Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | matrixin family protein | 0.0143 | 0.2025 | 0.102 |
Trichomonas vaginalis | macrophage migration inhibitory factor, mif, putative | 0.0273 | 0.6481 | 0.5 |
Loa Loa (eye worm) | macrophage migration inhibitory factor | 0.0273 | 0.6481 | 0.6038 |
Schistosoma mansoni | ADAMTS5 peptidase (M12 family) | 0.0085 | 0.0022 | 0.0066 |
Loa Loa (eye worm) | matrixin family protein | 0.0131 | 0.162 | 0.0564 |
Onchocerca volvulus | Matrix metalloproteinase homolog | 0.0131 | 0.162 | 1 |
Onchocerca volvulus | Matrilysin homolog | 0.0131 | 0.162 | 1 |
Entamoeba histolytica | macrophage migration inhibitory factor-like protein | 0.0273 | 0.6481 | 0.5 |
Brugia malayi | metalloprotease disintegrin 16 with thrombospondin type I motif | 0.0085 | 0.0022 | 0.0033 |
Plasmodium vivax | macrophage migration inhibitory factor, putative | 0.0273 | 0.6481 | 0.5 |
Toxoplasma gondii | macrophage migration inhibitory factor, putative | 0.0273 | 0.6481 | 0.5 |
Echinococcus multilocularis | matrix metallopeptidase 7 (M10 family) | 0.0215 | 0.4491 | 1 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0273 | 0.6481 | 0.5 |
Echinococcus granulosus | Blood coagulation inhibitor Disintegrin | 0.0112 | 0.0972 | 0.2128 |
Echinococcus multilocularis | adam 17 protease | 0.0179 | 0.3254 | 0.7233 |
Schistosoma mansoni | ADAM17 peptidase (M12 family) | 0.0179 | 0.3254 | 1 |
Echinococcus granulosus | matrix metallopeptidase 7 M10 family | 0.0215 | 0.4491 | 1 |
Leishmania major | macrophage migration inhibitory factor-like protein | 0.0273 | 0.6481 | 0.5 |
Giardia lamblia | Macrophage migration inhibitory factor | 0.0273 | 0.6481 | 0.5 |
Echinococcus granulosus | adam 17 protease | 0.0197 | 0.3865 | 0.86 |
Brugia malayi | Bm-MIF-1, identical | 0.0273 | 0.6481 | 1 |
Leishmania major | macrophage migration inhibitory factor-like protein | 0.0273 | 0.6481 | 0.5 |
Plasmodium falciparum | macrophage migration inhibitory factor | 0.0273 | 0.6481 | 0.5 |
Echinococcus multilocularis | Blood coagulation inhibitor, Disintegrin | 0.0112 | 0.0972 | 0.2128 |
Brugia malayi | Matrixin family protein | 0.0143 | 0.2025 | 0.3124 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
CC50 (ADMET) | > 100 ug ml-1 | Cytotoxicity against Vero cells by MTT assay | ChEMBL. | 17696514 |
CC50 (ADMET) | > 100 ug ml-1 | Cytotoxicity against human foreskin fibroblast cells by MTT assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 25 % | Antimycobacterial activity against Mycobacterium avium ATCC 25291 at 50 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 25 % | Antimycobacterial activity against Mycobacterium avium ATCC 25291 at 10 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 50 % | Antimycobacterial activity against Mycobacterium bovis BCG at 1 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 50 % | Antimycobacterial activity against Mycobacterium tuberculosis H37Ra at 1 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 50 % | Antimycobacterial activity against Mycobacterium tuberculosis H37Ra at 1 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 90 % | Antimycobacterial activity against Mycobacterium avium ATCC 25291 at 100 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 100 % | Antimycobacterial activity against Mycobacterium tuberculosis H37Ra at 100 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 100 % | Antimycobacterial activity against Mycobacterium bovis BCG at 100 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 100 % | Antimycobacterial activity against Mycobacterium bovis BCG at 50 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 100 % | Antimycobacterial activity against Mycobacterium bovis BCG at 10 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 100 % | Antimycobacterial activity against Mycobacterium tuberculosis H37Ra at 50 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 100 % | Antimycobacterial activity against Mycobacterium tuberculosis H37Ra at 10 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 100 % | Antimycobacterial activity against Mycobacterium tuberculosis H37Ra at 100 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 100 % | Antimycobacterial activity against Mycobacterium tuberculosis H37Ra at 50 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
Inhibition (functional) | = 100 % | Antimycobacterial activity against Mycobacterium tuberculosis H37Ra at 10 uM by microplate alamar blue assay | ChEMBL. | 17696514 |
MIC (functional) | = 100 ug ml-1 | Antibacterial activity against Bacillus subtilis ATCC 6633 | ChEMBL. | 17696514 |
MIC (functional) | = 100 ug ml-1 | Antibacterial activity against Streptococcus pneumoniae ATCC 49619 | ChEMBL. | 17696514 |
MIC (functional) | = 100 ug ml-1 | Antibacterial activity against Streptococcus pyogenes ATCC 19615 | ChEMBL. | 17696514 |
MIC90 (functional) | = 1 ug ml-1 | Antimycobacterial activity against Mycobacterium bovis BCG by microplate alamar blue assay | ChEMBL. | 17696514 |
MIC90 (functional) | = 1 ug ml-1 | Antimycobacterial activity against Mycobacterium tuberculosis H37Ra by microplate alamar blue assay | ChEMBL. | 17696514 |
MIC90 (functional) | = 1 ug ml-1 | Antimycobacterial activity against Mycobacterium tuberculosis H37Ra by microplate alamar blue assay | ChEMBL. | 17696514 |
MIC90 (functional) | = 100 ug ml-1 | Antimycobacterial activity against Mycobacterium avium ATCC 25291 by microplate alamar blue assay | ChEMBL. | 17696514 |
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.