Compile Data Set for Download or QSAR

Found 121 hits with Last Name = 'oleksyszyn' and Initial = 'j'   

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
Aminopeptidase N (Sus scrofa (Pig))	BDBM50244147 ((4-methoxybenzyl)carbamothioyl(1-aminopentyl)phosp...) Show SMILES CCCCC(N)=P(O)(O)C(=S)NCc1ccc(OC)cc1 Show InChI InChI=1S/C14H23N2O3PS/c1-3-4-5-13(15)20(17,18)14(21)16-10-11-6-8-12(19-2)9-7-11/h6-9,17-18H,3-5,10,15H2,1-2H3,(H,16,21)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	143	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N				Bioorg Med Chem Lett 18: 3734-6 (2008) Article DOI: 10.1016/j.bmcl.2008.05.050 BindingDB Entry DOI: 10.7270/Q2H41R6T
					More data for this Ligand-Target Pair
Cytosol aminopeptidase (Homo sapiens (Human))	BDBM50316047 (1-amino-2-methylbutylphosphonic acid monophenylest...) Show SMILES CC(C)CC(N)P(O)(=O)Oc1ccccc1 Show InChI InChI=1S/C11H18NO3P/c1-9(2)8-11(12)16(13,14)15-10-6-4-3-5-7-10/h3-7,9,11H,8,12H2,1-2H3,(H,13,14)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	230	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of leucine aminopeptidase				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Cytosol aminopeptidase (Homo sapiens (Human))	BDBM50129679 ((1-Amino-3-methyl-butyl)-phosphonic acid | 1-amino...) Show SMILES CC(C)CC(N)P(O)(O)=O Show InChI InChI=1S/C5H14NO3P/c1-4(2)3-5(6)10(7,8)9/h4-5H,3,6H2,1-2H3,(H2,7,8,9)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid PDB UniChem Patents Similars	Article PubMed	230	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of leucine aminopeptidase				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Cytosol aminopeptidase (Homo sapiens (Human))	BDBM50316048 (1-amino-2-phenylethylphosphonic acid monophenyl es...) Show SMILES NC(Cc1ccccc1)P(O)(=O)Oc1ccccc1 Show InChI InChI=1S/C14H16NO3P/c15-14(11-12-7-3-1-4-8-12)19(16,17)18-13-9-5-2-6-10-13/h1-10,14H,11,15H2,(H,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	420	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of leucine aminopeptidase				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Cytosol aminopeptidase (Homo sapiens (Human))	BDBM50024592 ((S)-1-Ammonium-2-phenyl-ethanephosphonic acid anio...) Show SMILES [NH3+][C@H](Cc1ccccc1)P(O)([O-])=O Show InChI InChI=1S/C8H12NO3P/c9-8(13(10,11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,9H2,(H2,10,11,12)/t8-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	420	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of leucine aminopeptidase				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Glutamyl endopeptidase (Staphylococcus aureus)	BDBM50435121 (CHEMBL2391716) Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)NC(CCC(O)=O)P(=O)(Oc1ccccc1)Oc1ccccc1 |r| Show InChI InChI=1S/C36H46N3O9P/c1-25(2)23-29(37-33(42)30(24-26-15-9-6-10-16-26)38-35(44)46-36(3,4)5)34(43)39-31(21-22-32(40)41)49(45,47-27-17-11-7-12-18-27)48-28-19-13-8-14-20-28/h6-20,25,29-31H,21-24H2,1-5H3,(H,37,42)(H,38,44)(H,39,43)(H,40,41)/t29-,30-,31?/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of Staphylococcus aureus endoproteinase GluC using Ac-Phe-Leu-Glu-ACC as substrate after 30 mins				Bioorg Med Chem Lett 23: 1412-5 (2013) Article DOI: 10.1016/j.bmcl.2012.12.074 BindingDB Entry DOI: 10.7270/Q2SX6FKB
