Compile Data Set for Download or QSAR

Found 28 hits of Enzyme Inhibition Constant Data   

TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071664(5-Amino-2-[1-(3,5-dibromo-4-hydroxy-phenyl)-meth-(...)copy SMILEScopy InChI
Affinity DataIC50: 32nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071667(5-Amino-2-[1-(3,5-dichloro-4-hydroxy-phenyl)-meth-...)copy SMILEScopy InChI
Affinity DataIC50: 102nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071666(2-(3,5-Dibromo-4-hydroxy-benzylidene)-5,6-dimethox...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071677(2-[1-(3,5-Dibromo-4-hydroxy-phenyl)-meth-(E)-ylide...)copy SMILEScopy InChI
Affinity DataIC50: 144nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071668(2-(3,5-Dichloro-4-hydroxy-benzylidene)-5,6-dimetho...)copy SMILEScopy InChI
Affinity DataIC50: 310nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071664(5-Amino-2-[1-(3,5-dibromo-4-hydroxy-phenyl)-meth-(...)copy SMILEScopy InChI
Affinity DataIC50: 460nMAssay Description:Inhibition of Src tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071676(4-Amino-2-[1-(3,5-dibromo-4-hydroxy-phenyl)-meth-(...)copy SMILEScopy InChI
Affinity DataIC50: 470nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071665(5-Amino-2-[1-(3,4-dihydroxy-phenyl)-meth-(E)-ylide...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071670(6-Amino-2-[1-(3,5-dibromo-4-hydroxy-phenyl)-meth-(...)copy SMILEScopy InChI
Affinity DataIC50: 710nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071669(2-(3,5-Dibromo-4-hydroxy-benzylidene)-indan-1,3-di...)copy SMILEScopy InChI
Affinity DataIC50: 740nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071682(2-[1-(3-Bromo-4-hydroxy-5-methoxy-phenyl)-meth-(E)...)copy SMILEScopy InChI
Affinity DataIC50: 880nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071678(5-Bromo-2-[1-(3,5-dibromo-4-hydroxy-phenyl)-meth-(...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071675(2-[1-(3,5-Dichloro-4-hydroxy-phenyl)-meth-(Z)-ylid...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071681(2-[1-(3,4-Dihydroxy-phenyl)-meth-(E)-ylidene]-5-me...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071673(5-Amino-2-[1-(4-hydroxy-3,5-dimethoxy-phenyl)-meth...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071680(2-(3-Bromo-4-hydroxy-5-methoxy-benzylidene)-5,6-di...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071667(5-Amino-2-[1-(3,5-dichloro-4-hydroxy-phenyl)-meth-...)copy SMILEScopy InChI
Affinity DataIC50: 3.50E+3nMAssay Description:Inhibition of Src tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetcAMP-dependent protein kinase catalytic subunit alpha/beta/gamma(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071667(5-Amino-2-[1-(3,5-dichloro-4-hydroxy-phenyl)-meth-...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of Protein Kinase A (PKA)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071674(2-[1-(3,4-Dihydroxy-phenyl)-meth-(Z)-ylidene]-5-ni...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071671(5,6-Dichloro-2-(4-hydroxy-3-methoxy-benzylidene)-i...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071683(2-[1-(3,4-Dihydroxy-phenyl)-meth-(Z)-ylidene]-4-ni...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071672(2-[1-(3,5-Dibromo-4-hydroxy-phenyl)-meth-(E)-ylide...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071679(5-Amino-2-[1-(3,5-dibromo-4-hydroxy-phenyl)-meth-(...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50067024(2-(3,4-Dihydroxy-benzylidene)-indan-1,3-dione | CH...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50045936((E)-4-(3,5-dihydroxystyryl)benzene-1,2-diol | (E)-...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetcAMP-dependent protein kinase catalytic subunit alpha/beta/gamma(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071664(5-Amino-2-[1-(3,5-dibromo-4-hydroxy-phenyl)-meth-(...)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibition of Protein Kinase A (PKA)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetcAMP-dependent protein kinase catalytic subunit alpha/beta/gamma(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071677(2-[1-(3,5-Dibromo-4-hydroxy-phenyl)-meth-(E)-ylide...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of Protein Kinase A (PKA)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
R. W. Johnson Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50071677(2-[1-(3,5-Dibromo-4-hydroxy-phenyl)-meth-(E)-ylide...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of Src tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M3VPubMed
* indicates data uncertainty>20%