Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | sodium bile acid cotransporter | 0.0423 | 1 | 1 |
Loa Loa (eye worm) | TAR-binding protein | 0.0067 | 0.0386 | 0.0386 |
Echinococcus multilocularis | sodium bile acid cotransporter | 0.0423 | 1 | 1 |
Onchocerca volvulus | 0.0423 | 1 | 0.5 | |
Brugia malayi | RNA recognition motif domain containing protein | 0.0067 | 0.0386 | 0.0386 |
Schistosoma mansoni | sodium-bile acid cotransporter related | 0.0172 | 0.3207 | 0.2934 |
Echinococcus granulosus | sodium bile acid cotransporter | 0.0423 | 1 | 1 |
Schistosoma mansoni | sodium-bile acid cotransporter | 0.0252 | 0.5367 | 0.518 |
Echinococcus multilocularis | sodium bile acid cotransporter | 0.0423 | 1 | 1 |
Brugia malayi | TAR-binding protein | 0.0067 | 0.0386 | 0.0386 |
Echinococcus multilocularis | sodium bile acid cotransporter | 0.0423 | 1 | 1 |
Echinococcus granulosus | sodium bile acid cotransporter | 0.0423 | 1 | 1 |
Schistosoma mansoni | sodium-bile acid cotransporter related | 0.0423 | 1 | 1 |
Loa Loa (eye worm) | RNA binding protein | 0.0067 | 0.0386 | 0.0386 |
Loa Loa (eye worm) | hypothetical protein | 0.0423 | 1 | 1 |
Loa Loa (eye worm) | RNA recognition domain-containing protein domain-containing protein | 0.0067 | 0.0386 | 0.0386 |
Brugia malayi | RNA binding protein | 0.0067 | 0.0386 | 0.0386 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
pKa (ADMET) | = 7.28 | Acid dissociation constant was determined | ChEMBL. | 7277388 |
Suppression (functional) | = 5 % | Immunological activity in mice as the percentage of suppression of the cellular response to EI4 tumor cells at 10 mg/kg | ChEMBL. | 7277388 |
Suppression (functional) | = 5 % | Immunological activity in mice as the percentage of suppression of the cellular response to EI4 tumor cells at 10 mg/kg | ChEMBL. | 7277388 |
Suppression (functional) | = 51 % | Compound was evaluated for immunological activity in mice as the percentage of suppression of the humoral response to EI4 tumor cells at 10 mg/kg, po | ChEMBL. | 7277388 |
Suppression (functional) | = 51 % | Compound was evaluated for immunological activity in mice as the percentage of suppression of the humoral response to EI4 tumor cells at 10 mg/kg, po | ChEMBL. | 7277388 |
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.