Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Glutamate [NMDA] receptor subunit epsilon 3 | Starlite/ChEMBL | References |
Rattus norvegicus | Glutamate NMDA receptor | Starlite/ChEMBL | References |
Rattus norvegicus | Serotonin transporter | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | serotonin transporter b | 0.0073 | 0.439 | 0.5 |
Echinococcus granulosus | serotonin transporter | 0.0073 | 0.439 | 0.439 |
Loa Loa (eye worm) | norepinephrine transporter | 0.0073 | 0.439 | 0.5 |
Onchocerca volvulus | 0.0073 | 0.439 | 0.5 | |
Treponema pallidum | sodium- and chloride- dependent transporter | 0.0073 | 0.439 | 0.5 |
Schistosoma mansoni | glutamate receptor NMDA | 0.0085 | 1 | 1 |
Brugia malayi | Sodium:neurotransmitter symporter family protein | 0.0073 | 0.439 | 0.5 |
Echinococcus multilocularis | serotonin transporter | 0.0073 | 0.439 | 0.439 |
Loa Loa (eye worm) | hypothetical protein | 0.0073 | 0.439 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0073 | 0.439 | 0.5 |
Echinococcus multilocularis | glutamate (NMDA) receptor subunit | 0.0085 | 1 | 1 |
Loa Loa (eye worm) | solute carrier family 6 member 4 | 0.0073 | 0.439 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0073 | 0.439 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 0.35 uM | Inhibition of [3H]-MK-801 binding to NMDA receptor from rat cerebral cortical synaptic membrane | ChEMBL. | 8941398 |
IC50 (binding) | = 0.35 uM | Inhibition of [3H]-MK-801 binding to N-methyl-D-aspartate glutamate receptor of rat cerebral cortical synaptic membrane | ChEMBL. | 9719604 |
IC50 (binding) | = 0.35 uM | Inhibition of [3H]-MK-801 binding to NMDA receptor from rat cerebral cortical synaptic membrane | ChEMBL. | 8941398 |
IC50 (binding) | = 0.35 uM | Inhibition of [3H]-MK-801 binding to N-methyl-D-aspartate glutamate receptor of rat cerebral cortical synaptic membrane | ChEMBL. | 9719604 |
IC50 (functional) | = 2.3 uM | Concentration required to inhibit of N-methyl-D-aspartic acid (NMDA) receptor produced by oocytes | ChEMBL. | 8941398 |
IC50 (functional) | = 2.3 uM | Concentration required to inhibit of N-methyl-D-aspartic acid (NMDA) receptor produced by oocytes | ChEMBL. | 8941398 |
IC50 (binding) | = 6.5 uM | Inhibition of [3H]-MK-801 binding to NMDA receptor from rat cerebral cortical synaptic membrane | ChEMBL. | 8941398 |
IC50 (binding) | = 6.5 uM | Inhibition of [3H]-MK-801 binding to N-methyl-D-aspartate glutamate receptor of rat cerebral cortical synaptic membrane | ChEMBL. | 9719604 |
IC50 (binding) | = 6.5 uM | Inhibition of [3H]-MK-801 binding to NMDA receptor from rat cerebral cortical synaptic membrane | ChEMBL. | 8941398 |
IC50 (binding) | = 6.5 uM | Inhibition of [3H]-MK-801 binding to N-methyl-D-aspartate glutamate receptor of rat cerebral cortical synaptic membrane | ChEMBL. | 9719604 |
Inhibition (functional) | = 50 % | Percentage inhibition of N-methyl-D-aspartic acid (NMDA) receptor produced by oocytes | ChEMBL. | 8941398 |
Inhibition (functional) | = 50 % | Percentage inhibition of N-methyl-D-aspartic acid (NMDA) receptor produced by oocytes | ChEMBL. | 8941398 |
Ki (binding) | = 0.014 uM | Inhibition of [3H]-paroxetine binding on serotonin transporter of rat cerebral cortical synaptic membrane | ChEMBL. | 8941398 |
Ki (binding) | = 0.014 uM | Inhibition of Serotonin transporter in cerebral cortical synaptic membrane of rats using [3H]-paroxetine | ChEMBL. | 9719604 |
Ki (binding) | = 0.014 uM | Inhibition of [3H]-paroxetine binding on serotonin transporter of rat cerebral cortical synaptic membrane | ChEMBL. | 8941398 |
Ki (binding) | = 0.014 uM | Inhibition of Serotonin transporter in cerebral cortical synaptic membrane of rats using [3H]-paroxetine | ChEMBL. | 9719604 |
Ki (binding) | = 2.4 uM | Inhibition of [3H]-paroxetine binding on serotonin transporter of rat cerebral cortical synaptic membrane | ChEMBL. | 8941398 |
Ki (binding) | = 2.4 uM | Inhibition of Serotonin transporter in cerebral cortical synaptic membrane of rats using [3H]-paroxetine | ChEMBL. | 9719604 |
Ki (binding) | = 2.4 uM | Inhibition of [3H]-paroxetine binding on serotonin transporter of rat cerebral cortical synaptic membrane | ChEMBL. | 8941398 |
Ki (binding) | = 2.4 uM | Inhibition of Serotonin transporter in cerebral cortical synaptic membrane of rats using [3H]-paroxetine | ChEMBL. | 9719604 |
Selectivity index (binding) | = 0.04 | Ratio of 5 HT inhibition to NMDA receptor binding | ChEMBL. | 8941398 |
Selectivity index (binding) | = 0.37 | Ratio of 5 HT inhibition to NMDA receptor binding | ChEMBL. | 8941398 |
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.