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

Curated by ChEMBL
LigandPNGBDBM50501643(CHEMBL4065191)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501643(CHEMBL4065191)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501640(CHEMBL4102509)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50590206(CHEMBL4117853)copy SMILES
Affinity DataKi:  19nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2183BHPPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127702(CHEMBL3629697)copy SMILEScopy InChI
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
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501638(CHEMBL4091389)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501638(CHEMBL4091389)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127703(CHEMBL3629696)copy SMILEScopy InChI
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
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127703(CHEMBL3629696)copy SMILEScopy InChI
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
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127703(CHEMBL3629696)copy SMILEScopy InChI
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
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127703(CHEMBL3629696)copy SMILEScopy InChI
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
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
LigandPNGBDBM50559955(CHEMBL4776007)copy SMILES
Affinity DataKi:  29nMAssay Description:Inhibition of rat liver ST6Gal-1 by HPLC-based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M69DRPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501642(CHEMBL3629698)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501642(CHEMBL3629698)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501637(CHEMBL4063545)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501637(CHEMBL4063545)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
LigandPNGBDBM50501640(CHEMBL4102509)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M69DRPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501644(CHEMBL4097206)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501644(CHEMBL4097206)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501641(CHEMBL4081024)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501641(CHEMBL4081024)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501639(CHEMBL4083608)copy SMILEScopy InChI
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
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127706(CHEMBL3629692)copy SMILEScopy InChI
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
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127706(CHEMBL3629692)copy SMILEScopy InChI
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
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127704(CHEMBL3629694)copy SMILEScopy InChI
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
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127705(CHEMBL3629693)copy SMILEScopy InChI
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
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127707(CHEMBL3629691)copy SMILEScopy InChI
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
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127709(CHEMBL3629689)copy SMILEScopy InChI
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
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127709(CHEMBL3629689)copy SMILEScopy InChI
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
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50590208(CHEMBL5185498)copy SMILES
Affinity DataKi:  6.00E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2183BHPPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50590208(CHEMBL5185498)copy SMILES
Affinity DataKi:  6.00E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2183BHPPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50590209(CHEMBL5175639)copy SMILES
Affinity DataKi:  6.70E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2183BHPPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50590209(CHEMBL5175639)copy SMILES
Affinity DataKi:  6.70E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2183BHPPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50559954(CHEMBL4755740)copy SMILES
Affinity DataKi:  8.50E+3nMAssay Description:Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M69DRPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50559951(CHEMBL4751247)copy SMILES
Affinity DataKi:  1.92E+4nMAssay Description:Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M69DRPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50559952(CHEMBL4743892)copy SMILES
Affinity DataKi:  2.03E+4nMAssay Description:Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M69DRPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50590207(CHEMBL5180951)copy SMILES
Affinity DataKi:  4.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2183BHPPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50590207(CHEMBL5180951)copy SMILES
Affinity DataKi:  4.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2183BHPPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50559953(CHEMBL4757654)copy SMILES
Affinity DataKi:  5.55E+4nMAssay Description:Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M69DRPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50559953(CHEMBL4757654)copy SMILES
Affinity DataKi:  5.55E+4nMAssay Description:Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M69DRPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Rattus norvegicus)
University of Colorado

Curated by ChEMBL
LigandPNGBDBM50310540(((2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)...)copy SMILEScopy InChI
Affinity DataKi:  6.40E+4nMAssay Description:Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liverMore data for this Ligand-Target Pair
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50559950(CHEMBL4745184)copy SMILES
Affinity DataKi:  3.06E+5nMAssay Description:Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M69DRPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50559950(CHEMBL4745184)copy SMILES
Affinity DataKi:  3.06E+5nMAssay Description:Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M69DRPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Rattus norvegicus)
University of Colorado

Curated by ChEMBL
LigandPNGBDBM50366837(CHEMBL608619)copy SMILEScopy InChI
Affinity DataKi:  3.70E+5nMAssay Description:Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liverMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FJ2HBMPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Rattus norvegicus)
University of Colorado

Curated by ChEMBL
LigandPNGBDBM50366833(CHEMBL608928)copy SMILEScopy InChI
Affinity DataKi:  7.30E+5nMAssay Description:Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liverMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FJ2HBMPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Rattus norvegicus)
University of Colorado

Curated by ChEMBL
LigandPNGBDBM50366836(CHEMBL610554)copy SMILEScopy InChI
Affinity DataKi:  1.70E+6nMAssay Description:Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liverMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FJ2HBMPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Rattus norvegicus)
University of Colorado

Curated by ChEMBL
LigandPNGBDBM50366835(CHEMBL609514)copy SMILEScopy InChI
Affinity DataKi:  2.20E+6nMAssay Description:Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liverMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FJ2HBMPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Rattus norvegicus)
University of Colorado

Curated by ChEMBL
LigandPNGBDBM50366838(CHEMBL609215)copy SMILEScopy InChI
Affinity DataKi:  2.40E+6nMAssay Description:Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liverMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FJ2HBMPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Rattus norvegicus)
University of Colorado

Curated by ChEMBL
LigandPNGBDBM50366832(CHEMBL609516)copy SMILEScopy InChI
Affinity DataKi:  2.50E+6nMAssay Description:Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liverMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FJ2HBMPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Rattus norvegicus)
University of Colorado

Curated by ChEMBL
LigandPNGBDBM50366834(CHEMBL609800)copy SMILEScopy InChI
Affinity DataKi:  3.80E+6nMAssay Description:Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liverMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FJ2HBMPubMed
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