BDBM50084036 CHEMBL3425671

SMILES COc1cc(ccc1Nc1ncc(Cl)c(Oc2cccc(NC(C)=O)c2)n1)N1CCN(C)CC1

InChI Key InChIKey=RHYMWMBUICSCMV-UHFFFAOYSA-N

Data  8 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50084036   

TargetEpidermal growth factor receptor(Human)
Technische Universit£T Dortmund

Curated by ChEMBL
LigandPNGBDBM50084036(CHEMBL3425671)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of wild type N-terminal His6-tagged human EGFR kinase domain (702 to 1016 residues) expressed in Sf9 cells pre-incubated for 30 mins befor...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Human)
Technische Universit£T Dortmund

Curated by ChEMBL
LigandPNGBDBM50084036(CHEMBL3425671)
Affinity DataIC50:  490nMAssay Description:Inhibition of GST-tagged human recombinant EGFR catalytic domain (668 to 1210 amino acids) L858R mutant expressed in Sf9 cells pre-incubated for 30 m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Human)
Technische Universit£T Dortmund

Curated by ChEMBL
LigandPNGBDBM50084036(CHEMBL3425671)
Affinity DataIC50:  180nMAssay Description:Inhibition of GST-tagged human recombinant EGFR catalytic domain (668 to 1210 amino acids) T790M/L858R mutant expressed in Sf9 cells pre-incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Human)
Technische Universit£T Dortmund

Curated by ChEMBL
LigandPNGBDBM50084036(CHEMBL3425671)
Affinity DataIC50:  3.27E+3nMAssay Description:Inhibition of EGFR E746_A750 deletion mutant in human PC9 cells assessed as reduction in cell viability after 72 hrs by MTT assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Human)
Technische Universit£T Dortmund

Curated by ChEMBL
LigandPNGBDBM50084036(CHEMBL3425671)
Affinity DataIC50:  1.74E+4nMAssay Description:Inhibition of EGFR in human NCI-H460 cells assessed as reduction in cell viability after 72 hrs by MTT assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Mouse)
St. John'S University

Curated by ChEMBL
LigandPNGBDBM50084036(CHEMBL3425671)
Affinity DataIC50:  2.91E+3nMAssay Description:Inhibition of ABL in mouse BAF3 cells assessed as reduction in cell viability after 72 hrs by MTT assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Mouse)
St. John'S University

Curated by ChEMBL
LigandPNGBDBM50084036(CHEMBL3425671)
Affinity DataIC50:  5.56E+3nMAssay Description:Inhibition of ABL T315I mutant in mouse BAF3 cells assessed as reduction in cell viability after 72 hrs by MTT assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Human)
Technische Universit£T Dortmund

Curated by ChEMBL
LigandPNGBDBM50084036(CHEMBL3425671)
Affinity DataIC50:  6.10E+3nMAssay Description:Inhibition of EGFR E746_A750 deletion/T790M mutant in human growth-resistant PC9 cells assessed as reduction in cell viability after 72 hrs by MTT as...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed