Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | progesterone receptor | Starlite/ChEMBL | References |
Homo sapiens | nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) | Starlite/ChEMBL | References |
Homo sapiens | nuclear receptor subfamily 3, group C, member 2 | Starlite/ChEMBL | References |
Homo sapiens | androgen receptor | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | steroid hormone receptor | 0.004 | 0.5 | 0.5 |
Brugia malayi | nuclear hormone receptor | 0.004 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-40 | 0.004 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-1 | 0.004 | 0.5 | 0.5 |
Echinococcus granulosus | ecdysone induced protein 78C | 0.004 | 0.5 | 0.5 |
Echinococcus multilocularis | nuclear receptor 2DBD gamma | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-49 | 0.004 | 0.5 | 0.5 |
Brugia malayi | Ligand-binding domain of nuclear hormone receptor family protein | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear Hormone Receptor family member | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | nuclear receptor 2DBD-gamma | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | Tr4/Tr2 (homologue) | 0.004 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-19 | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | FTZ-F1 nuclear receptor-like protein | 0.004 | 0.5 | 0.5 |
Brugia malayi | Steroid receptor seven-up type 2 | 0.004 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-14 | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | nuclear hormone receptor | 0.004 | 0.5 | 0.5 |
Echinococcus multilocularis | ecdysone induced protein 78C | 0.004 | 0.5 | 0.5 |
Onchocerca volvulus | Steroid hormone receptor family member cnr14 homolog | 0.004 | 0.5 | 0.5 |
Echinococcus granulosus | nuclear receptor 2DBD gamma | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | photoreceptor-specific nuclear receptor related | 0.004 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor-like 1 | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-40 | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | nuclear hormone receptor nor-1/nor-2 | 0.004 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-19 | 0.004 | 0.5 | 0.5 |
Echinococcus multilocularis | nuclear receptor 2DBD gamma | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.004 | 0.5 | 0.5 |
Brugia malayi | nuclear receptor NHR-88 | 0.004 | 0.5 | 0.5 |
Echinococcus multilocularis | thyroid hormone receptor alpha | 0.004 | 0.5 | 0.5 |
Echinococcus granulosus | Nuclear hormone receptor family member nhr 41 | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-14 | 0.004 | 0.5 | 0.5 |
Echinococcus granulosus | FTZ F1 alpha | 0.004 | 0.5 | 0.5 |
Brugia malayi | Ligand-binding domain of nuclear hormone receptor family protein | 0.004 | 0.5 | 0.5 |
Echinococcus multilocularis | FTZ F1 alpha | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-41 | 0.004 | 0.5 | 0.5 |
Echinococcus granulosus | nuclear receptor 2DBD gamma | 0.004 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-31 | 0.004 | 0.5 | 0.5 |
Echinococcus multilocularis | COUP TF:Svp nuclear hormone receptor | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | retinoic acid receptor RXR | 0.004 | 0.5 | 0.5 |
Echinococcus multilocularis | FTZ F1 nuclear receptor protein | 0.004 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-25 | 0.004 | 0.5 | 0.5 |
Onchocerca volvulus | Protein ultraspiracle homolog | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | thyroid hormone receptor | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-1 | 0.004 | 0.5 | 0.5 |
Echinococcus granulosus | retinoic acid receptor rxr beta a | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.004 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-41 | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | RAR-like nuclear receptor | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | thyroid hormone receptor | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | steroid hormone receptor | 0.004 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-25 | 0.004 | 0.5 | 0.5 |
Echinococcus granulosus | FTZ F1 nuclear receptor protein | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | coup transcription factor | 0.004 | 0.5 | 0.5 |
Brugia malayi | photoreceptor-specific nuclear receptor | 0.004 | 0.5 | 0.5 |
Echinococcus granulosus | COUP TF:Svp nuclear hormone receptor | 0.004 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-49 | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | steroid hormone receptor ad4bp | 0.004 | 0.5 | 0.5 |
Schistosoma mansoni | retinoid-x-receptor (RXR) | 0.004 | 0.5 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-31 | 0.004 | 0.5 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-3 | 0.004 | 0.5 | 0.5 |
Onchocerca volvulus | Bile acid receptor homolog | 0.004 | 0.5 | 0.5 |
Onchocerca volvulus | 0.004 | 0.5 | 0.5 | |
Echinococcus granulosus | hepatocyte nuclear factor 4 alpha | 0.004 | 0.5 | 0.5 |
Echinococcus multilocularis | Nuclear hormone receptor family member nhr 41 | 0.004 | 0.5 | 0.5 |
Echinococcus multilocularis | hepatocyte nuclear factor 4 alpha | 0.004 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 5.7 nM | Binding affinity against human Glucocorticoid receptor (GR) using [3H]-dexamethasone as radioligand | ChEMBL. | 15081010 |
IC50 (binding) | = 5.7 nM | Inhibition of [3H]-dexamethasone binding to glucocorticoid receptor | ChEMBL. | 15261264 |
IC50 (binding) | = 5.7 nM | Binding affinity against human Glucocorticoid receptor (GR) using [3H]-dexamethasone as radioligand | ChEMBL. | 15081010 |
IC50 (binding) | = 5.7 nM | Inhibition of [3H]-dexamethasone binding to glucocorticoid receptor | ChEMBL. | 15261264 |
IC50 (functional) | = 210 nM | Functional activity towards human Glucocorticoid receptor in genetically engineered cell line containing glucocorticoid response element and reporter gene encoding a secreted form of alkaline phosphatase | ChEMBL. | 15081010 |
IC50 (functional) | = 210 nM | Inhibition of glucocorticoid receptor dexamethasone response | ChEMBL. | 15261264 |
IC50 (functional) | = 210 nM | Functional activity towards human Glucocorticoid receptor in genetically engineered cell line containing glucocorticoid response element and reporter gene encoding a secreted form of alkaline phosphatase | ChEMBL. | 15081010 |
IC50 (functional) | = 210 nM | Inhibition of glucocorticoid receptor dexamethasone response | ChEMBL. | 15261264 |
IC50 (binding) | = 300 nM | Displacement of [3H]-dexamethasone from human androgen receptor | ChEMBL. | 15081010 |
IC50 (binding) | = 300 nM | Displacement of [3H]-dexamethasone from human androgen receptor | ChEMBL. | 15081010 |
IC50 (binding) | = 790 nM | Displacement of [3H]-dexamethasone from human progesterone receptor | ChEMBL. | 15081010 |
IC50 (binding) | = 790 nM | Displacement of [3H]-dexamethasone from human progesterone receptor | ChEMBL. | 15081010 |
IC50 (binding) | = 4000 nM | Displacement of [3H]-dexamethasone from human mineralocorticoid receptor | ChEMBL. | 15081010 |
IC50 (binding) | = 4000 nM | Displacement of [3H]-dexamethasone from human mineralocorticoid receptor | ChEMBL. | 15081010 |
T1/2 (ADMET) | 0 min | Half-life of the compound was determined in rat microsomes; not determined | ChEMBL. | 15261264 |
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.