Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | thyroid hormone receptor | 0.1489 | 0.1731 | 1 |
Echinococcus multilocularis | thyroid hormone receptor alpha | 0.1489 | 0.1731 | 1 |
Echinococcus granulosus | Mitotic checkpoint protein PRCC C terminal | 0.1254 | 0 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor-like 1 | 0.2499 | 0.9184 | 1 |
Schistosoma mansoni | thyroid hormone receptor | 0.1489 | 0.1731 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (binding) | 0 | Induction of pBR322 cross-linking in absence of irradiation by alkaline agarose gel assay | ChEMBL. | 18047263 |
Activity (binding) | 0 | Induction of pBR322 cross-linking after irradiation at 20 mM at pH 5.5 by alkaline agarose gel assay | ChEMBL. | 18047263 |
Activity (binding) | = 2.5 uM | Induction of pBR322 cross-linking after irradiation by alkaline agarose gel assay | ChEMBL. | 18047263 |
CC50 (functional) | > 200 uM | Cytotoxicity against human LoVo cells after 24 hrs by MTT assay | ChEMBL. | 18047263 |
CC50 (functional) | > 200 uM | Cytotoxicity against human LoVo cells after 24 hrs by MTT assay | ChEMBL. | 18047263 |
EC50 (functional) | > 200 uM | Photocytotoxicity against UV irradiated human LoVo cells after 24 hrs by MTT assay | ChEMBL. | 18047263 |
EC50 (functional) | > 200 uM | Photocytotoxicity against UV irradiated human LoVo cells after 24 hrs by MTT assay | ChEMBL. | 18047263 |
LogP | = 4.28 | Partition coefficient, log P of the compound | ChEMBL. | 18047263 |
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.