BDBM50008909 CHEMBL3237620
SMILES [H][C@@]1(O[C@H]2[C@H](O)[C@@H](CO)O[C@@]([H])(O[C@H]3[C@H](O)[C@@H](O)[C@]([H])(O[C@H]4[C@H](O)[C@@H](CO)O[C@@]([H])(O[C@H]5[C@H](O)[C@@H](O)[C@H](O)O[C@@H]5C(O)=O)[C@@H]4NC(C)=O)O[C@@H]3C(O)=O)[C@@H]2NC(C)=O)O[C@@H]([C@@H](O[C@]2([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2NC(C)=O)[C@H](O)[C@H]1O)C(O)=O
InChI Key InChIKey=XPUFUQLOOZFGID-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50008909
Affinity DataKd: 3.88E+4nMAssay Description:Binding affinity to immobilized recombinant human CD44 hyaluronan binding domain by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataKd: 5.84E+4nMAssay Description:Binding affinity to immobilized recombinant mouse CD44 hyaluronan binding domain by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.08E+5nMAssay Description:Inhibition of recombinant human hyaluronan binding domain of CD44 binding to immobilized polymeric hyaluronan by surface plasmon resonance assayMore data for this Ligand-Target Pair