BDBM50247707 CHEMBL454166::N-((3S,4R)-6-cyano-3-hydroxy-2,2-dimethylchroman-4-yl)benzo[d][1,3]dioxole-5-carboxamide

SMILES: CC1(C)Oc2ccc(cc2[C@@H](NC(=O)c2ccc3OCOc3c2)[C@@H]1O)C#N

InChI Key: InChIKey=LCMULRGEZDKTHJ-MSOLQXFVSA-N

Data: 1 EC50

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 = 50247707   

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
Sulfonylurea receptor 2, Kir6.2 (Homo sapiens (Human))	BDBM50247707 (CHEMBL454166 | N-((3S,4R)-6-cyano-3-hydroxy-2,2-di...) Show SMILES CC1(C)Oc2ccc(cc2[C@@H](NC(=O)c2ccc3OCOc3c2)[C@@H]1O)C#N |r| Show InChI InChI=1S/C20H18N2O5/c1-20(2)18(23)17(13-7-11(9-21)3-5-14(13)27-20)22-19(24)12-4-6-15-16(8-12)26-10-25-15/h3-8,17-18,23H,10H2,1-2H3,(H,22,24)/t17-,18+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	810	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Channel opening activity at SUR2B/Kir6.2 potassium ATP channel in human TE671 cells assessed as isometric force by FLIPR				Bioorg Med Chem 17: 855-66 (2009) Article DOI: 10.1016/j.bmc.2008.11.055 BindingDB Entry DOI: 10.7270/Q2N017FM
					More data for this Ligand-Target Pair