					More data for this Ligand-Target Pair
Glutamyl endopeptidase (Staphylococcus aureus)	BDBM50435123 (CHEMBL2391713) Show SMILES CC(C)C[C@H](NC(=O)OC(C)(C)C)C(=O)NC(CCC(O)=O)P(=O)(Oc1ccccc1)Oc1ccccc1 |r| Show InChI InChI=1S/C27H37N2O8P/c1-19(2)18-22(28-26(33)35-27(3,4)5)25(32)29-23(16-17-24(30)31)38(34,36-20-12-8-6-9-13-20)37-21-14-10-7-11-15-21/h6-15,19,22-23H,16-18H2,1-5H3,(H,28,33)(H,29,32)(H,30,31)/t22-,23?/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of Staphylococcus aureus endoproteinase GluC using Ac-Phe-Leu-Glu-ACC as substrate after 30 mins				Bioorg Med Chem Lett 23: 1412-5 (2013) Article DOI: 10.1016/j.bmcl.2012.12.074 BindingDB Entry DOI: 10.7270/Q2SX6FKB
					More data for this Ligand-Target Pair
Glutamyl endopeptidase (Staphylococcus aureus)	BDBM50435124 (CHEMBL2390964) Show SMILES OC(=O)CCC(NC(=O)OCc1ccccc1)P(=O)(Oc1ccccc1)Oc1ccccc1 Show InChI InChI=1S/C24H24NO7P/c26-23(27)17-16-22(25-24(28)30-18-19-10-4-1-5-11-19)33(29,31-20-12-6-2-7-13-20)32-21-14-8-3-9-15-21/h1-15,22H,16-18H2,(H,25,28)(H,26,27)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of Staphylococcus aureus endoproteinase GluC using Ac-Phe-Leu-Glu-ACC as substrate after 30 mins				Bioorg Med Chem Lett 23: 1412-5 (2013) Article DOI: 10.1016/j.bmcl.2012.12.074 BindingDB Entry DOI: 10.7270/Q2SX6FKB
					More data for this Ligand-Target Pair
Glutamyl endopeptidase (Staphylococcus aureus)	BDBM50435117 (CHEMBL2391722) Show SMILES CC(C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)NC(CCC(O)=O)P(=O)(Oc1ccccc1)Oc1ccccc1 |r| Show InChI InChI=1S/C35H44N3O9P/c1-24(2)31(38-32(41)28(23-25-15-9-6-10-16-25)36-34(43)45-35(3,4)5)33(42)37-29(21-22-30(39)40)48(44,46-26-17-11-7-12-18-26)47-27-19-13-8-14-20-27/h6-20,24,28-29,31H,21-23H2,1-5H3,(H,36,43)(H,37,42)(H,38,41)(H,39,40)/t28-,29?,31-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.15E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of Staphylococcus aureus endoproteinase GluC using Ac-Phe-Leu-Glu-ACC as substrate after 30 mins				Bioorg Med Chem Lett 23: 1412-5 (2013) Article DOI: 10.1016/j.bmcl.2012.12.074 BindingDB Entry DOI: 10.7270/Q2SX6FKB
					More data for this Ligand-Target Pair
Glutamyl endopeptidase (Staphylococcus aureus)	BDBM50435119 (CHEMBL2391719) Show SMILES C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)NC(CCC(O)=O)P(=O)(Oc1ccccc1)Oc1ccccc1 |r| Show InChI InChI=1S/C33H40N3O9P/c1-23(34-31(40)27(22-24-14-8-5-9-15-24)35-32(41)43-33(2,3)4)30(39)36-28(20-21-29(37)38)46(42,44-25-16-10-6-11-17-25)45-26-18-12-7-13-19-26/h5-19,23,27-28H,20-22H2,1-4H3,(H,34,40)(H,35,41)(H,36,39)(H,37,38)/t23-,27-,28?/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of Staphylococcus aureus endoproteinase GluC using Ac-Phe-Leu-Glu-ACC as substrate after 30 mins				Bioorg Med Chem Lett 23: 1412-5 (2013) Article DOI: 10.1016/j.bmcl.2012.12.074 BindingDB Entry DOI: 10.7270/Q2SX6FKB
					More data for this Ligand-Target Pair
