null

SMILES: [#6]\[#6](-[#6])=[#6]\[#6](=O)-[#8]-c1cccnc1-[#6](=O)-[#7]-c1nccs1

InChI Key: InChIKey=HXMWBPFAEQPIPD-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50129646   

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))	BDBM50129646 (3-Methyl-but-2-enoic acid 2-(thiazol-2-ylcarbamoyl...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6](=O)-[#8]-c1cccnc1-[#6](=O)-[#7]-c1nccs1 Show InChI InChI=1S/C14H13N3O3S/c1-9(2)8-11(18)20-10-4-3-5-15-12(10)13(19)17-14-16-6-7-21-14/h3-8H,1-2H3,(H,16,17,19)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory activity against Methionine aminopeptidase 1 from Escherichia coli				J Med Chem 46: 2631-40 (2003) Article DOI: 10.1021/jm0300532 BindingDB Entry DOI: 10.7270/Q2CF9QTC
					More data for this Ligand-Target Pair
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50129646 (3-Methyl-but-2-enoic acid 2-(thiazol-2-ylcarbamoyl...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6](=O)-[#8]-c1cccnc1-[#6](=O)-[#7]-c1nccs1 Show InChI InChI=1S/C14H13N3O3S/c1-9(2)8-11(18)20-10-4-3-5-15-12(10)13(19)17-14-16-6-7-21-14/h3-8H,1-2H3,(H,16,17,19)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	490	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory activity against type I methionine aminopeptidase from Saccharomyces cerevisiae				J Med Chem 46: 2631-40 (2003) Article DOI: 10.1021/jm0300532 BindingDB Entry DOI: 10.7270/Q2CF9QTC
					More data for this Ligand-Target Pair