null

SMILES: COC(Cc1scnc1C(=O)Nc1nccs1)c1ccccc1OC

InChI Key: InChIKey=AILNQGROYLAXCK-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50170367   

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
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50170367 (5-[2-Methoxy-2-(2-methoxy-phenyl)-ethyl]-thiazole-...) Show SMILES COC(Cc1scnc1C(=O)Nc1nccs1)c1ccccc1OC Show InChI InChI=1S/C17H17N3O3S2/c1-22-12-6-4-3-5-11(12)13(23-2)9-14-15(19-10-25-14)16(21)20-17-18-7-8-24-17/h3-8,10,13H,9H2,1-2H3,(H,18,20,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	35	n/a	n/a	n/a	n/a	n/a	n/a
Shanghai Graduate School of the Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory concentration against EcMetAP1 enzyme activity				Bioorg Med Chem Lett 15: 4130-5 (2005) Article DOI: 10.1016/j.bmcl.2005.06.005 BindingDB Entry DOI: 10.7270/Q2FN15RH
					More data for this Ligand-Target Pair
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50170367 (5-[2-Methoxy-2-(2-methoxy-phenyl)-ethyl]-thiazole-...) Show SMILES COC(Cc1scnc1C(=O)Nc1nccs1)c1ccccc1OC Show InChI InChI=1S/C17H17N3O3S2/c1-22-12-6-4-3-5-11(12)13(23-2)9-14-15(19-10-25-14)16(21)20-17-18-7-8-24-17/h3-8,10,13H,9H2,1-2H3,(H,18,20,21)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	570	n/a	n/a	n/a	n/a	n/a	n/a
Shanghai Graduate School of the Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory concentration against ScMetAP1 enzyme activity				Bioorg Med Chem Lett 15: 4130-5 (2005) Article DOI: 10.1016/j.bmcl.2005.06.005 BindingDB Entry DOI: 10.7270/Q2FN15RH
					More data for this Ligand-Target Pair