BDBM50505586 CHEMBL4472432

SMILES: NC1=Nc2cc(OCCCN3CCCC3)c(OCC3CC3)cc2C11CCCC1

InChI Key: InChIKey=LBOYBJFHDJIIDQ-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 = 50505586   

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
Histone-lysine N-methyltransferase EHMT1/EHMT2 (Homo sapiens (Human))	BDBM50505586 (CHEMBL4472432) Show SMILES NC1=Nc2cc(OCCCN3CCCC3)c(OCC3CC3)cc2C11CCCC1 |t:1| Show InChI InChI=1S/C23H33N3O2/c24-22-23(8-1-2-9-23)18-14-20(28-16-17-6-7-17)21(15-19(18)25-22)27-13-5-12-26-10-3-4-11-26/h14-15,17H,1-13,16H2,(H2,24,25)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of G9a (unknown origin) by scintillation proximity Assay				J Med Chem 62: 9008-9025 (2019) Article DOI: 10.1021/acs.jmedchem.9b00562
					More data for this Ligand-Target Pair
Spindlin-1 (Homo sapiens)	BDBM50505586 (CHEMBL4472432) Show SMILES NC1=Nc2cc(OCCCN3CCCC3)c(OCC3CC3)cc2C11CCCC1 |t:1| Show InChI InChI=1S/C23H33N3O2/c24-22-23(8-1-2-9-23)18-14-20(28-16-17-6-7-17)21(15-19(18)25-22)27-13-5-12-26-10-3-4-11-26/h14-15,17H,1-13,16H2,(H2,24,25)	PDB MMDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.12E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Displacement of trimethylated biotinylated histone H3 peptide from recombinant human His-tagged SPIN1 (26 to 262 residues) expressed in Escherichia c...				J Med Chem 62: 9008-9025 (2019) Article DOI: 10.1021/acs.jmedchem.9b00562
					More data for this Ligand-Target Pair