Compile Data Set for Download or QSAR

Found 127 hits with Last Name = 'luo' and Initial = 'ql'   

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))	BDBM50129663 (3-But-3-enoylamino-pyridine-2-carboxylic acid thia...) Show SMILES C=CCC(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C13H12N4O2S/c1-2-4-10(18)16-9-5-3-6-14-11(9)12(19)17-13-15-7-8-20-13/h2-3,5-8H,1,4H2,(H,16,18)(H,15,17,19)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	130	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)	BDBM50129648 (3-(4-Methyl-pent-3-enoylamino)-pyridine-2-carboxyl...) Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-[#6](=O)-[#7]-c1cccnc1-[#6](=O)-[#7]-c1nccs1 Show InChI InChI=1S/C15H16N4O2S/c1-10(2)5-6-12(20)18-11-4-3-7-16-13(11)14(21)19-15-17-8-9-22-15/h3-5,7-9H,6H2,1-2H3,(H,18,20)(H,17,19,21)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	140	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
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50129660 (3-(3-Methyl-but-3-enoylamino)-pyridine-2-carboxyli...) Show SMILES CC(=C)CC(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C14H14N4O2S/c1-9(2)8-11(19)17-10-4-3-5-15-12(10)13(20)18-14-16-6-7-21-14/h3-7H,1,8H2,2H3,(H,17,19)(H,16,18,20)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	150	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 (Escherichia coli (strain K12))	BDBM17847 (CHEMBL327579 | pyridine-2-carboxylic acid inhibito...) Show SMILES CC(C)(C)OC(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C14H16N4O3S/c1-14(2,3)21-13(20)17-9-5-4-6-15-10(9)11(19)18-12-16-7-8-22-12/h4-8H,1-3H3,(H,17,20)(H,16,18,19)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	180	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)	BDBM50129642 (CHEMBL86427 | Phenyl-acetic acid 2-(thiazol-2-ylca...) Show SMILES O=C(Cc1ccccc1)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C17H13N3O3S/c21-14(11-12-5-2-1-3-6-12)23-13-7-4-8-18-15(13)16(22)20-17-19-9-10-24-17/h1-10H,11H2,(H,19,20,22)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	200	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
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50129640 (3-(3-Methyl-but-2-enoylamino)-pyridine-2-carboxyli...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6](=O)-[#7]-c1cccnc1-[#6](=O)-[#7]-c1nccs1 Show InChI InChI=1S/C14H14N4O2S/c1-9(2)8-11(19)17-10-4-3-5-15-12(10)13(20)18-14-16-6-7-21-14/h3-8H,1-2H3,(H,17,19)(H,16,18,20)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	220	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 (Escherichia coli (strain K12))	BDBM50129648 (3-(4-Methyl-pent-3-enoylamino)-pyridine-2-carboxyl...) Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-[#6](=O)-[#7]-c1cccnc1-[#6](=O)-[#7]-c1nccs1 Show InChI InChI=1S/C15H16N4O2S/c1-10(2)5-6-12(20)18-11-4-3-7-16-13(11)14(21)19-15-17-8-9-22-15/h3-5,7-9H,6H2,1-2H3,(H,18,20)(H,17,19,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	240	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 (Escherichia coli (strain K12))	BDBM50129672 (3-Propionylamino-pyridine-2-carboxylic acid thiazo...) Show SMILES CCC(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C12H12N4O2S/c1-2-9(17)15-8-4-3-5-13-10(8)11(18)16-12-14-6-7-19-12/h3-7H,2H2,1H3,(H,15,17)(H,14,16,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory concentration against Escherichia coli methionine aminopeptidase 1				Bioorg Med Chem Lett 15: 635-8 (2005) Article DOI: 10.1016/j.bmcl.2004.11.034 BindingDB Entry DOI: 10.7270/Q2222T7R
					More data for this Ligand-Target Pair
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50129672 (3-Propionylamino-pyridine-2-carboxylic acid thiazo...) Show SMILES CCC(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C12H12N4O2S/c1-2-9(17)15-8-4-3-5-13-10(8)11(18)16-12-14-6-7-19-12/h3-7H,2H2,1H3,(H,15,17)(H,14,16,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	260	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 (Escherichia coli (strain K12))	BDBM50129674 (3-(2-Methyl-but-2-enoylamino)-pyridine-2-carboxyli...) Show SMILES C\C=C(/C)C(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C14H14N4O2S/c1-3-9(2)12(19)17-10-5-4-6-15-11(10)13(20)18-14-16-7-8-21-14/h3-8H,1-2H3,(H,17,19)(H,16,18,20)/b9-3+	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	280	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 (Escherichia coli (strain K12))	BDBM50129657 (3-(2-Fluoro-benzoylamino)-pyridine-2-carboxylic ac...) Show SMILES Fc1ccccc1C(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C16H11FN4O2S/c17-11-5-2-1-4-10(11)14(22)20-12-6-3-7-18-13(12)15(23)21-16-19-8-9-24-16/h1-9H,(H,20,22)(H,19,21,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	280	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)	BDBM50129669 (3-(5-Methyl-hex-4-enoylamino)-pyridine-2-carboxyli...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#6]-[#6](=O)-[#7]-c1cccnc1-[#6](=O)-[#7]-c1nccs1 Show InChI InChI=1S/C16H18N4O2S/c1-11(2)5-3-7-13(21)19-12-6-4-8-17-14(12)15(22)20-16-18-9-10-23-16/h4-6,8-10H,3,7H2,1-2H3,(H,19,21)(H,18,20,22)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	310	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
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50129649 (CHEMBL315098 | Cyclohexanecarboxylic acid 2-(thiaz...) Show SMILES O=C(Oc1cccnc1C(=O)Nc1nccs1)C1CCCCC1 Show InChI InChI=1S/C16H17N3O3S/c20-14(19-16-18-9-10-23-16)13-12(7-4-8-17-13)22-15(21)11-5-2-1-3-6-11/h4,7-11H,1-3,5-6H2,(H,18,19,20)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	320	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
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50129635 (3-Formylamino-pyridine-2-carboxylic acid thiazol-2...) Show SMILES O=CNc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C10H8N4O2S/c15-6-13-7-2-1-3-11-8(7)9(16)14-10-12-4-5-17-10/h1-6H,(H,13,15)(H,12,14,16)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	320	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
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50129635 (3-Formylamino-pyridine-2-carboxylic acid thiazol-2...) Show SMILES O=CNc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C10H8N4O2S/c15-6-13-7-2-1-3-11-8(7)9(16)14-10-12-4-5-17-10/h1-6H,(H,13,15)(H,12,14,16)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	330	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 (Escherichia coli (strain K12))	BDBM50129670 (3-(2,2,2-Trifluoro-acetylamino)-pyridine-2-carboxy...) Show SMILES FC(F)(F)C(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C11H7F3N4O2S/c12-11(13,14)9(20)17-6-2-1-3-15-7(6)8(19)18-10-16-4-5-21-10/h1-5H,(H,17,20)(H,16,18,19)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	340	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)	BDBM17849 (3-(2,2-dimethylpropanamido)-N-(1,3-thiazol-2-yl)py...) Show SMILES CC(C)(C)C(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C14H16N4O2S/c1-14(2,3)12(20)17-9-5-4-6-15-10(9)11(19)18-13-16-7-8-21-13/h4-8H,1-3H3,(H,17,20)(H,16,18,19)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	340	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
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50129672 (3-Propionylamino-pyridine-2-carboxylic acid thiazo...) Show SMILES CCC(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C12H12N4O2S/c1-2-9(17)15-8-4-3-5-13-10(8)11(18)16-12-14-6-7-19-12/h3-7H,2H2,1H3,(H,15,17)(H,14,16,18)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	350	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
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50129672 (3-Propionylamino-pyridine-2-carboxylic acid thiazo...) Show SMILES CCC(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C12H12N4O2S/c1-2-9(17)15-8-4-3-5-13-10(8)11(18)16-12-14-6-7-19-12/h3-7H,2H2,1H3,(H,15,17)(H,14,16,18)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	350	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory concentration against Saccharomyces cerevisiae methionine aminopeptidase 1				Bioorg Med Chem Lett 15: 635-8 (2005) Article DOI: 10.1016/j.bmcl.2004.11.034 BindingDB Entry DOI: 10.7270/Q2222T7R
					More data for this Ligand-Target Pair
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50129656 (3-Hexanoylamino-pyridine-2-carboxylic acid thiazol...) Show SMILES CCCCCC(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C15H18N4O2S/c1-2-3-4-7-12(20)18-11-6-5-8-16-13(11)14(21)19-15-17-9-10-22-15/h5-6,8-10H,2-4,7H2,1H3,(H,18,20)(H,17,19,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	380	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 (Escherichia coli (strain K12))	BDBM50129656 (3-Hexanoylamino-pyridine-2-carboxylic acid thiazol...) Show SMILES CCCCCC(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C15H18N4O2S/c1-2-3-4-7-12(20)18-11-6-5-8-16-13(11)14(21)19-15-17-9-10-22-15/h5-6,8-10H,2-4,7H2,1H3,(H,18,20)(H,17,19,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	380	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory concentration against Escherichia coli methionine aminopeptidase 1				Bioorg Med Chem Lett 15: 635-8 (2005) Article DOI: 10.1016/j.bmcl.2004.11.034 BindingDB Entry DOI: 10.7270/Q2222T7R
					More data for this Ligand-Target Pair
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50129663 (3-But-3-enoylamino-pyridine-2-carboxylic acid thia...) Show SMILES C=CCC(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C13H12N4O2S/c1-2-4-10(18)16-9-5-3-6-14-11(9)12(19)17-13-15-7-8-20-13/h2-3,5-8H,1,4H2,(H,16,18)(H,15,17,19)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	380	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
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50129650 (CHEMBL314448 | Propionic acid 2-(thiazol-2-ylcarba...) Show SMILES CCC(=O)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C12H11N3O3S/c1-2-9(16)18-8-4-3-5-13-10(8)11(17)15-12-14-6-7-19-12/h3-7H,2H2,1H3,(H,14,15,17)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	380	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
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50129641 (2-Methyl-but-2-enoic acid 2-(thiazol-2-ylcarbamoyl...) Show SMILES C\C=C(/C)C(=O)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C14H13N3O3S/c1-3-9(2)13(19)20-10-5-4-6-15-11(10)12(18)17-14-16-7-8-21-14/h3-8H,1-2H3,(H,16,17,18)/b9-3+	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	390	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
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50129666 (3-Phenylacetylamino-pyridine-2-carboxylic acid thi...) Show SMILES O=C(Cc1ccccc1)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C17H14N4O2S/c22-14(11-12-5-2-1-3-6-12)20-13-7-4-8-18-15(13)16(23)21-17-19-9-10-24-17/h1-10H,11H2,(H,20,22)(H,19,21,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	400	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
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM17849 (3-(2,2-dimethylpropanamido)-N-(1,3-thiazol-2-yl)py...) Show SMILES CC(C)(C)C(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C14H16N4O2S/c1-14(2,3)12(20)17-9-5-4-6-15-10(9)11(19)18-13-16-7-8-21-13/h4-8H,1-3H3,(H,17,20)(H,16,18,19)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	540	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 (Escherichia coli (strain K12))	BDBM50129642 (CHEMBL86427 | Phenyl-acetic acid 2-(thiazol-2-ylca...) Show SMILES O=C(Cc1ccccc1)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C17H13N3O3S/c21-14(11-12-5-2-1-3-6-12)23-13-7-4-8-18-15(13)16(22)20-17-19-9-10-24-17/h1-10H,11H2,(H,19,20,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	540	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)	BDBM50129675 (2-Methoxy-benzoic acid 2-(thiazol-2-ylcarbamoyl)-p...) Show SMILES COc1ccccc1C(=O)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C17H13N3O4S/c1-23-12-6-3-2-5-11(12)16(22)24-13-7-4-8-18-14(13)15(21)20-17-19-9-10-25-17/h2-10H,1H3,(H,19,20,21)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	550	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
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50129638 (3-Nitro-benzoic acid 2-(thiazol-2-ylcarbamoyl)-pyr...) Show SMILES [O-][N+](=O)c1cccc(c1)C(=O)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C16H10N4O5S/c21-14(19-16-18-7-8-26-16)13-12(5-2-6-17-13)25-15(22)10-3-1-4-11(9-10)20(23)24/h1-9H,(H,18,19,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	600	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 (Escherichia coli (strain K12))	BDBM50129669 (3-(5-Methyl-hex-4-enoylamino)-pyridine-2-carboxyli...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#6]-[#6](=O)-[#7]-c1cccnc1-[#6](=O)-[#7]-c1nccs1 Show InChI InChI=1S/C16H18N4O2S/c1-11(2)5-3-7-13(21)19-12-6-4-8-17-14(12)15(22)20-16-18-9-10-23-16/h4-6,8-10H,3,7H2,1-2H3,(H,19,21)(H,18,20,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	610	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)	BDBM50129656 (3-Hexanoylamino-pyridine-2-carboxylic acid thiazol...) Show SMILES CCCCCC(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C15H18N4O2S/c1-2-3-4-7-12(20)18-11-6-5-8-16-13(11)14(21)19-15-17-9-10-22-15/h5-6,8-10H,2-4,7H2,1H3,(H,18,20)(H,17,19,21)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	620	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory concentration against Saccharomyces cerevisiae methionine aminopeptidase 1				Bioorg Med Chem Lett 15: 635-8 (2005) Article DOI: 10.1016/j.bmcl.2004.11.034 BindingDB Entry DOI: 10.7270/Q2222T7R
					More data for this Ligand-Target Pair
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50129656 (3-Hexanoylamino-pyridine-2-carboxylic acid thiazol...) Show SMILES CCCCCC(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C15H18N4O2S/c1-2-3-4-7-12(20)18-11-6-5-8-16-13(11)14(21)19-15-17-9-10-22-15/h5-6,8-10H,2-4,7H2,1H3,(H,18,20)(H,17,19,21)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	620	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
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50129636 (2,2-Dimethyl-propionic acid 2-(thiazol-2-ylcarbamo...) Show SMILES CC(C)(C)C(=O)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C14H15N3O3S/c1-14(2,3)12(19)20-9-5-4-6-15-10(9)11(18)17-13-16-7-8-21-13/h4-8H,1-3H3,(H,16,17,18)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	680	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 (Escherichia coli (strain K12))	BDBM50129664 (3-(3-Fluoro-benzoylamino)-pyridine-2-carboxylic ac...) Show SMILES Fc1cccc(c1)C(=O)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C16H11FN4O2S/c17-11-4-1-3-10(9-11)14(22)20-12-5-2-6-18-13(12)15(23)21-16-19-7-8-24-16/h1-9H,(H,20,22)(H,19,21,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	710	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)	BDBM50129640 (3-(3-Methyl-but-2-enoylamino)-pyridine-2-carboxyli...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6](=O)-[#7]-c1cccnc1-[#6](=O)-[#7]-c1nccs1 Show InChI InChI=1S/C14H14N4O2S/c1-9(2)8-11(19)17-10-4-3-5-15-12(10)13(20)18-14-16-6-7-21-14/h3-8H,1-2H3,(H,17,19)(H,16,18,20)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	770	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
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50160043 (3-Benzyloxy-pyridine-2-carboxylic acid thiazol-2-y...) Show SMILES O=C(Nc1nccs1)c1ncccc1OCc1ccccc1 Show InChI InChI=1S/C16H13N3O2S/c20-15(19-16-18-9-10-22-16)14-13(7-4-8-17-14)21-11-12-5-2-1-3-6-12/h1-10H,11H2,(H,18,19,20)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	770	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory concentration against Saccharomyces cerevisiae methionine aminopeptidase 1				Bioorg Med Chem Lett 15: 635-8 (2005) Article DOI: 10.1016/j.bmcl.2004.11.034 BindingDB Entry DOI: 10.7270/Q2222T7R
					More data for this Ligand-Target Pair
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50129636 (2,2-Dimethyl-propionic acid 2-(thiazol-2-ylcarbamo...) Show SMILES CC(C)(C)C(=O)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C14H15N3O3S/c1-14(2,3)12(19)20-9-5-4-6-15-10(9)11(18)17-13-16-7-8-21-13/h4-8H,1-3H3,(H,16,17,18)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	780	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
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50129666 (3-Phenylacetylamino-pyridine-2-carboxylic acid thi...) Show SMILES O=C(Cc1ccccc1)Nc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C17H14N4O2S/c22-14(11-12-5-2-1-3-6-12)20-13-7-4-8-18-15(13)16(23)21-17-19-9-10-24-17/h1-10H,11H2,(H,20,22)(H,19,21,23)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	820	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
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50129655 (2-Fluoro-benzoic acid 2-(thiazol-2-ylcarbamoyl)-py...) Show SMILES Fc1ccccc1C(=O)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C16H10FN3O3S/c17-11-5-2-1-4-10(11)15(22)23-12-6-3-7-18-13(12)14(21)20-16-19-8-9-24-16/h1-9H,(H,19,20,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	830	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 (Escherichia coli (strain K12))	BDBM50129659 (3-(Cyclohexanecarbonyl-amino)-pyridine-2-carboxyli...) Show SMILES O=C(Nc1cccnc1C(=O)Nc1nccs1)C1CCCCC1 Show InChI InChI=1S/C16H18N4O2S/c21-14(11-5-2-1-3-6-11)19-12-7-4-8-17-13(12)15(22)20-16-18-9-10-23-16/h4,7-11H,1-3,5-6H2,(H,19,21)(H,18,20,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	870	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)	BDBM50129658 (2-Iodo-benzoic acid 2-(thiazol-2-ylcarbamoyl)-pyri...) Show SMILES Ic1ccccc1C(=O)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C16H10IN3O3S/c17-11-5-2-1-4-10(11)15(22)23-12-6-3-7-18-13(12)14(21)20-16-19-8-9-24-16/h1-9H,(H,19,20,21)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	890	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
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50129652 (3-Benzoylamino-pyridine-2-carboxylic acid thiazol-...) Show SMILES O=C(Nc1cccnc1C(=O)Nc1nccs1)c1ccccc1 Show InChI InChI=1S/C16H12N4O2S/c21-14(11-5-2-1-3-6-11)19-12-7-4-8-17-13(12)15(22)20-16-18-9-10-23-16/h1-10H,(H,19,21)(H,18,20,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	890	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 (Escherichia coli (strain K12))	BDBM50129639 (3-Fluoro-benzoic acid 2-(thiazol-2-ylcarbamoyl)-py...) Show SMILES Fc1cccc(c1)C(=O)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C16H10FN3O3S/c17-11-4-1-3-10(9-11)15(22)23-12-5-2-6-18-13(12)14(21)20-16-19-7-8-24-16/h1-9H,(H,19,20,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	950	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 (Escherichia coli (strain K12))	BDBM50160054 (5-But-3-enoylamino-pyridine-2-carboxylic acid thia...) Show SMILES C=CCC(=O)Nc1ccc(nc1)C(=O)Nc1nccs1 Show InChI InChI=1S/C13H12N4O2S/c1-2-3-11(18)16-9-4-5-10(15-8-9)12(19)17-13-14-6-7-20-13/h2,4-8H,1,3H2,(H,16,18)(H,14,17,19)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.01E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory concentration against Escherichia coli methionine aminopeptidase 1				Bioorg Med Chem Lett 15: 635-8 (2005) Article DOI: 10.1016/j.bmcl.2004.11.034 BindingDB Entry DOI: 10.7270/Q2222T7R
					More data for this Ligand-Target Pair
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50129637 (CHEMBL315903 | Hexanoic acid 2-(thiazol-2-ylcarbam...) Show SMILES CCCCCC(=O)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C15H17N3O3S/c1-2-3-4-7-12(19)21-11-6-5-8-16-13(11)14(20)18-15-17-9-10-22-15/h5-6,8-10H,2-4,7H2,1H3,(H,17,18,20)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.02E+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)	BDBM50129671 (Benzoic acid 2-(thiazol-2-ylcarbamoyl)-pyridin-3-y...) Show SMILES O=C(Nc1nccs1)c1ncccc1OC(=O)c1ccccc1 Show InChI InChI=1S/C16H11N3O3S/c20-14(19-16-18-9-10-23-16)13-12(7-4-8-17-13)22-15(21)11-5-2-1-3-6-11/h1-10H,(H,18,19,20)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.03E+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 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
Methionine aminopeptidase 1 (Saccharomyces cerevisiae)	BDBM50129671 (Benzoic acid 2-(thiazol-2-ylcarbamoyl)-pyridin-3-y...) Show SMILES O=C(Nc1nccs1)c1ncccc1OC(=O)c1ccccc1 Show InChI InChI=1S/C16H11N3O3S/c20-14(19-16-18-9-10-23-16)13-12(7-4-8-17-13)22-15(21)11-5-2-1-3-6-11/h1-10H,(H,18,19,20)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.03E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibitory concentration against Saccharomyces cerevisiae methionine aminopeptidase 1				Bioorg Med Chem Lett 15: 635-8 (2005) Article DOI: 10.1016/j.bmcl.2004.11.034 BindingDB Entry DOI: 10.7270/Q2222T7R
					More data for this Ligand-Target Pair
Methionine aminopeptidase (Escherichia coli (strain K12))	BDBM50129644 (4-Fluoro-benzoic acid 2-(thiazol-2-ylcarbamoyl)-py...) Show SMILES Fc1ccc(cc1)C(=O)Oc1cccnc1C(=O)Nc1nccs1 Show InChI InChI=1S/C16H10FN3O3S/c17-11-5-3-10(4-6-11)15(22)23-12-2-1-7-18-13(12)14(21)20-16-19-8-9-24-16/h1-9H,(H,19,20,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.10E+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 (Escherichia coli (strain K12))	BDBM50129671 (Benzoic acid 2-(thiazol-2-ylcarbamoyl)-pyridin-3-y...) Show SMILES O=C(Nc1nccs1)c1ncccc1OC(=O)c1ccccc1 Show InChI InChI=1S/C16H11N3O3S/c20-14(19-16-18-9-10-23-16)13-12(7-4-8-17-13)22-15(21)11-5-2-1-3-6-11/h1-10H,(H,18,19,20)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.22E+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

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