Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | Nuclear hormone receptor family member nhr-31 | 0.005 | 0.5 | 0.5 |
Echinococcus multilocularis | COUP TF:Svp nuclear hormone receptor | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | retinoic acid receptor RXR | 0.005 | 0.5 | 0.5 |
Echinococcus multilocularis | FTZ F1 nuclear receptor protein | 0.005 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-25 | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | thyroid hormone receptor | 0.005 | 0.5 | 0.5 |
Onchocerca volvulus | Protein ultraspiracle homolog | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-1 | 0.005 | 0.5 | 0.5 |
Echinococcus granulosus | retinoic acid receptor rxr beta a | 0.005 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-41 | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | RAR-like nuclear receptor | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | thyroid hormone receptor | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | steroid hormone receptor | 0.005 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-25 | 0.005 | 0.5 | 0.5 |
Echinococcus granulosus | FTZ F1 nuclear receptor protein | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | coup transcription factor | 0.005 | 0.5 | 0.5 |
Echinococcus granulosus | COUP TF:Svp nuclear hormone receptor | 0.005 | 0.5 | 0.5 |
Brugia malayi | photoreceptor-specific nuclear receptor | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | retinoid-x-receptor (RXR) | 0.005 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-49 | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | steroid hormone receptor ad4bp | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-31 | 0.005 | 0.5 | 0.5 |
Onchocerca volvulus | 0.005 | 0.5 | 0.5 | |
Echinococcus granulosus | hepatocyte nuclear factor 4 alpha | 0.005 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-3 | 0.005 | 0.5 | 0.5 |
Onchocerca volvulus | Bile acid receptor homolog | 0.005 | 0.5 | 0.5 |
Echinococcus multilocularis | hepatocyte nuclear factor 4 alpha | 0.005 | 0.5 | 0.5 |
Echinococcus multilocularis | Nuclear hormone receptor family member nhr 41 | 0.005 | 0.5 | 0.5 |
Brugia malayi | nuclear hormone receptor | 0.005 | 0.5 | 0.5 |
Brugia malayi | steroid hormone receptor | 0.005 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-40 | 0.005 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-1 | 0.005 | 0.5 | 0.5 |
Echinococcus multilocularis | nuclear receptor 2DBD gamma | 0.005 | 0.5 | 0.5 |
Echinococcus granulosus | ecdysone induced protein 78C | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear Hormone Receptor family member | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | nuclear receptor 2DBD-gamma | 0.005 | 0.5 | 0.5 |
Brugia malayi | Ligand-binding domain of nuclear hormone receptor family protein | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-49 | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | Tr4/Tr2 (homologue) | 0.005 | 0.5 | 0.5 |
Brugia malayi | Steroid receptor seven-up type 2 | 0.005 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-14 | 0.005 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-19 | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | FTZ-F1 nuclear receptor-like protein | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | nuclear hormone receptor | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.005 | 0.5 | 0.5 |
Echinococcus granulosus | nuclear receptor 2DBD gamma | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.005 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor-like 1 | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | photoreceptor-specific nuclear receptor related | 0.005 | 0.5 | 0.5 |
Echinococcus multilocularis | ecdysone induced protein 78C | 0.005 | 0.5 | 0.5 |
Onchocerca volvulus | Steroid hormone receptor family member cnr14 homolog | 0.005 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-19 | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-40 | 0.005 | 0.5 | 0.5 |
Schistosoma mansoni | nuclear hormone receptor nor-1/nor-2 | 0.005 | 0.5 | 0.5 |
Echinococcus multilocularis | thyroid hormone receptor alpha | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-14 | 0.005 | 0.5 | 0.5 |
Echinococcus granulosus | Nuclear hormone receptor family member nhr 41 | 0.005 | 0.5 | 0.5 |
Echinococcus granulosus | FTZ F1 alpha | 0.005 | 0.5 | 0.5 |
Echinococcus multilocularis | nuclear receptor 2DBD gamma | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.005 | 0.5 | 0.5 |
Brugia malayi | nuclear receptor NHR-88 | 0.005 | 0.5 | 0.5 |
Echinococcus multilocularis | FTZ F1 alpha | 0.005 | 0.5 | 0.5 |
Brugia malayi | Ligand-binding domain of nuclear hormone receptor family protein | 0.005 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-41 | 0.005 | 0.5 | 0.5 |
Echinococcus granulosus | nuclear receptor 2DBD gamma | 0.005 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Inhibition (functional) | = 2.5 % | Inhibition of carrageenan-induced rat's paw edema (CPE) after peroral administration of 100 mg/kg dose. | ChEMBL. | 1552506 |
Inhibition (functional) | = 4.6 % | Inhibition of Zymosan-induced rat's paw edema(ZPE) after peroral administration of 100 mg/kg dose. | ChEMBL. | 1552506 |
Inhibition (functional) | = 15.4 % | Compound was tested for the inhibition of rat reversed passive Arthus pleurisy after peroral administration of 100 mg/kg dose at 3.77*10e6 no of cells with 3.86*10e6 cells of control | ChEMBL. | 1552506 |
Inhibition (functional) | = 18.1 % | Compound was tested for the inhibition of rat reversed passive Arthus pleurisy after peroral administration of 100 mg/kg dose at 0.64 mL of exudate volume with 0.79 mL of control (injected intrapleurally) | ChEMBL. | 1552506 |
Swelling (functional) | = 66.3 % | Antiinflammatory activity of the compound on Zymosan-induced rat's paw edema(ZPE) after peroral administration of 100 mg/kg dose with control swelling of 69.5% | ChEMBL. | 1552506 |
Swelling (functional) | = 69.9 % | Antiinflammatory activity of the compound on Carrageenan rat's paw edema(CPE) after peroral administration of 100 mg/kg dose with control swelling of 63.7% | ChEMBL. | 1552506 |
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.