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Found 34 Enz. Inhib. hit(s) with all data for entry = 50028880
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50045936((E)-4-(3,5-dihydroxystyryl)benzene-1,2-diol | (E)-...)
Affinity DataIC50:  6.60E+4nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279912(4-(Phenyl-hydrazonomethyl)-benzene-1,2-diol | CHEM...)
Affinity DataIC50:  7.00E+4nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279914(4-[(2,4-Dinitro-phenyl)-hydrazonomethyl]-benzene-1...)
Affinity DataIC50:  1.44E+5nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (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 phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279909(4-(Pyridin-2-yl-hydrazonomethyl)-benzene-1,2-diol ...)
Affinity DataIC50:  2.27E+5nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279904(2-[(4-Methoxy-phenyl)-hydrazonomethyl]-benzene-1,4...)
Affinity DataIC50:  3.10E+5nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279910(3-[(4-Methoxy-phenyl)-hydrazonomethyl]-benzene-1,2...)
Affinity DataIC50:  3.10E+5nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279902(4-(Phenyl-hydrazonomethyl)-benzene-1,3-diol | CHEM...)
Affinity DataIC50:  3.50E+5nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279919(4-[(2,4-Dinitro-phenyl)-hydrazonomethyl]-benzene-1...)
Affinity DataIC50:  3.52E+5nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279907(CHEMBL68997 | N-Pyridin-2-yl-N'-[1-pyridin-3-yl-me...)
Affinity DataIC50:  4.00E+5nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279925(4-[(4-Bromo-phenyl)-hydrazonomethyl]-benzene-1,3-d...)
Affinity DataIC50:  5.21E+5nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (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 phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279911(4-[(4-Bromo-phenyl)-hydrazonomethyl]-benzene-1,2-d...)
Affinity DataIC50:  5.99E+5nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279903(4-[(4-Methoxy-phenyl)-hydrazonomethyl]-benzene-1,2...)
Affinity DataIC50:  7.43E+5nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279920(4-[(2,4-Dinitro-phenyl)-hydrazonomethyl]-benzene-1...)
Affinity DataIC50:  1.01E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279896(4-(Pyridin-2-yl-hydrazonomethyl)-benzene-1,3-diol ...)
Affinity DataIC50:  1.01E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279917(4-[(4-Bromo-phenyl)-hydrazonomethyl]-benzene-1,2,3...)
Affinity DataIC50:  1.04E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279921(3-(Phenyl-hydrazonomethyl)-benzene-1,2-diol | CHEM...)
Affinity DataIC50:  1.26E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279898(CHEMBL62881 | N-Phenyl-N'-[1-pyridin-3-yl-meth-(E)...)
Affinity DataIC50:  1.32E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279899(4-(Phenyl-hydrazonomethyl)-benzene-1,2,3-triol | C...)
Affinity DataIC50:  1.57E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279905(2-Methoxy-5-(phenyl-hydrazonomethyl)-phenol | CHEM...)
Affinity DataIC50:  2.11E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279908(4-Bromo-2-[(4-bromo-phenyl)-hydrazonomethyl]-pheno...)
Affinity DataIC50: >2.16E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279906(5-[(4-Bromo-phenyl)-hydrazonomethyl]-2-methoxy-phe...)
Affinity DataIC50: >2.49E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279918(3-[(2,4-Dinitro-phenyl)-hydrazonomethyl]-benzene-1...)
Affinity DataIC50: >2.51E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279913(2-Methoxy-4-(phenyl-hydrazonomethyl)-phenol | CHEM...)
Affinity DataIC50:  2.59E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279901(4-Bromo-2-(phenyl-hydrazonomethyl)-phenol | CHEMBL...)
Affinity DataIC50: >2.61E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279924(CHEMBL67586 | N-(4-Bromo-phenyl)-N'-[1-pyridin-2-y...)
Affinity DataIC50: >2.90E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279900(CHEMBL67159 | N-(4-Bromo-phenyl)-N'-[1-pyridin-4-y...)
Affinity DataIC50: >2.90E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279928(CHEMBL69089 | N-(4-Bromo-phenyl)-N'-[1-pyridin-3-y...)
Affinity DataIC50: >2.90E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279922(CHEMBL307304 | N-[1-(3-Nitro-phenyl)-meth-(E)-ylid...)
Affinity DataIC50: >3.32E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279923(CHEMBL69572 | N-[1-(4-Nitro-phenyl)-meth-(E)-ylide...)
Affinity DataIC50: >3.32E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279916(2-(Phenyl-hydrazonomethyl)-benzene-1,4-diol | CHEM...)
Affinity DataIC50: >3.50E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279915(CHEMBL69762 | N-Phenyl-N'-[1-pyridin-2-yl-meth-(E)...)
Affinity DataIC50: >4.06E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279927(CHEMBL303617 | N-Phenyl-N'-[1-pyridin-4-yl-meth-(E...)
Affinity DataIC50: >4.06E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article