BDBM50400782 CHEMBL2204999

SMILES: CC(C)n1ncc2c(cc(cc12)C1CC1)C(=O)NCc1c(C)cc(C)[nH]c1=O

InChI Key: InChIKey=CXHIBWJWKWWABQ-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 = 50400782   

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 EZH2 (Homo sapiens (Human))	BDBM50400782 (CHEMBL2204999) Show SMILES CC(C)n1ncc2c(cc(cc12)C1CC1)C(=O)NCc1c(C)cc(C)[nH]c1=O Show InChI InChI=1S/C22H26N4O2/c1-12(2)26-20-9-16(15-5-6-15)8-17(19(20)11-24-26)21(27)23-10-18-13(3)7-14(4)25-22(18)28/h7-9,11-12,15H,5-6,10H2,1-4H3,(H,23,27)(H,25,28)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.51E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of EZH2-mediated proliferation of human LNCaP cells after 6 days by chemiluminescence analysis				ACS Med Chem Lett 3: 1091-1096 (2012) Article DOI: 10.1021/ml3003346 BindingDB Entry DOI: 10.7270/Q2NK3G60
					More data for this Ligand-Target Pair