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Compile Data Set for Download or QSAR

Found 40 hits of ki data for polymerid = 50006995   
Target/Host
(Institution)		LigandTarget/Host
Links		Ligand
Links		Trg + Lig
Links		Ki
nM		ΔG°
kJ/mole		IC50
nM		Kd
nM		EC50/IC50
nM		koff
s-1		kon
M-1s-1		pHTemp
°C
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501643
PNG
(CHEMBL4065191)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ccn(-[#6@@H]-2-[#8]-[#6@H](-[#6]-[#8]P([#8-])(=O)[#8]-[#6](-[#6]-[#7]-[#6](=O)-c3ccccc3)P([#8-])([#8-])=O)-[#6@@H](-[#8])-[#6@H]-2-[#8])c(=O)n1 |r|
Show InChI InChI=1S/C18H24N4O12P2.3Na/c19-12-6-7-22(18(26)21-12)17-15(24)14(23)11(33-17)9-32-36(30,31)34-13(35(27,28)29)8-20-16(25)10-4-2-1-3-5-10;;;/h1-7,11,13-15,17,23-24H,8-9H2,(H,20,25)(H,30,31)(H2,19,21,26)(H2,27,28,29);;;/q;3*+1/p-3/t11-,13?,14-,15-,17-;;;/m1.../s1
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 16n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501643
PNG
(CHEMBL4065191)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ccn(-[#6@@H]-2-[#8]-[#6@H](-[#6]-[#8]P([#8-])(=O)[#8]-[#6](-[#6]-[#7]-[#6](=O)-c3ccccc3)P([#8-])([#8-])=O)-[#6@@H](-[#8])-[#6@H]-2-[#8])c(=O)n1 |r|
Show InChI InChI=1S/C18H24N4O12P2.3Na/c19-12-6-7-22(18(26)21-12)17-15(24)14(23)11(33-17)9-32-36(30,31)34-13(35(27,28)29)8-20-16(25)10-4-2-1-3-5-10;;;/h1-7,11,13-15,17,23-24H,8-9H2,(H,20,25)(H,30,31)(H2,19,21,26)(H2,27,28,29);;;/q;3*+1/p-3/t11-,13?,14-,15-,17-;;;/m1.../s1
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 16n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50590206
PNG
(CHEMBL4117853)
Show SMILES Nc1ccn([C@@H]2O[C@H](COP(O)(=O)O[C@@H](c3cccc(Oc4ccccc4)c3)P(O)(O)=O)[C@@H](O)[C@H]2O)c(=O)n1 |r|
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 19n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1039/d1md00079a
BindingDB Entry DOI: 10.7270/Q2183BHP
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50127702
PNG
(CHEMBL3629697)
Show SMILES [Na+].[Na+].[Na+].Nc1ccn([C@@H]2O[C@H](COP([O-])(=O)OC(c3cccc(Oc4ccccc4)c3)P([O-])([O-])=O)[C@@H](O)[C@H]2O)c(=O)n1 |r|
Show InChI InChI=1S/C22H25N3O12P2.3Na/c23-17-9-10-25(22(28)24-17)20-19(27)18(26)16(36-20)12-34-39(32,33)37-21(38(29,30)31)13-5-4-8-15(11-13)35-14-6-2-1-3-7-14;;;/h1-11,16,18-21,26-27H,12H2,(H,32,33)(H2,23,24,28)(H2,29,30,31);;;/q;3*+1/p-3/t16-,18-,19-,20-,21?;;;/m1.../s1
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 19n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...

