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BDBM50127707 CHEMBL3629691

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

InChI Key: InChIKey=FLBRVHHIVRRNJL-BEGKMLMKSA-K

Data: 1 KI

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50127707   
Target/Host
(Institution)		LigandTarget/Host
Links		Ligand
Links		Trg + Lig
Links		Ki
nM		ΔG°
kcal/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))		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
PDB

UniProtKB/SwissProt

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PC sid
UniChem

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Similars
PubMed
 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)


BindingDB Entry DOI: 10.7270/Q20V8FMQ
More data for this
Ligand-Target Pair