Compile Data Set for Download or QSAR
maximum 50k data
Found 30 Enz. Inhib. hit(s) with all data for entry = 50011854
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)
Affinity DataIC50:  800nMAssay Description:Inhibition of Cell division cycle 2 (CDK1)-cyclin BMore data for this Ligand-Target Pair
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111434(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of Cyclin-dependent kinase 5-p35nck5aMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111434(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)
Affinity DataIC50:  6.00E+3nMAssay Description:Inhibition of Cyclin-dependent kinase 2-cyclin AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM5718(2,6,9-Trisubstituted purine deriv. 26 | 2-{[6-(ben...)
Affinity DataIC50:  7.00E+3nMAssay Description:Inhibition of Cyclin-dependent kinase 5-p35nck5aMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

LigandPNGBDBM100152(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)
Affinity DataIC50:  1.80E+4nMAssay Description:Inhibition of Cell division cycle 2 (CDK1)-cyclin BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM100152(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)
Affinity DataIC50:  2.10E+4nMAssay Description:Inhibition of Cyclin-dependent kinase 5-p35nck5aMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111433(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)
Affinity DataIC50:  2.20E+4nMAssay Description:Inhibition of Cyclin-dependent kinase 2-cyclin AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111435(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)
Affinity DataIC50:  2.40E+4nMAssay Description:Inhibition of Cyclin-dependent kinase 5-p35nck5aMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50111434(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)
Affinity DataIC50:  2.50E+4nMAssay Description:Inhibition of Cyclin-dependent kinase 5-p35nck5aMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111435(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)
Affinity DataIC50:  3.00E+4nMAssay Description:Inhibition of Cyclin-dependent kinase 2-cyclin AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM100152(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)
Affinity DataIC50:  3.50E+4nMAssay Description:Inhibition of Cyclin-dependent kinase 2-cyclin AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50111435(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)
Affinity DataIC50:  4.20E+4nMAssay Description:Inhibition of Cell division cycle 2 (CDK1)-cyclin BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50111433(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)
Affinity DataIC50:  4.50E+4nMAssay Description:Inhibition of Cell division cycle 2 (CDK1)-cyclin BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Lyn(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111434(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Lyn tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111434(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of protein kinase CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111435(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of protein kinase CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM100152(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of protein kinase CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetO94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111433(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of protein kinase CMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111434(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Fyn kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111434(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111435(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM100152(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111433(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Fyn kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Lyn(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111435(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Lyn tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Lyn(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111433(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Lyn tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM100152(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Fyn kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Lyn(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM100152(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Lyn tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111433(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111435(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Fyn kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50111433(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)
Affinity DataIC50: >1.20E+6nMAssay Description:Inhibition of Cyclin-dependent kinase 5-p35nck5aMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed