BDBM50564250 CHEMBL4786167
SMILES O[C@@H]1CN[C@H](Cn2cc(COCC(COCc3cn(C[C@H]4NC[C@@H](O)[C@H]4O)nn3)(COCc3cn(C[C@H]4NC[C@@H](O)[C@H]4O)nn3)NC(=O)c3cc(cc(c3)C(=O)NC(COCc3cn(C[C@H]4NC[C@@H](O)[C@H]4O)nn3)(COCc3cn(C[C@H]4NC[C@@H](O)[C@H]4O)nn3)COCc3cn(C[C@H]4NC[C@@H](O)[C@H]4O)nn3)C(=O)NC(COCc3cn(C[C@H]4NC[C@@H](O)[C@H]4O)nn3)(COCc3cn(C[C@H]4NC[C@@H](O)[C@H]4O)nn3)COCc3cn(C[C@H]4NC[C@@H](O)[C@H]4O)nn3)nn2)[C@@H]1O
InChI Key InChIKey=BRBOWQWOZAWAHQ-UHFFFAOYSA-N
Data 1 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 1 hit for monomerid = 50564250
Affinity DataIC50: 2.86E+5nMAssay Description:Inhibition of human recombinant lysosomal alpha-GalA using 4-methylumbelliferyl-alpha-D-glucopyranoside as substrate preincubated for 45 mins followe...More data for this Ligand-Target Pair