Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Metabotropic glutamate receptor 5 | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | excitatory amino acid transporter 2 | 0.2612 | 1 | 1 |
Echinococcus multilocularis | sodium:dicarboxylate symporter | 0.1158 | 0.4381 | 0.4344 |
Echinococcus multilocularis | sodium:dicarboxylate symporter | 0.2612 | 1 | 1 |
Onchocerca volvulus | Excitatory amino acid transporter homolog | 0.2612 | 1 | 0.5 |
Echinococcus granulosus | excitatory amino acid transporter 3 | 0.2612 | 1 | 1 |
Chlamydia trachomatis | glutamate symporter | 0.2612 | 1 | 1 |
Echinococcus granulosus | metabotropic glutamate receptor 5 | 0.006 | 0.014 | 0.0075 |
Echinococcus multilocularis | neutral amino acid transporter excitatory amino acid transporter | 0.2612 | 1 | 1 |
Echinococcus granulosus | neutral amino acid transporter A | 0.2612 | 1 | 1 |
Schistosoma mansoni | metabotropic glutamate receptor | 0.0041 | 0.0066 | 0.0066 |
Echinococcus multilocularis | neutral amino acid transporter A | 0.2612 | 1 | 1 |
Echinococcus multilocularis | excitatory amino acid transporter 3 | 0.2612 | 1 | 1 |
Echinococcus granulosus | excitatory amino acid transporter 2 | 0.2612 | 1 | 1 |
Echinococcus granulosus | sodium:dicarboxylate symporter | 0.2612 | 1 | 1 |
Wolbachia endosymbiont of Brugia malayi | Na+/H+-dicarboxylate symporter | 0.2612 | 1 | 0.5 |
Brugia malayi | metabotropic glutamate receptor subtype 5a (mGluR5a), putative | 0.0044 | 0.0079 | 0.0079 |
Schistosoma mansoni | sodium/dicarboxylate symporter-related | 0.1158 | 0.4381 | 0.4381 |
Echinococcus granulosus | Excitatory amino acid transporter | 0.2612 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.006 | 0.014 | 0.0044 |
Echinococcus multilocularis | Excitatory amino acid transporter | 0.2612 | 1 | 1 |
Loa Loa (eye worm) | excitatory amino acid transporter | 0.2612 | 1 | 1 |
Treponema pallidum | glutamate/aspartate transporter | 0.1158 | 0.4381 | 0.5 |
Echinococcus multilocularis | neutral amino acid transporter A | 0.2612 | 1 | 1 |
Echinococcus granulosus | neutral amino acid transporter | 0.2612 | 1 | 1 |
Echinococcus multilocularis | Excitatory amino acid transporter | 0.2612 | 1 | 1 |
Echinococcus multilocularis | neutral amino acid transporter excitatory amino acid transporter | 0.1158 | 0.4381 | 0.4344 |
Echinococcus granulosus | excitatory amino acid transporter 2 | 0.2612 | 1 | 1 |
Schistosoma mansoni | sodium/dicarboxylate symporter-related | 0.1158 | 0.4381 | 0.4381 |
Echinococcus multilocularis | neutral amino acid transporter A | 0.2612 | 1 | 1 |
Treponema pallidum | glutamate transporter | 0.1158 | 0.4381 | 0.5 |
Schistosoma mansoni | solute carrier family 1 (glial high affinity glutamate transporter | 0.2612 | 1 | 1 |
Schistosoma mansoni | metabotropic glutamate receptor 2 3 (mglur group 2) | 0.0056 | 0.0123 | 0.0123 |
Mycobacterium tuberculosis | Probable C4-dicarboxylate-transport transmembrane protein DctA | 0.2612 | 1 | 0.5 |
Echinococcus granulosus | neutral amino acid transporter A | 0.2612 | 1 | 1 |
Brugia malayi | Metabotropic glutamate receptor precursor. | 0.0049 | 0.0097 | 0.0097 |
Echinococcus granulosus | Excitatory amino acid transporter | 0.2612 | 1 | 1 |
Echinococcus multilocularis | metabotropic glutamate receptor 5 | 0.006 | 0.014 | 0.0075 |
Echinococcus multilocularis | excitatory amino acid transporter 2 | 0.2612 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 669 nM | Negative allosteric modulation of rat mGluR5 receptor expressed in HEK293 cells assessed as intracellular calcium flux after 170 seconds by FLIPR assay | ChEMBL. | 23850200 |
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.