Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | histone deacetylase 1 | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | Furin-like cysteine rich region family protein | 0.0537 | 0.0305 | 0.0305 |
Schistosoma mansoni | tyrosine kinase | 0.0518 | 0.0285 | 0.0285 |
Echinococcus multilocularis | epidermal growth factor receptor | 0.0537 | 0.0305 | 0.0305 |
Echinococcus granulosus | insulin growth factor 1 receptor beta | 0.1169 | 0.0976 | 0.0976 |
Echinococcus granulosus | sodium bile acid cotransporter | 0.9673 | 1 | 1 |
Loa Loa (eye worm) | TK/ALK protein kinase | 0.2102 | 0.1966 | 0.1966 |
Schistosoma mansoni | sodium-bile acid cotransporter related | 0.3922 | 0.3898 | 0.3898 |
Echinococcus multilocularis | sodium bile acid cotransporter | 0.9673 | 1 | 1 |
Echinococcus granulosus | epidermal growth factor receptor | 0.0537 | 0.0305 | 0.0305 |
Echinococcus granulosus | insulin receptor | 0.1169 | 0.0976 | 0.0976 |
Schistosoma mansoni | sodium-bile acid cotransporter related | 0.9673 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.9673 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0632 | 0.0406 | 0.0406 |
Loa Loa (eye worm) | hypothetical protein | 0.1834 | 0.1681 | 0.1681 |
Echinococcus granulosus | sodium bile acid cotransporter | 0.9673 | 1 | 1 |
Schistosoma mansoni | tyrosine kinase | 0.0537 | 0.0305 | 0.0305 |
Echinococcus multilocularis | sodium bile acid cotransporter | 0.9673 | 1 | 1 |
Echinococcus granulosus | melanoma receptor tyrosine protein kinase | 0.0537 | 0.0305 | 0.0305 |
Echinococcus multilocularis | insulin growth factor 1 receptor beta | 0.1169 | 0.0976 | 0.0976 |
Schistosoma mansoni | tyrosine kinase | 0.0518 | 0.0285 | 0.0285 |
Schistosoma mansoni | tyrosine kinase | 0.1169 | 0.0976 | 0.0976 |
Onchocerca volvulus | 0.9673 | 1 | 1 | |
Schistosoma mansoni | tyrosine kinase | 0.0518 | 0.0285 | 0.0285 |
Brugia malayi | Protein kinase domain containing protein | 0.1169 | 0.0976 | 0.0976 |
Schistosoma mansoni | tyrosine kinase | 0.0537 | 0.0305 | 0.0305 |
Schistosoma mansoni | sodium-bile acid cotransporter | 0.5751 | 0.5838 | 0.5838 |
Echinococcus multilocularis | epidermal growth factor receptor | 0.0537 | 0.0305 | 0.0305 |
Schistosoma mansoni | tyrosine kinase | 0.1169 | 0.0976 | 0.0976 |
Brugia malayi | Protein kinase domain containing protein | 0.0651 | 0.0426 | 0.0426 |
Schistosoma mansoni | tyrosine kinase | 0.0537 | 0.0305 | 0.0305 |
Brugia malayi | Protein kinase domain containing protein | 0.2102 | 0.1966 | 0.1966 |
Echinococcus granulosus | sodium bile acid cotransporter | 0.9673 | 1 | 1 |
Loa Loa (eye worm) | TK/EGFR protein kinase | 0.0537 | 0.0305 | 0.0305 |
Loa Loa (eye worm) | TK/INSR protein kinase | 0.1169 | 0.0976 | 0.0976 |
Echinococcus multilocularis | sodium bile acid cotransporter | 0.9673 | 1 | 1 |
Echinococcus multilocularis | insulin receptor | 0.1169 | 0.0976 | 0.0976 |
Echinococcus granulosus | epidermal growth factor receptor | 0.0537 | 0.0305 | 0.0305 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 200 nM | Inhibitory concentration against recombinant human Histone deacetylase 1 | ChEMBL. | 14613312 |
IC50 (binding) | = 200 nM | Inhibition against partially purified human histone deacetylase 1 (HDAC-1) | ChEMBL. | 12061890 |
IC50 (binding) | = 200 nM | Inhibitory concentration against recombinant human Histone deacetylase 1 | ChEMBL. | 14613312 |
IC50 (binding) | = 200 nM | Inhibition against partially purified human histone deacetylase 1 (HDAC-1) | ChEMBL. | 12061890 |
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.
2 literature references were collected for this gene.