | ChEMBL. | 17127059 |
Ki (binding) | = 2 nM | Binding affinity to rat SERT | ChEMBL. | 17107798 |
Ki (binding) | = 2 nM | Binding affinity to human histamine H3 receptor | ChEMBL. | 17107798 |
Ki (binding) | = 2 nM | Binding affinity at human histamine H3 | ChEMBL. | 17765543 |
Ki (binding) | = 2 nM | Binding affinity at rat SERT | ChEMBL. | 17127059 |
Ki (binding) | = 2 nM | Binding affinity at human histamine H3 receptor | ChEMBL. | 17127059 |
Ki (binding) | = 2 nM | Binding affinity to rat SERT | ChEMBL. | 17107798 |
Ki (binding) | = 2 nM | Binding affinity to human histamine H3 receptor | ChEMBL. | 17107798 |
Ki (binding) | = 2 nM | Binding affinity at human histamine H3 | ChEMBL. | 17765543 |
Ki (binding) | = 2 nM | Binding affinity at rat SERT | ChEMBL. | 17127059 |
Ki (binding) | = 2 nM | Binding affinity at human histamine H3 receptor | ChEMBL. | 17127059 |
Ki (binding) | = 5.1 nM | Binding affinity to human SERT | ChEMBL. | 17107798 |
Ki (binding) | = 5.1 nM | Binding affinity at human SERT | ChEMBL. | 17765543 |
Ki (binding) | = 5.1 nM | Binding affinity at human SERT | ChEMBL. | 17127059 |
Ki (binding) | = 5.1 nM | Binding affinity to human SERT | ChEMBL. | 17107798 |
Ki (binding) | = 5.1 nM | Binding affinity at human SERT | ChEMBL. | 17765543 |
Ki (binding) | = 5.1 nM | Binding affinity at human SERT | ChEMBL. | 17127059 |
pA2 (functional) | = 9.22 | Antagonist activity at human histamine H3 receptor | ChEMBL. | 17127059 |
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.
3 literature references were collected for this gene.