null

SMILES Cc1c(oc2ccc(C)cc12)-c1n(nc2c1c(N)n[nH]c2=O)-c1ccc(NC(=O)C=C)cc1

InChI Key InChIKey=HKMTYQNMRIBAHX-UHFFFAOYSA-N

PDB links: 1 PDB ID matches this monomer.

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 19 hits for monomerid = 50504104   

TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataKi:  1.90nMAssay Description:Irreversible inhibition of human FGFR1 using poly (Glu, Tyr)4:1 as substrate measured after 60 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetFibroblast growth factor receptor 3(Homo sapiens (Human))TBA
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 150nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human EGFR using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISA relative to controlMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetReceptor tyrosine-protein kinase erbB-4(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human ERbb4 using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISA relative to controlMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human ABL using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISA relative to controlMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay Description:Inhibition of human FGFR1 using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetFibroblast growth factor receptor 3(Homo sapiens (Human))TBA
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibition of human FGFR3 using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human PDGFRbeta using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human ERG by patch-clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human c-Src using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISA relative to controlMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human ALK using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISA relative to controlMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetVascular endothelial growth factor receptor 1(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human VEGFR1 using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:Inhibition of human FGFR2 using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetFibroblast growth factor receptor 4(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Inhibition of human FGFR4 using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetReceptor tyrosine-protein kinase erbB-2(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human ERbb2 using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISA relative to controlMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human c-MET using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISA relative to controlMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 4.80nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails
TargetEphrin type-A receptor 2(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human EPHA2 using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISA relative to controlMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Shanghai University

Curated by ChEMBL
LigandPNGBDBM50504104(CHEMBL4446835)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human VEGFR2 using poly (Glu, Tyr)4:1 as substrate measured after 60 mins by ELISAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP85D8PubMed