null

SMILES CCOC(=O)c1ccc(cc1)-c1cn(-c2ccccc2)c2ncnc(N)c12

InChI Key InChIKey=KPNHRZBBKFZVMF-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 7 hits for monomerid = 50088914   

TargetTyrosine-protein kinase ABL1/ABL2(Homo sapiens (Human))
Novartis Pharma AG

Curated by ChEMBL
LigandPNGBDBM50088914(4-(4-Amino-7-phenyl-7H-pyrrolo[2,3-d]pyrimidin-5-y...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Tested in vitro for inhibition of non-receptor tyrosine kinase v-AblMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R78DG4PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Gallus gallus (Chicken))
Novartis Pharma AG

Curated by ChEMBL
LigandPNGBDBM50088914(4-(4-Amino-7-phenyl-7H-pyrrolo[2,3-d]pyrimidin-5-y...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Tested for inhibition of protein tyrosine kinase c-Src phosphorylationMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R78DG4PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Novartis Pharma AG

Curated by ChEMBL
LigandPNGBDBM50088914(4-(4-Amino-7-phenyl-7H-pyrrolo[2,3-d]pyrimidin-5-y...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Tested in vitro for inhibition of KDR-receptor tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R78DG4PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))TBA
LigandPNGBDBM50088914(4-(4-Amino-7-phenyl-7H-pyrrolo[2,3-d]pyrimidin-5-y...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of c-Src kinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BZ68ZH
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Novartis Pharma AG

Curated by ChEMBL
LigandPNGBDBM50088914(4-(4-Amino-7-phenyl-7H-pyrrolo[2,3-d]pyrimidin-5-y...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Tested in vitro for inhibition of EGF-receptor tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R78DG4PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))TBA
LigandPNGBDBM50088914(4-(4-Amino-7-phenyl-7H-pyrrolo[2,3-d]pyrimidin-5-y...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of c-SrcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC8434PubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Novartis Pharma AG

Curated by ChEMBL
LigandPNGBDBM50088914(4-(4-Amino-7-phenyl-7H-pyrrolo[2,3-d]pyrimidin-5-y...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Tested in vitro for inhibition of serine/threonine kinase Cdc2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R78DG4PubMed