Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | jun-related protein | 0.0068 | 0.1276 | 0.5 |
Echinococcus granulosus | Basic leucine zipper bZIP transcription factor | 0.0083 | 1 | 0.5 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription factor | 0.0083 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0081 | 0.8724 | 0.5 |
Echinococcus multilocularis | jun protein | 0.0083 | 1 | 0.5 |
Echinococcus granulosus | jun protein | 0.0083 | 1 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0068 | 0.1276 | 0.5 |
Onchocerca volvulus | 0.0065 | 0 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Half duration (functional) | = 58 min | Antihypertensive activity by the increase in the vertebral blood flow in anesthetized dogs expressed as duration of half of the maximum change in blood flow. | ChEMBL. | 1995892 |
Increase in CBF (functional) | > 0.5 ml min-1 | Increase in the coronary blood flow (CBF) was determined in isolated guinea pig heart at a dose of 30 microg/heart | ChEMBL. | 1995892 |
Potency ratio (functional) | = 0.16 | Antihypertensive activity expressed as the ratio of the potency evaluated by increased vertebral blood flow (VBF) of the compound to that of diltiazem. | ChEMBL. | 1995892 |
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.