Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.1433 | 1 | 1 |
Echinococcus granulosus | nuclear factor of activated T cells 5 | 0.0483 | 0.2904 | 1 |
Echinococcus multilocularis | Ankyrin | 0.0095 | 0.0006 | 0.0021 |
Onchocerca volvulus | 0.1433 | 1 | 0.5 | |
Schistosoma mansoni | retinoblastoma-binding protein 4 (rbbp4) | 0.0095 | 0.0006 | 1 |
Echinococcus multilocularis | nuclear factor of activated T cells 5 | 0.0483 | 0.2904 | 1 |
Echinococcus granulosus | Ankyrin | 0.0095 | 0.0006 | 0.0021 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
GI50 (functional) | > 10 uM | Inhibition of the growth of human breast cancer MCF-7 cells done for 2 h at 37 degree C with compound | ChEMBL. | 16078843 |
GI50 (functional) | > 10 uM | Inhibition of the growth of human breast cancer MCF-7 cells done for 2 h at 37 degree C with compound | ChEMBL. | 16078843 |
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.