Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | Copper type II ascorbate-dependent monooxygenase, C-terminal domain containing protein | 0.0123 | 0.3581 | 0.3581 |
Echinococcus multilocularis | peptidyl glycine alpha amidating monooxygenase | 0.0231 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0231 | 1 | 1 |
Schistosoma mansoni | peptidyl-glycine monooxygenase | 0.0231 | 1 | 1 |
Echinococcus granulosus | peptidyl glycine alpha amidating monooxygenase | 0.0231 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
LC50 (ADMET) | 0 | Cytotoxicity against rat N-ras transformed NRK N/4.2 cells after 5 days | ChEMBL. | 17035024 |
LC50 (ADMET) | = 20 uM | Cytotoxicity against rat H-ras transformed NRK H/1.2 cells after 5 days | ChEMBL. | 17035024 |
LC50 (ADMET) | = 21.5 uM | Cytotoxicity against rat NRK 52E cells after 5 days | ChEMBL. | 17035024 |
LC50 (ADMET) | > 33 uM | Cytotoxicity against rat K-ras transformed NRK K/1 cells after 5 days | ChEMBL. | 17035024 |
LC50 (ADMET) | > 33 uM | Cytotoxicity against mouse 3LL cells after 5 days | ChEMBL. | 17035024 |
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.