Glutamyl endopeptidase (Staphylococcus aureus)	BDBM50435120 (CHEMBL2391718) Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)OC(C)(C)C)C(=O)NC(CCC(O)=O)P(=O)(Oc1ccccc1)Oc1ccccc1 |r| Show InChI InChI=1S/C32H44N3O11P/c1-21(2)20-25(33-29(40)24(16-18-27(36)37)34-31(42)44-32(3,4)5)30(41)35-26(17-19-28(38)39)47(43,45-22-12-8-6-9-13-22)46-23-14-10-7-11-15-23/h6-15,21,24-26H,16-20H2,1-5H3,(H,33,40)(H,34,42)(H,35,41)(H,36,37)(H,38,39)/t24-,25-,26?/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.50E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of Staphylococcus aureus endoproteinase GluC using Ac-Phe-Leu-Glu-ACC as substrate after 30 mins				Bioorg Med Chem Lett 23: 1412-5 (2013) Article DOI: 10.1016/j.bmcl.2012.12.074 BindingDB Entry DOI: 10.7270/Q2SX6FKB
					More data for this Ligand-Target Pair
Glutamyl endopeptidase (Staphylococcus aureus)	BDBM50435116 (CHEMBL2391724) Show SMILES CC(C)[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)OC(C)(C)C)C(=O)NC(CCC(O)=O)P(=O)(Oc1ccccc1)Oc1ccccc1 |r| Show InChI InChI=1S/C31H42N3O11P/c1-20(2)27(34-28(39)23(16-18-25(35)36)32-30(41)43-31(3,4)5)29(40)33-24(17-19-26(37)38)46(42,44-21-12-8-6-9-13-21)45-22-14-10-7-11-15-22/h6-15,20,23-24,27H,16-19H2,1-5H3,(H,32,41)(H,33,40)(H,34,39)(H,35,36)(H,37,38)/t23-,24?,27-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.95E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of Staphylococcus aureus endoproteinase GluC using Ac-Phe-Leu-Glu-ACC as substrate after 30 mins				Bioorg Med Chem Lett 23: 1412-5 (2013) Article DOI: 10.1016/j.bmcl.2012.12.074 BindingDB Entry DOI: 10.7270/Q2SX6FKB
					More data for this Ligand-Target Pair
Glutamyl endopeptidase (Staphylococcus aureus)	BDBM50435125 (CHEMBL2391726) Show SMILES CC(=O)NC(CCC(O)=O)P(=O)(Oc1ccccc1)Oc1ccccc1 Show InChI InChI=1S/C18H20NO6P/c1-14(20)19-17(12-13-18(21)22)26(23,24-15-8-4-2-5-9-15)25-16-10-6-3-7-11-16/h2-11,17H,12-13H2,1H3,(H,19,20)(H,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	1.11E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of Staphylococcus aureus endoproteinase GluC using Ac-Phe-Leu-Glu-ACC as substrate after 30 mins				Bioorg Med Chem Lett 23: 1412-5 (2013) Article DOI: 10.1016/j.bmcl.2012.12.074 BindingDB Entry DOI: 10.7270/Q2SX6FKB
					More data for this Ligand-Target Pair
Glutamyl endopeptidase (Staphylococcus aureus)	BDBM50435118 (CHEMBL2391721) Show SMILES C[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)OC(C)(C)C)C(=O)NC(CCC(O)=O)P(=O)(Oc1ccccc1)Oc1ccccc1 |r| Show InChI InChI=1S/C29H38N3O11P/c1-19(30-27(38)22(15-17-24(33)34)31-28(39)41-29(2,3)4)26(37)32-23(16-18-25(35)36)44(40,42-20-11-7-5-8-12-20)43-21-13-9-6-10-14-21/h5-14,19,22-23H,15-18H2,1-4H3,(H,30,38)(H,31,39)(H,32,37)(H,33,34)(H,35,36)/t19-,22-,23?/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.29E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of Staphylococcus aureus endoproteinase GluC using Ac-Phe-Leu-Glu-ACC as substrate after 30 mins				Bioorg Med Chem Lett 23: 1412-5 (2013) Article DOI: 10.1016/j.bmcl.2012.12.074 BindingDB Entry DOI: 10.7270/Q2SX6FKB
					More data for this Ligand-Target Pair
Glutamyl endopeptidase (Staphylococcus aureus)	BDBM50435122 (CHEMBL2391714) Show SMILES CC(C)[C@H](NC(=O)OC(C)(C)C)C(=O)NC(CCC(O)=O)P(=O)(Oc1ccccc1)Oc1ccccc1 |r| Show InChI InChI=1S/C26H35N2O8P/c1-18(2)23(28-25(32)34-26(3,4)5)24(31)27-21(16-17-22(29)30)37(33,35-19-12-8-6-9-13-19)36-20-14-10-7-11-15-20/h6-15,18,21,23H,16-17H2,1-5H3,(H,27,31)(H,28,32)(H,29,30)/t21?,23-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.33E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of Staphylococcus aureus endoproteinase GluC using Ac-Phe-Leu-Glu-ACC as substrate after 30 mins				Bioorg Med Chem Lett 23: 1412-5 (2013) Article DOI: 10.1016/j.bmcl.2012.12.074 BindingDB Entry DOI: 10.7270/Q2SX6FKB
