Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | jun proto-oncogene | Starlite/ChEMBL | References |
Homo sapiens | v-rel avian reticuloendotheliosis viral oncogene homolog A | References | |
Homo sapiens | nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target/s | Ortholog Group |
---|---|---|---|
Echinococcus multilocularis | jun protein | Get druggable targets OG5_131442 | All targets in OG5_131442 |
Echinococcus granulosus | jun protein | Get druggable targets OG5_131442 | All targets in OG5_131442 |
Loa Loa (eye worm) | hypothetical protein | Get druggable targets OG5_131442 | All targets in OG5_131442 |
Brugia malayi | bZIP transcription factor family protein | Get druggable targets OG5_131442 | All targets in OG5_131442 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription factor | Get druggable targets OG5_131442 | All targets in OG5_131442 |
Echinococcus granulosus | Basic leucine zipper bZIP transcription factor | Get druggable targets OG5_131442 | All targets in OG5_131442 |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | Basic leucine zipper bZIP transcription factor | 0.0101 | 0.337 | 0.337 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription factor | 0.0101 | 0.337 | 0.337 |
Echinococcus multilocularis | Ankyrin | 0.0018 | 0.0006 | 0.0006 |
Schistosoma mansoni | jun-related protein | 0.0082 | 0.2608 | 1 |
Onchocerca volvulus | 0.008 | 0.2497 | 0.5 | |
Brugia malayi | bZIP transcription factor family protein | 0.0101 | 0.337 | 1 |
Echinococcus multilocularis | nuclear factor of activated T cells 5 | 0.0267 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0099 | 0.3258 | 1 |
Schistosoma mansoni | retinoblastoma-binding protein 4 (rbbp4) | 0.0018 | 0.0006 | 0.0023 |
Echinococcus granulosus | Ankyrin | 0.0018 | 0.0006 | 0.0006 |
Echinococcus granulosus | jun protein | 0.0101 | 0.337 | 0.337 |
Echinococcus multilocularis | jun protein | 0.0101 | 0.337 | 0.337 |
Schistosoma mansoni | hypothetical protein | 0.0082 | 0.2608 | 1 |
Brugia malayi | hypothetical protein | 0.008 | 0.2497 | 0.7409 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 0.2 uM | Concentration required to inhibit activator protein-1(AP-1) mediated transcriptional activation in human Jurkat T-cells | ChEMBL. | 11052805 |
IC50 (binding) | = 0.2 uM | Concentration required to inhibit activator protein-1(AP-1) mediated transcriptional activation in human Jurkat T-cells | ChEMBL. | 11052805 |
IC50 (binding) | = 0.2 uM | Inhibition of AP-1-mediated transcriptional activation in human Jurkat cells by luciferase reporter gene assay | ChEMBL. | 24831826 |
IC50 (binding) | = 0.6 uM | Concentration required to inhibit nuclear factor-kappa B) mediated transcriptional activation in human Jurkat T-cells. | ChEMBL. | 11052805 |
IC50 (binding) | = 0.6 uM | Concentration required to inhibit nuclear factor-kappa B) mediated transcriptional activation in human Jurkat T-cells. | ChEMBL. | 11052805 |
IC50 (binding) | = 0.6 uM | Inhibition of NF-kappaB-mediated transcriptional activation in human Jurkat cells by luciferase reporter gene assay | ChEMBL. | 24831826 |
Permeability (ADMET) | = 0.0000031 cm s-1 | Compound was tested for permeability in Caco-2 cells by HPLC method | ChEMBL. | 11052805 |
Permeability (ADMET) | = 0.0000031 cm s-1 | Compound was tested for permeability in Caco-2 cells by HPLC method | ChEMBL. | 11052805 |
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.