Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | lactate dehydrogenase a | 0.00522164 | 1 | 1 |
Onchocerca volvulus | Chorion peroxidase homolog | 0.00443967 | 0.474103 | 0.5 |
Onchocerca volvulus | Peroxidase homolog | 0.00443967 | 0.474103 | 0.5 |
Toxoplasma gondii | lactate dehydrogenase LDH2 | 0.00522164 | 1 | 0.5 |
Echinococcus multilocularis | L lactate dehydrogenase B chain | 0.00522164 | 1 | 1 |
Brugia malayi | lactate dehydrogenase. | 0.00522164 | 1 | 1 |
Toxoplasma gondii | lactate dehydrogenase LDH1 | 0.00522164 | 1 | 0.5 |
Toxoplasma gondii | malate dehydrogenase MDH | 0.00522164 | 1 | 0.5 |
Onchocerca volvulus | 0.00443967 | 0.474103 | 0.5 | |
Onchocerca volvulus | 0.00443967 | 0.474103 | 0.5 | |
Leishmania major | malate dehydrogenase, putative | 0.00522164 | 1 | 0.5 |
Plasmodium vivax | malate dehydrogenase, putative | 0.00522164 | 1 | 0.5 |
Echinococcus multilocularis | peroxidasin | 0.00443967 | 0.474103 | 0.474103 |
Echinococcus multilocularis | lactate dehydrogenase a | 0.00522164 | 1 | 1 |
Onchocerca volvulus | Peroxidase homolog | 0.00443967 | 0.474103 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.00522164 | 1 | 1 |
Onchocerca volvulus | 0.00443967 | 0.474103 | 0.5 | |
Onchocerca volvulus | Peroxidasin homolog | 0.00443967 | 0.474103 | 0.5 |
Onchocerca volvulus | Peroxidasin homolog | 0.00443967 | 0.474103 | 0.5 |
Echinococcus granulosus | peroxidasin | 0.00443967 | 0.474103 | 0.474103 |
Echinococcus granulosus | lactate dehydrogenase a | 0.00522164 | 1 | 1 |
Plasmodium vivax | lactate dehydrogenase | 0.00522164 | 1 | 0.5 |
Plasmodium falciparum | malate dehydrogenase | 0.00522164 | 1 | 0.5 |
Schistosoma mansoni | malate dehydrogenase | 0.00522164 | 1 | 1 |
Echinococcus multilocularis | lactate dehydrogenase a | 0.00522164 | 1 | 1 |
Echinococcus granulosus | lactate dehydrogenase protein | 0.00522164 | 1 | 1 |
Onchocerca volvulus | Dual oxidase homolog | 0.00443967 | 0.474103 | 0.5 |
Plasmodium falciparum | L-lactate dehydrogenase | 0.00522164 | 1 | 0.5 |
Echinococcus granulosus | L lactate dehydrogenase B chain | 0.00522164 | 1 | 1 |
Wolbachia endosymbiont of Brugia malayi | malate dehydrogenase | 0.00522164 | 1 | 0.5 |
Echinococcus multilocularis | lactate dehydrogenase protein | 0.00522164 | 1 | 1 |
Echinococcus granulosus | lactate dehydrogenase a | 0.00522164 | 1 | 1 |
Entamoeba histolytica | malate dehydrogenase, putative | 0.00522164 | 1 | 0.5 |
Schistosoma mansoni | L-lactate dehydrogenase | 0.00522164 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (functional) | NOVARTIS: Antimalarial liver stage activity measured as a greater than 50% reduction in Plasmodium yoelii schizont area in HepG2-A16-CD81 cells at 10uM compound concentration, determined by immuno-fluorescence. | ChEMBL. | 22096101 | |
CC50 (functional) | = 6.27 uM | Huh7 cytotoxicity for Pf inhibitors | Novartis-GNF Malaria Box. | No reference |
CC50 | = 6.27 uM | NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7) | ChEMBL. | 18579783 |
EC50 (functional) | = 0.2787 uM | W2 Pf proliferation inhibition | Novartis-GNF Malaria Box. | No reference |
EC50 (functional) | = 0.2787 uM | NOVARTIS: Inhibition of Plasmodium falciparum W2 (drug-resistant) proliferation in erythrocyte-based infection assay | ChEMBL. | 18579783 |
EC50 (functional) | = 0.521 uM | PF proliferation inhibition 3D7 | Novartis-GNF Malaria Box. | No reference |
EC50 (functional) | = 0.521 uM | NOVARTIS: Inhibition of Plasmodium falciparum 3D7 (drug-susceptible) proliferation in erythrocyte-based infection assay | ChEMBL. | 18579783 |
IFI promiscuity index | = 0.09434 | IFI promiscuity index | Novartis-GNF Malaria Box. | No reference |
Species name | Source | Reference | Is orphan |
---|---|---|---|
Plasmodium falciparum | ChEMBL23 | 18579783 |
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.