Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Plasmodium falciparum | dipeptidyl aminopeptidase 2 | 0.0206 | 1 | 1 |
Onchocerca volvulus | 0.015 | 0.5617 | 0.5 | |
Loa Loa (eye worm) | hypothetical protein | 0.015 | 0.5617 | 0.5 |
Brugia malayi | hypothetical protein | 0.015 | 0.5617 | 0.5 |
Plasmodium falciparum | dipeptidyl aminopeptidase 1 | 0.0206 | 1 | 1 |
Plasmodium vivax | dipeptidyl aminopeptidase 1, putative | 0.0206 | 1 | 1 |
Plasmodium vivax | dipeptidyl aminopeptidase 2, putative | 0.0206 | 1 | 1 |
Schistosoma mansoni | dipeptidyl-peptidase I (C01 family) | 0.0206 | 1 | 0.5 |
Trichomonas vaginalis | Clan CA, family C1, cathepsin B-like cysteine peptidase | 0.0128 | 0.3886 | 0.5 |
Toxoplasma gondii | cathepsin CPC1 | 0.0206 | 1 | 1 |
Toxoplasma gondii | preprocathepsin c precursor, putative | 0.0206 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Delta mean survival time (functional) | = 0.2 | Antimalarial activity of the compound was measured in mice infected with Plasmodium berghei by subcutaneous administraton at 40 mg/kg | ChEMBL. | 1404226 |
Delta mean survival time (functional) | = 0.8 | Antimalarial activity measured in mice infected with Plasmodium berghei by subcutaneous administraton of 160 mg/kg | ChEMBL. | 1404226 |
Delta mean survival time (functional) | = 2.2 | Antimalarial activity of the compound was measured against mice infected with Plasmodium berghei by subcutaneous administraton of 640 mg/kg dose | ChEMBL. | 1404226 |
Delta mean survival time (functional) | = 0.2 | Antimalarial activity of the compound was measured in mice infected with Plasmodium berghei by subcutaneous administraton at 40 mg/kg | ChEMBL. | 1404226 |
Delta mean survival time (functional) | = 0.8 | Antimalarial activity measured in mice infected with Plasmodium berghei by subcutaneous administraton of 160 mg/kg | ChEMBL. | 1404226 |
Delta mean survival time (functional) | = 2.2 | Antimalarial activity of the compound was measured against mice infected with Plasmodium berghei by subcutaneous administraton of 640 mg/kg dose | ChEMBL. | 1404226 |
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.