Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0534 | 1 | 0.5 |
Onchocerca volvulus | 0.0534 | 1 | 1 | |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0534 | 1 | 0.5 |
Toxoplasma gondii | PAN domain-containing protein | 0.035 | 0.283 | 0.5 |
Toxoplasma gondii | PAN domain-containing protein | 0.035 | 0.283 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0534 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0534 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
ED50 (functional) | 0 uM kg-1 | Tested orally (po) in rats for antagonism of stereotypies induced by amphetamine; NT = Not Tested | ChEMBL. | 6134833 |
ED50 (functional) | 0 uM kg-1 | Ability to induce catalepsy, an effect normally related to clinical extrapyramidal side effects; NT = Not Tested | ChEMBL. | 6134833 |
ED50 (functional) | = 37 uM kg-1 | Compound (administered intraperitoneally) was assessed for neuroleptic activity to antagonize methyl phenidate induced stereotypes in mice | ChEMBL. | 6134833 |
ED50 (functional) | = 37 uM kg-1 | Compound (administered intraperitoneally) was assessed for neuroleptic activity to antagonize methyl phenidate induced stereotypes in mice | ChEMBL. | 6134833 |
ED50 (functional) | > 95 uM kg-1 | Compound (administered intraperitoneally) was assessed for neuroleptic activity to antagonize methyl phenidate induced stereotypes in mice | ChEMBL. | 6134833 |
ED50 (functional) | > 95 uM kg-1 | Compound (administered intraperitoneally) was assessed for neuroleptic activity to antagonize methyl phenidate induced stereotypes in mice | ChEMBL. | 6134833 |
IC50 (binding) | nM | Ability to displace [3H]-haloperidol from rat striatal membranes, in order to measure its intrinsic affinity for the dopamine (DA) receptor;NT=Not Tested | ChEMBL. | 6134833 |
IC50 (binding) | 0 nM | Ability to displace [3H]-haloperidol from rat striatal membranes, in order to measure its intrinsic affinity for the dopamine (DA) receptor;NT=Not Tested | ChEMBL. | 6134833 |
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.