Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Toxoplasma gondii | PAN domain-containing protein | 0.1232 | 0.7412 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.1277 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.1277 | 1 | 0.5 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.1277 | 1 | 0.5 |
Toxoplasma gondii | PAN domain-containing protein | 0.1232 | 0.7412 | 0.5 |
Onchocerca volvulus | 0.1277 | 1 | 1 | |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.1277 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
MIC (functional) | > 8 uM | Antitubercular activity against Mycobacterium tuberculosis H37Rv by MABA method | ChEMBL. | 21069962 |
MIC (functional) | > 32 uM | Antitubercular activity against Mycobacterium tuberculosis H37Rv by LORA method | ChEMBL. | 21069962 |
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.