Compile Data Set for Download or QSAR

Found 69 hits Enz. Inhib. hit(s) with Target = 'CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,6-sialyltransferase'   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Beta-galactoside alpha-2,6-sialyltransferase 1 (Homo sapiens (Human))	BDBM50501643 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	16	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	16	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	19	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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))	BDBM50501640 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	19	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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))	BDBM50127702 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	19	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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))	BDBM50501638 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	28	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	28	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	28	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	28	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (Rattus norvegicus)	BDBM50559955 (CHEMBL4776007) 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@@H](-[#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	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	29	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rat liver ST6Gal-1 by HPLC-based assay				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))	BDBM50501642 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	29	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	29	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (Rattus norvegicus)	BDBM50501640 (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	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of rat liver ST6Gal-1 using p-nitrophenyl-DL-alanine measured up to 20 mins by HPLC analysis				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))	BDBM50501644 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	106	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	106	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	200	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	200	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	224	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	436	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	436	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	865	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	1.51E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	4.31E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	5.85E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	5.85E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	6.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	6.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	8.50E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.92E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.03E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	4.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	4.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5.55E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5.55E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (Rattus norvegicus)	BDBM50310540 (((2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)...) Show SMILES Nc1ccn([C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]2O)c(=O)n1 |r| Show InChI InChI=1S/C9H14N3O8P/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H2,10,11,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	6.40E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Colorado Curated by ChEMBL					Assay Description Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liver				Bioorg Med Chem Lett 13: 301-4 (2002) BindingDB Entry DOI: 10.7270/Q2FJ2HBM
					More data for this Ligand-Target Pair				3D Structure (crystal)
Beta-galactoside alpha-2,6-sialyltransferase 1 (Homo sapiens (Human))	BDBM50559950 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.06E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (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| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.06E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/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 (Rattus norvegicus)	BDBM50366837 (CHEMBL608619) Show SMILES Nc1ccn(C2O[C@H](COP(O)(=O)OCC(O)=O)[C@@H](O)[C@H]2O)c(=O)n1 |r| Show InChI InChI=1S/C11H16N3O10P/c12-6-1-2-14(11(19)13-6)10-9(18)8(17)5(24-10)3-22-25(20,21)23-4-7(15)16/h1-2,5,8-10,17-18H,3-4H2,(H,15,16)(H,20,21)(H2,12,13,19)/t5-,8-,9-,10?/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.70E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Colorado Curated by ChEMBL					Assay Description Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liver				Bioorg Med Chem Lett 13: 301-4 (2002) BindingDB Entry DOI: 10.7270/Q2FJ2HBM
