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Found 85 with Last Name = 'winska' and Initial = 'p'
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50156670(2-(dimethylamino)-4,5,6,7-tetrabromo-1H-benzimidaz...)
Affinity DataKi:  40nMAssay Description:Binding affinity to CK2alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM11323(4,5,6,7-tetrabromo-1H-1,2,3-benzotriazole | 4,5,6,...)
Affinity DataKi:  270nMAssay Description:The activity of CK2α was tested using P81 filter isotopic assay, as it was described earlier [Łukowska-Chojnacka et al., Bioorg. Med. Chem....More data for this Ligand-Target Pair
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM11323(4,5,6,7-tetrabromo-1H-1,2,3-benzotriazole | 4,5,6,...)
Affinity DataKi:  400nMAssay Description:Binding affinity to CK2alpha (unknown origin)More data for this Ligand-Target Pair
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50156669(4,5,6,7-TETRABROMO-BENZIMIDAZOLE | 4,5,6,7-tetrabr...)
Affinity DataKi:  680nMAssay Description:The activity of CK2α was tested using P81 filter isotopic assay, as it was described earlier [Łukowska-Chojnacka et al., Bioorg. Med. Chem....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM222400(1-[3-(4,5,6,7-Tetrabromo-1H-benzimidazol-1-yl)prop...)
Affinity DataKi:  910nMAssay Description:The activity of CK2α was tested using P81 filter isotopic assay, as it was described earlier [Łukowska-Chojnacka et al., Bioorg. Med. Chem....More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50156669(4,5,6,7-TETRABROMO-BENZIMIDAZOLE | 4,5,6,7-tetrabr...)
Affinity DataKi:  1.03E+3nMAssay Description:Inhibition of recombinant human CK2alpha using RRRDDDSDDD substrate peptide by scintillation counter in presence of [32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50140937(CHEMBL3754770)
Affinity DataKi:  1.11E+3nMAssay Description:Inhibition of recombinant human CK2alpha using RRRDDDSDDD substrate peptide by scintillation counter in presence of [32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50140938(CHEMBL3752778)
Affinity DataKi:  1.27E+3nMAssay Description:Inhibition of recombinant human CK2alpha using RRRDDDSDDD substrate peptide by scintillation counter in presence of [32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50141038(CHEMBL3753165)
Affinity DataKi:  1.42E+3nMAssay Description:Inhibition of recombinant human CK2alpha using RRRDDDSDDD substrate peptide by scintillation counter in presence of [32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50140939(CHEMBL3753027)
Affinity DataKi:  1.63E+3nMAssay Description:Inhibition of recombinant human CK2alpha using RRRDDDSDDD substrate peptide by scintillation counter in presence of [32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50276733(1-(3-chloropropyl)-4,5,6,7-tetrabromo-1H-benzimida...)
Affinity DataKi:  1.78E+3nMAssay Description:The activity of CK2α was tested using P81 filter isotopic assay, as it was described earlier [Łukowska-Chojnacka et al., Bioorg. Med. Chem....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM222398(1-[2-(4,5,6,7-Tetrabromo-1H-benzimidazol-1-yl)ethy...)
Affinity DataKi:  1.96E+3nMAssay Description:The activity of CK2α was tested using P81 filter isotopic assay, as it was described earlier [Łukowska-Chojnacka et al., Bioorg. Med. Chem....More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM222402(4,5,6-tribromo-7-methyl-1H-benzimidazole (13))
Affinity DataKi:  2.26E+3nMAssay Description:The activity of CK2α was tested using P81 filter isotopic assay, as it was described earlier [Łukowska-Chojnacka et al., Bioorg. Med. Chem....More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM222396(1-(2-Azidoethyl)-4,5,6,7-tetrabromo-1H-benzimidazo...)
Affinity DataKi:  2.34E+3nMAssay Description:The activity of CK2α was tested using P81 filter isotopic assay, as it was described earlier [Łukowska-Chojnacka et al., Bioorg. Med. Chem....More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM222401(3-{1-[3-(4,5,6,7-Tetrabromo-1H-benzimidazol-1-yl)p...)
Affinity DataKi:  2.37E+3nMAssay Description:The activity of CK2α was tested using P81 filter isotopic assay, as it was described earlier [Łukowska-Chojnacka et al., Bioorg. Med. Chem....More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50141053(CHEMBL3751908)
Affinity DataKi:  2.42E+3nMAssay Description:Inhibition of recombinant human CK2alpha using RRRDDDSDDD substrate peptide by scintillation counter in presence of [32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM222403(1-[3-(4,5,6,7-Tetrabromo-2H-benzotriazol-2-yl)prop...)
