Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | coagulation factor X | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | choline:ethanolamine kinase | 0.0041 | 0.941 | 0.941 |
Echinococcus granulosus | carboxylesterase 5A | 0.0042 | 1 | 1 |
Echinococcus granulosus | acetylcholinesterase | 0.0042 | 1 | 1 |
Plasmodium falciparum | choline kinase | 0.0041 | 0.941 | 0.5 |
Echinococcus multilocularis | acetylcholinesterase | 0.0042 | 1 | 1 |
Loa Loa (eye worm) | carboxylesterase | 0.0042 | 1 | 1 |
Echinococcus granulosus | acetylcholinesterase | 0.0042 | 1 | 1 |
Brugia malayi | Choline/ethanolamine kinase family protein | 0.0041 | 0.941 | 0.941 |
Toxoplasma gondii | phosphotransferase enzyme family protein | 0.0041 | 0.941 | 1 |
Echinococcus multilocularis | carboxylesterase 5A | 0.0042 | 1 | 1 |
Brugia malayi | Carboxylesterase family protein | 0.0042 | 1 | 1 |
Loa Loa (eye worm) | acetylcholinesterase 1 | 0.0042 | 1 | 1 |
Plasmodium vivax | choline kinase, putative | 0.0041 | 0.941 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0042 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0042 | 1 | 1 |
Onchocerca volvulus | Arrow homolog | 0.0016 | 0 | 0.5 |
Echinococcus multilocularis | choline:ethanolamine kinase | 0.0041 | 0.941 | 0.941 |
Loa Loa (eye worm) | choline/ethanolamine kinase | 0.0041 | 0.941 | 0.941 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0042 | 1 | 1 |
Echinococcus multilocularis | acetylcholinesterase | 0.0042 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (functional) | = 0.85 uM | Anticoagulant potency in human plasma assessed as concentration required to double prothrombin time after 4 mins | ChEMBL. | 18077174 |
Activity (functional) | = 14 uM | Anticoagulant potency in mouse plasma assessed as concentration required to double prothrombin time after 4 mins | ChEMBL. | 18077174 |
Activity (functional) | = 14 uM | Anticoagulant potency in mouse plasma assessed as concentration required to double prothrombin time after 4 mins | ChEMBL. | 18077174 |
IC50 (binding) | = 0.037 uM | Inhibition of human factor 10a | ChEMBL. | 18077174 |
IC50 (binding) | = 0.037 uM | Inhibition of human factor 10a | ChEMBL. | 18077174 |
Ratio (functional) | = 1 | Ex vivo anticoagulant potency in ICR mouse blood at 30 mg/kg, po after 1 hr expressed as ratio of prothrombin time in drug treated animal to control | ChEMBL. | 18077174 |
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.