					More data for this Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1 (Rattus norvegicus)	BDBM50366833 (CHEMBL608928) Show SMILES Nc1ccn(C2O[C@H](COP(O)(=O)N[C@@H](Cc3c[nH]c4ccccc34)C(O)=O)[C@@H](O)[C@H]2O)c(=O)n1 |r| Show InChI InChI=1S/C20H24N5O9P/c21-15-5-6-25(20(30)23-15)18-17(27)16(26)14(34-18)9-33-35(31,32)24-13(19(28)29)7-10-8-22-12-4-2-1-3-11(10)12/h1-6,8,13-14,16-18,22,26-27H,7,9H2,(H,28,29)(H2,21,23,30)(H2,24,31,32)/t13-,14+,16+,17+,18?/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	7.30E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Colorado Curated by ChEMBL					Assay Description Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liver				Bioorg Med Chem Lett 13: 301-4 (2002) BindingDB Entry DOI: 10.7270/Q2FJ2HBM
					More data for this Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1 (Rattus norvegicus)	BDBM50366836 (CHEMBL610554) Show SMILES C[C@H](NP(O)(=O)OC[C@H]1OC([C@H](O)[C@@H]1O)n1ccc(N)nc1=O)C(O)=O |r| Show InChI InChI=1S/C12H19N4O9P/c1-5(11(19)20)15-26(22,23)24-4-6-8(17)9(18)10(25-6)16-3-2-7(13)14-12(16)21/h2-3,5-6,8-10,17-18H,4H2,1H3,(H,19,20)(H2,13,14,21)(H2,15,22,23)/t5-,6+,8+,9+,10?/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.70E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Colorado Curated by ChEMBL					Assay Description Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liver				Bioorg Med Chem Lett 13: 301-4 (2002) BindingDB Entry DOI: 10.7270/Q2FJ2HBM
					More data for this Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1 (Rattus norvegicus)	BDBM50366835 (CHEMBL609514) Show SMILES Nc1ccn(C2O[C@H](COP(O)(=O)N[C@@H](CC(O)=O)C(O)=O)[C@@H](O)[C@H]2O)c(=O)n1 |r| Show InChI InChI=1S/C13H19N4O11P/c14-7-1-2-17(13(24)15-7)11-10(21)9(20)6(28-11)4-27-29(25,26)16-5(12(22)23)3-8(18)19/h1-2,5-6,9-11,20-21H,3-4H2,(H,18,19)(H,22,23)(H2,14,15,24)(H2,16,25,26)/t5-,6+,9+,10+,11?/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.20E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Colorado Curated by ChEMBL					Assay Description Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liver				Bioorg Med Chem Lett 13: 301-4 (2002) BindingDB Entry DOI: 10.7270/Q2FJ2HBM
					More data for this Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1 (Rattus norvegicus)	BDBM50366838 (CHEMBL609215) Show SMILES Nc1ccn(C2O[C@H](COP(O)(=O)NCC(O)=O)[C@@H](O)[C@H]2O)c(=O)n1 |r| Show InChI InChI=1S/C11H17N4O9P/c12-6-1-2-15(11(20)14-6)10-9(19)8(18)5(24-10)4-23-25(21,22)13-3-7(16)17/h1-2,5,8-10,18-19H,3-4H2,(H,16,17)(H2,12,14,20)(H2,13,21,22)/t5-,8-,9-,10?/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.40E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Colorado Curated by ChEMBL					Assay Description Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liver				Bioorg Med Chem Lett 13: 301-4 (2002) BindingDB Entry DOI: 10.7270/Q2FJ2HBM
					More data for this Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1 (Rattus norvegicus)	BDBM50366832 (CHEMBL609516) Show SMILES CC(C)C[C@H](NP(O)(=O)OC[C@H]1OC([C@H](O)[C@@H]1O)n1ccc(N)nc1=O)C(O)=O |r| Show InChI InChI=1S/C15H25N4O9P/c1-7(2)5-8(14(22)23)18-29(25,26)27-6-9-11(20)12(21)13(28-9)19-4-3-10(16)17-15(19)24/h3-4,7-9,11-13,20-21H,5-6H2,1-2H3,(H,22,23)(H2,16,17,24)(H2,18,25,26)/t8-,9+,11+,12+,13?/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.50E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Colorado Curated by ChEMBL					Assay Description Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liver				Bioorg Med Chem Lett 13: 301-4 (2002) BindingDB Entry DOI: 10.7270/Q2FJ2HBM
					More data for this Ligand-Target Pair
Beta-galactoside alpha-2,6-sialyltransferase 1 (Rattus norvegicus)	BDBM50366834 (CHEMBL609800) Show SMILES Nc1ccn(C2O[C@H](COP(O)(=O)N[C@@H](Cc3ccccc3)C(O)=O)[C@@H](O)[C@H]2O)c(=O)n1 |r| Show InChI InChI=1S/C18H23N4O9P/c19-13-6-7-22(18(27)20-13)16-15(24)14(23)12(31-16)9-30-32(28,29)21-11(17(25)26)8-10-4-2-1-3-5-10/h1-7,11-12,14-16,23-24H,8-9H2,(H,25,26)(H2,19,20,27)(H2,21,28,29)/t11-,12+,14+,15+,16?/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.80E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Colorado Curated by ChEMBL					Assay Description Inhibitory activity evaluated against alpha-2,6-sialyltransferase from rat liver				Bioorg Med Chem Lett 13: 301-4 (2002) BindingDB Entry DOI: 10.7270/Q2FJ2HBM
					More data for this Ligand-Target Pair

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