Compile Data Set for Download or QSAR

Found 58 hits of Enzyme Inhibition Constant Data   

TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181669(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataKi:  500nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181675(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataKi:  1.10E+3nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181669(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataKi:  5.30E+3nMAssay Description:Inhibitory activity against IRKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181670(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataKi:  8.80E+3nMAssay Description:Inhibitory activity against IRKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181675(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataKi:  9.00E+3nMAssay Description:Inhibitory activity against IRKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 400nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181670(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181674(6'-methoxy-6-oxo-1,6-dihydro-[3,3']bipyridinyl-5-c...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibitory activity against IRKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor/Nucleophosmin(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181670(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+3nMAssay Description:Antiproliferative activity against human NPM-ALK positive anaplastic large cell lymphoma karpas299 cell lineMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181671(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+3nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetBreakpoint cluster region protein/Tyrosine-protein kinase ABL1(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181670(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 3.80E+3nMAssay Description:Antiproliferative activity against human BCR-ABL positive chronic myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181679(5-(2-methyl-benzothiazol-5-yl)-2-oxo-1,2-dihydro-p...)copy SMILEScopy InChI
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibitory activity against Flt3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181670(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibitory activity against Flt3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181682(2-oxo-5-quinoxalin-6-yl-1,2-dihydro-pyridine-3-car...)copy SMILEScopy InChI
Affinity DataIC50: 5.50E+3nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor/Nucleophosmin(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181670(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+3nMAssay Description:Antiproliferative activity against murine BaF3 cell line expressing NPM-ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181682(2-oxo-5-quinoxalin-6-yl-1,2-dihydro-pyridine-3-car...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibitory activity against IRKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibitory activity against IGF1RMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181673(5-(3,4,5-trimethoxyphenyl)-2-oxo-1,2-dihydro-pyrid...)copy SMILEScopy InChI
Affinity DataIC50: 7.50E+3nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor/Nucleophosmin(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 7.50E+3nMAssay Description:Antiproliferative activity against human NPM-ALK positive anaplastic large cell lymphoma karpas299 cell lineMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor/Nucleophosmin(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181675(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 9.40E+3nMAssay Description:Antiproliferative activity against human NPM-ALK positive anaplastic large cell lymphoma karpas299 cell lineMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetBreakpoint cluster region protein/Tyrosine-protein kinase ABL1(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 9.50E+3nMAssay Description:Antiproliferative activity against human BCR-ABL positive chronic myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor/Nucleophosmin(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181669(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 1.12E+4nMAssay Description:Antiproliferative activity against human NPM-ALK positive anaplastic large cell lymphoma karpas299 cell lineMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetBreakpoint cluster region protein/Tyrosine-protein kinase ABL1(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181669(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 1.29E+4nMAssay Description:Antiproliferative activity against human BCR-ABL positive chronic myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor/Nucleophosmin(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181675(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 1.37E+4nMAssay Description:Antiproliferative activity against murine BaF3 cell line expressing NPM-ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181674(6'-methoxy-6-oxo-1,6-dihydro-[3,3']bipyridinyl-5-c...)copy SMILEScopy InChI
Affinity DataIC50: 1.38E+4nMAssay Description:Inhibitory activity against IRKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181683(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 1.38E+4nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181676(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 1.45E+4nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetBreakpoint cluster region protein/Tyrosine-protein kinase ABL1(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181675(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 1.46E+4nMAssay Description:Antiproliferative activity against human BCR-ABL positive chronic myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181670(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibitory activity against IGF1RMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181679(5-(2-methyl-benzothiazol-5-yl)-2-oxo-1,2-dihydro-p...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibitory activity against IRKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor/Nucleophosmin(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 1.74E+4nMAssay Description:Antiproliferative activity against murine BaF3 cell line expressing NPM-ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181680(6-oxo-1,6-dihydro-[3,4']bipyridinyl-5-carboxylic a...)copy SMILEScopy InChI
Affinity DataIC50: 1.95E+4nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181669(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against IGF1RMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181675(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against AblMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against SrcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181670(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against AblMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181675(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against Flt3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181669(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against SrcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181669(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against AblMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181670(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against SrcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181675(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against SrcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against AblMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181675(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against IGF1RMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181669(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against Flt3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181677(5-benzo[1,3]dioxol-5-yl-2-methoxy-N-[4-(4-methyl-p...)copy SMILEScopy InChI
Affinity DataIC50: 2.03E+4nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor/Nucleophosmin(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181669(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+4nMAssay Description:Antiproliferative activity against murine BaF3 cell line expressing NPM-ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181678(5-benzo[1,3]dioxol-5-yl-2-chloro-N-[4-(4-methyl-pi...)copy SMILEScopy InChI
Affinity DataIC50: 2.68E+4nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181678(5-benzo[1,3]dioxol-5-yl-2-chloro-N-[4-(4-methyl-pi...)copy SMILEScopy InChI
Affinity DataIC50: 2.73E+4nMAssay Description:Inhibitory activity against IRKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
Displayed 1 to 50 (of 58 total ) | Next | Last >>* indicates data uncertainty>20%