J Med Chem 58: 7972-90 (2015)


Article DOI: 10.1021/acs.jmedchem.5b01181
BindingDB Entry DOI: 10.7270/Q20V8FMQ
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501640
PNG
(CHEMBL4102509)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ccn(-[#6@@H]-2-[#8]-[#6@H](-[#6]-[#8]P([#8-])(=O)[#8]-[#6@@H](-c3cccc(-[#8]-c4ccccc4)c3)P([#8-])([#8-])=O)-[#6@@H](-[#8])-[#6@H]-2-[#8])c(=O)n1 |r|
Show InChI InChI=1S/C22H25N3O12P2.3Na/c23-17-9-10-25(22(28)24-17)20-19(27)18(26)16(36-20)12-34-39(32,33)37-21(38(29,30)31)13-5-4-8-15(11-13)35-14-6-2-1-3-7-14;;;/h1-11,16,18-21,26-27H,12H2,(H,32,33)(H2,23,24,28)(H2,29,30,31);;;/q;3*+1/p-3/t16-,18-,19-,20-,21-;;;/m1.../s1
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 19n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501638
PNG
(CHEMBL4091389)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ccn(-[#6@@H]-2-[#8]-[#6@H](-[#6]-[#8]P([#8-])(=O)[#8]-[#6](-[#6](=O)-[#7]-3-[#6]-[#6]-[#6]-[#6]-[#6]-3)P([#8-])([#8-])=O)-[#6@@H](-[#8])-[#6@H]-2-[#8])c(=O)n1 |r|
Show InChI InChI=1S/C16H26N4O12P2.3Na/c17-10-4-7-20(16(24)18-10)14-12(22)11(21)9(31-14)8-30-34(28,29)32-15(33(25,26)27)13(23)19-5-2-1-3-6-19;;;/h4,7,9,11-12,14-15,21-22H,1-3,5-6,8H2,(H,28,29)(H2,17,18,24)(H2,25,26,27);;;/q;3*+1/p-3/t9-,11-,12-,14-,15?;;;/m1.../s1
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 20n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501638
PNG
(CHEMBL4091389)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ccn(-[#6@@H]-2-[#8]-[#6@H](-[#6]-[#8]P([#8-])(=O)[#8]-[#6](-[#6](=O)-[#7]-3-[#6]-[#6]-[#6]-[#6]-[#6]-3)P([#8-])([#8-])=O)-[#6@@H](-[#8])-[#6@H]-2-[#8])c(=O)n1 |r|
Show InChI InChI=1S/C16H26N4O12P2.3Na/c17-10-4-7-20(16(24)18-10)14-12(22)11(21)9(31-14)8-30-34(28,29)32-15(33(25,26)27)13(23)19-5-2-1-3-6-19;;;/h4,7,9,11-12,14-15,21-22H,1-3,5-6,8H2,(H,28,29)(H2,17,18,24)(H2,25,26,27);;;/q;3*+1/p-3/t9-,11-,12-,14-,15?;;;/m1.../s1
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 20n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50127703
PNG
(CHEMBL3629696)
Show SMILES [Na+].[Na+].[Na+].CC(=O)NC[C@@H]1CCC(OP([O-])(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)n2ccc(N)nc2=O)([C@H]1OCc1ccccc1)P([O-])([O-])=O |r|
Show InChI InChI=1S/C24H34N4O13P2.3Na/c1-14(29)26-11-16-7-9-24(42(33,34)35,21(16)38-12-15-5-3-2-4-6-15)41-43(36,37)39-13-17-19(30)20(31)22(40-17)28-10-8-18(25)27-23(28)32;;;/h2-6,8,10,16-17,19-22,30-31H,7,9,11-13H2,1H3,(H,26,29)(H,36,37)(H2,25,27,32)(H2,33,34,35);;;/q;3*+1/p-3/t16-,17+,19+,20+,21-,22+,24?;;;/m0.../s1
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 28n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...

J Med Chem 58: 7972-90 (2015)


Article DOI: 10.1021/acs.jmedchem.5b01181
BindingDB Entry DOI: 10.7270/Q20V8FMQ
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50127703
PNG
(CHEMBL3629696)
Show SMILES [Na+].[Na+].[Na+].CC(=O)NC[C@@H]1CCC(OP([O-])(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)n2ccc(N)nc2=O)([C@H]1OCc1ccccc1)P([O-])([O-])=O |r|
Show InChI InChI=1S/C24H34N4O13P2.3Na/c1-14(29)26-11-16-7-9-24(42(33,34)35,21(16)38-12-15-5-3-2-4-6-15)41-43(36,37)39-13-17-19(30)20(31)22(40-17)28-10-8-18(25)27-23(28)32;;;/h2-6,8,10,16-17,19-22,30-31H,7,9,11-13H2,1H3,(H,26,29)(H,36,37)(H2,25,27,32)(H2,33,34,35);;;/q;3*+1/p-3/t16-,17+,19+,20+,21-,22+,24?;;;/m0.../s1
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 28n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...

J Med Chem 58: 7972-90 (2015)


Article DOI: 10.1021/acs.jmedchem.5b01181
BindingDB Entry DOI: 10.7270/Q20V8FMQ
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50127703
PNG
(CHEMBL3629696)
Show SMILES [Na+].[Na+].[Na+].CC(=O)NC[C@@H]1CCC(OP([O-])(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)n2ccc(N)nc2=O)([C@H]1OCc1ccccc1)P([O-])([O-])=O |r|
Show InChI InChI=1S/C24H34N4O13P2.3Na/c1-14(29)26-11-16-7-9-24(42(33,34)35,21(16)38-12-15-5-3-2-4-6-15)41-43(36,37)39-13-17-19(30)20(31)22(40-17)28-10-8-18(25)27-23(28)32;;;/h2-6,8,10,16-17,19-22,30-31H,7,9,11-13H2,1H3,(H,26,29)(H,36,37)(H2,25,27,32)(H2,33,34,35);;;/q;3*+1/p-3/t16-,17+,19+,20+,21-,22+,24?;;;/m0.../s1
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 28n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50127703
PNG
(CHEMBL3629696)
Show SMILES [Na+].[Na+].[Na+].CC(=O)NC[C@@H]1CCC(OP([O-])(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)n2ccc(N)nc2=O)([C@H]1OCc1ccccc1)P([O-])([O-])=O |r|
Show InChI InChI=1S/C24H34N4O13P2.3Na/c1-14(29)26-11-16-7-9-24(42(33,34)35,21(16)38-12-15-5-3-2-4-6-15)41-43(36,37)39-13-17-19(30)20(31)22(40-17)28-10-8-18(25)27-23(28)32;;;/h2-6,8,10,16-17,19-22,30-31H,7,9,11-13H2,1H3,(H,26,29)(H,36,37)(H2,25,27,32)(H2,33,34,35);;;/q;3*+1/p-3/t16-,17+,19+,20+,21-,22+,24?;;;/m0.../s1
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 28n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501642
PNG
(CHEMBL3629698)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#6]-[#6](=O)-[#7]-[#6@@H]-1-[#6@@H](-[#8])-[#6]=[#6](-[#8]-[#6@H]-1-[#8]-c1ccccc1)-[#6](-[#8]P([#8-])(=O)[#8]-[#6]-[#6@H]-1-[#8]-[#6@H](-[#6@H](-[#8])-[#6@@H]-1-[#8])-n1ccc(-[#7])nc1=O)P([#8-])([#8-])=O |r,c:7|
Show InChI InChI=1S/C23H30N4O15P2.3Na/c1-11(28)25-17-13(29)9-14(41-21(17)39-12-5-3-2-4-6-12)22(43(33,34)35)42-44(36,37)38-10-15-18(30)19(31)20(40-15)27-8-7-16(24)26-23(27)32;;;/h2-9,13,15,17-22,29-31H,10H2,1H3,(H,25,28)(H,36,37)(H2,24,26,32)(H2,33,34,35);;;/q;3*+1/p-3/t13-,15+,17+,18+,19+,20+,21+,22?;;;/m0.../s1
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 29n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501642
PNG
(CHEMBL3629698)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#6]-[#6](=O)-[#7]-[#6@@H]-1-[#6@@H](-[#8])-[#6]=[#6](-[#8]-[#6@H]-1-[#8]-c1ccccc1)-[#6](-[#8]P([#8-])(=O)[#8]-[#6]-[#6@H]-1-[#8]-[#6@H](-[#6@H](-[#8])-[#6@@H]-1-[#8])-n1ccc(-[#7])nc1=O)P([#8-])([#8-])=O |r,c:7|
Show InChI InChI=1S/C23H30N4O15P2.3Na/c1-11(28)25-17-13(29)9-14(41-21(17)39-12-5-3-2-4-6-12)22(43(33,34)35)42-44(36,37)38-10-15-18(30)19(31)20(40-15)27-8-7-16(24)26-23(27)32;;;/h2-9,13,15,17-22,29-31H,10H2,1H3,(H,25,28)(H,36,37)(H2,24,26,32)(H2,33,34,35);;;/q;3*+1/p-3/t13-,15+,17+,18+,19+,20+,21+,22?;;;/m0.../s1
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UniChem
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 29n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501637
PNG
(CHEMBL4063545)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ccn(-[#6@@H]-2-[#8]-[#6@H](-[#6]-[#8]P([#8-])(=O)[#8]-[#6](-[#6](=O)-[#7]-3-[#6]-[#6]-[#6]-[#6]-3)P([#8-])([#8-])=O)-[#6@@H](-[#8])-[#6@H]-2-[#8])c(=O)n1 |r|
Show InChI InChI=1S/C15H24N4O12P2.3Na/c16-9-3-6-19(15(23)17-9)13-11(21)10(20)8(30-13)7-29-33(27,28)31-14(32(24,25)26)12(22)18-4-1-2-5-18;;;/h3,6,8,10-11,13-14,20-21H,1-2,4-5,7H2,(H,27,28)(H2,16,17,23)(H2,24,25,26);;;/q;3*+1/p-3/t8-,10-,11-,13-,14?;;;/m1.../s1
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UniProtKB/SwissProt

