BDBM50148934 CHEMBL3770842

SMILES: CC(=O)N1N=C(OC1c1ccc(Cl)c(Cl)c1)c1ccc(C)cc1

InChI Key: InChIKey=WQMGPMPSDQLUCP-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 = 50148934   

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
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50148934 (CHEMBL3770842) Show SMILES CC(=O)N1N=C(OC1c1ccc(Cl)c(Cl)c1)c1ccc(C)cc1 |c:4| Show InChI InChI=1S/C17H14Cl2N2O2/c1-10-3-5-12(6-4-10)16-20-21(11(2)22)17(23-16)13-7-8-14(18)15(19)9-13/h3-9,17H,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Cagliari Curated by ChEMBL					Assay Description Inhibition of human recombinant MAO-B expressed in baculovirus infected BTI cells using p-tyramine as substrate after 15 mins by Amplex Red-based flu...				Eur J Med Chem 108: 542-52 (2016) BindingDB Entry DOI: 10.7270/Q2GX4DFK
					More data for this Ligand-Target Pair