Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | metabotropic glutamate receptor | 0.05 | 0.5304 | 0.5392 |
Onchocerca volvulus | Excitatory amino acid transporter homolog | 0.0457 | 0.4438 | 0.5 |
Mycobacterium tuberculosis | Probable C4-dicarboxylate-transport transmembrane protein DctA | 0.0457 | 0.4438 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0735 | 1 | 1 |
Echinococcus multilocularis | metabotropic glutamate receptor 5 | 0.0735 | 1 | 1 |
Chlamydia trachomatis | glutamate symporter | 0.0457 | 0.4438 | 0.5 |
Loa Loa (eye worm) | glutamate receptor | 0.0597 | 0.7241 | 0.7241 |
Loa Loa (eye worm) | excitatory amino acid transporter | 0.0457 | 0.4438 | 0.4438 |
Echinococcus multilocularis | metabotropic glutamate receptor 2 | 0.05 | 0.5304 | 0.1557 |
Schistosoma mansoni | solute carrier family 1 (glial high affinity glutamate transporter | 0.0457 | 0.4438 | 0.4275 |
Schistosoma mansoni | metabotropic glutamate receptor 2 3 (mglur group 2) | 0.0679 | 0.8878 | 1 |
Brugia malayi | Excitatory amino acid transporter | 0.0457 | 0.4438 | 0.5418 |
Echinococcus granulosus | metabotropic glutamate receptor 2 | 0.05 | 0.5304 | 0.1557 |
Brugia malayi | metabotropic glutamate receptor subtype 5a (mGluR5a), putative | 0.0541 | 0.6119 | 0.8166 |
Wolbachia endosymbiont of Brugia malayi | Na+/H+-dicarboxylate symporter | 0.0457 | 0.4438 | 1 |
Brugia malayi | Metabotropic glutamate receptor precursor. | 0.0597 | 0.7241 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 2 uM | Inhibitory concentration against glutamate uptake in HEK cells expressing human Excitatory amino acid transporter 3 | ChEMBL. | 16165356 |
IC50 (binding) | = 3 uM | Inhibitory concentration against glutamate uptake in HEK cells expressing human Excitatory amino acid transporter 1 | ChEMBL. | 16165356 |
IC50 (binding) | = 13 uM | Inhibitory concentration against glutamate uptake in HEK cells expressing human Excitatory amino acid transporter 2 | ChEMBL. | 16165356 |
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.