Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Metabotropic glutamate receptor 5 | Starlite/ChEMBL | References |
Homo sapiens | glutamate receptor, metabotropic 5 | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | sodium-bile acid cotransporter related | 0.0615 | 0.3862 | 0.3862 |
Onchocerca volvulus | 0.1516 | 1 | 0.5 | |
Echinococcus multilocularis | metabotropic glutamate receptor 5 | 0.012 | 0.0495 | 0.0268 |
Echinococcus multilocularis | sodium bile acid cotransporter | 0.1516 | 1 | 1 |
Schistosoma mansoni | metabotropic glutamate receptor | 0.0082 | 0.0233 | 0.0233 |
Brugia malayi | Metabotropic glutamate receptor precursor. | 0.0098 | 0.0341 | 0.0341 |
Echinococcus granulosus | sodium bile acid cotransporter | 0.1516 | 1 | 1 |
Brugia malayi | metabotropic glutamate receptor subtype 5a (mGluR5a), putative | 0.0089 | 0.0279 | 0.0279 |
Loa Loa (eye worm) | hypothetical protein | 0.1516 | 1 | 1 |
Schistosoma mansoni | metabotropic glutamate receptor 2 3 (mglur group 2) | 0.0111 | 0.0433 | 0.0433 |
Schistosoma mansoni | sodium-bile acid cotransporter related | 0.1516 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.012 | 0.0495 | 0.0159 |
Echinococcus granulosus | sodium bile acid cotransporter | 0.1516 | 1 | 1 |
Echinococcus multilocularis | sodium bile acid cotransporter | 0.1516 | 1 | 1 |
Echinococcus granulosus | metabotropic glutamate receptor 5 | 0.012 | 0.0495 | 0.0268 |
Echinococcus multilocularis | sodium bile acid cotransporter | 0.1516 | 1 | 1 |
Schistosoma mansoni | sodium-bile acid cotransporter | 0.0901 | 0.5813 | 0.5813 |
Echinococcus granulosus | sodium bile acid cotransporter | 0.1516 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 2 nM | In vitro potency against human recombinant mGlu5 receptor was determined by [Ca2+] flux assay using glutamate as agonist | ChEMBL. | 15225713 |
IC50 (functional) | = 2 nM | In vitro potency against human recombinant mGlu5 receptor was determined by [Ca2+] flux assay using glutamate as agonist | ChEMBL. | 15225713 |
IC50 (functional) | = 82.6 nM | Activity in agonist-induced phosphoinositide hydrolysis in CHO cells expressing mGluR5a | ChEMBL. | 16451073 |
IC50 (functional) | = 82.6 nM | Activity in agonist-induced phosphoinositide hydrolysis in CHO cells expressing mGluR5a | ChEMBL. | 16451073 |
Ki (binding) | = 10 nM | Displacement by compound of [3H]-3-methoxy-5-(pyridin-2-ylethynyl)pyridine from rat cortical membranes | ChEMBL. | 15225713 |
Ki (binding) | = 10 nM | Displacement by compound of [3H]-3-methoxy-5-(pyridin-2-ylethynyl)pyridine from rat cortical membranes | ChEMBL. | 15225713 |
logD (ADMET) | = 3.9 | logD value of the compound was determined | ChEMBL. | 15225713 |
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.