Compile Data Set for Download or QSAR
Found 61 with Last Name = 'moravcová' and Initial = 'd'
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132192(CHEMBL102871 | N*2*-(4-Amino-cyclohexyl)-N*6*-(3-c...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM27216((2R)-2-({6-[(3-chlorophenyl)amino]-9-(propan-2-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
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
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)copy SMILEScopy InChI
Affinity DataIC50: 450nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
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
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
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
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
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132199(3-{[8-Chloro-2-(1-hydroxymethyl-propylamino)-9-iso...)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+3nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
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
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132196(2-(6-Benzylamino-9-isopropyl-8-methyl-9H-purin-2-y...)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
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
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132197(2-(6-Benzylamino-9-isopropyl-8-mercapto-9H-purin-2...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
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
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132193(2-[8-Chloro-6-(3-chloro-phenylamino)-9-isopropyl-9...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132198(CHEMBL103567 | N*2*-(4-Amino-cyclohexyl)-N*6*-(3-c...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132189(2-(6-Benzylamino-9-isopropyl-8-nitro-9H-purin-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
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
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132190(2-(6-Benzylamino-8-chloro-9-isopropyl-9H-purin-2-y...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
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
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
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
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
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132195(6-Benzylamino-2-(1-hydroxymethyl-propylamino)-9-is...)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+4nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
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
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132188(2-(8-Amino-6-benzylamino-9-isopropyl-9H-purin-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+4nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
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
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132191(2-(6-Benzylamino-8-bromo-9-isopropyl-9H-purin-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132200(2-(6-Benzylamino-9-isopropyl-8-propoxy-9H-purin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50132194(2-[6-Benzylamino-8-(3-hydroxy-propylamino)-9-isopr...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against Cyclin dependent kinase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q270820NPubMed
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
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