Affinity DataKi:  2.47E+3nMAssay Description:The activity of CK2α was tested using P81 filter isotopic assay, as it was described earlier [Łukowska-Chojnacka et al., Bioorg. Med. Chem....More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50140975(CHEMBL3751963)
Affinity DataKi:  2.49E+3nMAssay Description:Inhibition of recombinant human CK2alpha using RRRDDDSDDD substrate peptide by scintillation counter in presence of [32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50141040(CHEMBL3753068)
Affinity DataKi:  2.51E+3nMAssay Description:Inhibition of recombinant human CK2alpha using RRRDDDSDDD substrate peptide by scintillation counter in presence of [32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50140947(CHEMBL3753482)
Affinity DataKi:  2.77E+3nMAssay Description:Inhibition of recombinant human CK2alpha using RRRDDDSDDD substrate peptide by scintillation counter in presence of [32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM222404(3-{1-[3-(4,5,6,7-Tetrabromo-2H-benzotriazol-2-yl)p...)
Affinity DataKi:  3.16E+3nMAssay Description:The activity of CK2α was tested using P81 filter isotopic assay, as it was described earlier [Łukowska-Chojnacka et al., Bioorg. Med. Chem....More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM222397(1-(3-Azidopropyl)-4,5,6,7-tetrabromo-1H-benzimidaz...)
Affinity DataKi:  3.28E+3nMAssay Description:The activity of CK2α was tested using P81 filter isotopic assay, as it was described earlier [Łukowska-Chojnacka et al., Bioorg. Med. Chem....More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50140952(CHEMBL3754483)
Affinity DataKi:  5.03E+3nMAssay Description:Inhibition of recombinant human CK2alpha using RRRDDDSDDD substrate peptide by scintillation counter in presence of [32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM222399(3-{1-[2-(4,5,6,7-Tetrabromo-1H-benzimidazol-1-yl)e...)
Affinity DataKi:  5.37E+3nMAssay Description:The activity of CK2α was tested using P81 filter isotopic assay, as it was described earlier [Łukowska-Chojnacka et al., Bioorg. Med. Chem....More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068350(CHEMBL3402303)
Affinity DataIC50:  2nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068302(CHEMBL3402305)
Affinity DataIC50:  10nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068306(CHEMBL3402304)
Affinity DataIC50:  20nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM11323(4,5,6,7-tetrabromo-1H-1,2,3-benzotriazole | 4,5,6,...)
Affinity DataIC50:  320nMAssay Description:Inhibition of human CK2alpha using RRRDDDSDDD peptide substrate by P81 filter-binding assayMore data for this Ligand-Target Pair
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068345(CHEMBL3402314)
Affinity DataIC50:  340nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068344(CHEMBL3402313)
Affinity DataIC50:  520nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068348(CHEMBL3402296)
Affinity DataIC50:  720nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068296(CHEMBL3402310)
Affinity DataIC50:  750nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50052080(CHEMBL3322700)
Affinity DataIC50:  800nMAssay Description:Inhibition of human CK2alpha using RRRDDDSDDD peptide substrate by P81 filter-binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068334(CHEMBL3402299)
Affinity DataIC50:  810nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068297(CHEMBL3402309)
Affinity DataIC50:  830nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068299(CHEMBL3402308)
Affinity DataIC50:  930nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068301(CHEMBL3402306)
Affinity DataIC50:  1.08E+3nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068342(CHEMBL3402312)
Affinity DataIC50:  1.33E+3nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068349(CHEMBL3402311)
Affinity DataIC50:  1.78E+3nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068306(CHEMBL3402304)
Affinity DataIC50:  1.83E+3nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068290(CHEMBL3402293)
Affinity DataIC50:  1.87E+3nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068293(CHEMBL3400171)
Affinity DataIC50:  1.98E+3nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50052077(CHEMBL3322704)
Affinity DataIC50:  2.17E+3nMAssay Description:Inhibition of human CK2alpha using RRRDDDSDDD peptide substrate by P81 filter-binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068338(CHEMBL3402298)
Affinity DataIC50:  2.32E+3nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50052088(CHEMBL3322699)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibition of human CK2alpha using RRRDDDSDDD peptide substrate by P81 filter-binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50052079(CHEMBL3322701)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibition of human CK2alpha using RRRDDDSDDD peptide substrate by P81 filter-binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068288(CHEMBL3402295)
Affinity DataIC50:  2.73E+3nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068300(CHEMBL3402307)
Affinity DataIC50:  3.41E+3nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Warsaw University Of Technology

Curated by ChEMBL
LigandPNGBDBM50052078(CHEMBL3322702)
Affinity DataIC50:  3.60E+3nMAssay Description:Inhibition of human CK2alpha using RRRDDDSDDD peptide substrate by P81 filter-binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jagiellonian University

Curated by ChEMBL
LigandPNGBDBM50068291(CHEMBL3402292)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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