Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | ryanodine receptor 44f | 0.0343 | 0.1645 | 1 |
Schistosoma mansoni | inositol 145-trisphosphate receptor | 0.0596 | 0.7075 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.039 | 0.2657 | 0.3809 |
Leishmania major | hypothetical protein, conserved | 0.0275 | 0.0189 | 0.5 |
Echinococcus multilocularis | ryanodine receptor 44f | 0.0343 | 0.1645 | 1 |
Schistosoma mansoni | ryanodine receptor related | 0.0479 | 0.457 | 0.4331 |
Trypanosoma cruzi | inositol 1,4,5-trisphosphate receptor, putative | 0.0404 | 0.2962 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0458 | 0.4113 | 0.9289 |
Trypanosoma brucei | inositol 1,4,5-trisphosphate receptor | 0.0404 | 0.2962 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0467 | 0.4302 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Arrhythmias times (functional) | = 429 | Effect of the compound (30 mg/kg, iv) on coronary reperfusion-induced arrhythmias was assessed in anesthetized rats.(Intervals of ventricular tachycardia (VT)+ventricular fibrillation (VF) within 600 s. | ChEMBL. | 1578489 |
Inhibition (functional) | = 1 % | Inhibition of lipid peroxidation in rat liver microsomes. | ChEMBL. | 1578489 |
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.