Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0482 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0482 | 1 | 1 |
Echinococcus granulosus | serotonin transporter | 0.0482 | 1 | 0.5 |
Trypanosoma brucei | C-8 sterol isomerase, putative | 0.0358 | 0.5844 | 0.5 |
Schistosoma mansoni | sodium/chloride dependent transporter | 0.0482 | 1 | 0.5 |
Loa Loa (eye worm) | norepinephrine transporter | 0.0482 | 1 | 1 |
Leishmania major | C-8 sterol isomerase-like protein | 0.0358 | 0.5844 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0358 | 0.5844 | 0.5844 |
Loa Loa (eye worm) | serotonin transporter b | 0.0482 | 1 | 1 |
Echinococcus multilocularis | serotonin transporter | 0.0482 | 1 | 0.5 |
Trypanosoma cruzi | C-8 sterol isomerase, putative | 0.0358 | 0.5844 | 0.5 |
Schistosoma mansoni | norepinephrine/norepinephrine transporter | 0.0482 | 1 | 0.5 |
Loa Loa (eye worm) | solute carrier family 6 member 4 | 0.0482 | 1 | 1 |
Onchocerca volvulus | 0.0482 | 1 | 0.5 | |
Loa Loa (eye worm) | hypothetical protein | 0.0482 | 1 | 1 |
Treponema pallidum | sodium- and chloride- dependent transporter | 0.0482 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 5.9 uM | The concentration required for inhibition of Human inducible nitric oxide synthase (iNOS) isoform | ChEMBL. | 11931623 |
IC50 (binding) | = 35 uM | The concentration required for inhibition of Human Neuronal nitric oxide synthase (nNOS) | ChEMBL. | 11931623 |
IC50 (binding) | = 138 uM | The concentration required for inhibition of Human endothelial nitric oxide synthase (eNOS) isoform | ChEMBL. | 11931623 |
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.