BDBM50445359 CHEMBL3104257

SMILES: CC(=NNC(=O)c1ccc(Cl)c(Br)c1)c1cc(Cl)ccc1O

InChI Key: InChIKey=ATFNCVWMHFTCOK-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 = 50445359   

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
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM50445359 (CHEMBL3104257) Show SMILES CC(=NNC(=O)c1ccc(Cl)c(Br)c1)c1cc(Cl)ccc1O |w:2.2| Show InChI InChI=1S/C15H11BrCl2N2O2/c1-8(11-7-10(17)3-5-14(11)21)19-20-15(22)9-2-4-13(18)12(16)6-9/h2-7,21H,1H3,(H,20,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Utah Curated by ChEMBL					Assay Description Inhibition of LSD1 (unknown origin) using dimethyl K4 peptide as substrate assessed as resorufin level by spectrophotometric analysis				J Med Chem 56: 9496-508 (2014) Article DOI: 10.1021/jm400870h BindingDB Entry DOI: 10.7270/Q2Z60QJ7
					More data for this Ligand-Target Pair