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50024592 ((S)-1-Ammonium-2-phenyl-ethanephosphonic acid anio...) Show SMILES [NH3+][C@H](Cc1ccccc1)P(O)([O-])=O Show InChI InChI=1S/C8H12NO3P/c9-8(13(10,11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,9H2,(H2,10,11,12)/t8-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.75E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of aminopeptidase N				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50316048 (1-amino-2-phenylethylphosphonic acid monophenyl es...) Show SMILES NC(Cc1ccccc1)P(O)(=O)Oc1ccccc1 Show InChI InChI=1S/C14H16NO3P/c15-14(11-12-7-3-1-4-8-12)19(16,17)18-13-9-5-2-6-10-13/h1-10,14H,11,15H2,(H,16,17)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	2.75E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of aminopeptidase N				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50316047 (1-amino-2-methylbutylphosphonic acid monophenylest...) Show SMILES CC(C)CC(N)P(O)(=O)Oc1ccccc1 Show InChI InChI=1S/C11H18NO3P/c1-9(2)8-11(12)16(13,14)15-10-6-4-3-5-7-10/h3-7,9,11H,8,12H2,1-2H3,(H,13,14)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.30E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of aminopeptidase N				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50129679 ((1-Amino-3-methyl-butyl)-phosphonic acid | 1-amino...) Show SMILES CC(C)CC(N)P(O)(O)=O Show InChI InChI=1S/C5H14NO3P/c1-4(2)3-5(6)10(7,8)9/h4-5H,3,6H2,1-2H3,(H2,7,8,9)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid PDB UniChem Patents Similars	Article PubMed	5.30E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of aminopeptidase N				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50184648 (CHEMBL378976 | [benzyloxycarbonylamino-(4-guanidin...) Show SMILES [#6]-[#16]-c1ccc(-[#8]P(=O)([#8]-c2ccc(-[#16]-[#6])cc2)[#6](-[#7]-[#6](=O)-[#8]-[#6]-c2ccccc2)-c2ccc(cc2)\[#7]=[#6](\[#7])-[#7])cc1 Show InChI InChI=1S/C30H31N4O5PS2/c1-41-26-16-12-24(13-17-26)38-40(36,39-25-14-18-27(42-2)19-15-25)28(22-8-10-23(11-9-22)33-29(31)32)34-30(35)37-20-21-6-4-3-5-7-21/h3-19,28H,20H2,1-2H3,(H,34,35)(H4,31,32,33)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	26	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of human uPA by chromogenic assay using Cbz-Val-Gly-Arg-pNA as chromogenic substrate				Bioorg Med Chem Lett 16: 2886-90 (2006) Article DOI: 10.1016/j.bmcl.2006.03.002 BindingDB Entry DOI: 10.7270/Q22N51WR
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50184646 (CHEMBL379814 | [benzyloxycarbonylamino-(4-guanidin...) Show SMILES [#6]S(=O)(=O)c1ccc(-[#8]P(=O)([#8]-c2ccc(cc2)S([#6])(=O)=O)[#6](-[#7]-[#6](=O)-[#8]-[#6]-c2ccccc2)-c2ccc(cc2)\[#7]=[#6](\[#7])-[#7])cc1 Show InChI InChI=1S/C30H31N4O9PS2/c1-45(37,38)26-16-12-24(13-17-26)42-44(36,43-25-14-18-27(19-15-25)46(2,39)40)28(22-8-10-23(11-9-22)33-29(31)32)34-30(35)41-20-21-6-4-3-5-7-21/h3-19,28H,20H2,1-2H3,(H,34,35)(H4,31,32,33)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	53	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of human uPA by chromogenic assay using Cbz-Val-Gly-Arg-pNA as chromogenic substrate				Bioorg Med Chem Lett 16: 2886-90 (2006) Article DOI: 10.1016/j.bmcl.2006.03.002 BindingDB Entry DOI: 10.7270/Q22N51WR
