Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | glucagon-like peptide 1 receptor | Starlite/ChEMBL | No references |
Homo sapiens | isocitrate dehydrogenase 1 (NADP+), soluble | Starlite/ChEMBL | No references |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Loa Loa (eye worm) | pigment dispersing factor receptor c | glucagon-like peptide 1 receptor | 463 aa | 388 aa | 25.8 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | calcium-activated potassium channel | 0.0115 | 0.0586 | 0.1367 |
Loa Loa (eye worm) | hypothetical protein | 0.0058 | 0.0055 | 0.0336 |
Schistosoma mansoni | serine-rich repeat protein | 0.0266 | 0.1982 | 0.4805 |
Brugia malayi | Calcitonin receptor-like protein seb-1 | 0.006 | 0.0077 | 0.0287 |
Echinococcus multilocularis | voltage dependent calcium channel subunit | 0.0516 | 0.4287 | 0.4269 |
Trypanosoma cruzi | ion transport protein, putative | 0.0098 | 0.0423 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0266 | 0.1982 | 0.4805 |
Schistosoma mansoni | calcium-activated potassium channel | 0.011 | 0.0534 | 0.1239 |
Schistosoma mansoni | dihydropyridine-sensitive l-type calcium channel | 0.0495 | 0.4092 | 1 |
Echinococcus multilocularis | voltage dependent calcium channel subunit | 0.1134 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.006 | 0.0077 | 0.0471 |
Leishmania major | ion transport protein-like protein | 0.0098 | 0.0423 | 0.5 |
Brugia malayi | Cache domain containing protein | 0.0228 | 0.1631 | 1 |
Echinococcus granulosus | small conductance calcium activated potassium | 0.0115 | 0.0586 | 0.0557 |
Schistosoma mansoni | hypothetical protein | 0.0115 | 0.0586 | 0.1367 |
Trypanosoma cruzi | ion transport protein, putative | 0.0098 | 0.0423 | 0.5 |
Loa Loa (eye worm) | pigment dispersing factor receptor c | 0.006 | 0.0077 | 0.0471 |
Echinococcus multilocularis | small conductance calcium activated potassium | 0.0115 | 0.0586 | 0.0557 |
Loa Loa (eye worm) | hypothetical protein | 0.0115 | 0.0586 | 0.3595 |
Brugia malayi | Corticotropin releasing factor receptor 2 precursor, putative | 0.006 | 0.0077 | 0.0287 |
Echinococcus granulosus | voltage dependent calcium channel subunit | 0.0516 | 0.4287 | 0.4269 |
Loa Loa (eye worm) | hypothetical protein | 0.0228 | 0.1631 | 1 |
Schistosoma mansoni | dihydropyridine-sensitive l-type calcium channel | 0.0249 | 0.1825 | 0.4418 |
Loa Loa (eye worm) | GTP-binding regulatory protein Gs alpha-S chain | 0.0055 | 0.0031 | 0.019 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Potency (functional) | 11.2202 uM | PubChem BioAssay. qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode). (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 18.3564 uM | PubChem BioAssay. qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 31.6228 uM | PubChem BioAssay. qHTS for Inhibitors of ATXN expression. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 50.1187 uM | PubChem BioAssay. qHTS of PTHR Inhibitors: Primary Screen. (Class of assay: confirmatory) | ChEMBL. | No reference |
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.