BDBM50512622 CHEMBL4521601

SMILES: COc1cc2c(NC3CCN(C)CC3)nc(nc2cc1C(N)=O)N1CCCN(C)CC1

InChI Key: InChIKey=NHEULNLHTGCYGU-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 = 50512622   

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))	BDBM50512622 (CHEMBL4521601) Show SMILES COc1cc2c(NC3CCN(C)CC3)nc(nc2cc1C(N)=O)N1CCCN(C)CC1 Show InChI InChI=1S/C22H33N7O2/c1-27-7-4-8-29(12-11-27)22-25-18-13-17(20(23)30)19(31-3)14-16(18)21(26-22)24-15-5-9-28(2)10-6-15/h13-15H,4-12H2,1-3H3,(H2,23,30)(H,24,25,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	642	n/a	n/a	n/a	n/a	n/a	n/a
Mercachem BV Curated by ChEMBL					Assay Description Inhibition of N-terminal GST tagged human recombinant EHMT1 (794 to 1294 residues) expressed in baculovirus infected Sf9 insect cells assessed as red...				Bioorg Med Chem Lett 29: 2516-2524 (2019) Article DOI: 10.1016/j.bmcl.2019.06.012
					More data for this Ligand-Target Pair
Histone-lysine N-methyltransferase EHMT1/EHMT2 (Homo sapiens (Human))	BDBM50512622 (CHEMBL4521601) Show SMILES COc1cc2c(NC3CCN(C)CC3)nc(nc2cc1C(N)=O)N1CCCN(C)CC1 Show InChI InChI=1S/C22H33N7O2/c1-27-7-4-8-29(12-11-27)22-25-18-13-17(20(23)30)19(31-3)14-16(18)21(26-22)24-15-5-9-28(2)10-6-15/h13-15H,4-12H2,1-3H3,(H2,23,30)(H,24,25,26)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.63E+3	n/a	n/a	n/a	n/a	n/a	n/a
Mercachem BV Curated by ChEMBL					Assay Description Inhibition of N-terminal GST tagged human recombinant EHMT2 (785 to 1210 residues) expressed in baculovirus infected Sf9 insect cells assessed as red...				Bioorg Med Chem Lett 29: 2516-2524 (2019) Article DOI: 10.1016/j.bmcl.2019.06.012
					More data for this Ligand-Target Pair