Compile Data Set for Download or QSAR

Found 37 hits of Enzyme Inhibition Constant Data   

TargetCyclin-T1/Cyclin-dependent kinase 9(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM7266(14-bromo-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 64nMAssay Description:Inhibition of human recombinant CDK9/cyclin T expressed in insect cells assessed as incorporation of [gamma-33P]-ATP in to pRB fragment (773 to 928) ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-T1/Cyclin-dependent kinase 9(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346235(9-azapaullone | CHEMBL1782168)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of human recombinant CDK9/cyclin T expressed in insect cells assessed as incorporation of [gamma-33P]-ATP in to pRB fragment (773 to 928) ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-T1/Cyclin-dependent kinase 9(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346237(9-Oxy-5,12-dihydro-7H-5,9,12-triaza-dibenzo[a,e]az...)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Inhibition of human recombinant CDK9/cyclin T expressed in insect cells assessed as incorporation of [gamma-33P]-ATP in to pRB fragment (773 to 928) ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM7266(14-bromo-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 400nMAssay Description:Inhibition of CDK1/cyclin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM7266(14-bromo-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 780nMAssay Description:Inhibition of human recombinant CDK2/cyclin A assessed as incorporation of [gamma-33P]-ATP into histone H1 substrate after 30 mins by scintillation c...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-T1/Cyclin-dependent kinase 9(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM7287(8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,17}]octad...)copy SMILEScopy InChI
Affinity DataIC50: 810nMAssay Description:Inhibition of human recombinant CDK9/cyclin T expressed in insect cells assessed as incorporation of [gamma-33P]-ATP in to pRB fragment (773 to 928) ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM7266(14-bromo-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human recombinant CDK5/p25 assessed as incorporation of [gamma-33P]-ATP into histone H1 substrate after 30 mins by scintillation counti...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346235(9-azapaullone | CHEMBL1782168)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of human recombinant CDK2/cyclin A assessed as incorporation of [gamma-33P]-ATP into histone H1 substrate after 30 mins by scintillation c...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM7287(8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,17}]octad...)copy SMILEScopy InChI
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibition of human recombinant CDK2/cyclin A assessed as incorporation of [gamma-33P]-ATP into histone H1 substrate after 30 mins by scintillation c...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346235(9-azapaullone | CHEMBL1782168)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of human recombinant CDK5/p25 assessed as incorporation of [gamma-33P]-ATP into histone H1 substrate after 30 mins by scintillation counti...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM7287(8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,17}]octad...)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibition of human recombinant CDK5/p25 assessed as incorporation of [gamma-33P]-ATP into histone H1 substrate after 30 mins by scintillation counti...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346237(9-Oxy-5,12-dihydro-7H-5,9,12-triaza-dibenzo[a,e]az...)copy SMILEScopy InChI
Affinity DataIC50: 6.20E+3nMAssay Description:Inhibition of human recombinant CDK2/cyclin A assessed as incorporation of [gamma-33P]-ATP into histone H1 substrate after 30 mins by scintillation c...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM7287(8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,17}]octad...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of CDK1/cyclin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346237(9-Oxy-5,12-dihydro-7H-5,9,12-triaza-dibenzo[a,e]az...)copy SMILEScopy InChI
Affinity DataIC50: 7.30E+3nMAssay Description:Inhibition of human recombinant CDK5/p25 assessed as incorporation of [gamma-33P]-ATP into histone H1 substrate after 30 mins by scintillation counti...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-T1/Cyclin-dependent kinase 9(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346236(9-Benzyl-6-oxo-5,6,7,12-tetrahydro-5,12-diaza-9-az...)copy SMILEScopy InChI
Affinity DataIC50: 7.40E+3nMAssay Description:Inhibition of human recombinant CDK9/cyclin T expressed in insect cells assessed as incorporation of [gamma-33P]-ATP in to pRB fragment (773 to 928) ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetGlycogen synthase kinase 3(Plasmodium falciparum (isolate 3D7))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346237(9-Oxy-5,12-dihydro-7H-5,9,12-triaza-dibenzo[a,e]az...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of Plasmodium falciparum GSK3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
LigandPNGBDBM7287(8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,17}]octad...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of rat recombinant GST-fused DYRK1A expressed in Escherichia coli assessed as assessed as incorporation of [gamma-33P]-ATP into myelin bas...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCasein kinase I isoform alpha(Sus scrofa)
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346235(9-azapaullone | CHEMBL1782168)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of porcine brain CK1 assessed as incorporation of [gamma-33P]-ATP into RRKHAAIGpSAYSITA substrate after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetGlycogen synthase kinase 3(Plasmodium falciparum (isolate 3D7))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346236(9-Benzyl-6-oxo-5,6,7,12-tetrahydro-5,12-diaza-9-az...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of Plasmodium falciparum GSK3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetGlycogen synthase kinase 3(Plasmodium falciparum (isolate 3D7))
Trinity College

