Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | jun-related protein | 0.007 | 0.5531 | 0.5 |
Onchocerca volvulus | 0.0067 | 0.4877 | 0.5 | |
Echinococcus granulosus | Basic leucine zipper bZIP transcription factor | 0.0086 | 1 | 0.5 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription factor | 0.0086 | 1 | 0.5 |
Echinococcus multilocularis | jun protein | 0.0086 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0083 | 0.9346 | 1 |
Brugia malayi | hypothetical protein | 0.0067 | 0.4877 | 0.4877 |
Schistosoma mansoni | hypothetical protein | 0.007 | 0.5531 | 0.5 |
Echinococcus granulosus | jun protein | 0.0086 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Potency (functional) | = 28.1838 um | PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1). (Class of assay: confirmatory) [Related pubchem assays: 1030 (qHTS Validation Assay for Inhibitors of aldehyde dehydrogenase 1 (ALDH1A1))] | ChEMBL. | No reference |
Potency (functional) | 100 uM | PUBCHEM_BIOASSAY: HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488962] | ChEMBL. | No reference |
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.