BDBM50299428 2-{7-[(3-Hydroxybenzyl)oxy]-2-oxo-2H-chromen-4-yl}acetamide::CHEMBL574191

SMILES: NC(=O)Cc1cc(=O)oc2cc(OCc3cccc(O)c3)ccc12

InChI Key: InChIKey=DPWLNJLKZUDWPZ-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50299428   

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
Monoamine oxidase (Rattus norvegicus (rat))	BDBM50299428 (2-{7-[(3-Hydroxybenzyl)oxy]-2-oxo-2H-chromen-4-yl}...) Show SMILES NC(=O)Cc1cc(=O)oc2cc(OCc3cccc(O)c3)ccc12 Show InChI InChI=1S/C18H15NO5/c19-17(21)7-12-8-18(22)24-16-9-14(4-5-15(12)16)23-10-11-2-1-3-13(20)6-11/h1-6,8-9,20H,7,10H2,(H2,19,21)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.27E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universita degli Studi di Bari Curated by ChEMBL					Assay Description Inhibition of MAO-A from Wistar rat brain by radioenzymatic assay				J Med Chem 52: 6685-706 (2009) Article DOI: 10.1021/jm9010127 BindingDB Entry DOI: 10.7270/Q2DR2VJ6
					More data for this Ligand-Target Pair
Monoamine Oxidase Type B (MAO-B) (Rattus norvegicus (rat))	BDBM50299428 (2-{7-[(3-Hydroxybenzyl)oxy]-2-oxo-2H-chromen-4-yl}...) Show SMILES NC(=O)Cc1cc(=O)oc2cc(OCc3cccc(O)c3)ccc12 Show InChI InChI=1S/C18H15NO5/c19-17(21)7-12-8-18(22)24-16-9-14(4-5-15(12)16)23-10-11-2-1-3-13(20)6-11/h1-6,8-9,20H,7,10H2,(H2,19,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universita degli Studi di Bari Curated by ChEMBL					Assay Description Inhibition of MAO-B from Wistar rat brain by radioenzymatic assay				J Med Chem 52: 6685-706 (2009) Article DOI: 10.1021/jm9010127 BindingDB Entry DOI: 10.7270/Q2DR2VJ6
					More data for this Ligand-Target Pair