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50184644 (CHEMBL377857 | [benzyloxycarbonylamino-(4-guanidin...) Show SMILES [#6]C([#6])([#6])c1ccc(-[#8]P(=O)([#8]-c2ccc(cc2)C([#6])([#6])[#6])[#6](-[#7]-[#6](=O)-[#8]-[#6]-c2ccccc2)-c2ccc(cc2)\[#7]=[#6](\[#7])-[#7])cc1 Show InChI InChI=1S/C36H43N4O5P/c1-35(2,3)27-14-20-30(21-15-27)44-46(42,45-31-22-16-28(17-23-31)36(4,5)6)32(26-12-18-29(19-13-26)39-33(37)38)40-34(41)43-24-25-10-8-7-9-11-25/h7-23,32H,24H2,1-6H3,(H,40,41)(H4,37,38,39)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	98	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of human uPA by chromogenic assay using Cbz-Val-Gly-Arg-pNA as chromogenic substrate				Bioorg Med Chem Lett 16: 2886-90 (2006) Article DOI: 10.1016/j.bmcl.2006.03.002 BindingDB Entry DOI: 10.7270/Q22N51WR
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50184647 (CHEMBL378778 | [benzyloxycarbonylamino-(4-guanidin...) Show SMILES [#6]C([#6])([#6])[#6]C([#6])([#6])c1ccc(-[#8]P(=O)([#8]-c2ccc(cc2)C([#6])([#6])[#6]C([#6])([#6])[#6])[#6](-[#7]-[#6](=O)-[#8]-[#6]-c2ccccc2)-c2ccc(cc2)\[#7]=[#6](\[#7])-[#7])cc1 Show InChI InChI=1S/C44H59N4O5P/c1-41(2,3)29-43(7,8)33-18-24-36(25-19-33)52-54(50,53-37-26-20-34(21-27-37)44(9,10)30-42(4,5)6)38(32-16-22-35(23-17-32)47-39(45)46)48-40(49)51-28-31-14-12-11-13-15-31/h11-27,38H,28-30H2,1-10H3,(H,48,49)(H4,45,46,47)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	204	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of human uPA by chromogenic assay using Cbz-Val-Gly-Arg-pNA as chromogenic substrate				Bioorg Med Chem Lett 16: 2886-90 (2006) Article DOI: 10.1016/j.bmcl.2006.03.002 BindingDB Entry DOI: 10.7270/Q22N51WR
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50184640 (CHEMBL378396 | [benzyloxycarbonylamino-(4-guanidin...) Show SMILES [#6]-[#6](-[#6])-c1ccc(-[#8]P(=O)([#8]-c2ccc(cc2)-[#6](-[#6])-[#6])[#6](-[#7]-[#6](=O)-[#8]-[#6]-c2ccccc2)-c2ccc(cc2)\[#7]=[#6](\[#7])-[#7])cc1 Show InChI InChI=1S/C34H39N4O5P/c1-23(2)26-12-18-30(19-13-26)42-44(40,43-31-20-14-27(15-21-31)24(3)4)32(28-10-16-29(17-11-28)37-33(35)36)38-34(39)41-22-25-8-6-5-7-9-25/h5-21,23-24,32H,22H2,1-4H3,(H,38,39)(H4,35,36,37)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	208	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of human uPA by chromogenic assay using Cbz-Val-Gly-Arg-pNA as chromogenic substrate				Bioorg Med Chem Lett 16: 2886-90 (2006) Article DOI: 10.1016/j.bmcl.2006.03.002 BindingDB Entry DOI: 10.7270/Q22N51WR
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50204146 (1-amino-2-phenylethyl(1-hydroxy-3-phenylpropyl)pho...) Show SMILES NC(Cc1ccccc1)P(O)(O)C(=O)CCc1ccccc1 Show InChI InChI=1S/C17H22NO3P/c18-16(13-15-9-5-2-6-10-15)22(20,21)17(19)12-11-14-7-3-1-4-8-14/h1-10,16,20-22H,11-13,18H2	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of APN				Bioorg Med Chem Lett 17: 1516-9 (2007) Article DOI: 10.1016/j.bmcl.2007.01.028 BindingDB Entry DOI: 10.7270/Q2C24W3B
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50184645 (CHEMBL209091 | [benzyloxycarbonylamino-(4-guanidin...) Show SMILES [#6]-c1ccc(-[#8]P(=O)([#8]-c2ccc(-[#6])cc2)[#6](-[#7]-[#6](=O)-[#8]-[#6]-c2ccccc2)-c2ccc(cc2)\[#7]=[#6](\[#7])-[#7])cc1 Show InChI InChI=1S/C30H31N4O5P/c1-21-8-16-26(17-9-21)38-40(36,39-27-18-10-22(2)11-19-27)28(24-12-14-25(15-13-24)33-29(31)32)34-30(35)37-20-23-6-4-3-5-7-23/h3-19,28H,20H2,1-2H3,(H,34,35)(H4,31,32,33)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	370	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of human uPA by chromogenic assay using Cbz-Val-Gly-Arg-pNA as chromogenic substrate				Bioorg Med Chem Lett 16: 2886-90 (2006) Article DOI: 10.1016/j.bmcl.2006.03.002 BindingDB Entry DOI: 10.7270/Q22N51WR
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM50244150 ((4-methoxybenzyl)carbamothioyl(1-amino-3-phenylpro...) Show SMILES COc1ccc(CNC(=S)P(O)(O)=C(N)CCc2ccccc2)cc1 Show InChI InChI=1S/C18H23N2O3PS/c1-23-16-10-7-15(8-11-16)13-20-18(25)24(21,22)17(19)12-9-14-5-3-2-4-6-14/h2-8,10-11,21-22H,9,12-13,19H2,1H3,(H,20,25)	PDB 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
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N				Bioorg Med Chem Lett 18: 3734-6 (2008) Article DOI: 10.1016/j.bmcl.2008.05.050 BindingDB Entry DOI: 10.7270/Q2H41R6T
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50184642 (CHEMBL378782 | [benzyloxycarbonylamino-(4-guanidin...) Show SMILES [#7]\[#6](-[#7])=[#7]\c1ccc(cc1)-[#6](-[#7]-[#6](=O)-[#8]-[#6]-c1ccccc1)P(=O)([#8]-c1ccc2ccccc2c1)[#8]-c1ccc2ccccc2c1 Show InChI InChI=1S/C36H31N4O5P/c37-35(38)39-31-18-14-28(15-19-31)34(40-36(41)43-24-25-8-2-1-3-9-25)46(42,44-32-20-16-26-10-4-6-12-29(26)22-32)45-33-21-17-27-11-5-7-13-30(27)23-33/h1-23,34H,24H2,(H,40,41)(H4,37,38,39)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	455	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of human uPA by chromogenic assay using Cbz-Val-Gly-Arg-pNA as chromogenic substrate				Bioorg Med Chem Lett 16: 2886-90 (2006) Article DOI: 10.1016/j.bmcl.2006.03.002 BindingDB Entry DOI: 10.7270/Q22N51WR
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM50316042 (1-amino-3-phenylpropylphosphonic acid mono-(4-isop...) Show SMILES CC(C)c1ccc(OP(O)(=O)C(N)CCc2ccccc2)cc1 Show InChI InChI=1S/C18H24NO3P/c1-14(2)16-9-11-17(12-10-16)22-23(20,21)18(19)13-8-15-6-4-3-5-7-15/h3-7,9-12,14,18H,8,13,19H2,1-2H3,(H,20,21)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N using Leu-AMC as substrate				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM50244148 (1-amino-3-methylbutyl(hexylcarbamothioyl)phosphini...) Show SMILES CCCCCCNC(=S)P(O)(O)=C(N)CC(C)C Show InChI InChI=1S/C12H27N2O2PS/c1-4-5-6-7-8-14-12(18)17(15,16)11(13)9-10(2)3/h10,15-16H,4-9,13H2,1-3H3,(H,14,18)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N				Bioorg Med Chem Lett 18: 3734-6 (2008) Article DOI: 10.1016/j.bmcl.2008.05.050 BindingDB Entry DOI: 10.7270/Q2H41R6T
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50204160 (1-amino-2-methylpropyl(1-hydroxy-3-phenylpropyl)ph...) Show SMILES CC(C)C(N)P(O)(O)C(=O)CCc1ccccc1 Show InChI InChI=1S/C13H22NO3P/c1-10(2)13(14)18(16,17)12(15)9-8-11-6-4-3-5-7-11/h3-7,10,13,16-18H,8-9,14H2,1-2H3	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of APN				Bioorg Med Chem Lett 17: 1516-9 (2007) Article DOI: 10.1016/j.bmcl.2007.01.028 BindingDB Entry DOI: 10.7270/Q2C24W3B
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50204163 (CHEMBL227345 | alpha1-(1-amino-3-methylbutane)-alp...) Show SMILES CC(C)CC(N)=P(O)(O)C(=O)NCc1ccccc1 Show InChI InChI=1S/C13H21N2O3P/c1-10(2)8-12(14)19(17,18)13(16)15-9-11-6-4-3-5-7-11/h3-7,10,17-18H,8-9,14H2,1-2H3,(H,15,16)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	530	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of APN				Bioorg Med Chem Lett 17: 1516-9 (2007) Article DOI: 10.1016/j.bmcl.2007.01.028 BindingDB Entry DOI: 10.7270/Q2C24W3B
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50184643 (CHEMBL379807 | [benzyloxycarbonylamino-(4-guanidin...) Show SMILES [#7]\[#6](-[#7])=[#7]\c1ccc(cc1)-[#6](-[#7]-[#6](=O)-[#8]-[#6]-c1ccccc1)P(=O)([#8]-c1ccccc1)[#8]-c1ccccc1 Show InChI InChI=1S/C28H27N4O5P/c29-27(30)31-23-18-16-22(17-19-23)26(32-28(33)35-20-21-10-4-1-5-11-21)38(34,36-24-12-6-2-7-13-24)37-25-14-8-3-9-15-25/h1-19,26H,20H2,(H,32,33)(H4,29,30,31)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	532	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of human uPA by chromogenic assay using Cbz-Val-Gly-Arg-pNA as chromogenic substrate				Bioorg Med Chem Lett 16: 2886-90 (2006) Article DOI: 10.1016/j.bmcl.2006.03.002 BindingDB Entry DOI: 10.7270/Q22N51WR
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50204159 (CHEMBL226863 | alpha1-(1-amino-1-phenylmethane)-al...) Show SMILES NC(Cc1ccccc1)P(O)(O)C(=O)Cc1ccccc1 Show InChI InChI=1S/C16H20NO3P/c17-15(11-13-7-3-1-4-8-13)21(19,20)16(18)12-14-9-5-2-6-10-14/h1-10,15,19-21H,11-12,17H2	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	550	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of APN				Bioorg Med Chem Lett 17: 1516-9 (2007) Article DOI: 10.1016/j.bmcl.2007.01.028 BindingDB Entry DOI: 10.7270/Q2C24W3B
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50204161 (CHEMBL227290 | bis-alpha-(1-amino-1-phenylmethane)...) Show SMILES NC(Cc1ccccc1)P(O)(O)C(=N)Cc1ccccc1 Show InChI InChI=1S/C16H21N2O2P/c17-15(11-13-7-3-1-4-8-13)21(19,20)16(18)12-14-9-5-2-6-10-14/h1-10,15,18-21H,11-12,17H2	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of APN				Bioorg Med Chem Lett 17: 1516-9 (2007) Article DOI: 10.1016/j.bmcl.2007.01.028 BindingDB Entry DOI: 10.7270/Q2C24W3B
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM50244108 ((4-methoxybenzyl)carbamothioyl(1-aminobutyl)phosph...) Show SMILES CCCC(N)=P(O)(O)C(=S)NCc1ccc(OC)cc1 Show InChI InChI=1S/C13H21N2O3PS/c1-3-4-12(14)19(16,17)13(20)15-9-10-5-7-11(18-2)8-6-10/h5-8,16-17H,3-4,9,14H2,1-2H3,(H,15,20)	PDB UniProtKB/SwissProt 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
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N				Bioorg Med Chem Lett 18: 3734-6 (2008) Article DOI: 10.1016/j.bmcl.2008.05.050 BindingDB Entry DOI: 10.7270/Q2H41R6T
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50204157 (CHEMBL227340 | alpha1-(1-amino-1-phenylmethane)-al...) Show SMILES NC(Cc1ccccc1)P(O)(O)C(=N)CCc1ccccc1 Show InChI InChI=1S/C17H23N2O2P/c18-16(12-11-14-7-3-1-4-8-14)22(20,21)17(19)13-15-9-5-2-6-10-15/h1-10,17-18,20-22H,11-13,19H2	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of APN				Bioorg Med Chem Lett 17: 1516-9 (2007) Article DOI: 10.1016/j.bmcl.2007.01.028 BindingDB Entry DOI: 10.7270/Q2C24W3B
