Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Ovis aries | Cyclooxygenase-1 | Starlite/ChEMBL | References |
Homo sapiens | prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase) | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | peroxidasin | 0.0079 | 0.5 | 0.5 |
Onchocerca volvulus | Chorion peroxidase homolog | 0.0079 | 0.5 | 0.5 |
Brugia malayi | Peroxidasin | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Brugia malayi | Animal haem peroxidase family protein | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Echinococcus granulosus | peroxidasin | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Brugia malayi | Blistered cuticle protein 3 | 0.0079 | 0.5 | 0.5 |
Onchocerca volvulus | Peroxidase homolog | 0.0079 | 0.5 | 0.5 |
Onchocerca volvulus | Peroxidase homolog | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Echinococcus multilocularis | peroxidasin | 0.0079 | 0.5 | 0.5 |
Brugia malayi | Animal haem peroxidase family protein | 0.0079 | 0.5 | 0.5 |
Onchocerca volvulus | 0.0079 | 0.5 | 0.5 | |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | blistered cuticle protein 3 | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | animal heme peroxidase | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Brugia malayi | Animal haem peroxidase family protein | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Onchocerca volvulus | Peroxidasin homolog | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Brugia malayi | Animal haem peroxidase family protein | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | animal heme peroxidase | 0.0079 | 0.5 | 0.5 |
Schistosoma mansoni | peroxidasin | 0.0079 | 0.5 | 0.5 |
Brugia malayi | Animal haem peroxidase family protein | 0.0079 | 0.5 | 0.5 |
Onchocerca volvulus | Dual oxidase homolog | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Onchocerca volvulus | 0.0079 | 0.5 | 0.5 | |
Loa Loa (eye worm) | animal heme peroxidase | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Onchocerca volvulus | Peroxidasin homolog | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | animal heme peroxidase | 0.0079 | 0.5 | 0.5 |
Onchocerca volvulus | 0.0079 | 0.5 | 0.5 | |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 470 nM | Inhibition of ovine COX-1 using [14C] arachidonic acid as substrate preincubated for 17 mins before substrate addition measured after 3 mins by thin-layer chromatographic analysis | ChEMBL. | 22263894 |
IC50 (binding) | = 495 nM | Inhibition of COX-1 in human OVCAR3 cells using [14C] arachidonic acid as substrate preincubated for 30 mins before substrate addition measured after 30 mins | ChEMBL. | 22263894 |
Inhibition (binding) | = 15 % | Inhibition of mouse COX-2 using [14C] arachidonic acid as substrate at 4 uM preincubated for 17 mins before substrate addition measured after 3 mins by thin-layer chromatographic analysis | ChEMBL. | 22263894 |
Inhibition (binding) | = 99 % | Inhibition of ovine COX-1 using [14C] arachidonic acid as substrate at 4 uM preincubated for 17 mins before substrate addition measured after 3 mins by thin-layer chromatographic analysis | ChEMBL. | 22263894 |
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.