BDBM50236424 CHEMBL4081750

SMILES: Cn1cnc2[nH]c(cc12)C(=O)Nc1ccccc1

InChI Key: InChIKey=KHOHCORZUZEUFA-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 = 50236424   

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
LSD1/CoREST complex (Homo sapiens (Human))	BDBM50236424 (CHEMBL4081750) Show SMILES Cn1cnc2[nH]c(cc12)C(=O)Nc1ccccc1 Show InChI InChI=1S/C13H12N4O/c1-17-8-14-12-11(17)7-10(16-12)13(18)15-9-5-3-2-4-6-9/h2-8,16H,1H3,(H,15,18)	PDB MMDB UniProtKB/SwissProt DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
European Institute of Oncology Curated by ChEMBL					Assay Description Inhibition of [3H]raclopride binding to Dopamine receptor D2 of rat striatum membranes				J Med Chem 60: 1673-1692 (2017) Article DOI: 10.1021/acs.jmedchem.6b01018 BindingDB Entry DOI: 10.7270/Q26112KN
					More data for this Ligand-Target Pair