BDBM50151149 CHEMBL3769639

SMILES: FC(F)(F)c1ccc(CCCCOC(=O)N[C@H]2CNC2=O)cc1

InChI Key: InChIKey=XFGRAAXRZBSWNY-LBPRGKRZSA-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 = 50151149   

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
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM50151149 (CHEMBL3769639) Show SMILES FC(F)(F)c1ccc(CCCCOC(=O)N[C@H]2CNC2=O)cc1 |r| Show InChI InChI=1S/C15H17F3N2O3/c16-15(17,18)11-6-4-10(5-7-11)3-1-2-8-23-14(22)20-12-9-19-13(12)21/h4-7,12H,1-3,8-9H2,(H,19,21)(H,20,22)/t12-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	73	n/a	n/a	n/a	n/a	n/a	n/a
Italian Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human NAAA expressed in HEK293 cells preincubated for 10 mins followed by N-(4-methyl-2-oxo-chromen-7-yl)-hexadecanamide substrate addi...				Eur J Med Chem 111: 138-59 (2016) BindingDB Entry DOI: 10.7270/Q2GQ70MX
					More data for this Ligand-Target Pair