Compile Data Set for Download or QSAR

Found 8 hits Enz. Inhib. hit(s) with all data for entry = 50014030   

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 1 (Homo sapiens (Human))	BDBM50137352 ((S)-2-Amino-hexanoic acid hydroxy-[(2-pyridin-2-yl...) Show SMILES CCCC[C@H](N)C(=O)N(O)CC(=O)NCCc1ccccn1 Show InChI InChI=1S/C15H24N4O3/c1-2-3-7-13(16)15(21)19(22)11-14(20)18-10-8-12-6-4-5-9-17-12/h4-6,9,13,22H,2-3,7-8,10-11,16H2,1H3,(H,18,20)/t13-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	3.30E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Ohio State University Curated by ChEMBL					Assay Description Inhibitory activity of the compound against Methionine aminopeptidase 1				Bioorg Med Chem Lett 14: 77-9 (2003) BindingDB Entry DOI: 10.7270/Q2DV1J90
					More data for this Ligand-Target Pair
Methionine aminopeptidase 1 (Homo sapiens (Human))	BDBM50137355 ((S)-2-Amino-N-hydroxy-4-methylsulfanyl-N-[(2-pyrid...) Show SMILES CSCC[C@H](N)C(=O)N(O)CC(=O)NCCc1ccccn1 Show InChI InChI=1S/C14H22N4O3S/c1-22-9-6-12(15)14(20)18(21)10-13(19)17-8-5-11-4-2-3-7-16-11/h2-4,7,12,21H,5-6,8-10,15H2,1H3,(H,17,19)/t12-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	4.80E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Ohio State University Curated by ChEMBL					Assay Description Inhibitory activity of the compound against Methionine aminopeptidase 1				Bioorg Med Chem Lett 14: 77-9 (2003) BindingDB Entry DOI: 10.7270/Q2DV1J90
					More data for this Ligand-Target Pair
Methionine aminopeptidase 2 (Homo sapiens (Human))	BDBM50137355 ((S)-2-Amino-N-hydroxy-4-methylsulfanyl-N-[(2-pyrid...) Show SMILES CSCC[C@H](N)C(=O)N(O)CC(=O)NCCc1ccccn1 Show InChI InChI=1S/C14H22N4O3S/c1-22-9-6-12(15)14(20)18(21)10-13(19)17-8-5-11-4-2-3-7-16-11/h2-4,7,12,21H,5-6,8-10,15H2,1H3,(H,17,19)/t12-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	9.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Ohio State University Curated by ChEMBL					Assay Description Inhibitory activity of the compound against Methionine aminopeptidase 2				Bioorg Med Chem Lett 14: 77-9 (2003) BindingDB Entry DOI: 10.7270/Q2DV1J90
					More data for this Ligand-Target Pair
Methionine aminopeptidase 2 (Homo sapiens (Human))	BDBM50137352 ((S)-2-Amino-hexanoic acid hydroxy-[(2-pyridin-2-yl...) Show SMILES CCCC[C@H](N)C(=O)N(O)CC(=O)NCCc1ccccn1 Show InChI InChI=1S/C15H24N4O3/c1-2-3-7-13(16)15(21)19(22)11-14(20)18-10-8-12-6-4-5-9-17-12/h4-6,9,13,22H,2-3,7-8,10-11,16H2,1H3,(H,18,20)/t13-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	1.64E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Ohio State University Curated by ChEMBL					Assay Description Inhibitory activity of the compound against Methionine aminopeptidase 2				Bioorg Med Chem Lett 14: 77-9 (2003) BindingDB Entry DOI: 10.7270/Q2DV1J90
					More data for this Ligand-Target Pair
Methionine aminopeptidase 1 (Homo sapiens (Human))	BDBM50137354 (CHEMBL164406 | [((R)-2-Amino-propionyl)-hydroxy-am...) Show SMILES C[C@@H](N)C(=O)N(O)CC(O)=O Show InChI InChI=1S/C5H10N2O4/c1-3(6)5(10)7(11)2-4(8)9/h3,11H,2,6H2,1H3,(H,8,9)/t3-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	1.80E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Ohio State University Curated by ChEMBL					Assay Description Inhibitory activity of the compound against Methionine aminopeptidase 1				Bioorg Med Chem Lett 14: 77-9 (2003) BindingDB Entry DOI: 10.7270/Q2DV1J90
					More data for this Ligand-Target Pair
Methionine aminopeptidase 1 (Homo sapiens (Human))	BDBM50137353 (CHEMBL349154 | [((S)-2-Amino-4-methylsulfanyl-buty...) Show SMILES CSCC[C@H](N)C(=O)N(O)CC(O)=O Show InChI InChI=1S/C7H14N2O4S/c1-14-3-2-5(8)7(12)9(13)4-6(10)11/h5,13H,2-4,8H2,1H3,(H,10,11)/t5-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	3.90E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Ohio State University Curated by ChEMBL					Assay Description Inhibitory activity of the compound against Methionine aminopeptidase 1				Bioorg Med Chem Lett 14: 77-9 (2003) BindingDB Entry DOI: 10.7270/Q2DV1J90
					More data for this Ligand-Target Pair
Methionine aminopeptidase 2 (Homo sapiens (Human))	BDBM50137354 (CHEMBL164406 | [((R)-2-Amino-propionyl)-hydroxy-am...) Show SMILES C[C@@H](N)C(=O)N(O)CC(O)=O Show InChI InChI=1S/C5H10N2O4/c1-3(6)5(10)7(11)2-4(8)9/h3,11H,2,6H2,1H3,(H,8,9)/t3-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	6.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Ohio State University Curated by ChEMBL					Assay Description Inhibitory activity of the compound against Methionine aminopeptidase 2				Bioorg Med Chem Lett 14: 77-9 (2003) BindingDB Entry DOI: 10.7270/Q2DV1J90
					More data for this Ligand-Target Pair
Methionine aminopeptidase 2 (Homo sapiens (Human))	BDBM50137353 (CHEMBL349154 | [((S)-2-Amino-4-methylsulfanyl-buty...) Show SMILES CSCC[C@H](N)C(=O)N(O)CC(O)=O Show InChI InChI=1S/C7H14N2O4S/c1-14-3-2-5(8)7(12)9(13)4-6(10)11/h5,13H,2-4,8H2,1H3,(H,10,11)/t5-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	1.30E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Ohio State University Curated by ChEMBL					Assay Description Inhibitory activity of the compound against Methionine aminopeptidase 2				Bioorg Med Chem Lett 14: 77-9 (2003) BindingDB Entry DOI: 10.7270/Q2DV1J90
					More data for this Ligand-Target Pair