| Experimental Information |
| |
| Enzymatic Activity |
| Molecule Id | EGIN0000682 |
| PMID | 8627606 |
| Assay Used | Inhibition of the phosphorylation of a 14-residue fragment of phospholipase C-ç1 by EGFR |
| Experimently Validated | Yes |
| EGFR (IC50) | 0.13 nM |
| HER2 (IC50) | - |
| 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 the Isomeric 4-[(3-Bromophenyl)amino]pyrido[d]-pyrimidines as Potent ATP Binding Site Inhibitors of the Tyrosine Kinase Function of the Epidermal Growth Factor Receptor |
| Extra | - |
| |
