BDBM50384921 CHEMBL2036510

SMILES: CCCCc1c(C)nc2ccc(OC)cc2c1SCCCO

InChI Key: InChIKey=WDCVXZDKKAIRLQ-UHFFFAOYSA-N

Data: 2 KI

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 = 50384921   

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
Peptide N-myristoyltransferase 2 (Homo sapiens (Human))	BDBM50384921 (CHEMBL2036510) Show SMILES CCCCc1c(C)nc2ccc(OC)cc2c1SCCCO Show InChI InChI=1S/C18H25NO2S/c1-4-5-7-15-13(2)19-17-9-8-14(21-3)12-16(17)18(15)22-11-6-10-20/h8-9,12,20H,4-7,10-11H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Imperial College London Curated by ChEMBL					Assay Description Inhibition of human N-myristoyltransferase 2 using human pp60Src92-16 amino acids) as substrate				J Med Chem 55: 3578-82 (2012) Article DOI: 10.1021/jm300040p BindingDB Entry DOI: 10.7270/Q2BC40KN
					More data for this Ligand-Target Pair
Myristoyl-CoA:protein N-myristoyltransferase (Nmt) (Homo sapiens (Human))	BDBM50384921 (CHEMBL2036510) Show SMILES CCCCc1c(C)nc2ccc(OC)cc2c1SCCCO Show InChI InChI=1S/C18H25NO2S/c1-4-5-7-15-13(2)19-17-9-8-14(21-3)12-16(17)18(15)22-11-6-10-20/h8-9,12,20H,4-7,10-11H2,1-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Imperial College London Curated by ChEMBL					Assay Description Inhibition of human N-myristoyltransferase 1 using human pp60Src92-16 amino acids) as substrate				J Med Chem 55: 3578-82 (2012) Article DOI: 10.1021/jm300040p BindingDB Entry DOI: 10.7270/Q2BC40KN
					More data for this Ligand-Target Pair