BDBM50339275 (2R,3S,4S,5S,6R)-2-(hexylsulfonyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol::CHEMBL1689641

SMILES: CCCCCCS(=O)(=O)[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O

InChI Key: InChIKey=SROORBDBUHCJSN-LDMBFOFVSA-N

Data: 1 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 1 hit for monomerid = 50339275   

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
Mannosyl-oligosaccharide alpha-1,2-mannosidase isoform B (Drosophila melanogaster)	BDBM50339275 ((2R,3S,4S,5S,6R)-2-(hexylsulfonyl)-6-(hydroxymethy...) Show SMILES CCCCCCS(=O)(=O)[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O |r| Show InChI InChI=1S/C12H24O7S/c1-2-3-4-5-6-20(17,18)12-11(16)10(15)9(14)8(7-13)19-12/h8-16H,2-7H2,1H3/t8-,9-,10+,11+,12-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.50E+6	n/a	n/a	n/a	n/a	n/a	n/a
Slovak Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of Drosophila melanogaster GM2b by spectrophotometry				Eur J Med Chem 46: 944-52 (2011) Article DOI: 10.1016/j.ejmech.2011.01.012 BindingDB Entry DOI: 10.7270/Q2MS3TQM
					More data for this Ligand-Target Pair