Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | calcium channel, voltage-dependent, L type, alpha 1C subunit | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trypanosoma cruzi | Voltage-dependent calcium channel subunit, putative | 0.0056 | 0.0019 | 0.5 |
Loa Loa (eye worm) | calcium channel | 0.0093 | 0.0303 | 0.0157 |
Onchocerca volvulus | Matrilysin homolog | 0.0085 | 0.0238 | 1 |
Schistosoma mansoni | high voltage-activated calcium channel Cav1 | 0.0093 | 0.0303 | 0.0303 |
Loa Loa (eye worm) | hypothetical protein | 0.0093 | 0.0303 | 0.0157 |
Onchocerca volvulus | Matrix metalloproteinase homolog | 0.0085 | 0.0238 | 1 |
Wolbachia endosymbiont of Brugia malayi | extracellular metallopeptidase | 0.0992 | 0.7333 | 0.5 |
Schistosoma mansoni | family A2 unassigned peptidase (A02 family) | 0.0242 | 0.1472 | 0.1472 |
Schistosoma mansoni | matrix metallopeptidase-9 (M10 family) | 0.0091 | 0.0285 | 0.0285 |
Schistosoma mansoni | polycystin 1-related | 0.0087 | 0.0259 | 0.0259 |
Echinococcus multilocularis | matrix metallopeptidase 7 (M10 family) | 0.0139 | 0.0661 | 1 |
Schistosoma mansoni | high voltage-activated calcium channel Cav2A | 0.0093 | 0.0303 | 0.0303 |
Loa Loa (eye worm) | angiotensin-converting enzyme family protein | 0.0613 | 0.437 | 1 |
Echinococcus granulosus | matrix metallopeptidase 7 M10 family | 0.0139 | 0.0661 | 1 |
Brugia malayi | Voltage-gated calcium channel, L-type, alpha subunit. C. elegans egl-19 ortholog | 0.0093 | 0.0303 | 0.0694 |
Schistosoma mansoni | voltage-gated cation channel | 0.0093 | 0.0303 | 0.0303 |
Brugia malayi | Angiotensin-converting enzyme family protein | 0.0613 | 0.437 | 1 |
Trypanosoma brucei | Voltage-dependent calcium channel subunit, putative | 0.0056 | 0.0019 | 0.5 |
Brugia malayi | Matrixin family protein | 0.0092 | 0.0298 | 0.0682 |
Loa Loa (eye worm) | matrixin family protein | 0.0092 | 0.0298 | 0.0144 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
EC50 (functional) | > 30 uM | In vitro contraction of rabbit aorta strips. | ChEMBL. | 7837222 |
IC50 (functional) | = 20 uM | In vitro inhibition of potassium-induced contractions in rabbit aorta strips. | ChEMBL. | 7837222 |
Kd (binding) | = 2.7 uM | Displacement of [3H]-nitrendipine from dihydropyridine receptor of guinea pig myocardial membranes | ChEMBL. | 7837222 |
Kd (binding) | = 2.7 uM | Displacement of [3H]-nitrendipine from dihydropyridine receptor of guinea pig myocardial membranes | ChEMBL. | 7837222 |
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.