BDBM50388328 CHEMBL2059505
SMILES CCCCCCCCCCCCCCCCCC(=O)NCCCO[C@@H]1O[C@H](COS([O-])(=O)=O)[C@@H](O[C@H]2O[C@H](COS([O-])(=O)=O)[C@@H](O[C@H]3O[C@H](COS([O-])(=O)=O)[C@@H](OS([O-])(=O)=O)[C@H](OS([O-])(=O)=O)[C@H]3OS([O-])(=O)=O)[C@H](OS([O-])(=O)=O)[C@H]2OS([O-])(=O)=O)[C@H](OS([O-])(=O)=O)[C@H]1OS([O-])(=O)=O
InChI Key InChIKey=OBNDKQCXTGZBFN-ZOJVXTOCSA-D
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50388328
Affinity DataKi: 11.3nMAssay Description:Inhibition of human recombinant heparanase after 2 to 24 hrs by WST1 dye based fondaparinux assayMore data for this Ligand-Target Pair
Affinity DataKd: 530nMAssay Description:Binding affinity to FGF-2 by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataKd: 32.2nMAssay Description:Binding affinity to FGF-1 by surface plasmon resonance assayMore data for this Ligand-Target Pair