null

SMILES CN(CCN(C)Cc1ccc(cc1)C(=O)Nc1ccc2ncnc(Nc3cccc(Cl)c3)c2c1)CCn1nc(-c2ccc(Cl)cc2)c2c(N)ncnc12

InChI Key InChIKey=OEJQOBRQZABLAP-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50282192   

TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Hunan University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50282192(CHEMBL4163321)copy SMILEScopy InChI
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibition of Src kinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D79DX7PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50282192(CHEMBL4163321)copy SMILEScopy InChI
Affinity DataIC50: 320nMAssay Description:Inhibitory activity to dihydrofolate reductase in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Hunan University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50282192(CHEMBL4163321)copy SMILEScopy InChI
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibitory activity to dihydrofolate reductase in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails
TargetEpidermal growth factor receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50282192(CHEMBL4163321)copy SMILEScopy InChI
Affinity DataIC50: 320nMAssay Description:Inhibition of human A431 cells derived EGFR by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D79DX7PubMed