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UniChem
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 60n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501637
PNG
(CHEMBL4063545)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ccn(-[#6@@H]-2-[#8]-[#6@H](-[#6]-[#8]P([#8-])(=O)[#8]-[#6](-[#6](=O)-[#7]-3-[#6]-[#6]-[#6]-[#6]-3)P([#8-])([#8-])=O)-[#6@@H](-[#8])-[#6@H]-2-[#8])c(=O)n1 |r|
Show InChI InChI=1S/C15H24N4O12P2.3Na/c16-9-3-6-19(15(23)17-9)13-11(21)10(20)8(30-13)7-29-33(27,28)31-14(32(24,25)26)12(22)18-4-1-2-5-18;;;/h3,6,8,10-11,13-14,20-21H,1-2,4-5,7H2,(H,27,28)(H2,16,17,23)(H2,24,25,26);;;/q;3*+1/p-3/t8-,10-,11-,13-,14?;;;/m1.../s1
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 60n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501644
PNG
(CHEMBL4097206)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ccn(-[#6@@H]-2-[#8]-[#6@H](-[#6]-[#8]P([#8-])(=O)[#8]-[#6](-[#6](=O)-[#7]-c3ccccc3)P([#8-])([#8-])=O)-[#6@@H](-[#8])-[#6@H]-2-[#8])c(=O)n1 |r|
Show InChI InChI=1S/C17H22N4O12P2.3Na/c18-11-6-7-21(17(25)20-11)15-13(23)12(22)10(32-15)8-31-35(29,30)33-16(34(26,27)28)14(24)19-9-4-2-1-3-5-9;;;/h1-7,10,12-13,15-16,22-23H,8H2,(H,19,24)(H,29,30)(H2,18,20,25)(H2,26,27,28);;;/q;3*+1/p-3/t10-,12-,13-,15-,16?;;;/m1.../s1
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 106n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501644
PNG
(CHEMBL4097206)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ccn(-[#6@@H]-2-[#8]-[#6@H](-[#6]-[#8]P([#8-])(=O)[#8]-[#6](-[#6](=O)-[#7]-c3ccccc3)P([#8-])([#8-])=O)-[#6@@H](-[#8])-[#6@H]-2-[#8])c(=O)n1 |r|
Show InChI InChI=1S/C17H22N4O12P2.3Na/c18-11-6-7-21(17(25)20-11)15-13(23)12(22)10(32-15)8-31-35(29,30)33-16(34(26,27)28)14(24)19-9-4-2-1-3-5-9;;;/h1-7,10,12-13,15-16,22-23H,8H2,(H,19,24)(H,29,30)(H2,18,20,25)(H2,26,27,28);;;/q;3*+1/p-3/t10-,12-,13-,15-,16?;;;/m1.../s1
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 106n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501641
PNG
(CHEMBL4081024)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ccn(-[#6@@H]-2-[#8]-[#6@H](-[#6]-[#8]P([#8-])(=O)[#8]-[#6](-c3ccccc3)P([#8-])([#8-])=O)-[#6@@H](-[#8])-[#6@H]-2-[#8])c(=O)n1 |r|
