Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Onchocerca volvulus | Chitinase | Starlite/ChEMBL | References |
Onchocerca volvulus | |
References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Onchocerca volvulus | Putative endochitinase | 0.0102 | 0.3645 | 0.2052 |
Onchocerca volvulus | Putative endochitinase | 0.0102 | 0.3645 | 0.2052 |
Loa Loa (eye worm) | microfilarial chitinase | 0.0088 | 0.1641 | 0.1641 |
Echinococcus multilocularis | Hepatocellular carcinoma associated antigen 59 | 0.0144 | 1 | 0.5 |
Mycobacterium tuberculosis | Possible chitinase | 0.0078 | 0 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0144 | 1 | 0.5 |
Echinococcus granulosus | Hepatocellular carcinoma associated antigen 59 | 0.0144 | 1 | 0.5 |
Mycobacterium ulcerans | chitinase/cellulase | 0.0078 | 0 | 0.5 |
Onchocerca volvulus | 0.0144 | 1 | 1 | |
Loa Loa (eye worm) | hypothetical protein | 0.0144 | 1 | 1 |
Mycobacterium ulcerans | chitinase/cellulase | 0.0078 | 0 | 0.5 |
Onchocerca volvulus | Putative endochitinase | 0.0102 | 0.3645 | 0.2052 |
Onchocerca volvulus | 0.0144 | 1 | 1 | |
Leishmania major | chitinase | 0.0091 | 0.2004 | 0.5 |
Brugia malayi | endochitinase | 0.0102 | 0.3645 | 0.2052 |
Loa Loa (eye worm) | hypothetical protein | 0.0144 | 1 | 1 |
Plasmodium falciparum | conserved protein, unknown function | 0.0144 | 1 | 0.5 |
Loa Loa (eye worm) | chitinase I | 0.0091 | 0.2004 | 0.2004 |
Brugia malayi | Endochitinase | 0.0102 | 0.3645 | 0.2052 |
Loa Loa (eye worm) | cuticular endochitinase | 0.0091 | 0.2004 | 0.2004 |
Plasmodium vivax | hypothetical protein, conserved | 0.0144 | 1 | 0.5 |
Toxoplasma gondii | hypothetical protein | 0.0144 | 1 | 0.5 |
Entamoeba histolytica | chitinase, putative | 0.0091 | 0.2004 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Drug uptake (ADMET) | = 0.22 nmol/mg | Drug uptake in late stage L4 Caenorhabditis elegans at 10 uM after 6 hrs by LC-MS analysis | ChEMBL. | 25815157 |
IC50 (binding) | = 3.49 uM | Inhibition of L3 larval stage of Onchocerca volvulus chitinase using 4-methylumbelliferyl-N-N'-N''-beta-chitotrioside as substrate assessed as release of 4-methylumbelliferone measured for 10 mins by fluorescence assay | ChEMBL. | 25815157 |
Inhibition (functional) | = 45 % | Antionchocerciasis activity against L3 larval stage of Onchocerca volvulus assessed as inhibition of parasite molting at 1 uM treated for 24 hrs prior to complete medium and PBMC addition measured after 6 days by inverted microscopic analysis | ChEMBL. | 25815157 |
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.