| Experimental Information |
| |
| Enzymatic Activity |
| Molecule Id | EGIN0000003 |
| PMID | 16777410 |
| Assay Used | Inhibition of ErbB-1 and ErbB-2 tyrosine Kinase activity was evaluated in Enzyme assays using the purified recombinant human intracellular domain of each receptor and Cellular assay |
| Experimently Validated | Yes |
| EGFR (IC50) | 12 nM |
| HER2 (IC50) | 10 nM |
| HER4 (IC50) | - |
| Mutant L858R (IC50) | - |
| Mutant T790M (IC50) | - |
| Double Mutant (IC50) | - |
| Average ERBB2 and ERBB1 (IC50) | - |
| Inhibition EGFR (%) | - |
| Inhibitory Concentration | - |
| Inhibition HER2 (%) | - |
| Inhibitory Concentration | - |
| Ki (EGFR) | - |
| Ki (HER2) | - |
| Ki (HER4) | - |
| Kd (EGFR) | - |
| Kd (L858R) | - |
| Kd (T790M) | - |
| Kd (L858R/T790M) | - |
| Kd (Other mutation) | - |
| Note | The paper describes 6-furanylquinazoline series of dual ErbB-1/ErbB-2 tyrosine kinase inhibitors |
| Extra | - |
| |
