Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Adenosine A1 receptor | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | insulin receptor | 0.0143 | 0.0064 | 0.0062 |
Echinococcus granulosus | sodium bile acid cotransporter | 1.2457 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0077 | 0.0011 | 0.0009 |
Loa Loa (eye worm) | TK/ALK protein kinase | 0.0257 | 0.0156 | 0.0154 |
Brugia malayi | Protein kinase domain containing protein | 0.0079 | 0.0013 | 0.0011 |
Brugia malayi | Protein kinase domain containing protein | 0.0143 | 0.0064 | 0.0062 |
Echinococcus multilocularis | sodium bile acid cotransporter | 1.2457 | 1 | 1 |
Schistosoma mansoni | sodium-bile acid cotransporter | 0.7406 | 0.5924 | 0.5924 |
Echinococcus granulosus | sodium bile acid cotransporter | 1.2457 | 1 | 1 |
Schistosoma mansoni | tyrosine kinase | 0.0066 | 0.0002 | 0.0002 |
Loa Loa (eye worm) | TK/INSR protein kinase | 0.0143 | 0.0064 | 0.0062 |
Schistosoma mansoni | sodium-bile acid cotransporter related | 1.2457 | 1 | 1 |
Echinococcus multilocularis | insulin receptor | 0.0143 | 0.0064 | 0.0062 |
Loa Loa (eye worm) | hypothetical protein | 1.2457 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0224 | 0.013 | 0.0128 |
Echinococcus multilocularis | sodium bile acid cotransporter | 1.2457 | 1 | 1 |
Schistosoma mansoni | tyrosine kinase | 0.0066 | 0.0002 | 0.0002 |
Echinococcus multilocularis | insulin growth factor 1 receptor beta | 0.0143 | 0.0064 | 0.0062 |
Echinococcus granulosus | insulin growth factor 1 receptor beta | 0.0143 | 0.0064 | 0.0062 |
Schistosoma mansoni | tyrosine kinase | 0.0066 | 0.0002 | 0.0002 |
Echinococcus multilocularis | sodium bile acid cotransporter | 1.2457 | 1 | 1 |
Schistosoma mansoni | sodium-bile acid cotransporter related | 0.5051 | 0.4025 | 0.4025 |
Schistosoma mansoni | tyrosine kinase | 0.0143 | 0.0064 | 0.0064 |
Echinococcus granulosus | sodium bile acid cotransporter | 1.2457 | 1 | 1 |
Schistosoma mansoni | tyrosine kinase | 0.0143 | 0.0064 | 0.0064 |
Brugia malayi | Protein kinase domain containing protein | 0.0257 | 0.0156 | 0.0154 |
Onchocerca volvulus | 1.2457 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
k' (ADMET) | = 1.81 | Hydrophobicity index | ChEMBL. | 1895305 |
Ki (binding) | = 1.7 uM | Binding affinity against adenosine A1 receptor in rat cortex by using [3H]- PIA as a radioligand | ChEMBL. | 1895305 |
Ki (binding) | = 1.7 uM | Binding affinity against adenosine A1 receptor in rat cortex by using [3H]- PIA as a radioligand | ChEMBL. | 1895305 |
Ki (binding) | = 30 uM | Tested for inhibition of rat PC12 adenylate cyclase stimulation by using NECA as a radioligand | ChEMBL. | 1895305 |
Ki (binding) | = 30 uM | Tested for inhibition of rat PC12 adenylate cyclase stimulation by using NECA as a radioligand | ChEMBL. | 1895305 |
Ki (binding) | = 39 uM | Binding affinity against adenosine A2 receptor in rat striatum by using [3H]-NECA as a radioligand | ChEMBL. | 1895305 |
Ki (binding) | = 39 uM | Binding affinity against adenosine A2 receptor in rat striatum by using [3H]-NECA as a radioligand | ChEMBL. | 1895305 |
Selectivity ratio (binding) | = 23 | It is the ratio of Ki value of A1 receptor to that of A2 receptor. | ChEMBL. | 1895305 |
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.