BDBM50585315 CHEMBL5070579
SMILES COc1cc(N(C)CCN(C)CC#C)c(NC(=O)C=C)cc1Nc1nccc(Nc2ccn(C)n2)n1
InChI Key InChIKey=IFKCLMDEPDCIBC-UHFFFAOYSA-N
Data 3 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 5 hits for monomerid = 50585315
TargetEpidermal growth factor receptor(Human)
Beijing Institute of Pharmacology and Toxicology
Curated by ChEMBL
Beijing Institute of Pharmacology and Toxicology
Curated by ChEMBL
Affinity DataIC50: 8.60nMAssay Description:Inhibition of EGFR T790M/C797S double mutant (unknown origin) using flurogenic substrate in presence of ATP by HTRF assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Human)
Beijing Institute of Pharmacology and Toxicology
Curated by ChEMBL
Beijing Institute of Pharmacology and Toxicology
Curated by ChEMBL
Affinity DataIC50: 8.60nMAssay Description:Inhibition of EGFR L858R/T790M (unknown origin)More data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Human)
Beijing Institute of Pharmacology and Toxicology
Curated by ChEMBL
Beijing Institute of Pharmacology and Toxicology
Curated by ChEMBL
Affinity DataIC50: 22nMAssay Description:Inhibition of EGFR del19 (unknown origin) using flurogenic substrate in presence of ATP by HTRF assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Human)
Beijing Institute of Pharmacology and Toxicology
Curated by ChEMBL
Beijing Institute of Pharmacology and Toxicology
Curated by ChEMBL
Affinity DataIC50: 51nMAssay Description:Inhibition of wild type EGFR (unknown origin) using flurogenic substrate in presence of ATP by HTRF assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Human)
Beijing Institute of Pharmacology and Toxicology
Curated by ChEMBL
Beijing Institute of Pharmacology and Toxicology
Curated by ChEMBL
Affinity DataIC50: 51nMAssay Description:Inhibition of wild-type EGFR (unknown origin)More data for this Ligand-Target Pair
