BDBM50127240 CHEMBL3629807

SMILES: COc1ccc(\C=C\c2cc(OC)cc(OC)c2\C=C\C(=O)c2cc3ccc(Br)cc3oc2=O)cc1

InChI Key: InChIKey=VUIHXXXAELJOFV-RTYMFESYSA-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 = 50127240   

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))	BDBM50127240 (CHEMBL3629807) Show SMILES COc1ccc(\C=C\c2cc(OC)cc(OC)c2\C=C\C(=O)c2cc3ccc(Br)cc3oc2=O)cc1 Show InChI InChI=1S/C29H23BrO6/c1-33-22-10-5-18(6-11-22)4-7-19-14-23(34-2)17-28(35-3)24(19)12-13-26(31)25-15-20-8-9-21(30)16-27(20)36-29(25)32/h4-17H,1-3H3/b7-4+,13-12+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.53E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hefei University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant human MAOB using p-tyramine as substrate assessed as H2O2 production preincubated for 15 mins followed by substrate additio...				Eur J Med Chem 103: 185-90 (2015) BindingDB Entry DOI: 10.7270/Q29C7070
					More data for this Ligand-Target Pair
Amine oxidase (flavin-containing) A (Homo sapiens (Human))	BDBM50127240 (CHEMBL3629807) Show SMILES COc1ccc(\C=C\c2cc(OC)cc(OC)c2\C=C\C(=O)c2cc3ccc(Br)cc3oc2=O)cc1 Show InChI InChI=1S/C29H23BrO6/c1-33-22-10-5-18(6-11-22)4-7-19-14-23(34-2)17-28(35-3)24(19)12-13-26(31)25-15-20-8-9-21(30)16-27(20)36-29(25)32/h4-17H,1-3H3/b7-4+,13-12+	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.01E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hefei University of Technology Curated by ChEMBL					Assay Description Inhibition of recombinant human MAOA using p-tyramine as substrate assessed as H2O2 production preincubated for 15 mins followed by substrate additio...				Eur J Med Chem 103: 185-90 (2015) BindingDB Entry DOI: 10.7270/Q29C7070
					More data for this Ligand-Target Pair