Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Leishmania major | fatty-acid desaturase, putative | 0.195 | 1 | 0.5 |
Onchocerca volvulus | 0.195 | 1 | 0.5 | |
Plasmodium falciparum | stearoyl-CoA desaturase | 0.1765 | 0.8695 | 0.5 |
Mycobacterium tuberculosis | Possible penicillin-binding protein | 0.053 | 0 | 0.5 |
Onchocerca volvulus | 0.195 | 1 | 0.5 | |
Trypanosoma brucei | fatty acid desaturase, putative | 0.195 | 1 | 0.5 |
Brugia malayi | acyl-CoA desaturase | 0.1765 | 0.8695 | 0.5 |
Loa Loa (eye worm) | acyl-CoA desaturase | 0.1765 | 0.8695 | 0.5 |
Plasmodium vivax | stearoyl-CoA desaturase (acyl-CoA desaturase, faty acid desaturase), putative | 0.1765 | 0.8695 | 0.5 |
Trypanosoma cruzi | fatty acid desaturase, putative | 0.195 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IZ (functional) | = 0 mm | Antibacterial activity against Escherichia coli at 50 uL/well by well diffusion assay | ChEMBL. | 21185109 |
IZ (functional) | = 0 mm | Antifungal activity against Candida albicans at 50 uL/well by well diffusion assay | ChEMBL. | 21185109 |
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.