BDBM50501642 CHEMBL3629698

SMILES CC(=O)N[C@@H]1[C@@H](O)C=C(O[C@H]1Oc1ccccc1)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=QQLNDVODCNFGAI-UHFFFAOYSA-K

Data  2 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50501642   

TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
Peking University

Curated by ChEMBL
LigandPNGBDBM50501642(CHEMBL3629698)
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
In Depth
Date in BDB:
9/5/2020
Entry Details Article
PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Human)
Peking University

Curated by ChEMBL
LigandPNGBDBM50501642(CHEMBL3629698)
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
In Depth
Date in BDB:
9/5/2020
Entry Details Article
PubMed