BDBM50384911 CHEMBL2036500

SMILES: CCc1c(C)nc2ccc(OC)cc2c1SCCC#N

InChI Key: InChIKey=XWQDUNPYGOGWBB-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 = 50384911   

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
Myristoyl-CoA:protein N-myristoyltransferase (Nmt) (Homo sapiens (Human))	BDBM50384911 (CHEMBL2036500) Show SMILES CCc1c(C)nc2ccc(OC)cc2c1SCCC#N Show InChI InChI=1S/C16H18N2OS/c1-4-13-11(2)18-15-7-6-12(19-3)10-14(15)16(13)20-9-5-8-17/h6-7,10H,4-5,9H2,1-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.56E+4	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
Peptide N-myristoyltransferase 2 (Homo sapiens (Human))	BDBM50384911 (CHEMBL2036500) Show SMILES CCc1c(C)nc2ccc(OC)cc2c1SCCC#N Show InChI InChI=1S/C16H18N2OS/c1-4-13-11(2)18-15-7-6-12(19-3)10-14(15)16(13)20-9-5-8-17/h6-7,10H,4-5,9H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.32E+4	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