Compile Data Set for Download or QSAR

Found 4 hits Enz. Inhib. hit(s) with Target = 'Methionine aminopeptidase' and Ligand = 'BDBM50175439'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50175439 (5-(2-NITROPHENYL)-2-FUROIC ACID | 5-(2-nitrophenyl...) Show SMILES OC(=O)c1ccc(o1)-c1ccccc1[N+]([O-])=O Show InChI InChI=1S/C11H7NO5/c13-11(14)10-6-5-9(17-10)7-3-1-2-4-8(7)12(15)16/h1-6H,(H,13,14)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank MMDB PDB Article PubMed	n/a	n/a	1.08E+3	n/a	n/a	n/a	n/a	n/a	n/a
Graduate School of Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory activity against Mn(II) form of Escherichia coli MetAP				Bioorg Med Chem Lett 15: 5386-91 (2005) Article DOI: 10.1016/j.bmcl.2005.09.019 BindingDB Entry DOI: 10.7270/Q2HH6JNV
					More data for this Ligand-Target Pair				3D Structure (crystal)
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50175439 (5-(2-NITROPHENYL)-2-FUROIC ACID | 5-(2-nitrophenyl...) Show SMILES OC(=O)c1ccc(o1)-c1ccccc1[N+]([O-])=O Show InChI InChI=1S/C11H7NO5/c13-11(14)10-6-5-9(17-10)7-3-1-2-4-8(7)12(15)16/h1-6H,(H,13,14)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank MMDB PDB Article PubMed	n/a	n/a	1.20E+5	n/a	n/a	n/a	n/a	n/a	n/a
Graduate School of Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory activity against Co(II) form of Escherichia coli MetAP				Bioorg Med Chem Lett 15: 5386-91 (2005) Article DOI: 10.1016/j.bmcl.2005.09.019 BindingDB Entry DOI: 10.7270/Q2HH6JNV
					More data for this Ligand-Target Pair				3D Structure (crystal)
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50175439 (5-(2-NITROPHENYL)-2-FUROIC ACID | 5-(2-nitrophenyl...) Show SMILES OC(=O)c1ccc(o1)-c1ccccc1[N+]([O-])=O Show InChI InChI=1S/C11H7NO5/c13-11(14)10-6-5-9(17-10)7-3-1-2-4-8(7)12(15)16/h1-6H,(H,13,14)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank MMDB PDB Article PubMed	n/a	n/a	1.75E+5	n/a	n/a	n/a	n/a	n/a	n/a
Graduate School of Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory activity against Ni(II) form of Escherichia coli MetAP				Bioorg Med Chem Lett 15: 5386-91 (2005) Article DOI: 10.1016/j.bmcl.2005.09.019 BindingDB Entry DOI: 10.7270/Q2HH6JNV
					More data for this Ligand-Target Pair				3D Structure (crystal)
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50175439 (5-(2-NITROPHENYL)-2-FUROIC ACID | 5-(2-nitrophenyl...) Show SMILES OC(=O)c1ccc(o1)-c1ccccc1[N+]([O-])=O Show InChI InChI=1S/C11H7NO5/c13-11(14)10-6-5-9(17-10)7-3-1-2-4-8(7)12(15)16/h1-6H,(H,13,14)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank MMDB PDB Article PubMed	n/a	n/a	1.78E+5	n/a	n/a	n/a	n/a	n/a	n/a
Graduate School of Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory activity against Fe(II) form of Escherichia coli MetAP				Bioorg Med Chem Lett 15: 5386-91 (2005) Article DOI: 10.1016/j.bmcl.2005.09.019 BindingDB Entry DOI: 10.7270/Q2HH6JNV
					More data for this Ligand-Target Pair				3D Structure (crystal)