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Found 72 with Last Name = 'bretner' and Initial = 'm'
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50022238((R)-5-Fluoro-1-((4S,5R)-4-hydroxy-5-methylphosphat...)
Affinity DataKi:  10nMAssay Description:Apparent Ki value of the compound was measured by competitive inhibition of Thymidylate Synthases from Ehrlich Carcinoma cells of mouseMore data for this Ligand-Target Pair
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50022238((R)-5-Fluoro-1-((4S,5R)-4-hydroxy-5-methylphosphat...)
Affinity DataKi:  20nMAssay Description:Time-independent inhibition of thymidylate synthase from parenteral L1210 cellsMore data for this Ligand-Target Pair
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50022238((R)-5-Fluoro-1-((4S,5R)-4-hydroxy-5-methylphosphat...)
Affinity DataKi:  20nMAssay Description:Apparent Ki value of the compound was measured by competitive inhibition of Thymidylate Synthases from L1210 cells of mouseMore data for this Ligand-Target Pair
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50022238((R)-5-Fluoro-1-((4S,5R)-4-hydroxy-5-methylphosphat...)
Affinity DataKi:  30nMAssay Description:Time-independent inhibition of thymidylate synthase from FdUrd-resistant L1210 cellsMore data for this Ligand-Target Pair
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
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50042594(CHEMBL120677 | Phosphoric acid mono-[5-(5-fluoro-4...)
Affinity DataKi:  70nMAssay Description:Apparent Ki value of the compound was measured by competitive inhibition of Thymidylate Synthase from L1210 cells of mouseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50042594(CHEMBL120677 | Phosphoric acid mono-[5-(5-fluoro-4...)
Affinity DataKi:  140nMAssay Description:Apparent Ki value of the compound was measured by competitive inhibition of Thymidylate Synthase from Ehrlich Carcinoma cells of mouseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50028374(CHEMBL278466 | Phosphoric acid mono-[5-(5-chloro-2...)
Affinity DataKi:  150nMAssay Description:Time-independent inhibition of thymidylate synthase from FdUrd-resistant L1210 cellsMore 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
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50028374(CHEMBL278466 | Phosphoric acid mono-[5-(5-chloro-2...)
Affinity DataKi:  300nMAssay Description:Time-independent inhibition of thymidylate synthase from parenteral L1210 cellsMore 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:  400nMAssay Description:Binding affinity to CK2alpha (unknown origin)More data for this Ligand-Target Pair
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094611(CHEMBL143376 | Phosphoric acid mono-[5-(5-bromo-2,...)
Affinity DataKi:  460nMAssay Description:Time-independent inhibition of thymidylate synthase from FdUrd-resistant L1210 cellsMore data for this Ligand-Target Pair
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:  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
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094619(1-(beta--D-2-Deoxyribofuranosyl)-4-hydroxyamino-5-...)
Affinity DataKi:  800nMAssay Description:Time-independent inhibition of thymidylate synthase from parenteral L1210 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094621(CHEMBL143398 | Phosphoric acid mono-[3-hydroxy-5-(...)
Affinity DataKi:  900nMAssay Description:Time-independent inhibition of thymidylate synthase from FdUrd-resistant L1210 cellsMore 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
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094619(1-(beta--D-2-Deoxyribofuranosyl)-4-hydroxyamino-5-...)
Affinity DataKi:  1.40E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from FdUrd-resistant L1210 cellsMore 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
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094611(CHEMBL143376 | Phosphoric acid mono-[5-(5-bromo-2,...)
Affinity DataKi:  1.50E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from parenteral L1210 cellsMore 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
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094610(1-(beta--D-2-Deoxyribofuranosyl)-4-hydroxyaminopyr...)
Affinity DataKi:  1.70E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from parenteral L1210 cellsMore 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
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094622(1-(beta--D-2-Deoxyribofuranosyl)-4-hydroxyamino-5-...)
Affinity DataKi:  1.91E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from parenteral L1210 cellsMore 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
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094622(1-(beta--D-2-Deoxyribofuranosyl)-4-hydroxyamino-5-...)
Affinity DataKi:  2.18E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from FdUrd-resistant L1210 cellsMore data for this Ligand-Target Pair
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
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094621(CHEMBL143398 | Phosphoric acid mono-[3-hydroxy-5-(...)
Affinity DataKi:  3.70E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from parenteral L1210 cellsMore data for this Ligand-Target Pair
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
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094618(1-(beta--D-2-Deoxyribofuranosyl)-4-hydroxyamino-5-...)
Affinity DataKi:  5.70E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from FdUrd-resistant L1210 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094623(CHEMBL142885 | Phosphoric acid mono-[3-hydroxy-5-(...)
Affinity DataKi:  6.99E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from FdUrd-resistant L1210 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50221257(4-(4,5-dihydro-5-thioxo-1,3,4-thiadiazol-2-yl)-1-(...)
Affinity DataKi:  7.30E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from parenteral L1210 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094618(1-(beta--D-2-Deoxyribofuranosyl)-4-hydroxyamino-5-...)
Affinity DataKi:  7.46E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from parenteral L1210 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094623(CHEMBL142885 | Phosphoric acid mono-[3-hydroxy-5-(...)
Affinity DataKi:  7.68E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from parenteral L1210 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094608(1-(beta--D-2-Deoxyribofuranosyl)-4-hydroxyamino-5-...)
Affinity DataKi:  8.40E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from FdUrd-resistant L1210 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094608(1-(beta--D-2-Deoxyribofuranosyl)-4-hydroxyamino-5-...)
Affinity DataKi:  8.50E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from parenteral L1210 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094610(1-(beta--D-2-Deoxyribofuranosyl)-4-hydroxyaminopyr...)
Affinity DataKi:  9.30E+3nMAssay Description:Time-independent inhibition of thymidylate synthase from FdUrd-resistant L1210 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Mus musculus)
Polish Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50094614(1-(beta--D-2-Deoxyribofuranosyl)-4-hydroxyamino-5-...)
Affinity DataKi:  3.21E+4nMAssay Description:Time-independent inhibition of thymidylate synthase from parenteral L1210 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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