Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | POT family protein | 0.0085 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 21.3 /uM | Inhibition of Flt1 expressed in mouse NIH3T3 cells by autoradiography | ChEMBL. | 18474428 |
IC50 (binding) | = 21.3 /uM | Inhibition of human A431 cell EGFRK assessed as 32P phosphorylation by scintillation counter | ChEMBL. | 18474428 |
IC50 (binding) | = 49 /uM | Inhibition of human bowes melanoma cell MMP2 | ChEMBL. | 18474428 |
IC50 (binding) | = 102 /uM | Inhibition of bovine arterial endothelial cell MMP9 | ChEMBL. | 18474428 |
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.