Show InChI InChI=1S/C16H21N3O11P2.3Na/c17-11-6-7-19(16(22)18-11)14-13(21)12(20)10(29-14)8-28-32(26,27)30-15(31(23,24)25)9-4-2-1-3-5-9;;;/h1-7,10,12-15,20-21H,8H2,(H,26,27)(H2,17,18,22)(H2,23,24,25);;;/q;3*+1/p-3/t10-,12-,13-,14-,15?;;;/m1.../s1
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 200n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501641
PNG
(CHEMBL4081024)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ccn(-[#6@@H]-2-[#8]-[#6@H](-[#6]-[#8]P([#8-])(=O)[#8]-[#6](-c3ccccc3)P([#8-])([#8-])=O)-[#6@@H](-[#8])-[#6@H]-2-[#8])c(=O)n1 |r|
Show InChI InChI=1S/C16H21N3O11P2.3Na/c17-11-6-7-19(16(22)18-11)14-13(21)12(20)10(29-14)8-28-32(26,27)30-15(31(23,24)25)9-4-2-1-3-5-9;;;/h1-7,10,12-15,20-21H,8H2,(H,26,27)(H2,17,18,22)(H2,23,24,25);;;/q;3*+1/p-3/t10-,12-,13-,14-,15?;;;/m1.../s1
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 200n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50501639
PNG
(CHEMBL4083608)
Show SMILES [Na;v0+].[Na;v0+].[Na;v0+].[#7]-c1ccn(-[#6@@H]-2-[#8]-[#6@H](-[#6]-[#8]P([#8-])(=O)[#8]-[#6](-[#6]-[#7]-3-[#6](=O)-[#6]-[#6]-[#6]-3=O)P([#8-])([#8-])=O)-[#6@@H](-[#8])-[#6@H]-2-[#8])c(=O)n1 |r|
Show InChI InChI=1S/C15H22N4O13P2.3Na/c16-8-3-4-18(15(24)17-8)14-13(23)12(22)7(31-14)6-30-34(28,29)32-11(33(25,26)27)5-19-9(20)1-2-10(19)21;;;/h3-4,7,11-14,22-23H,1-2,5-6H2,(H,28,29)(H2,16,17,24)(H2,25,26,27);;;/q;3*+1/p-3/t7-,11?,12-,13-,14-;;;/m1.../s1
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 224n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50127706
PNG
(CHEMBL3629692)
Show SMILES [Na+].[Na+].[Na+].[H][C@@]1(C[C@H](NC(C)=O)[C@@H](C1)OCc1ccccc1)C(OP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1ccc(N)nc1=O)P([O-])([O-])=O |r|
Show InChI InChI=1S/C24H34N4O13P2.3Na/c1-13(29)26-16-9-15(10-17(16)38-11-14-5-3-2-4-6-14)23(42(33,34)35)41-43(36,37)39-12-18-20(30)21(31)22(40-18)28-8-7-19(25)27-24(28)32;;;/h2-8,15-18,20-23,30-31H,9-12H2,1H3,(H,26,29)(H,36,37)(H2,25,27,32)(H2,33,34,35);;;/q;3*+1/p-3/t15-,16-,17+,18+,20+,21+,22+,23?;;;/m0.../s1
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 436n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...

