Compile Data Set for Download or QSAR

Found 128 hits of Enzyme Inhibition Constant Data   

TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)copy SMILEScopy InChI
Affinity DataIC50: 1.48E+3nMAssay Description:Inhibition of recombinant human SRC using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)copy SMILEScopy InChI
Affinity DataIC50: 1.91E+3nMAssay Description:Inhibition of recombinant human SRC using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)copy SMILEScopy InChI
Affinity DataIC50: 2.17E+3nMAssay Description:Inhibition of recombinant human SRC using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)copy SMILEScopy InChI
Affinity DataIC50: 2.24E+3nMAssay Description:Inhibition of recombinant human SRC using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibition of recombinant human IGF1-R using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of recombinant human SRC using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)copy SMILEScopy InChI
Affinity DataIC50: 2.42E+3nMAssay Description:Inhibition of recombinant human IGF1-R using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)copy SMILEScopy InChI
Affinity DataIC50: 2.46E+3nMAssay Description:Inhibition of recombinant human IGF1-R using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)copy SMILEScopy InChI
Affinity DataIC50: 2.77E+3nMAssay Description:Inhibition of recombinant human IGF1-R using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)copy SMILEScopy InChI
Affinity DataIC50: 3.16E+3nMAssay Description:Inhibition of recombinant human IGF1-R using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)copy SMILEScopy InChI
Affinity DataIC50: 4.16E+3nMAssay Description:Inhibition of recombinant human ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)copy SMILEScopy InChI
Affinity DataIC50: 4.35E+3nMAssay Description:Inhibition of recombinant human VEGF-R2 using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)copy SMILEScopy InChI
Affinity DataIC50: 4.36E+3nMAssay Description:Inhibition of recombinant human ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)copy SMILEScopy InChI
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibition of recombinant human VEGF-R2 using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)copy SMILEScopy InChI
Affinity DataIC50: 4.73E+3nMAssay Description:Inhibition of recombinant human ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)copy SMILEScopy InChI
Affinity DataIC50: 4.85E+3nMAssay Description:Inhibition of recombinant human VEGF-R2 using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)copy SMILEScopy InChI
Affinity DataIC50: 4.95E+3nMAssay Description:Inhibition of recombinant human VEGF-R2 using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)copy SMILEScopy InChI
Affinity DataIC50: 6.01E+3nMAssay Description:Inhibition of recombinant human VEGF-R2 using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)copy SMILEScopy InChI
Affinity DataIC50: 7.55E+3nMAssay Description:Inhibition of recombinant human ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)copy SMILEScopy InChI
Affinity DataIC50: 9.33E+3nMAssay Description:Inhibition of recombinant human ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)copy SMILEScopy InChI
Affinity DataIC50: 9.63E+3nMAssay Description:Inhibition of recombinant human FAK using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)copy SMILEScopy InChI
Affinity DataIC50: 9.92E+3nMAssay Description:Inhibition of recombinant human FAK using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)copy SMILEScopy InChI
Affinity DataIC50: 1.07E+4nMAssay Description:Inhibition of recombinant human FAK using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)copy SMILEScopy InChI
Affinity DataIC50: 1.32E+4nMAssay Description:Inhibition of recombinant human FAK using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)copy SMILEScopy InChI
Affinity DataIC50: 1.47E+4nMAssay Description:Inhibition of recombinant human AXLMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)copy SMILEScopy InChI
Affinity DataIC50: 1.69E+4nMAssay Description:Inhibition of recombinant human FAK using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)copy SMILEScopy InChI
Affinity DataIC50: 1.69E+4nMAssay Description:Inhibition of recombinant human AXLMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)copy SMILEScopy InChI
Affinity DataIC50: 2.02E+4nMAssay Description:Inhibition of recombinant human AXLMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)copy SMILEScopy InChI
Affinity DataIC50: 2.19E+4nMAssay Description:Inhibition of recombinant human AXLMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetAurora kinase B(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)copy SMILEScopy InChI
Affinity DataIC50: 2.51E+4nMAssay Description:Inhibition of recombinant human Aurora-B using tetra(LRRWLSG) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)copy SMILEScopy InChI
Affinity DataIC50: 2.75E+4nMAssay Description:Inhibition of wild type human MET using poly(Ala,Glu,Lys,Tyr) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)copy SMILEScopy InChI
Affinity DataIC50: 3.26E+4nMAssay Description:Inhibition of recombinant human AXLMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+4nMAssay Description:Inhibition of wild type human MET using poly(Ala,Glu,Lys,Tyr) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetAurora kinase B(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)copy SMILEScopy InChI
Affinity DataIC50: 3.81E+4nMAssay Description:Inhibition of recombinant human Aurora-B using tetra(LRRWLSG) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)copy SMILEScopy InChI
Affinity DataIC50: 4.76E+4nMAssay Description:Inhibition of wild type human MET using poly(Ala,Glu,Lys,Tyr) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetDual specificity mitogen-activated protein kinase kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)copy SMILEScopy InChI
Affinity DataIC50: 4.89E+4nMAssay Description:Inhibition of wild type human MEK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)copy SMILEScopy InChI
Affinity DataIC50: 7.15E+4nMAssay Description:Inhibition of wild type human MET using poly(Ala,Glu,Lys,Tyr) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)copy SMILEScopy InChI
Affinity DataIC50: 7.80E+4nMAssay Description:Inhibition of wild type human MET using poly(Ala,Glu,Lys,Tyr) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetAurora kinase B(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human Aurora-B using tetra(LRRWLSG) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human AKT1 using GSK3 (amino acids 14 to 27) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human AKT1 using GSK3 (amino acids 14 to 27) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetDual specificity mitogen-activated protein kinase kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358248(CHEMBL456294)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of wild type human MEK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetDual specificity mitogen-activated protein kinase kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358250(CALICOFEROL B)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of wild type human MEK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358250(CALICOFEROL B)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of wild type human MET using poly(Ala,Glu,Lys,Tyr) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetSerine/threonine-protein kinase Nek2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358249(CHEMBL515982)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human NEK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358250(CALICOFEROL B)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human PIM1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetSerine/threonine-protein kinase N1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human PRK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetSerine/threonine-protein kinase N1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358248(CHEMBL456294)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human PRK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetSerine/threonine-protein kinase N1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358250(CALICOFEROL B)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human PRK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358249(CHEMBL515982)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human VEGF-R2 using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1D38PubMed
Displayed 1 to 50 (of 128 total ) | Next | Last >>* indicates data uncertainty>20%