BDBM50565730 CHEMBL4792554
SMILES [H][C@@]1(O[C@H]([C@@H](O)CO)[C@H](O[C@]2([H])O[C@H](COS([O-])(=O)=O)[C@H](OS([O-])(=O)=O)[C@H](O[C@]3([H])OC(=C[C@H](O[C@]4([H])O[C@@H](C)[C@@H](OS([O-])(=O)=O)[C@@H](OS(O)(=O)=O)[C@@H]4O)[C@H]3O)C([O-])=O)[C@H]2NC(C)=O)[C@H](O)C([O-])=O)O[C@@H](C)[C@@H](OS([O-])(=O)=O)[C@@H](OS(O)(=O)=O)[C@@H]1O
InChI Key InChIKey=UGDHJVDQSUGNAZ-UHFFFAOYSA-H
Data 2 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50565730
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of human citrated plasma iXase (factor 8a-factor 9a complex) preincubated for 2 mins followed by factor 10 addition and measured after 1 m...More data for this Ligand-Target Pair
Affinity DataIC50: 1.29E+4nMAssay Description:Inhibition of factor 9a (unknown origin) binding to immobilized biotinylated oHG-11 by biolayer interferometryMore data for this Ligand-Target Pair