Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | transient receptor potential cation channel | 0.0072 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0072 | 0.5 | 0.5 |
Echinococcus granulosus | transient receptor potential cation channel | 0.0072 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0072 | 0.5 | 0.5 |
Echinococcus granulosus | transient receptor potential cation channel | 0.0072 | 0.5 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0072 | 0.5 | 0.5 |
Echinococcus multilocularis | transient receptor potential cation channel | 0.0072 | 0.5 | 0.5 |
Echinococcus multilocularis | transient receptor potential cation channel | 0.0072 | 0.5 | 0.5 |
Schistosoma mansoni | transient receptor potential channel | 0.0072 | 0.5 | 0.5 |
Schistosoma mansoni | transient receptor potential channel | 0.0072 | 0.5 | 0.5 |
Echinococcus granulosus | transient receptor potential cation channel | 0.0072 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Potency (functional) | = 56.2341 um | PUBCHEM_BIOASSAY: qHTS Fluorescence Polarization Assay for Inhibitors of MLL CXXC domain - DNA interaction. (Class of assay: confirmatory) [Related pubchem assays: 2698 (Summary assay.)] | ChEMBL. | No reference |
Potency (functional) | 75.6863 uM | PubChem BioAssay. qHTS Assay to Find Inhibitors of Pin1. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 89.1251 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of Polymerase Iota. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID588623] | 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.