Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | retinoic acid receptor rxr beta a | 0.0159 | 0.0359 | 0.5 |
Echinococcus multilocularis | retinoic acid receptor rxr beta a retinoic acid receptor rxr alpha a retinoic acid receptor rxr alpha | 0.0136 | 0 | 0.5 |
Loa Loa (eye worm) | nuclear receptor nhr-7B | 0.0765 | 0.9641 | 1 |
Schistosoma mansoni | retinoic acid receptor RXR | 0.0159 | 0.0359 | 0.5 |
Brugia malayi | nuclear hormone receptor | 0.0765 | 0.9641 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (functional) | = 0 | Anticonvulsant activity was evaluated by subcutaneous pentylenetetrazole (Metrazol) (sc Met) seizure test at dose 600 mg/kg; No activity | ChEMBL. | 3989820 |
Activity (functional) | = 0 | Anticonvulsant activity was evaluated by Neurologic toxicity (the rotorod test) at dose 600 mg/kg; No activity | ChEMBL. | 3989820 |
Activity (functional) | = 0 | Anticonvulsant activity was evaluated by maximal electroshock seizure (MES) test at dose 600 mg/kg; No activity | ChEMBL. | 3989820 |
Activity (functional) | = 0 | Anticonvulsant activity was evaluated by maximal electroshock seizure (MES) test at dose 600 mg/kg; No activity | ChEMBL. | 3989820 |
Activity (functional) | = 0 | Anticonvulsant activity was evaluated by subcutaneous pentylenetetrazole (Metrazol) (sc Met) seizure test at dose 600 mg/kg; No activity | ChEMBL. | 3989820 |
Activity (functional) | = 0 | Anticonvulsant activity was evaluated by Neurologic toxicity (the rotorod test) at dose 600 mg/kg; No activity | ChEMBL. | 3989820 |
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.