Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | chemokine (C-C motif) receptor 3 | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0119 | 0.0306 | 0.103 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Brugia malayi | Animal haem peroxidase family protein | 0.0303 | 0.2973 | 1 |
Brugia malayi | Animal haem peroxidase family protein | 0.0303 | 0.2973 | 1 |
Onchocerca volvulus | Huntingtin homolog | 0.0119 | 0.0306 | 0.103 |
Onchocerca volvulus | Chorion peroxidase homolog | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | animal heme peroxidase | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Toxoplasma gondii | EGF family domain-containing protein | 0.0098 | 0 | 0.5 |
Onchocerca volvulus | Dual oxidase homolog | 0.0303 | 0.2973 | 1 |
Echinococcus granulosus | survival motor neuron protein 1 | 0.023 | 0.1911 | 0.6428 |
Brugia malayi | Animal haem peroxidase family protein | 0.0303 | 0.2973 | 1 |
Brugia malayi | Blistered cuticle protein 3 | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0119 | 0.0306 | 0.103 |
Onchocerca volvulus | Peroxidase homolog | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Giardia lamblia | High cysteine protein | 0.0098 | 0 | 0.5 |
Onchocerca volvulus | 0.0303 | 0.2973 | 1 | |
Brugia malayi | hypothetical protein | 0.0119 | 0.0306 | 0.103 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Onchocerca volvulus | Peroxidase homolog | 0.0303 | 0.2973 | 1 |
Brugia malayi | hypothetical protein | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Onchocerca volvulus | 0.0303 | 0.2973 | 1 | |
Onchocerca volvulus | Peroxidasin homolog | 0.0303 | 0.2973 | 1 |
Echinococcus multilocularis | peroxidasin | 0.0303 | 0.2973 | 0.2973 |
Brugia malayi | hypothetical protein | 0.023 | 0.1911 | 0.6428 |
Onchocerca volvulus | Peroxidasin homolog | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | animal heme peroxidase | 0.0303 | 0.2973 | 1 |
Onchocerca volvulus | Huntingtin homolog | 0.0119 | 0.0306 | 0.103 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Onchocerca volvulus | 0.0303 | 0.2973 | 1 | |
Brugia malayi | Animal haem peroxidase family protein | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.023 | 0.1911 | 0.6428 |
Echinococcus granulosus | peroxidasin | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Schistosoma mansoni | peroxidasin | 0.0303 | 0.2973 | 1 |
Brugia malayi | Animal haem peroxidase family protein | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | animal heme peroxidase | 0.0303 | 0.2973 | 1 |
Echinococcus multilocularis | survival motor neuron protein 1 | 0.023 | 0.1911 | 0.1911 |
Loa Loa (eye worm) | blistered cuticle protein 3 | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Brugia malayi | Peroxidasin | 0.0303 | 0.2973 | 1 |
Schistosoma mansoni | peroxidasin | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | animal heme peroxidase | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0303 | 0.2973 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | nM | Inhibition of eotaxin-induced chemotaxis of human eosinophils; NT= Not tested | ChEMBL. | 15771462 |
IC50 (binding) | = 29 nM | Inhibition of [125I]-eotaxin binding to human C-C chemokine receptor type 3 expressed in CHO cells | ChEMBL. | 15771462 |
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.