Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | tachykinin peptides receptor 99D | 0.0432 | 0.613 | 0.5 |
Mycobacterium leprae | Probable S-nitrosomycothiol reductase MscR | 0.0212 | 0.2416 | 1 |
Mycobacterium tuberculosis | Probable zinc-type alcohol dehydrogenase AdhD (aldehyde reductase) | 0.0212 | 0.2416 | 0.2733 |
Loa Loa (eye worm) | alcohol dehydrogenase class III | 0.0212 | 0.2416 | 1 |
Mycobacterium ulcerans | zinc-dependent alcohol dehydrogenase | 0.0212 | 0.2416 | 0.2416 |
Mycobacterium tuberculosis | Probable zinc-type alcohol dehydrogenase (E subunit) AdhE1 | 0.0186 | 0.198 | 0.224 |
Onchocerca volvulus | Putative alcohol dehydrogenase | 0.0212 | 0.2416 | 1 |
Mycobacterium ulcerans | zinc-containing alcohol dehydrogenase NAD-dependent AdhB | 0.0212 | 0.2416 | 0.2416 |
Brugia malayi | Alcohol dehydrogenase class III | 0.0212 | 0.2416 | 1 |
Mycobacterium ulcerans | zinc-type alcohol dehydrogenase AdhD | 0.0212 | 0.2416 | 0.2416 |
Mycobacterium ulcerans | zinc-containing alcohol dehydrogenase NAD dependent AdhB | 0.0212 | 0.2416 | 0.2416 |
Wolbachia endosymbiont of Brugia malayi | O-methyltransferase | 0.0069 | 0 | 0.5 |
Mycobacterium tuberculosis | Possible zinc-containing alcohol dehydrogenase NAD dependent AdhB | 0.0186 | 0.198 | 0.224 |
Mycobacterium ulcerans | zinc-dependent alcohol dehydrogenase AdhE2 | 0.0212 | 0.2416 | 0.2416 |
Schistosoma mansoni | alcohol dehydrogenase | 0.0212 | 0.2416 | 1 |
Toxoplasma gondii | Zn-containing alcohol dehydrogenase | 0.0212 | 0.2416 | 0.5 |
Mycobacterium tuberculosis | Probable catechol-O-methyltransferase | 0.0593 | 0.8842 | 1 |
Echinococcus multilocularis | tachykinin peptides receptor 99D | 0.0432 | 0.613 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 4.8 uM | Cytotoxicity against human SK-N-SH cells after 72 hrs by MTT assay | ChEMBL. | 18164206 |
IC50 (functional) | = 4.8 uM | Cytotoxicity against human SK-N-SH cells after 72 hrs by MTT assay | ChEMBL. | 18164206 |
IC50 (functional) | = 4.8 uM | Cytotoxicity against human SK-N-SH cells after 72 hrs by MTT assay | ChEMBL. | 19819703 |
IC50 (functional) | = 6.9 uM | Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay | ChEMBL. | 18164206 |
IC50 (functional) | = 6.9 uM | Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay | ChEMBL. | 18164206 |
IC50 (functional) | = 6.9 uM | Cytotoxicity against human HeLa cells after 72 hrs by MTT assay | ChEMBL. | 19819703 |
IC50 (functional) | = 7.3 uM | Cytotoxicity against human HeLa cells after 72 hrs by MTT assay | ChEMBL. | 18164206 |
IC50 (functional) | = 7.3 uM | Cytotoxicity against human HeLa cells after 72 hrs by MTT assay | ChEMBL. | 18164206 |
IC50 (functional) | = 7.3 uM | Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay | ChEMBL. | 19819703 |
Species name | Source | Reference | Is orphan |
---|---|---|---|
Homo sapiens | ChEMBL23 | 18164206 |
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.