BDBM50058693 CHEMBL3326805

SMILES [H][C@@]1(O[C@@H]2[C@@H](CO[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@]3([H])O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3NC(C)=O)O[C@H](OC)[C@@H](O)[C@@]2([H])O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@]2([H])O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2NC(C)=O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1NC(C)=O

InChI Key InChIKey=ZAXWMEOHWABEBI-RCUVRXQASA-N

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 = 50058693   

TargetN-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 3(Homo sapiens (Human))
Riken-Max Planck Joint Research Center For Systems Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50058693(CHEMBL3326805)
Affinity DataKi:  1.50E+6nMAssay Description:Inhibition of human N-terminally His6-tagged N-acetylglucosaminyltransferase 3 expressed in HEK293T cells assessed as GN-GnGnbi-PAs molar ratio level...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 3(Homo sapiens (Human))
Riken-Max Planck Joint Research Center For Systems Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50058693(CHEMBL3326805)
Affinity DataKi:  1.40E+7nMAssay Description:Inhibition of human N-terminally His6-tagged N-acetylglucosaminyltransferase 3 expressed in HEK293T cells assessed as GN-GnGnbi-PAs molar ratio level...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed