BDBM50345019 (2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(3-(4-(pent-2-enyloxy)benzyl)phenyl)tetrahydro-2H-pyran-3,4,5-triol::CHEMBL1778657

SMILES: CC\C=C\COc1ccc(Cc2cccc(c2)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1

InChI Key: InChIKey=PYAANSFDGRQQCG-NFQFPNEVSA-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 = 50345019   

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
Low affinity sodium-glucose cotransporter (Homo sapiens (Human))	BDBM50345019 ((2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(3-(4-(pent-2...) Show SMILES CC\C=C\COc1ccc(Cc2cccc(c2)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1 |r| Show InChI InChI=1S/C24H30O6/c1-2-3-4-12-29-19-10-8-16(9-11-19)13-17-6-5-7-18(14-17)24-23(28)22(27)21(26)20(15-25)30-24/h3-11,14,20-28H,2,12-13,15H2,1H3/b4-3+/t20-,21-,22+,23-,24+/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	59.5	n/a	n/a	n/a	n/a	n/a	n/a
Green Cross Corporation Curated by ChEMBL					Assay Description Inhibition of human SGLT2 expressed in CHO cells using methyl-alpha-D-glucopyranoside by liquid scintillation counting				Bioorg Med Chem Lett 21: 3759-63 (2011) Article DOI: 10.1016/j.bmcl.2011.04.063 BindingDB Entry DOI: 10.7270/Q2NC61KM
					More data for this Ligand-Target Pair