Compile Data Set for Download or QSAR
Found 45 with Last Name = 'gianoncelli' and Initial = 'a'
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34046(iodinated benzimidazole, 9a)copy SMILEScopy InChI
Affinity DataKi:  19nM ΔG°:  -45.8kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34038(4,5,6,7-tetraiodobenzimidazole (TIBI), 1a)copy SMILEScopy InChI
Affinity DataKi:  23nM ΔG°:  -45.4kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34044(iodinated benzimidazole, 7a)copy SMILEScopy InChI
Affinity DataKi:  24nM ΔG°:  -45.2kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34051(iodinated benzimidazole, 14)copy SMILEScopy InChI
Affinity DataKi:  27nM ΔG°:  -44.9kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34052(iodinated benzimidazole, 15)copy SMILEScopy InChI
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34054(iodinated benzimidazole, 17)copy SMILEScopy InChI
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34053(iodinated benzimidazole, 16)copy SMILEScopy InChI
Affinity DataKi:  54nM ΔG°:  -43.2kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34048(iodinated benzimidazole, 11a)copy SMILEScopy InChI
Affinity DataKi:  70nM ΔG°:  -42.5kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34043(iodinated benzimidazole, 6a)copy SMILEScopy InChI
Affinity DataKi:  75nM ΔG°:  -42.3kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34050(iodinated benzimidazole, 13a)copy SMILEScopy InChI
Affinity DataKi:  90nM ΔG°:  -41.8kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34040(iodinated benzimidazole, 3a)copy SMILEScopy InChI
Affinity DataKi:  100nM ΔG°:  -41.6kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34047(iodinated benzimidazole, 10a)copy SMILEScopy InChI
Affinity DataKi:  120nM ΔG°:  -41.1kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34049(iodinated benzimidazole, 12a)copy SMILEScopy InChI
Affinity DataKi:  120nM ΔG°:  -41.1kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34056(iodinated benzimidazole, 23)copy SMILEScopy InChI
Affinity DataKi:  130nM ΔG°:  -40.9kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34055(iodinated benzimidazole, 21)copy SMILEScopy InChI
Affinity DataKi:  140nM ΔG°:  -40.7kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34039(iodinated benzimidazole, 2a)copy SMILEScopy InChI
Affinity DataKi:  160nM ΔG°:  -40.3kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34058(iodinated benzimidazole, 27)copy SMILEScopy InChI
Affinity DataKi:  160nM ΔG°:  -40.3kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34057(iodinated benzimidazole, 25)copy SMILEScopy InChI
Affinity DataKi:  180nM ΔG°:  -40.0kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34045(iodinated benzimidazole, 8a)copy SMILEScopy InChI
Affinity DataKi:  330nM ΔG°:  -38.5kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34041(iodinated benzimidazole, 4a)copy SMILEScopy InChI
Affinity DataKi:  460nM ΔG°:  -37.6kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34042(iodinated benzimidazole, 5a)copy SMILEScopy InChI
Affinity DataKi:  590nM ΔG°:  -37.0kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34059(brominated benzimidazole, 20)copy SMILEScopy InChI
Affinity DataKi:  1.34E+3nM ΔG°:  -34.9kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34060(brominated benzimidazole, 22)copy SMILEScopy InChI
Affinity DataKi:  1.45E+3nM ΔG°:  -34.7kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34062(brominated benzimidazole, 26)copy SMILEScopy InChI
Affinity DataKi:  1.51E+3nM ΔG°:  -34.6kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase II subunit alpha(Rattus norvegicus (Rat))
University of Padova

LigandPNGBDBM34061(brominated benzimidazole, 24)copy SMILEScopy InChI
Affinity DataKi:  1.91E+3nM ΔG°:  -34.0kJ/molepH: 7.5 T: 2°CAssay Description:Inhibitory effect of test compound was assessed in reaction buffer containing purified CK2, synthetic peptide substrate, and [gamma-33P]ATP. Assays w...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ860PPubMed
TargetCasein kinase I isoform delta(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094895(1,4-diamino-9,10-anthraquinone | 1,4-diamino-anthr...)copy SMILEScopy InChI
Affinity DataIC50: 330nMAssay Description:Inhibition of CK1deltaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetCasein kinase I isoform delta(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094893(1-Amino-4-hydroxy-anthraquinone | 1-hydroxy-4-amin...)copy SMILEScopy InChI
Affinity DataIC50: 660nMAssay Description:Inhibition of CK1deltaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetCasein kinase I isoform alpha(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50008516(IC261)copy SMILEScopy InChI
Affinity DataIC50: 1.24E+3nMAssay Description:Inhibition of CK1alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetCasein kinase I isoform delta(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50008516(IC261)copy SMILEScopy InChI
Affinity DataIC50: 2.57E+3nMAssay Description:Inhibition of CK1deltaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetHomeodomain-interacting protein kinase 2(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094895(1,4-diamino-9,10-anthraquinone | 1,4-diamino-anthr...)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibition of HIPK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094895(1,4-diamino-9,10-anthraquinone | 1,4-diamino-anthr...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibition of DYRK1aMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetCasein kinase I isoform alpha(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094895(1,4-diamino-9,10-anthraquinone | 1,4-diamino-anthr...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of CK1alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetCasein kinase I isoform alpha(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094893(1-Amino-4-hydroxy-anthraquinone | 1-hydroxy-4-amin...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of CK1alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetTyrosine-protein kinase Fgr(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094895(1,4-diamino-9,10-anthraquinone | 1,4-diamino-anthr...)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+4nMAssay Description:Inhibition of FgrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094895(1,4-diamino-9,10-anthraquinone | 1,4-diamino-anthr...)copy SMILEScopy InChI
Affinity DataIC50: 2.47E+4nMAssay Description:Inhibition of PIM1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetCasein kinase I isoform gamma-1(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094893(1-Amino-4-hydroxy-anthraquinone | 1-hydroxy-4-amin...)copy SMILEScopy InChI
Affinity DataIC50: 2.62E+4nMAssay Description:Inhibition of CK1gamma1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetCasein kinase I isoform gamma-1(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094895(1,4-diamino-9,10-anthraquinone | 1,4-diamino-anthr...)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+4nMAssay Description:Inhibition of CK1gamma1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetTyrosine-protein kinase SYK(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094895(1,4-diamino-9,10-anthraquinone | 1,4-diamino-anthr...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of SykMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetTyrosine-protein kinase Lyn(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094895(1,4-diamino-9,10-anthraquinone | 1,4-diamino-anthr...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of LynMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetTyrosine-protein kinase CSK(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094895(1,4-diamino-9,10-anthraquinone | 1,4-diamino-anthr...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of CSKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetCasein kinase I isoform alpha(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50240382(1,4-Dihydroxyanthrachinon | 1,4-dihydroxy-9,10-ant...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of CK1alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetCasein kinase I isoform gamma-1(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50240382(1,4-Dihydroxyanthrachinon | 1,4-dihydroxy-9,10-ant...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of CK1gamma1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetCasein kinase I isoform delta(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50240382(1,4-Dihydroxyanthrachinon | 1,4-dihydroxy-9,10-ant...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of CK1deltaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50094895(1,4-diamino-9,10-anthraquinone | 1,4-diamino-anthr...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of GST tagged ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed
TargetCasein kinase I isoform gamma-1(Homo sapiens (Human))
Università di Padova

Curated by ChEMBL
LigandPNGBDBM50008516(IC261)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of CK1gamma1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VGPPubMed