BDBM50424625 CHEMBL2313197

SMILES: Cc1ccc(c(C)c1)S(=O)(=O)N1CCC(CC1)C(=O)Nc1ccc(cc1)N1CCOCC1

InChI Key: InChIKey=PWCYXMRNEZRYAL-UHFFFAOYSA-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 = 50424625   

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
EBifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50424625 (CHEMBL2313197) Show SMILES Cc1ccc(c(C)c1)S(=O)(=O)N1CCC(CC1)C(=O)Nc1ccc(cc1)N1CCOCC1 Show InChI InChI=1S/C24H31N3O4S/c1-18-3-8-23(19(2)17-18)32(29,30)27-11-9-20(10-12-27)24(28)25-21-4-6-22(7-5-21)26-13-15-31-16-14-26/h3-8,17,20H,9-16H2,1-2H3,(H,25,28)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	250	n/a	n/a	n/a	n/a	n/a	n/a
Columbia University Curated by ChEMBL					Assay Description Inhibition of human sEH assessed as 6-methoxy-2-naphthaldehyde generation preincubated for 10 before addition of cyano(2-methyl-oxynaphthalen-6-yl)me...				Bioorg Med Chem Lett 23: 417-21 (2012) Article DOI: 10.1016/j.bmcl.2012.11.084 BindingDB Entry DOI: 10.7270/Q2Z60QBJ
					More data for this Ligand-Target Pair