Compile Data Set for Download or QSAR
Report error Found 69 Enz. Inhib. hit(s) with Target = 'Beta-galactoside alpha-2,6-sialyltransferase 1'
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50559957(CHEMBL4795501)
Affinity DataKd:  9nMAssay Description:Displacement of fluorescent probe from human ST6Gal-1 by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50559956(CHEMBL4794815)
Affinity DataKd:  22nMAssay Description:Displacement of fluorescent probe from human ST6Gal-1 by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50565994(CHEMBL3596261)
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50565990(CHEMBL4780118)
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50565988(CHEMBL4785533)
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50565989(CHEMBL4798770)
Affinity DataIC50: 4.33E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50566002(CHEMBL4776137)
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50565991(CHEMBL4785375)
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50566003(CHEMBL4793980)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50565992(CHEMBL4795609)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50566001(CHEMBL4797927)
Affinity DataIC50: 5.10E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50565997(CHEMBL4793269)
Affinity DataIC50: 5.40E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50566000(CHEMBL4800187)
Affinity DataIC50: 5.60E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50565998(CHEMBL4786588)
Affinity DataIC50: 5.70E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50566004(CHEMBL4777310)
Affinity DataIC50: 5.70E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50565996(CHEMBL4781666)
Affinity DataIC50: 6.70E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50565995(CHEMBL4790244)
Affinity DataIC50: 7.20E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50565999(CHEMBL4779174)
Affinity DataIC50: 7.50E+3nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50565993(CHEMBL4797481)
Affinity DataIC50: 1.58E+4nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501643(CHEMBL4065191)
Affinity DataKi:  16nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501643(CHEMBL4065191)
Affinity DataKi:  16nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50127702(CHEMBL3629697)
Affinity DataKi:  19nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501640(CHEMBL4102509)
Affinity DataKi:  19nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50590206(CHEMBL4117853)
Affinity DataKi:  19nMAssay Description:Inhibition of human ST6Gal IMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501638(CHEMBL4091389)
Affinity DataKi:  20nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501638(CHEMBL4091389)
Affinity DataKi:  20nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50127703(CHEMBL3629696)
Affinity DataKi:  28nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50127703(CHEMBL3629696)
Affinity DataKi:  28nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50127703(CHEMBL3629696)
Affinity DataKi:  28nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50127703(CHEMBL3629696)
Affinity DataKi:  28nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501642(CHEMBL3629698)
Affinity DataKi:  29nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Rat)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50559955(CHEMBL4776007)
Affinity DataKi:  29nMAssay Description:Inhibition of rat liver ST6Gal-1 by HPLC-based assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501642(CHEMBL3629698)
Affinity DataKi:  29nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501637(CHEMBL4063545)
Affinity DataKi:  60nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501637(CHEMBL4063545)
Affinity DataKi:  60nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Rat)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501640(CHEMBL4102509)
Affinity DataKi:  70nMAssay Description:Inhibition of rat liver ST6Gal-1 using p-nitrophenyl-DL-alanine measured up to 20 mins by HPLC analysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501644(CHEMBL4097206)
Affinity DataKi:  106nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501644(CHEMBL4097206)
Affinity DataKi:  106nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501641(CHEMBL4081024)
Affinity DataKi:  200nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501641(CHEMBL4081024)
Affinity DataKi:  200nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50501639(CHEMBL4083608)
Affinity DataKi:  224nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50127706(CHEMBL3629692)
Affinity DataKi:  436nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50127706(CHEMBL3629692)
Affinity DataKi:  436nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50127704(CHEMBL3629694)
Affinity DataKi:  865nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50127705(CHEMBL3629693)
Affinity DataKi:  1.51E+3nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50127707(CHEMBL3629691)
Affinity DataKi:  4.31E+3nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50127709(CHEMBL3629689)
Affinity DataKi:  5.85E+3nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50127709(CHEMBL3629689)
Affinity DataKi:  5.85E+3nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50590208(CHEMBL5185498)
Affinity DataKi:  6.00E+3nMAssay Description:Inhibition of recombinant human ST6Gal I incubated for 1 hrs in the presence of CMP-Neu5Ac as donor and LacNAc as acceptor by luminescence based CMP-...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong

Curated by ChEMBL
LigandPNGBDBM50590208(CHEMBL5185498)
Affinity DataKi:  6.00E+3nMAssay Description:Inhibition of recombinant human ST6Gal I incubated for 1 hrs in the presence of CMP-Neu5Ac as donor and LacNAc as acceptor by luminescence based CMP-...More data for this Ligand-Target Pair
In DepthDetails
PubMed
Displayed 1 to 50 (of 69 total ) | Next | Last >>
Jump to: