Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0072 | 1 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0072 | 1 | 1 |
Onchocerca volvulus | 0.0072 | 1 | 0.5 | |
Loa Loa (eye worm) | hypothetical protein | 0.0072 | 1 | 1 |
Brugia malayi | SEA domain containing protein | 0.0072 | 1 | 1 |
Onchocerca volvulus | 0.0072 | 1 | 0.5 | |
Onchocerca volvulus | 0.0072 | 1 | 0.5 | |
Onchocerca volvulus | 0.0072 | 1 | 0.5 | |
Onchocerca volvulus | 0.0072 | 1 | 0.5 | |
Loa Loa (eye worm) | DOMON domain-containing protein | 0.0072 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | > 100 uM | Antiproliferative activity against human MCF7 cells after 72 hrs by MTT assay | ChEMBL. | 24835982 |
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.