Compile Data Set for Download or QSAR
Found 46 Enz. Inhib. hit(s) with all data for entry = 50013584
LigandPNGBDBM50132175(2-[(3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-ylam...)copy SMILEScopy InChI
Affinity DataIC50: 440nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132169((3-Chloro-phenyl)-(3-isopropyl-1H-pyrazolo[4,3-d]p...)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132178(5-[(3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-ylam...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132183((3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl)-pen...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132185(Benzyl-(3-isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132172(3-[(3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-ylam...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132179(4-[(3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-ylam...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132174((3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl)-(4-...)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+3nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132167(CHEMBL103206 | Furan-2-ylmethyl-(3-isopropyl-1H-py...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132177(3-[(9-Isopropyl-9H-purin-6-ylamino)-methyl]-phenol...)copy SMILEScopy InChI
Affinity DataIC50: 3.10E+3nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM10641(6-(benzylamino)-9-isopropylpurine | CHEMBL85015 | ...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+3nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132176((9-Isopropyl-9H-purin-6-yl)-(4-methoxy-benzyl)-ami...)copy SMILEScopy InChI
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132171(4-[(9-Isopropyl-9H-purin-6-ylamino)-methyl]-phenol...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132170(2-[(9-Isopropyl-9H-purin-6-ylamino)-methyl]-phenol...)copy SMILEScopy InChI
Affinity DataIC50: 4.40E+3nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132186(5-[(9-Isopropyl-9H-purin-6-ylamino)-methyl]-2-meth...)copy SMILEScopy InChI
Affinity DataIC50: 4.50E+3nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132180((3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl)-(3-...)copy SMILEScopy InChI
Affinity DataIC50: 4.50E+3nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132173((3-Chloro-phenyl)-(9-isopropyl-9H-purin-6-yl)-amin...)copy SMILEScopy InChI
Affinity DataIC50: 5.90E+3nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132182((9-Isopropyl-9H-purin-6-yl)-pentyl-amine | CHEMBL9...)copy SMILEScopy InChI
Affinity DataIC50: 6.90E+3nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM5718(2,6,9-Trisubstituted purine deriv. 26 | 2-{[6-(ben...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132168(CHEMBL103798 | Furan-2-ylmethyl-(9-isopropyl-9H-pu...)copy SMILEScopy InChI
Affinity DataIC50: 9.10E+3nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132187((2-Bromo-benzyl)-(3-isopropyl-1H-pyrazolo[4,3-d]py...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132184((9-Isopropyl-9H-purin-6-yl)-(3-methyl-but-2-enyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+4nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132169((3-Chloro-phenyl)-(3-isopropyl-1H-pyrazolo[4,3-d]p...)copy SMILEScopy InChI
Affinity DataIC50: 1.84E+4nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132181((2-Bromo-benzyl)-(9-isopropyl-9H-purin-6-yl)-amine...)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+4nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132178(5-[(3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-ylam...)copy SMILEScopy InChI
Affinity DataIC50: 2.60E+4nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132187((2-Bromo-benzyl)-(3-isopropyl-1H-pyrazolo[4,3-d]py...)copy SMILEScopy InChI
Affinity DataIC50: 2.90E+4nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132174((3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl)-(4-...)copy SMILEScopy InChI
Affinity DataIC50: 4.60E+4nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132181((2-Bromo-benzyl)-(9-isopropyl-9H-purin-6-yl)-amine...)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+4nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132175(2-[(3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-ylam...)copy SMILEScopy InChI
Affinity DataIC50: 5.40E+4nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132173((3-Chloro-phenyl)-(9-isopropyl-9H-purin-6-yl)-amin...)copy SMILEScopy InChI
Affinity DataIC50: 5.40E+4nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132183((3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl)-pen...)copy SMILEScopy InChI
Affinity DataIC50: 6.10E+4nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132185(Benzyl-(3-isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-...)copy SMILEScopy InChI
Affinity DataIC50: 6.60E+4nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132172(3-[(3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-ylam...)copy SMILEScopy InChI
Affinity DataIC50: 8.80E+4nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132186(5-[(9-Isopropyl-9H-purin-6-ylamino)-methyl]-2-meth...)copy SMILEScopy InChI
Affinity DataIC50: 1.04E+5nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132179(4-[(3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-ylam...)copy SMILEScopy InChI
Affinity DataIC50: 1.12E+5nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM10641(6-(benzylamino)-9-isopropylpurine | CHEMBL85015 | ...)copy SMILEScopy InChI
Affinity DataIC50: 1.13E+5nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132170(2-[(9-Isopropyl-9H-purin-6-ylamino)-methyl]-phenol...)copy SMILEScopy InChI
Affinity DataIC50: 1.25E+5nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132182((9-Isopropyl-9H-purin-6-yl)-pentyl-amine | CHEMBL9...)copy SMILEScopy InChI
Affinity DataIC50: 1.44E+5nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132180((3-Isopropyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl)-(3-...)copy SMILEScopy InChI
Affinity DataIC50: 1.52E+5nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM5718(2,6,9-Trisubstituted purine deriv. 26 | 2-{[6-(ben...)copy SMILEScopy InChI
Affinity DataIC50: 1.63E+5nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132171(4-[(9-Isopropyl-9H-purin-6-ylamino)-methyl]-phenol...)copy SMILEScopy InChI
Affinity DataIC50: 1.67E+5nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132167(CHEMBL103206 | Furan-2-ylmethyl-(3-isopropyl-1H-py...)copy SMILEScopy InChI
Affinity DataIC50: 1.67E+5nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132177(3-[(9-Isopropyl-9H-purin-6-ylamino)-methyl]-phenol...)copy SMILEScopy InChI
Affinity DataIC50: 1.67E+5nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132168(CHEMBL103798 | Furan-2-ylmethyl-(9-isopropyl-9H-pu...)copy SMILEScopy InChI
Affinity DataIC50: 1.67E+5nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132176((9-Isopropyl-9H-purin-6-yl)-(4-methoxy-benzyl)-ami...)copy SMILEScopy InChI
Affinity DataIC50: 1.67E+5nMAssay Description:Inhibitory concentration against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed
LigandPNGBDBM50132184((9-Isopropyl-9H-purin-6-yl)-(3-methyl-but-2-enyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 1.67E+5nMAssay Description:In vitro antiproliferative activity against myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29Z948QPubMed