Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | lamin A/C | Starlite/ChEMBL | No references |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | SEA domain containing protein | 0.0145 | 0.9521 | 0.9518 |
Loa Loa (eye worm) | hypothetical protein | 0.0033 | 0.005 | 0.005 |
Loa Loa (eye worm) | intermediate filament tail domain-containing protein | 0.0033 | 0.005 | 0.005 |
Onchocerca volvulus | 0.0145 | 0.9521 | 0.9518 | |
Onchocerca volvulus | 0.0044 | 0.1026 | 0.098 | |
Leishmania major | hypothetical protein, conserved | 0.0044 | 0.1026 | 0.5 |
Plasmodium vivax | cysteine repeat modular protein 1, putative | 0.0044 | 0.1026 | 0.5 |
Loa Loa (eye worm) | DOMON domain-containing protein | 0.0145 | 0.9521 | 0.9521 |
Schistosoma mansoni | hypothetical protein | 0.0044 | 0.1026 | 0.103 |
Onchocerca volvulus | 0.015 | 1 | 1 | |
Brugia malayi | Kringle domain containing protein | 0.0044 | 0.1026 | 0.098 |
Brugia malayi | Protein kinase domain containing protein | 0.0044 | 0.1026 | 0.098 |
Loa Loa (eye worm) | TK/ROR protein kinase | 0.0044 | 0.1026 | 0.1026 |
Loa Loa (eye worm) | hypothetical protein | 0.0145 | 0.9521 | 0.9521 |
Onchocerca volvulus | 0.0145 | 0.9521 | 0.9518 | |
Toxoplasma gondii | kringle domain-containing protein | 0.0044 | 0.1026 | 0.5 |
Plasmodium falciparum | cysteine repeat modular protein 1 | 0.0044 | 0.1026 | 0.5 |
Onchocerca volvulus | 0.0145 | 0.9521 | 0.9518 | |
Loa Loa (eye worm) | hypothetical protein | 0.015 | 1 | 1 |
Echinococcus granulosus | tissue type plasminogen activator | 0.0044 | 0.1026 | 1 |
Echinococcus multilocularis | tissue type plasminogen activator | 0.0044 | 0.1026 | 1 |
Loa Loa (eye worm) | intermediate filament protein | 0.0033 | 0.005 | 0.005 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.0044 | 0.1026 | 0.5 |
Onchocerca volvulus | 0.0145 | 0.9521 | 0.9518 | |
Loa Loa (eye worm) | hypothetical protein | 0.0044 | 0.1026 | 0.1026 |
Schistosoma mansoni | hypothetical protein | 0.0145 | 0.9521 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Potency (functional) | = 1.122 um | PUBCHEM_BIOASSAY: qHTS Assay for Modulators of Lamin A Splicing. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 7.3753 uM | PUBCHEM_BIOASSAY: Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488752, AID488774, AID504848, AID504850] | ChEMBL. | No reference |
Potency (functional) | 100 uM | PUBCHEM_BIOASSAY: HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488962] | ChEMBL. | No reference |
Species name | Source | Reference | Is orphan |
---|---|---|---|
Plasmodium falciparum | ChEMBL23 |
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.