Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | tissue type plasminogen activator | 0.1121 | 0.1881 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.3899 | 0.9892 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.1121 | 0.1881 | 0.1902 |
Plasmodium falciparum | cysteine repeat modular protein 1 | 0.1121 | 0.1881 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.1121 | 0.1881 | 0.1881 |
Plasmodium vivax | cysteine repeat modular protein 1, putative | 0.1121 | 0.1881 | 0.5 |
Onchocerca volvulus | 0.343 | 0.8539 | 0.8633 | |
Echinococcus multilocularis | tissue type plasminogen activator | 0.1121 | 0.1881 | 1 |
Brugia malayi | Kringle domain containing protein | 0.1121 | 0.1881 | 0.1902 |
Mycobacterium ulcerans | hypothetical protein | 0.0469 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.3899 | 0.9892 | 1 |
Brugia malayi | Trypsin family protein | 0.3899 | 0.9892 | 1 |
Toxoplasma gondii | PAN domain-containing protein | 0.1497 | 0.2965 | 1 |
Brugia malayi | Protein kinase domain containing protein | 0.1121 | 0.1881 | 0.1902 |
Onchocerca volvulus | 0.1121 | 0.1881 | 0.1902 | |
Trypanosoma cruzi | hypothetical protein, conserved | 0.1121 | 0.1881 | 0.5 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0486 | 0.0048 | 0.0048 |
Leishmania major | hypothetical protein, conserved | 0.1121 | 0.1881 | 0.5 |
Onchocerca volvulus | 0.3899 | 0.9892 | 1 | |
Toxoplasma gondii | PAN domain-containing protein | 0.1497 | 0.2965 | 1 |
Loa Loa (eye worm) | TK/ROR protein kinase | 0.1121 | 0.1881 | 0.1902 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.3899 | 0.9892 | 0.9892 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
ID50 (functional) | 0 mg kg-1 | In vivo potency of the compound determined for AII-induced pressor response in normotensive rats, iv administration; Not tested | ChEMBL. | No reference |
pKB (functional) | = 7.2 | Antagonistic affinity (pKB) against angiotensin II receptor in rabbit aorta. | ChEMBL. | No reference |
pKB (functional) | = 7.2 | Antagonistic affinity (pKB) against angiotensin II receptor in rabbit aorta. | ChEMBL. | No reference |
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.