Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Onchocerca volvulus | Ribonuclease H1 homolog | 0.0637 | 0.2515 | 1 |
Schistosoma mansoni | protein kinase | 0.0054 | 0.0025 | 0.0024 |
Trypanosoma cruzi | ribonuclease H1, putative | 0.0637 | 0.2515 | 1 |
Trichomonas vaginalis | reverse transcriptase [C. elegans], putative | 0.0054 | 0.0025 | 0.0099 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0054 | 0.0026 | 0.0025 |
Brugia malayi | RNase H family protein | 0.0637 | 0.2515 | 1 |
Trypanosoma brucei | RNA helicase, putative | 0.2388 | 1 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0054 | 0.0025 | 0.0024 |
Mycobacterium tuberculosis | Possible maturase | 0.0054 | 0.0025 | 0.5 |
Echinococcus multilocularis | ribonuclease H1 | 0.0637 | 0.2515 | 1 |
Entamoeba histolytica | protein kinase, putative | 0.0095 | 0.0199 | 0.5 |
Treponema pallidum | ribonuclease H (rnhA) | 0.0637 | 0.2515 | 0.5 |
Brugia malayi | Ribonuclease 2-5A family protein | 0.0095 | 0.0199 | 0.0697 |
Brugia malayi | RNase H family protein | 0.0637 | 0.2515 | 1 |
Trichomonas vaginalis | reverse transcriptases, putative | 0.0054 | 0.0025 | 0.0099 |
Trichomonas vaginalis | ribonuclease H1, putative | 0.0637 | 0.2515 | 1 |
Toxoplasma gondii | ribonuclease HI protein | 0.0637 | 0.2515 | 0.5 |
Trypanosoma brucei | ingi protein (ORF1) | 0.0691 | 0.2747 | 0.2728 |
Echinococcus granulosus | serine:threonine protein kinase:endoribonuclease | 0.0095 | 0.0199 | 0.0697 |
Trypanosoma brucei | ingi protein (ORF1) | 0.0691 | 0.2747 | 0.2728 |
Leishmania major | ribonuclease H1, putative | 0.0637 | 0.2515 | 0.5 |
Schistosoma mansoni | scy1(yeast) protein kinase-like | 0.0054 | 0.0025 | 0.0024 |
Trypanosoma cruzi | ribonuclease H1, putative | 0.0637 | 0.2515 | 1 |
Echinococcus multilocularis | serine:threonine protein kinase:endoribonuclease | 0.0095 | 0.0199 | 0.0697 |
Trichomonas vaginalis | NeSL-1_NeSL reverse transcriptases, putative | 0.0054 | 0.0025 | 0.0099 |
Loa Loa (eye worm) | IRE protein kinase | 0.0095 | 0.0199 | 0.5 |
Wolbachia endosymbiont of Brugia malayi | ribonuclease HI | 0.0637 | 0.2515 | 0.5 |
Trypanosoma brucei | retrotransposon hot spot protein 4 (RHS4), interrupted | 0.0691 | 0.2747 | 0.2728 |
Schistosoma mansoni | phosphoglucomutase | 0.0637 | 0.2515 | 0.2514 |
Giardia lamblia | Ribonuclease H | 0.0637 | 0.2515 | 1 |
Trichomonas vaginalis | reverse transcriptases, putative | 0.0054 | 0.0025 | 0.0099 |
Brugia malayi | RNase H family protein | 0.0637 | 0.2515 | 1 |
Schistosoma mansoni | phosphoglucomutase | 0.0637 | 0.2515 | 0.2514 |
Schistosoma mansoni | hypothetical protein | 0.0054 | 0.0025 | 0.0024 |
Trypanosoma brucei | hypothetical protein, conserved | 0.0691 | 0.2747 | 0.2728 |
Trypanosoma brucei | unspecified product | 0.0691 | 0.2747 | 0.2728 |
Schistosoma mansoni | phosphoglucomutase | 0.0637 | 0.2515 | 0.2514 |
Trypanosoma brucei | ribonuclease H1 | 0.0637 | 0.2515 | 0.2497 |
Echinococcus granulosus | ribonuclease H1 | 0.0637 | 0.2515 | 1 |
Entamoeba histolytica | protein kinase, putative | 0.0095 | 0.0199 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
EC50 (functional) | nM | Effective concentration required for inhibition of interleukin-6 in mouse thioglycolate-elicited peritoneal exudate cell line using 49% radiolabeled dexamethasone; ND=not determined because single point inhibition at 3 uM was observed | ChEMBL. | 15911283 |
EC50 (functional) | 0 nM | Effective concentration required for induction of tyrosine aminotransferase in human HepG2 cells using 8% radiolabeled dexamethasone; ND.=not determined | ChEMBL. | 15911283 |
EC50 (functional) | 0 nM | Effective concentration required for induction of glutamine synthetase in human skeletal muscle cells using 0% radiolabeled dexamethasone; ND.=not determined | ChEMBL. | 15911283 |
EC50 (functional) | 0 nM | Effective concentration required for inhibition of interleukin-6 in human A549 lung carcinoma cell line using 20% radiolabeled dexamethasone; ND.=not determined because single point inhibition at 3 uM was observed | ChEMBL. | 15911283 |
EC50 (functional) | 0 nM | Effective concentration required for inhibition of interleukin-6 in mouse thioglycolate-elicited peritoneal exudate cell line using 49% radiolabeled dexamethasone; ND=not determined because single point inhibition at 3 uM was observed | ChEMBL. | 15911283 |
IC50 (binding) | = 65 nM | Inhibition of human glucocorticoid receptor alpha isoform | ChEMBL. | 15911283 |
IC50 (binding) | = 65 nM | Inhibition of human glucocorticoid receptor alpha isoform | ChEMBL. | 15911283 |
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.