TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
Affinity DataKd: 9nMAssay Description:Displacement of fluorescent probe from human ST6Gal-1 by fluorescence polarization assayMore data for this Ligand-Target Pair
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
Affinity DataKd: 22nMAssay Description:Displacement of fluorescent probe from human ST6Gal-1 by fluorescence polarization assayMore data for this Ligand-Target Pair
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
Ligand Info
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
Ligand Info
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
Ligand Info
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
Ligand Info
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
Ligand Info
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
Ligand Info
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
Affinity DataKi: 19nMAssay Description:Inhibition of human ST6Gal IMore data for this Ligand-Target Pair
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
University of Wollongong
Curated by ChEMBL
University of Wollongong
Curated by ChEMBL
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







































