Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Onchocerca volvulus | 0.2414 | 0.1336 | 0.1739 | |
Schistosoma mansoni | serine-rich repeat protein | 0.2517 | 0.1438 | 0.0693 |
Echinococcus granulosus | voltage dependent calcium channel subunit | 1.0717 | 0.9565 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.3147 | 0.2062 | 0.2062 |
Loa Loa (eye worm) | hypothetical protein | 0.3147 | 0.2062 | 0.2062 |
Onchocerca volvulus | 0.3147 | 0.2062 | 0.2684 | |
Echinococcus multilocularis | voltage dependent calcium channel subunit | 1.0717 | 0.9565 | 1 |
Brugia malayi | Trypsin family protein | 0.3147 | 0.2062 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.2158 | 0.1081 | 0.1081 |
Onchocerca volvulus | 0.8817 | 0.7681 | 1 | |
Schistosoma mansoni | dihydropyridine-sensitive l-type calcium channel | 0.4675 | 0.3576 | 1 |
Brugia malayi | Cache domain containing protein | 0.2158 | 0.1081 | 0.5245 |
Loa Loa (eye worm) | hypothetical protein | 1.1156 | 1 | 1 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.3147 | 0.2062 | 0.3407 |
Schistosoma mansoni | hypothetical protein | 0.2517 | 0.1438 | 0.0693 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.3147 | 0.2062 | 0.3407 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 5.54 uM | In vitro Inhibitory concentration against HL-60 human leukemia cell line; Tested by trypan blue exclusion test | ChEMBL. | 15953727 |
IC50 (functional) | = 24.36 uM | In vitro Inhibitory concentration against BEL-7402 human hepatocarcinoma cell line; Tested by sulforhodamine B colorimetric assay | ChEMBL. | 15953727 |
IC50 (functional) | = 32.99 uM | In vitro Inhibitory concentration against 3AO human ovarian carcinoma cell line; Tested by sulforhodamine B colorimetric assay | ChEMBL. | 15953727 |
IC50 (functional) | = 169.26 uM | In vitro Inhibitory Concentration against A549 human lung carcinoma cell line; Tested by sulforhodamine B colorimetric assay | ChEMBL. | 15953727 |
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.