BDBM50505582 CHEMBL4465568

SMILES: CCOc1cc2c(cc1OCCCN1CCCC1)N=C(N)C21CCCC1

InChI Key: InChIKey=OLVBPAFOEGMPRK-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 = 50505582   

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))	BDBM50505582 (CHEMBL4465568) Show SMILES CCOc1cc2c(cc1OCCCN1CCCC1)N=C(N)C21CCCC1 |t:20| Show InChI InChI=1S/C21H31N3O2/c1-2-25-18-14-16-17(23-20(22)21(16)8-3-4-9-21)15-19(18)26-13-7-12-24-10-5-6-11-24/h14-15H,2-13H2,1H3,(H2,22,23)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	120	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)	BDBM50505582 (CHEMBL4465568) Show SMILES CCOc1cc2c(cc1OCCCN1CCCC1)N=C(N)C21CCCC1 |t:20| Show InChI InChI=1S/C21H31N3O2/c1-2-25-18-14-16-17(23-20(22)21(16)8-3-4-9-21)15-19(18)26-13-7-12-24-10-5-6-11-24/h14-15H,2-13H2,1H3,(H2,22,23)	PDB MMDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.15E+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