Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | protein cereblon | 0.0316 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0316 | 0.5 | 0.5 |
Entamoeba histolytica | hypothetical protein, conserved | 0.0316 | 0.5 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0316 | 0.5 | 0.5 |
Echinococcus granulosus | protein cereblon | 0.0316 | 0.5 | 0.5 |
Onchocerca volvulus | Protein cereblon homolog | 0.0316 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
ED50 (functional) | = 93.75 mg kg-1 | Anticonvulsant activity in ICR mouse after 30 mins by MES test | ChEMBL. | 18479918 |
ED50 (functional) | = 93.75 mg kg-1 | Anticonvulsant activity in ICR mouse after 30 mins by MES test | ChEMBL. | 18479918 |
ED50 (functional) | = 96.88 mg kg-1 | Anticonvulsant activity against pentylenetetrazole-induced seizure in ICR mouse after 30 mins | ChEMBL. | 18479918 |
ED50 (functional) | = 96.88 mg kg-1 | Anticonvulsant activity against pentylenetetrazole-induced seizure in ICR mouse after 30 mins | ChEMBL. | 18479918 |
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.