J Med Chem 58: 7972-90 (2015)


Article DOI: 10.1021/acs.jmedchem.5b01181
BindingDB Entry DOI: 10.7270/Q20V8FMQ
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50127706
PNG
(CHEMBL3629692)
Show SMILES [Na+].[Na+].[Na+].[H][C@@]1(C[C@H](NC(C)=O)[C@@H](C1)OCc1ccccc1)C(OP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1ccc(N)nc1=O)P([O-])([O-])=O |r|
Show InChI InChI=1S/C24H34N4O13P2.3Na/c1-13(29)26-16-9-15(10-17(16)38-11-14-5-3-2-4-6-14)23(42(33,34)35)41-43(36,37)39-12-18-20(30)21(31)22(40-18)28-8-7-19(25)27-24(28)32;;;/h2-8,15-18,20-23,30-31H,9-12H2,1H3,(H,26,29)(H,36,37)(H2,25,27,32)(H2,33,34,35);;;/q;3*+1/p-3/t15-,16-,17+,18+,20+,21+,22+,23?;;;/m0.../s1
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 436n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...

J Med Chem 58: 7972-90 (2015)


Article DOI: 10.1021/acs.jmedchem.5b01181
BindingDB Entry DOI: 10.7270/Q20V8FMQ
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50127704
PNG
(CHEMBL3629694)
Show SMILES [Na+].[Na+].[Na+].[H][C@]1(C[C@@H](CNC(C)=O)[C@@H](C1)OCc1ccccc1)C(OP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1ccc(N)nc1=O)P([O-])([O-])=O |r|
Show InChI InChI=1S/C25H36N4O13P2.3Na/c1-14(30)27-11-17-9-16(10-18(17)39-12-15-5-3-2-4-6-15)24(43(34,35)36)42-44(37,38)40-13-19-21(31)22(32)23(41-19)29-8-7-20(26)28-25(29)33;;;/h2-8,16-19,21-24,31-32H,9-13H2,1H3,(H,27,30)(H,37,38)(H2,26,28,33)(H2,34,35,36);;;/q;3*+1/p-3/t16-,17+,18-,19-,21-,22-,23-,24?;;;/m1.../s1
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 865n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...

J Med Chem 58: 7972-90 (2015)


Article DOI: 10.1021/acs.jmedchem.5b01181
BindingDB Entry DOI: 10.7270/Q20V8FMQ
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50127705
PNG
(CHEMBL3629693)
Show SMILES [Na+].[Na+].[Na+].[H][C@]1(C[C@H](NC(C)=O)[C@@H](C1)OCc1ccccc1)C(OP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1ccc(N)nc1=O)P([O-])([O-])=O |r|
Show InChI InChI=1S/C24H34N4O13P2.3Na/c1-13(29)26-16-9-15(10-17(16)38-11-14-5-3-2-4-6-14)23(42(33,34)35)41-43(36,37)39-12-18-20(30)21(31)22(40-18)28-8-7-19(25)27-24(28)32;;;/h2-8,15-18,20-23,30-31H,9-12H2,1H3,(H,26,29)(H,36,37)(H2,25,27,32)(H2,33,34,35);;;/q;3*+1/p-3/t15-,16+,17-,18-,20-,21-,22-,23?;;;/m1.../s1
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 1.51E+3n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...

J Med Chem 58: 7972-90 (2015)


Article DOI: 10.1021/acs.jmedchem.5b01181
BindingDB Entry DOI: 10.7270/Q20V8FMQ
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50127707
PNG
(CHEMBL3629691)
Show SMILES [Na+].[Na+].[Na+].[H][C@]1(C[C@@H](O)[C@H](C1)NC(C)=O)C(OP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1ccc(N)nc1=O)P([O-])([O-])=O |r|
Show InChI InChI=1S/C17H28N4O13P2.3Na/c1-7(22)19-9-4-8(5-10(9)23)16(35(27,28)29)34-36(30,31)32-6-11-13(24)14(25)15(33-11)21-3-2-12(18)20-17(21)26;;;/h2-3,8-11,13-16,23-25H,4-6H2,1H3,(H,19,22)(H,30,31)(H2,18,20,26)(H2,27,28,29);;;/q;3*+1/p-3/t8-,9-,10+,11+,13+,14+,15+,16?;;;/m0.../s1
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 4.31E+3n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...

