Compile Data Set for Download or QSAR
maximum 50k data
Found 128 Enz. Inhib. hit(s) with all data for entry = 50034172
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
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 ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)
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 ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)
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 ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)
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 ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
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 ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)
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 ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)
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 ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)
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 ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)
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 ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)
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 ArticlePubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)
Affinity DataIC50:  4.16E+3nMAssay Description:Inhibition of recombinant human ALKMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)
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 ArticlePubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50:  4.36E+3nMAssay Description:Inhibition of recombinant human ALKMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)
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 ArticlePubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)
Affinity DataIC50:  4.73E+3nMAssay Description:Inhibition of recombinant human ALKMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
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 ArticlePubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)
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 ArticlePubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)
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 ArticlePubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)
Affinity DataIC50:  7.55E+3nMAssay Description:Inhibition of recombinant human ALKMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)
Affinity DataIC50:  9.33E+3nMAssay Description:Inhibition of recombinant human ALKMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)
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 ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)
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 ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
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 ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)
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 ArticlePubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)
Affinity DataIC50:  1.47E+4nMAssay Description:Inhibition of recombinant human AXLMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)
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 ArticlePubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)
Affinity DataIC50:  1.69E+4nMAssay Description:Inhibition of recombinant human AXLMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
Affinity DataIC50:  2.02E+4nMAssay Description:Inhibition of recombinant human AXLMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)
Affinity DataIC50:  2.19E+4nMAssay Description:Inhibition of recombinant human AXLMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase B(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)
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 ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
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 ArticlePubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)
Affinity DataIC50:  3.26E+4nMAssay Description:Inhibition of recombinant human AXLMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)
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 ArticlePubMed
TargetAurora kinase B(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358243(CHEMBL1922224)
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 ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)
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 ArticlePubMed
TargetDual specificity mitogen-activated protein kinase kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)
Affinity DataIC50:  4.89E+4nMAssay Description:Inhibition of wild type human MEK1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)
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 ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358247(ASTROGORGIADIOL)
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 ArticlePubMed
TargetAurora kinase B(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358250(CALICOFEROL B)
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 ArticlePubMed
TargetAurora kinase B(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358244(CALICOFEROL A)
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 ArticlePubMed
TargetAurora kinase B(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358248(CHEMBL456294)
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 ArticlePubMed
TargetAurora kinase B(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358249(CHEMBL515982)
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 ArticlePubMed
TargetAurora kinase B(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358245(CHEMBL1922225)
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 ArticlePubMed
TargetAurora kinase B(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358246(CHEMBL456936)
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 ArticlePubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358250(CALICOFEROL B)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human AXLMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358248(CHEMBL456294)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human FAK using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358249(CHEMBL515982)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human FAK using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358250(CALICOFEROL B)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human FAK using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358248(CHEMBL456294)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human IGF1-R using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50358249(CHEMBL515982)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human IGF1-R using poly(Glu,Tyr)4:1 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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