Curated by ChEMBL
LigandPNGBDBM7287(8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,17}]octad...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of Plasmodium falciparum GSK3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetGlycogen synthase kinase 3(Plasmodium falciparum (isolate 3D7))
Trinity College

Curated by ChEMBL
LigandPNGBDBM7266(14-bromo-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of Plasmodium falciparum GSK3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
LigandPNGBDBM50346237(9-Oxy-5,12-dihydro-7H-5,9,12-triaza-dibenzo[a,e]az...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of rat recombinant GST-fused DYRK1A expressed in Escherichia coli assessed as assessed as incorporation of [gamma-33P]-ATP into myelin bas...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCasein kinase I isoform alpha(Sus scrofa)
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346236(9-Benzyl-6-oxo-5,6,7,12-tetrahydro-5,12-diaza-9-az...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of porcine brain CK1 assessed as incorporation of [gamma-33P]-ATP into RRKHAAIGpSAYSITA substrate after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
LigandPNGBDBM50346235(9-azapaullone | CHEMBL1782168)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of rat recombinant GST-fused DYRK1A expressed in Escherichia coli assessed as assessed as incorporation of [gamma-33P]-ATP into myelin bas...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetDual specificity protein kinase CLK1(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346237(9-Oxy-5,12-dihydro-7H-5,9,12-triaza-dibenzo[a,e]az...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CLK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCasein kinase I isoform alpha(Sus scrofa)
Trinity College

Curated by ChEMBL
LigandPNGBDBM7287(8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,17}]octad...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of porcine brain CK1 assessed as incorporation of [gamma-33P]-ATP into RRKHAAIGpSAYSITA substrate after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
LigandPNGBDBM50346236(9-Benzyl-6-oxo-5,6,7,12-tetrahydro-5,12-diaza-9-az...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of rat recombinant GST-fused DYRK1A expressed in Escherichia coli assessed as assessed as incorporation of [gamma-33P]-ATP into myelin bas...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetDual specificity protein kinase CLK1(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346236(9-Benzyl-6-oxo-5,6,7,12-tetrahydro-5,12-diaza-9-az...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CLK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetDual specificity protein kinase CLK1(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346235(9-azapaullone | CHEMBL1782168)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CLK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetGlycogen synthase kinase 3(Plasmodium falciparum (isolate 3D7))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346235(9-azapaullone | CHEMBL1782168)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of Plasmodium falciparum GSK3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346236(9-Benzyl-6-oxo-5,6,7,12-tetrahydro-5,12-diaza-9-az...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant CDK5/p25 assessed as incorporation of [gamma-33P]-ATP into histone H1 substrate after 30 mins by scintillation counti...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetDual specificity protein kinase CLK1(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM7266(14-bromo-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CLK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCasein kinase I isoform alpha(Sus scrofa)
Trinity College

Curated by ChEMBL
LigandPNGBDBM7266(14-bromo-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of porcine brain CK1 assessed as incorporation of [gamma-33P]-ATP into RRKHAAIGpSAYSITA substrate after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCasein kinase I isoform alpha(Sus scrofa)
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346237(9-Oxy-5,12-dihydro-7H-5,9,12-triaza-dibenzo[a,e]az...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of porcine brain CK1 assessed as incorporation of [gamma-33P]-ATP into RRKHAAIGpSAYSITA substrate after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetCyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50346236(9-Benzyl-6-oxo-5,6,7,12-tetrahydro-5,12-diaza-9-az...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant CDK2/cyclin A assessed as incorporation of [gamma-33P]-ATP into histone H1 substrate after 30 mins by scintillation c...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
LigandPNGBDBM7266(14-bromo-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of rat recombinant GST-fused DYRK1A expressed in Escherichia coli assessed as assessed as incorporation of [gamma-33P]-ATP into myelin bas...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
TargetDual specificity protein kinase CLK1(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM7287(8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,17}]octad...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CLK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21836T2PubMed
* indicates data uncertainty>20%