Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Abrasion score (functional) | = 1 | Compound was tested for abrasion score in mice at a dose of 3.6 nmol/25 g of TTNPB and 28.8 nmol/25 g of the compound | ChEMBL. | 10201840 |
Abrasion score (functional) | = 3 | Compound was tested for abrasion score in mice at a dose of 3.6 nmol/25 g of TTNPB and 7.2 nmol/25 g of the compound | ChEMBL. | 10201840 |
Cutaneous toxicology score (functional) | = 3 | Compound was tested for cutaneous toxicity score in mice at a dose of 3.6 nmol/25 g of TTNPB and 28.8 nmol/25 g of the compound | ChEMBL. | 10201840 |
Cutaneous toxicology score (functional) | = 4.6 | Compound was tested for cutaneous toxicity score in mice at a dose of 3.6 nmol/25 g of TTNPB and 7.2 nmol/25 g of the compound | ChEMBL. | 10201840 |
Flaking score (functional) | = 2 | Compound was tested for flaking score in mice at a dose of 3.6 nmol/25 g of TTNPB and 7.2 nmol/25 g of the compound | ChEMBL. | 10201840 |
Flaking score (functional) | = 2 | Compound was tested for flaking score in mice at a dose of 3.6 nmol/25 g of TTNPB and 28.8 nmol/25 g of the compound | ChEMBL. | 10201840 |
Gain (functional) | = 1 % | Compound was tested for its effect on body weight gain in mice at a dose of 3.6 nmol/25 g of TTNPB and 28.8 nmol/25 g of the compound | ChEMBL. | 10201840 |
Gain (functional) | = 1 % | Compound was tested for its effect on body weight gain in mice at a dose of 3.6 nmol/25 g of TTNPB and 28.8 nmol/25 g of the compound | ChEMBL. | 10201840 |
Gain (functional) | = 6 % | Compound was tested for its effect on body weight gain in mice at a dose of 3.6 nmol/25 g of TTNPB and 7.2 nmol/25 g of the compound | ChEMBL. | 10201840 |
Gain (functional) | = 6 % | Compound was tested for its effect on body weight gain in mice at a dose of 3.6 nmol/25 g of TTNPB and 7.2 nmol/25 g of the compound | ChEMBL. | 10201840 |
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.