Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | Lysine-specific histone demethylase 1 | 0.1324 | 0.7881 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.1324 | 0.7881 | 0.8938 |
Brugia malayi | SWIRM domain containing protein | 0.1428 | 0.8817 | 1 |
Mycobacterium tuberculosis | Probable flavin-containing monoamine oxidase AofH (amine oxidase) (MAO) | 0.1217 | 0.6923 | 0.5 |
Echinococcus multilocularis | lysine specific histone demethylase 1A | 0.1324 | 0.7881 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.1428 | 0.8817 | 1 |
Onchocerca volvulus | 0.1428 | 0.8817 | 0.5 | |
Mycobacterium ulcerans | flavin-containing monoamine oxidase AofH | 0.156 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.1324 | 0.7881 | 0.8938 |
Echinococcus granulosus | lysine specific histone demethylase 1A | 0.1324 | 0.7881 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 70 uM | Reversible inhibition of human recombinant AChE using acetylthiocholine iodide as substrate measured at initial time point by Ellmans method | ChEMBL. | 24076173 |
IC50 (binding) | = 110 uM | Reversible inhibition of human recombinant AChE using acetylthiocholine iodide as substrate measured after 2 hrs by Ellmans method | ChEMBL. | 24076173 |
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.