BDBM50058694 CHEMBL3326806

SMILES [H][C@]1(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)[C@H](O)[C@@H](CO[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](OC)[C@H]1O

InChI Key InChIKey=VRIBKPUEENOKSF-RXSBVVMGSA-N

Data  2 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50058694   

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

Curated by ChEMBL
LigandPNGBDBM50058694(CHEMBL3326806)
Affinity DataKi:  1.20E+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
LigandPNGBDBM50058694(CHEMBL3326806)
Affinity DataKi:  1.40E+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