J Med Chem 58: 7972-90 (2015)


Article DOI: 10.1021/acs.jmedchem.5b01181
BindingDB Entry DOI: 10.7270/Q20V8FMQ
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50127709
PNG
(CHEMBL3629689)
Show SMILES [Na+].[Na+].[Na+].Nc1ccn([C@@H]2O[C@H](COP([O-])(=O)OC(C3CCCC3)P([O-])([O-])=O)[C@@H](O)[C@H]2O)c(=O)n1 |r|
Show InChI InChI=1S/C15H25N3O11P2.3Na/c16-10-5-6-18(15(21)17-10)13-12(20)11(19)9(28-13)7-27-31(25,26)29-14(30(22,23)24)8-3-1-2-4-8;;;/h5-6,8-9,11-14,19-20H,1-4,7H2,(H,25,26)(H2,16,17,21)(H2,22,23,24);;;/q;3*+1/p-3/t9-,11-,12-,13-,14?;;;/m1.../s1
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 5.85E+3n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...

J Med Chem 58: 7972-90 (2015)


Article DOI: 10.1021/acs.jmedchem.5b01181
BindingDB Entry DOI: 10.7270/Q20V8FMQ
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50127709
PNG
(CHEMBL3629689)
Show SMILES [Na+].[Na+].[Na+].Nc1ccn([C@@H]2O[C@H](COP([O-])(=O)OC(C3CCCC3)P([O-])([O-])=O)[C@@H](O)[C@H]2O)c(=O)n1 |r|
Show InChI InChI=1S/C15H25N3O11P2.3Na/c16-10-5-6-18(15(21)17-10)13-12(20)11(19)9(28-13)7-27-31(25,26)29-14(30(22,23)24)8-3-1-2-4-8;;;/h5-6,8-9,11-14,19-20H,1-4,7H2,(H,25,26)(H2,16,17,21)(H2,22,23,24);;;/q;3*+1/p-3/t9-,11-,12-,13-,14?;;;/m1.../s1
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 5.85E+3n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay 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 method

J Med Chem 60: 2135-2141 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01644
BindingDB Entry DOI: 10.7270/Q2XP77Z0
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50590208
PNG
(CHEMBL5185498)
Show SMILES O[C@@H]1[C@@H](COCc2cn(nn2)C(c2ccc(F)c(Oc3ccccc3)c2)P([O-])([O-])=O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O |r|
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 6.00E+3n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1039/d1md00079a
BindingDB Entry DOI: 10.7270/Q2183BHP
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50590208
PNG
(CHEMBL5185498)
Show SMILES O[C@@H]1[C@@H](COCc2cn(nn2)C(c2ccc(F)c(Oc3ccccc3)c2)P([O-])([O-])=O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O |r|
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 6.00E+3n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1039/d1md00079a
BindingDB Entry DOI: 10.7270/Q2183BHP
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50590209
PNG
(CHEMBL5175639)
Show SMILES O[C@@H]1[C@@H](COCc2cn(nn2)C(c2cccc(OC(F)(F)C(F)F)c2)P([O-])([O-])=O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O |r|
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 6.70E+3n/an/an/an/an/an/an/an/a


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Citation and Details

Article DOI: 10.1039/d1md00079a
BindingDB Entry DOI: 10.7270/Q2183BHP
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50590209
PNG
(CHEMBL5175639)
Show SMILES O[C@@H]1[C@@H](COCc2cn(nn2)C(c2cccc(OC(F)(F)C(F)F)c2)P([O-])([O-])=O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O |r|
PDB

UniProtKB/SwissProt

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UniChem
Article
PubMed
 6.70E+3n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1039/d1md00079a
BindingDB Entry DOI: 10.7270/Q2183BHP
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50559954
PNG
(CHEMBL4755740)
Show SMILES O[C@@H]1[C@@H](CNC(=O)OC(c2cc3ccccc3s2)P([O-])([O-])=O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O |r|
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UniProtKB/SwissProt

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UniChem
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PubMed
 8.50E+3n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)

Citation and Details

Article DOI: 10.1016/j.bmc.2020.115561
BindingDB Entry DOI: 10.7270/Q25M69DR
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50559951
PNG
(CHEMBL4751247)
Show SMILES O[C@H]1[C@@H](O)[C@@H](O[C@@H]1CNC(=O)OC(c1cccc(F)c1)P([O-])([O-])=O)n1ccc(=O)[nH]c1=O |r|
PDB

UniProtKB/SwissProt

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UniChem
Article
PubMed
 1.92E+4n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)

Citation and Details

Article DOI: 10.1016/j.bmc.2020.115561
BindingDB Entry DOI: 10.7270/Q25M69DR
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50559952
PNG
(CHEMBL4743892)
Show SMILES CCCOc1cccc(c1)C(OC(=O)NC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1ccc(=O)[nH]c1=O)P([O-])([O-])=O |r|
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UniProtKB/SwissProt

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UniChem
Article
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 2.03E+4n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)

Citation and Details

Article DOI: 10.1016/j.bmc.2020.115561
BindingDB Entry DOI: 10.7270/Q25M69DR
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50590207
PNG
(CHEMBL5180951)
Show SMILES O[C@@H]1[C@@H](COCc2cn(nn2)C(c2cccc(Oc3ccccc3)c2)P([O-])([O-])=O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O |r|
PDB

UniProtKB/SwissProt

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UniChem
Article
PubMed
 4.00E+4n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1039/d1md00079a
BindingDB Entry DOI: 10.7270/Q2183BHP
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50590207
PNG
(CHEMBL5180951)
Show SMILES O[C@@H]1[C@@H](COCc2cn(nn2)C(c2cccc(Oc3ccccc3)c2)P([O-])([O-])=O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O |r|
PDB

UniProtKB/SwissProt

GoogleScholar
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PC cid
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UniChem
Article
PubMed
 4.00E+4n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1039/d1md00079a
BindingDB Entry DOI: 10.7270/Q2183BHP
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50559953
PNG
(CHEMBL4757654)
Show SMILES O[C@H]1[C@@H](O)[C@@H](O[C@@H]1CNC(=O)OC(c1ccc(OC2CCCC2)cc1)P([O-])([O-])=O)n1ccc(=O)[nH]c1=O |r|
PDB

UniProtKB/SwissProt

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UniChem
Article
PubMed
 5.55E+4n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)

Citation and Details

Article DOI: 10.1016/j.bmc.2020.115561
BindingDB Entry DOI: 10.7270/Q25M69DR
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50559953
PNG
(CHEMBL4757654)
Show SMILES O[C@H]1[C@@H](O)[C@@H](O[C@@H]1CNC(=O)OC(c1ccc(OC2CCCC2)cc1)P([O-])([O-])=O)n1ccc(=O)[nH]c1=O |r|
PDB

UniProtKB/SwissProt

GoogleScholar
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PC cid
PC sid
UniChem
Article
PubMed
 5.55E+4n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)

Citation and Details

Article DOI: 10.1016/j.bmc.2020.115561
BindingDB Entry DOI: 10.7270/Q25M69DR
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50559950
PNG
(CHEMBL4745184)
Show SMILES O[C@H]1[C@@H](O)[C@@H](O[C@@H]1CNC(=O)OC(c1ccc(F)cc1)P([O-])([O-])=O)n1ccc(=O)[nH]c1=O |r|
PDB

UniProtKB/SwissProt

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UniChem
Article
PubMed
 3.06E+5n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)

Citation and Details

Article DOI: 10.1016/j.bmc.2020.115561
BindingDB Entry DOI: 10.7270/Q25M69DR
More data for this
Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1


(Homo sapiens (Human))		BDBM50559950
PNG
(CHEMBL4745184)
Show SMILES O[C@H]1[C@@H](O)[C@@H](O[C@@H]1CNC(=O)OC(c1ccc(F)cc1)P([O-])([O-])=O)n1ccc(=O)[nH]c1=O |r|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
 3.06E+5n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human N-terminal 6His-tagged ST6Gal-1 (Glu44 to Cys406 residues)

Citation and Details

Article DOI: 10.1016/j.bmc.2020.115561
BindingDB Entry DOI: 10.7270/Q25M69DR
More data for this
Ligand-Target Pair