Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | intestinal type alkaline phosphatase 1 | 0.0925 | 0.9554 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.033 | 0.0757 | 0.5 |
Echinococcus granulosus | alkaline phosphatase | 0.0925 | 0.9554 | 0.5 |
Schistosoma mansoni | 23-cyclic-nucleotide 2-phosphodiesterase | 0.046 | 0.2685 | 0.2192 |
Echinococcus granulosus | alkaline phosphatase intestinal gene 2 | 0.0925 | 0.9554 | 0.5 |
Echinococcus multilocularis | intestinal type alkaline phosphatase | 0.0925 | 0.9554 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0481 | 0.2988 | 0.2536 |
Brugia malayi | Trypsin family protein | 0.033 | 0.0757 | 0.5 |
Treponema pallidum | 5'-nucleotidase (ushA) | 0.0461 | 0.2705 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.033 | 0.0757 | 0.5 |
Echinococcus multilocularis | alkaline phosphatase | 0.0925 | 0.9554 | 0.5 |
Schistosoma mansoni | alkaline phosphatase | 0.0925 | 0.9554 | 1 |
Onchocerca volvulus | 0.033 | 0.0757 | 0.0757 | |
Echinococcus granulosus | intestinal type alkaline phosphatase 1 | 0.0925 | 0.9554 | 0.5 |
Echinococcus multilocularis | alkaline phosphatase, intestinal, gene 2 | 0.0925 | 0.9554 | 0.5 |
Schistosoma mansoni | 23-cyclic-nucleotide 2-phosphodiesterase | 0.0461 | 0.2705 | 0.2214 |
Toxoplasma gondii | 5'-nucleotidase, C-terminal domain-containing protein | 0.0461 | 0.2705 | 0.5 |
Echinococcus granulosus | intestinal type alkaline phosphatase | 0.0925 | 0.9554 | 0.5 |
Schistosoma mansoni | alkaline phosphatase | 0.0925 | 0.9554 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | > 100 uM | In vitro cytotoxicity against murine Leukemia L1210 cells. | ChEMBL. | 10229634 |
IC50 (functional) | > 100 uM | In vitro cytotoxicity of the compound against human oral epidermoid carcinoma KB cells. | ChEMBL. | 10229634 |
IC50 (functional) | > 100 uM | In vitro cytotoxicity against murine Leukemia L1210 cells. | ChEMBL. | 10229634 |
IC50 (functional) | > 100 uM | In vitro cytotoxicity of the compound against human oral epidermoid carcinoma KB cells. | ChEMBL. | 10229634 |
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.