Compile Data Set for Download or QSAR
Report error Found 34 Enz. Inhib. hit(s) with all data for entry = 50028880
TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50045936(CHEMBL69863 | 4-(3,5-dihydroxystyryl)benzene-1,2-d...)
Affinity DataIC50: 6.60E+4nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279912(4-(Phenyl-hydrazonomethyl)-benzene-1,2-diol | CHEM...)
Affinity DataIC50: 7.00E+4nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279914(4-[(2,4-Dinitro-phenyl)-hydrazonomethyl]-benzene-1...)
Affinity DataIC50: 1.44E+5nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279897(5-(Pyridin-2-yl-hydrazonomethyl)-benzene-1,2,3-tri...)
Affinity DataIC50: 1.79E+5nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279909(4-(Pyridin-2-yl-hydrazonomethyl)-benzene-1,2-diol ...)
Affinity DataIC50: 2.27E+5nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279904(2-[(4-Methoxy-phenyl)-hydrazonomethyl]-benzene-1,4...)
Affinity DataIC50: 3.10E+5nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279910(3-[(4-Methoxy-phenyl)-hydrazonomethyl]-benzene-1,2...)
Affinity DataIC50: 3.10E+5nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279902(4-(Phenyl-hydrazonomethyl)-benzene-1,3-diol | CHEM...)
Affinity DataIC50: 3.50E+5nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279919(4-[(2,4-Dinitro-phenyl)-hydrazonomethyl]-benzene-1...)
Affinity DataIC50: 3.52E+5nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279907(N-Pyridin-2-yl-N'-[1-pyridin-3-yl-meth-(E)-ylidene...)
Affinity DataIC50: 4.00E+5nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279925(4-[(4-Bromo-phenyl)-hydrazonomethyl]-benzene-1,3-d...)
Affinity DataIC50: 5.21E+5nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279926(4-(Pyridin-2-yl-hydrazonomethyl)-benzene-1,2,3-tri...)
Affinity DataIC50: 5.22E+5nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279911(4-[(4-Bromo-phenyl)-hydrazonomethyl]-benzene-1,2-d...)
Affinity DataIC50: 5.99E+5nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279903(4-[(4-Methoxy-phenyl)-hydrazonomethyl]-benzene-1,2...)
Affinity DataIC50: 7.43E+5nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279920(4-[(2,4-Dinitro-phenyl)-hydrazonomethyl]-benzene-1...)
Affinity DataIC50: 1.01E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279896(4-(Pyridin-2-yl-hydrazonomethyl)-benzene-1,3-diol ...)
Affinity DataIC50: 1.01E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279917(4-[(4-Bromo-phenyl)-hydrazonomethyl]-benzene-1,2,3...)
Affinity DataIC50: 1.04E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279921(3-(Phenyl-hydrazonomethyl)-benzene-1,2-diol | CHEM...)
Affinity DataIC50: 1.26E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279898(N-Phenyl-N'-[1-pyridin-3-yl-meth-(E)-ylidene]-hydr...)
Affinity DataIC50: 1.32E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279899(4-(Phenyl-hydrazonomethyl)-benzene-1,2,3-triol | C...)
Affinity DataIC50: 1.57E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279905(2-Methoxy-5-(phenyl-hydrazonomethyl)-phenol | CHEM...)
Affinity DataIC50: 2.11E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279908(4-Bromo-2-[(4-bromo-phenyl)-hydrazonomethyl]-pheno...)
Affinity DataIC50: 2.16E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279906(5-[(4-Bromo-phenyl)-hydrazonomethyl]-2-methoxy-phe...)
Affinity DataIC50: 2.49E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279918(3-[(2,4-Dinitro-phenyl)-hydrazonomethyl]-benzene-1...)
Affinity DataIC50: 2.51E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279913(2-Methoxy-4-(phenyl-hydrazonomethyl)-phenol | CHEM...)
Affinity DataIC50: 2.59E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279901(4-Bromo-2-(phenyl-hydrazonomethyl)-phenol | CHEMBL...)
Affinity DataIC50: 2.61E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279900(N-(4-Bromo-phenyl)-N'-[1-pyridin-4-yl-meth-(E)-yli...)
Affinity DataIC50: 2.90E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279924(N-(4-Bromo-phenyl)-N'-[1-pyridin-2-yl-meth-(E)-yli...)
Affinity DataIC50: 2.90E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279928(N-(4-Bromo-phenyl)-N'-[1-pyridin-3-yl-meth-(E)-yli...)
Affinity DataIC50: 2.90E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279922(N-[1-(3-Nitro-phenyl)-meth-(E)-ylidene]-N'-phenyl-...)
Affinity DataIC50: 3.32E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279923(CHEMBL69572 | cid_252617 | N-[1-(4-Nitro-phenyl)-m...)
Affinity DataIC50: 3.32E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279916(2-(Phenyl-hydrazonomethyl)-benzene-1,4-diol | CHEM...)
Affinity DataIC50: 3.50E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279915(N-Phenyl-N'-[1-pyridin-2-yl-meth-(E)-ylidene]-hydr...)
Affinity DataIC50: 4.06E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article

TargetTyrosine-protein kinase Lck(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50279927(N-Phenyl-N'-[1-pyridin-4-yl-meth-(E)-ylidene]-hydr...)
Affinity DataIC50: 4.06E+6nMAssay Description:Inhibitory concentration against phosphorylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2010
Entry Details Article