Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Toxoplasma gondii | histone lysine methyltransferase SET/SUV39 | 0.0029 | 0.0053 | 0.5 |
Schistosoma mansoni | jun-related protein | 0.0067 | 0.1898 | 1 |
Echinococcus granulosus | histone lysine methyltransferase setb | 0.0029 | 0.0053 | 0.0199 |
Onchocerca volvulus | 0.0065 | 0.1787 | 0.1743 | |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription | 0.0035 | 0.0347 | 0.1132 |
Loa Loa (eye worm) | pre-SET domain-containing protein family protein | 0.0204 | 0.8618 | 1 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription factor | 0.0082 | 0.2653 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0067 | 0.1898 | 1 |
Plasmodium vivax | SET domain protein, putative | 0.0029 | 0.0053 | 0.5 |
Entamoeba histolytica | hypothetical protein | 0.0035 | 0.0347 | 0.5 |
Brugia malayi | hypothetical protein | 0.0065 | 0.1787 | 0.2025 |
Echinococcus multilocularis | jun protein | 0.0082 | 0.2653 | 1 |
Brugia malayi | bZIP transcription factor family protein | 0.0082 | 0.2653 | 0.3036 |
Entamoeba histolytica | hypothetical protein | 0.0035 | 0.0347 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0035 | 0.0347 | 0.1596 |
Trichomonas vaginalis | set domain proteins, putative | 0.0232 | 1 | 0.5 |
Echinococcus granulosus | Basic leucine zipper bZIP transcription factor | 0.0082 | 0.2653 | 1 |
Echinococcus granulosus | Basic leucine zipper bZIP transcription | 0.0035 | 0.0347 | 0.1308 |
Loa Loa (eye worm) | hypothetical protein | 0.008 | 0.2543 | 0.2907 |
Echinococcus granulosus | jun protein | 0.0082 | 0.2653 | 1 |
Schistosoma mansoni | transcription factor LCR-F1 | 0.0035 | 0.0347 | 0.1596 |
Entamoeba histolytica | hypothetical protein | 0.0035 | 0.0347 | 0.5 |
Brugia malayi | hypothetical protein | 0.0035 | 0.0347 | 0.0344 |
Brugia malayi | Pre-SET motif family protein | 0.0204 | 0.8618 | 1 |
Entamoeba histolytica | hypothetical protein | 0.0035 | 0.0347 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (functional) | Antibacterial activity against Escherichia coli WF+ | ChEMBL. | 18584918 | |
GI50 (functional) | = 1.7 uM | Cytotoxicity against human A549 cells after 48 hrs by fluorescence assay | ChEMBL. | 19883086 |
GI50 (functional) | = 4.2 uM | Cytotoxicity against human NCI-H2009 cells after 48 hrs by fluorescence assay | ChEMBL. | 19883086 |
IC50 (functional) | = 49 uM | Growth inhibition of human COLO205 cells after 48 hrs by MTT assay | ChEMBL. | 19875299 |
IC50 (functional) | = 94 uM | Growth inhibition of human HepG2 cells after 48 hrs by MTT assay | ChEMBL. | 19875299 |
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.