Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Entamoeba histolytica | chitinase, putative | 0.0073 | 0.2004 | 0.5 |
Brugia malayi | Endochitinase | 0.0082 | 0.3645 | 0.2052 |
Plasmodium vivax | hypothetical protein, conserved | 0.0116 | 1 | 0.5 |
Toxoplasma gondii | hypothetical protein | 0.0116 | 1 | 0.5 |
Loa Loa (eye worm) | cuticular endochitinase | 0.0073 | 0.2004 | 0.2004 |
Loa Loa (eye worm) | chitinase I | 0.0073 | 0.2004 | 0.2004 |
Plasmodium falciparum | conserved protein, unknown function | 0.0116 | 1 | 0.5 |
Brugia malayi | endochitinase | 0.0082 | 0.3645 | 0.2052 |
Loa Loa (eye worm) | hypothetical protein | 0.0116 | 1 | 1 |
Onchocerca volvulus | 0.0116 | 1 | 1 | |
Leishmania major | chitinase | 0.0073 | 0.2004 | 0.5 |
Onchocerca volvulus | Putative endochitinase | 0.0082 | 0.3645 | 0.2052 |
Onchocerca volvulus | 0.0116 | 1 | 1 | |
Mycobacterium ulcerans | chitinase/cellulase | 0.0062 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0116 | 1 | 1 |
Mycobacterium ulcerans | chitinase/cellulase | 0.0062 | 0 | 0.5 |
Echinococcus granulosus | Hepatocellular carcinoma associated antigen 59 | 0.0116 | 1 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0116 | 1 | 0.5 |
Mycobacterium tuberculosis | Possible chitinase | 0.0062 | 0 | 0.5 |
Echinococcus multilocularis | Hepatocellular carcinoma associated antigen 59 | 0.0116 | 1 | 0.5 |
Loa Loa (eye worm) | microfilarial chitinase | 0.0071 | 0.1641 | 0.1641 |
Onchocerca volvulus | Putative endochitinase | 0.0082 | 0.3645 | 0.2052 |
Onchocerca volvulus | Putative endochitinase | 0.0082 | 0.3645 | 0.2052 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
CC50 (ADMET) | = 45.5 uM | Cytotoxicity against CEM cells after 5 days by MTT method | ChEMBL. | 17376679 |
EC50 (functional) | > 45.5 uM | Antiviral activity against HIV1 3B in CEM cells assessed as inhibition of viral-induced cytopathicity | ChEMBL. | 17376679 |
IC50 (binding) | = 28 uM | Inhibition of HIV1 recombinant integrase 3'-processing activity | ChEMBL. | 17376679 |
IC50 (binding) | = 34 uM | Inhibition of HIV1 recombinant integrase strand transfer activity | ChEMBL. | 17376679 |
MIC (functional) | > 6.25 ug ml-1 | Antimycobacterial activity against Mycobacterium tuberculosis by agar dilution method | ChEMBL. | 17376679 |
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.