Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium leprae | PROBABLE ACETOLACTATE SYNTHASE (LARGE SUBUNIT) ILVB (ACETOHYDROXY-ACID SYNTHASE) | 0.0218 | 1 | 0.5 |
Plasmodium falciparum | acyl-CoA synthetase | 0.0125 | 0.2525 | 0.5 |
Mycobacterium leprae | Probable Acetolactate synthase IlvG (Acetohydroxy-acid synthase)(ALS) | 0.0218 | 1 | 0.5 |
Mycobacterium tuberculosis | Probable acetolactate synthase IlvG (acetohydroxy-acid synthase)(ALS) | 0.0218 | 1 | 1 |
Schistosoma mansoni | acetolactate synthase | 0.0186 | 0.7458 | 0.5 |
Loa Loa (eye worm) | ILVBL protein | 0.0132 | 0.3106 | 1 |
Plasmodium vivax | acyl-CoA synthetase, putative | 0.0125 | 0.2525 | 0.5 |
Mycobacterium ulcerans | acetolactate synthase 1 catalytic subunit | 0.0218 | 1 | 1 |
Leishmania major | putative pyruvate/indole-pyruvate carboxylase, putative | 0.0125 | 0.2525 | 0.5 |
Schistosoma mansoni | acetolactate synthase | 0.0186 | 0.7458 | 0.5 |
Mycobacterium ulcerans | hypothetical protein | 0.0218 | 1 | 1 |
Mycobacterium ulcerans | putative oxalyl-CoA decarboxylase | 0.0218 | 1 | 1 |
Mycobacterium tuberculosis | Probable oxalyl-CoA decarboxylase OxcA | 0.0218 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Fluorescence intensity (binding) | = 24 | Oxidative desamination of the compound by bovine serum amine oxidase and expressed in terms of fluorescence intensity. | ChEMBL. | 9871574 |
Fluorescence intensity (binding) | = 24 | Oxidative desamination of the compound by bovine serum amine oxidase and expressed in terms of fluorescence intensity. | ChEMBL. | 9871574 |
IC50 (functional) | > 170 uM | Compound was tested for inhibitory concentration required to inhibit 50% of [14C]- putrescine uptake. | ChEMBL. | 9871574 |
IC50 (functional) | > 170 uM | Compound was tested for inhibitory concentration required to inhibit 50% of [14C]- putrescine uptake. | ChEMBL. | 9871574 |
IC50 (functional) | > 200 uM | Cytotoxic effect on L1210 leukemia cells. | ChEMBL. | 9871574 |
IC50 (functional) | > 200 uM | Cytotoxic effect on L1210 leukemia cells. | ChEMBL. | 9871574 |
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.