BDBM50299750 (1S,3R,4S,5R,6R,7S)-4,5-Dihydroxy-3-(hydroxymethyl)-2-oxabicyclo[4.1.0]heptan-7-amine::CHEMBL574865

SMILES: N[C@@H]1[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]12

InChI Key: InChIKey=HZXSVTMGRQQZKC-JEUCJEOGSA-N

Data: 2 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50299750   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Beta-glucosidase (Homo sapiens (Human))	BDBM50299750 ((1S,3R,4S,5R,6R,7S)-4,5-Dihydroxy-3-(hydroxymethyl...) Show SMILES N[C@@H]1[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]12 |r| Show InChI InChI=1S/C7H13NO4/c8-4-3-6(11)5(10)2(1-9)12-7(3)4/h2-7,9-11H,1,8H2/t2-,3?,4+,5-,6-,7+/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Leiden University Curated by ChEMBL					Assay Description Inhibition of human GBA2				Bioorg Med Chem Lett 19: 6600-3 (2009) Article DOI: 10.1016/j.bmcl.2009.10.022 BindingDB Entry DOI: 10.7270/Q2736QZB
					More data for this Ligand-Target Pair
Lysosomal alpha-glucosidase (Homo sapiens (Human))	BDBM50299750 ((1S,3R,4S,5R,6R,7S)-4,5-Dihydroxy-3-(hydroxymethyl...) Show SMILES N[C@@H]1[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]12 |r| Show InChI InChI=1S/C7H13NO4/c8-4-3-6(11)5(10)2(1-9)12-7(3)4/h2-7,9-11H,1,8H2/t2-,3?,4+,5-,6-,7+/m1/s1	PDB NCI pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Leiden University Curated by ChEMBL					Assay Description Inhibition of human lysosomal alpha glucosidase				Bioorg Med Chem Lett 19: 6600-3 (2009) Article DOI: 10.1016/j.bmcl.2009.10.022 BindingDB Entry DOI: 10.7270/Q2736QZB
					More data for this Ligand-Target Pair