Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | Trypsin family protein | 0.0098 | 0.0475 | 0.5 |
Schistosoma mansoni | sphingosine kinase A B | 0.0317 | 1 | 1 |
Schistosoma mansoni | sphingoid long chain base kinase | 0.0317 | 1 | 1 |
Onchocerca volvulus | 0.0098 | 0.0475 | 1 | |
Mycobacterium ulcerans | hypothetical protein | 0.0317 | 1 | 0.5 |
Entamoeba histolytica | hypothetical protein, conserved | 0.0317 | 1 | 0.5 |
Mycobacterium tuberculosis | Conserved protein | 0.0317 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0317 | 1 | 1 |
Echinococcus multilocularis | sphingosine kinase 1 | 0.0317 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Potency (functional) | 89.1251 uM | PubChem BioAssay. qHTS of PTHR Inhibitors: Primary Screen. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 100 uM | PUBCHEM_BIOASSAY: Inhibitors of TCP-1 ring complex (TRiC) of Methanococcus maripaludis (MmCpn): qHTS. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488991] | 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.