Compile Data Set for Download or QSAR
Report error Found 51 Enz. Inhib. hit(s) with all data for entry = 50012092
TargetTyrosine-protein kinase Lck(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 15nMAssay Description:Inhibition of human p56 Lck tyrosine kinase (lck64-509)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lyn(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 29nMAssay Description:Inhibition of human p56 Lyn tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 41nMAssay Description:Inhibition of human Tyrosine-protein kinase CSKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 42nMAssay Description:Inhibition of Src protein tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114591(5-(4-Phenoxy-phenyl)-7-(tetrahydro-furan-3-yl)-7H-...)
Affinity DataIC50: 42nMAssay Description:Inhibition of human p56 Lck tyrosine kinase (lck64-509)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114582(7-Isoxazolidin-4-yl-5-(4-phenoxy-phenyl)-7H-pyrrol...)
Affinity DataIC50: 46nMAssay Description:Inhibition of human p56 Lck tyrosine kinase (lck64-509)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Blk(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 46nMAssay Description:Inhibition of human B lymphoid tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Fyn(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 59nMAssay Description:Inhibition of human p55 Fyn tyrosine kinase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114583(5-(4-Phenoxy-phenyl)-7-(4-piperidin-1-yl-cyclohexy...)
Affinity DataIC50: 82nMAssay Description:Inhibition of human p56 Lck tyrosine kinase (lck64-509)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50092228(7-Cyclopentyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-...)
Affinity DataIC50: 100nMAssay Description:Inhibition of human p56 Lck tyrosine kinase (lck64-509)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114590(5-(4-Phenoxy-phenyl)-7-(tetrahydro-pyran-4-yl)-7H-...)
Affinity DataIC50: 120nMAssay Description:Inhibition of human p56 Lck tyrosine kinase (lck64-509)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114586(2-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)
Affinity DataIC50: 130nMAssay Description:Inhibition of human p56 Lck tyrosine kinase (lck64-509)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114587(5-(4-Phenoxy-phenyl)-7-piperidin-4-yl-7H-pyrrolo[2...)
Affinity DataIC50: 170nMAssay Description:Inhibition of human p56 Lck tyrosine kinase (lck64-509)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114588(5-(4-Phenoxy-phenyl)-7-pyrrolidin-3-yl-7H-pyrrolo[...)
Affinity DataIC50: 240nMAssay Description:Inhibition of human p56 Lck tyrosine kinase (lck64-509)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM8793(CHEMBL45177 | 7-[4-(4-methylpiperazin-1-yl)cyclohe...)
Affinity DataIC50: 240nMAssay Description:Inhibition of human p56 Lck tyrosine kinase (lck64-509)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiopoietin-1 receptor(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 250nMAssay Description:Inhibition of TIE-2 kinase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114583(5-(4-Phenoxy-phenyl)-7-(4-piperidin-1-yl-cyclohexy...)
Affinity DataIC50: 298nMAssay Description:Inhibition of Src protein tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114591(5-(4-Phenoxy-phenyl)-7-(tetrahydro-furan-3-yl)-7H-...)
Affinity DataIC50: 320nMAssay Description:Inhibition of Src protein tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Blk(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM8793(CHEMBL45177 | 7-[4-(4-methylpiperazin-1-yl)cyclohe...)
Affinity DataIC50: 370nMAssay Description:Inhibition of human B lymphoid tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114582(7-Isoxazolidin-4-yl-5-(4-phenoxy-phenyl)-7H-pyrrol...)
Affinity DataIC50: 390nMAssay Description:Inhibition of Src protein tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lyn(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM8793(CHEMBL45177 | 7-[4-(4-methylpiperazin-1-yl)cyclohe...)
Affinity DataIC50: 430nMAssay Description:Inhibition of human p56 Lyn tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114589(5-(4-Phenoxy-phenyl)-7-(4-piperidin-1-yl-cyclohexy...)
Affinity DataIC50: 520nMAssay Description:Inhibition of human p56 Lck tyrosine kinase (lck64-509)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50092228(7-Cyclopentyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-...)
Affinity DataIC50: 560nMAssay Description:Inhibition of Src protein tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114584(7-(2-Amino-ethyl)-5-(4-phenoxy-phenyl)-7H-pyrrolo[...)
Affinity DataIC50: 890nMAssay Description:Inhibition of human p56 Lck tyrosine kinase (lck64-509)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114590(5-(4-Phenoxy-phenyl)-7-(tetrahydro-pyran-4-yl)-7H-...)
Affinity DataIC50: 1.12E+3nMAssay Description:Inhibition of Src protein tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM8793(CHEMBL45177 | 7-[4-(4-methylpiperazin-1-yl)cyclohe...)
