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 |
---|---|---|---|---|
Brugia malayi | RNase H family protein | 0.0637 | 0.2515 | 1 |
Trichomonas vaginalis | ribonuclease H1, putative | 0.0637 | 0.2515 | 1 |
Trichomonas vaginalis | reverse transcriptases, putative | 0.0054 | 0.0025 | 0.0099 |
Toxoplasma gondii | ribonuclease HI protein | 0.0637 | 0.2515 | 0.5 |
Brugia malayi | Ribonuclease 2-5A family protein | 0.0095 | 0.0199 | 0.0697 |
Entamoeba histolytica | protein kinase, putative | 0.0095 | 0.0199 | 0.5 |
Treponema pallidum | ribonuclease H (rnhA) | 0.0637 | 0.2515 | 0.5 |
Trypanosoma cruzi | ribonuclease H1, putative | 0.0637 | 0.2515 | 1 |
Schistosoma mansoni | scy1(yeast) protein kinase-like | 0.0054 | 0.0025 | 0.0024 |
Trypanosoma brucei | ingi protein (ORF1) | 0.0691 | 0.2747 | 0.2728 |
Leishmania major | ribonuclease H1, putative | 0.0637 | 0.2515 | 0.5 |
Echinococcus granulosus | serine:threonine protein kinase:endoribonuclease | 0.0095 | 0.0199 | 0.0697 |
Trypanosoma brucei | ingi protein (ORF1) | 0.0691 | 0.2747 | 0.2728 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0054 | 0.0026 | 0.0025 |
Schistosoma mansoni | protein kinase | 0.0054 | 0.0025 | 0.0024 |
Trichomonas vaginalis | reverse transcriptase [C. elegans], putative | 0.0054 | 0.0025 | 0.0099 |
Trypanosoma cruzi | ribonuclease H1, putative | 0.0637 | 0.2515 | 1 |
Onchocerca volvulus | Ribonuclease H1 homolog | 0.0637 | 0.2515 | 1 |
Mycobacterium tuberculosis | Possible maturase | 0.0054 | 0.0025 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0054 | 0.0025 | 0.0024 |
Echinococcus multilocularis | ribonuclease H1 | 0.0637 | 0.2515 | 1 |
Brugia malayi | RNase H family protein | 0.0637 | 0.2515 | 1 |
Trypanosoma brucei | RNA helicase, putative | 0.2388 | 1 | 1 |
Schistosoma mansoni | phosphoglucomutase | 0.0637 | 0.2515 | 0.2514 |
Trypanosoma brucei | unspecified product | 0.0691 | 0.2747 | 0.2728 |
Trypanosoma brucei | hypothetical protein, conserved | 0.0691 | 0.2747 | 0.2728 |
Schistosoma mansoni | hypothetical protein | 0.0054 | 0.0025 | 0.0024 |
Brugia malayi | RNase H family protein | 0.0637 | 0.2515 | 1 |
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 |
Wolbachia endosymbiont of Brugia malayi | ribonuclease HI | 0.0637 | 0.2515 | 0.5 |
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 |
Echinococcus multilocularis | serine:threonine protein kinase:endoribonuclease | 0.0095 | 0.0199 | 0.0697 |
Trichomonas vaginalis | reverse transcriptases, putative | 0.0054 | 0.0025 | 0.0099 |
Giardia lamblia | Ribonuclease H | 0.0637 | 0.2515 | 1 |
Schistosoma mansoni | phosphoglucomutase | 0.0637 | 0.2515 | 0.2514 |
Trypanosoma brucei | retrotransposon hot spot protein 4 (RHS4), interrupted | 0.0691 | 0.2747 | 0.2728 |
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 46% 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 2% 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 7% 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 2% 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 46% radiolabeled dexamethasone; ND.=not determined because single point inhibition at 3 uM was observed | ChEMBL. | 15911283 |
IC50 (binding) | = 12 nM | Inhibition of human glucocorticoid receptor alpha isoform | ChEMBL. | 15911283 |
IC50 (binding) | = 12 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.