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