BDBM50195463 CHEMBL3939705

SMILES: O=C1c2ccccc2-c2onc3c(cc(NCCN4CCCC4)c1c23)N1CCN(CC1)c1ccccc1

InChI Key: InChIKey=CFLCCLSHOUOYIN-UHFFFAOYSA-N

Data: 1 IC50

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Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50195463   

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 EHMT2 (Homo sapiens (Human))	BDBM50195463 (CHEMBL3939705) Show SMILES O=C1c2ccccc2-c2onc3c(cc(NCCN4CCCC4)c1c23)N1CCN(CC1)c1ccccc1 Show InChI InChI=1S/C30H31N5O2/c36-29-22-10-4-5-11-23(22)30-27-26(29)24(31-12-15-33-13-6-7-14-33)20-25(28(27)32-37-30)35-18-16-34(17-19-35)21-8-2-1-3-9-21/h1-5,8-11,20,31H,6-7,12-19H2	PDB UniProtKB/SwissProt UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.22E+3	n/a	n/a	n/a	n/a	n/a	n/a
China Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of G9a (unknown origin) using biotinylated-histone H3 (1 to 21 residues)/S-adenosyl-methionine as substrate/methyl donor after 3 hrs by Al...				Bioorg Med Chem 24: 6102-6108 (2016) Article DOI: 10.1016/j.bmc.2016.09.071 BindingDB Entry DOI: 10.7270/Q29C70D7
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