BDBM50151148 CHEMBL3769700

SMILES: O=C(N[C@H]1CNC1=O)OCc1ccc2CCCc2c1

InChI Key: InChIKey=WEAVXTAWMQIIJU-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 = 50151148   

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))	BDBM50151148 (CHEMBL3769700) Show SMILES O=C(N[C@H]1CNC1=O)OCc1ccc2CCCc2c1 |r| Show InChI InChI=1S/C14H16N2O3/c17-13-12(7-15-13)16-14(18)19-8-9-4-5-10-2-1-3-11(10)6-9/h4-6,12H,1-3,7-8H2,(H,15,17)(H,16,18)/t12-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	130	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