Affinity DataIC50: 1.19E+3nMAssay Description:Inhibition of Src protein tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 1.19E+3nMAssay Description:Inhibition of Vascular endothelial growth factor receptor 2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114586(2-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)
Affinity DataIC50: 1.47E+3nMAssay Description:Inhibition of Src protein tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114587(5-(4-Phenoxy-phenyl)-7-piperidin-4-yl-7H-pyrrolo[2...)
Affinity DataIC50: 1.78E+3nMAssay Description:Inhibition of Src protein tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Fyn(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM8793(CHEMBL45177 | 7-[4-(4-methylpiperazin-1-yl)cyclohe...)
Affinity DataIC50: 2.03E+3nMAssay Description:Inhibition of human p55 Fyn tyrosine kinase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114588(5-(4-Phenoxy-phenyl)-7-pyrrolidin-3-yl-7H-pyrrolo[...)
Affinity DataIC50: 2.36E+3nMAssay Description:Inhibition of Src protein tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM8793(CHEMBL45177 | 7-[4-(4-methylpiperazin-1-yl)cyclohe...)
Affinity DataIC50: 4.27E+3nMAssay Description:Inhibition of human Csk tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50092228(7-Cyclopentyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-...)
Affinity DataIC50: 4.44E+3nMAssay Description:Inhibition of Vascular endothelial growth factor receptor 2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiopoietin-1 receptor(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114591(5-(4-Phenoxy-phenyl)-7-(tetrahydro-furan-3-yl)-7H-...)
Affinity DataIC50: 5.15E+3nMAssay Description:Inhibition of TIE-2 kinase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114589(5-(4-Phenoxy-phenyl)-7-(4-piperidin-1-yl-cyclohexy...)
Affinity DataIC50: 5.46E+3nMAssay Description:Inhibition of Src protein tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiopoietin-1 receptor(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM8793(CHEMBL45177 | 7-[4-(4-methylpiperazin-1-yl)cyclohe...)
Affinity DataIC50: 5.85E+3nMAssay Description:Inhibition of TIE-2 kinase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiopoietin-1 receptor(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114582(7-Isoxazolidin-4-yl-5-(4-phenoxy-phenyl)-7H-pyrrol...)
Affinity DataIC50: 6.62E+3nMAssay Description:Inhibition of TIE-2 kinase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiopoietin-1 receptor(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50092228(7-Cyclopentyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-...)
Affinity DataIC50: 9.07E+3nMAssay Description:Inhibition of TIE-2 kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM8793(CHEMBL45177 | 7-[4-(4-methylpiperazin-1-yl)cyclohe...)
Affinity DataIC50: 1.07E+4nMAssay Description:Inhibition of Vascular endothelial growth factor receptor 2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiopoietin-1 receptor(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114590(5-(4-Phenoxy-phenyl)-7-(tetrahydro-pyran-4-yl)-7H-...)
Affinity DataIC50: 1.16E+4nMAssay Description:Inhibition of TIE-2 kinase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiopoietin-1 receptor(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114589(5-(4-Phenoxy-phenyl)-7-(4-piperidin-1-yl-cyclohexy...)
Affinity DataIC50: 1.22E+4nMAssay Description:Inhibition of TIE-2 kinase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiopoietin-1 receptor(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114586(2-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)
Affinity DataIC50: 1.67E+4nMAssay Description:Inhibition of TIE-2 kinase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHepatocyte growth factor receptor(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of cMet kinase (Inactive at 1 mM ATP)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase ZAP-70(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Zeta-chain (TCR) associated protein kinase 70kDa, Zap70 (Inactive at 1 mM ATP)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCyclin-dependent kinase 1(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Cell division control protein 2, Cdk-1 (Inactive at 1 mM ATP)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetInsulin receptor(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of insulin receptor kinase (Inactive at 1 mM ATP)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Protein kinase C (Inactive at 1 mM ATP)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlatelet-derived growth factor receptor alpha/beta(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114585((R)-7-[4-(4-Methyl-piperazin-1-yl)-cyclohexyl]-5-(...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Platelet-derived growth factor receptor (Inactive at 1 mM ATP)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiopoietin-1 receptor(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114587(5-(4-Phenoxy-phenyl)-7-piperidin-4-yl-7H-pyrrolo[2...)
Affinity DataIC50: 2.14E+4nMAssay Description:Inhibition of TIE-2 kinase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Abbott Bioresearch Center

Curated by ChEMBL
LigandPNGBDBM50114584(7-(2-Amino-ethyl)-5-(4-phenoxy-phenyl)-7H-pyrrolo[...)
Affinity DataIC50: 3.23E+4nMAssay Description:Inhibition of Src protein tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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