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM50244146 (1-aminopentyl(phenethylcarbamothioyl)phosphinic ac...) Show SMILES CCCCC(N)=P(O)(O)C(=S)NCCc1ccccc1 Show InChI InChI=1S/C14H23N2O2PS/c1-2-3-9-13(15)19(17,18)14(20)16-11-10-12-7-5-4-6-8-12/h4-8,17-18H,2-3,9-11,15H2,1H3,(H,16,20)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	730	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N				Bioorg Med Chem Lett 18: 3734-6 (2008) Article DOI: 10.1016/j.bmcl.2008.05.050 BindingDB Entry DOI: 10.7270/Q2H41R6T
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50204149 (CHEMBL390323 | bis-alpha-(1-amino-3-phenylpropane)...) Show SMILES NC(CCc1ccccc1)P(O)(O)C(=N)CCc1ccccc1 Show InChI InChI=1S/C18H25N2O2P/c19-17(13-11-15-7-3-1-4-8-15)23(21,22)18(20)14-12-16-9-5-2-6-10-16/h1-10,17,20-23H,11-14,19H2	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	830	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of APN				Bioorg Med Chem Lett 17: 1516-9 (2007) Article DOI: 10.1016/j.bmcl.2007.01.028 BindingDB Entry DOI: 10.7270/Q2C24W3B
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50204148 (CHEMBL227347 | alpha1-(1-amino-2-methylpropane)-al...) Show SMILES CC(C)C(N)=P(O)(O)C(=O)NCc1ccccc1 Show InChI InChI=1S/C12H19N2O3P/c1-9(2)11(13)18(16,17)12(15)14-8-10-6-4-3-5-7-10/h3-7,9,16-17H,8,13H2,1-2H3,(H,14,15)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	930	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of APN				Bioorg Med Chem Lett 17: 1516-9 (2007) Article DOI: 10.1016/j.bmcl.2007.01.028 BindingDB Entry DOI: 10.7270/Q2C24W3B
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50204150 (1-amino-3-methylbutyl(1-hydroxy-3-phenylpropyl)pho...) Show SMILES CC(C)CC(N)P(O)(O)C(=O)CCc1ccccc1 Show InChI InChI=1S/C14H24NO3P/c1-11(2)10-13(15)19(17,18)14(16)9-8-12-6-4-3-5-7-12/h3-7,11,13,17-19H,8-10,15H2,1-2H3	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of APN				Bioorg Med Chem Lett 17: 1516-9 (2007) Article DOI: 10.1016/j.bmcl.2007.01.028 BindingDB Entry DOI: 10.7270/Q2C24W3B
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM50316033 (1-aminopentylphosphonic acid mono-(4-methylphenyl)...) Show SMILES CCCCC(N)P(O)(=O)Oc1ccc(C)cc1 Show InChI InChI=1S/C12H20NO3P/c1-3-4-5-12(13)17(14,15)16-11-8-6-10(2)7-9-11/h6-9,12H,3-5,13H2,1-2H3,(H,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N using Leu-AMC as substrate				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM50316028 (1-aminopropylphosphonic acid mono-(4-tbutylphenyl)...) Show SMILES CCC(N)P(O)(=O)Oc1ccc(cc1)C(C)(C)C Show InChI InChI=1S/C13H22NO3P/c1-5-12(14)18(15,16)17-11-8-6-10(7-9-11)13(2,3)4/h6-9,12H,5,14H2,1-4H3,(H,15,16)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N using Leu-AMC as substrate				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM50244106 ((4-methoxybenzyl)carbamothioyl(1-aminoethyl)phosph...) Show SMILES COc1ccc(CNC(=S)P(O)(O)=C(C)N)cc1 Show InChI InChI=1S/C11H17N2O3PS/c1-8(12)17(14,15)11(18)13-7-9-3-5-10(16-2)6-4-9/h3-6,14-15H,7,12H2,1-2H3,(H,13,18)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.12E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N				Bioorg Med Chem Lett 18: 3734-6 (2008) Article DOI: 10.1016/j.bmcl.2008.05.050 BindingDB Entry DOI: 10.7270/Q2H41R6T
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM50244110 (1-amino-2-methylpropyl(hexylcarbamothioyl)phosphin...) Show SMILES CCCCCCNC(=S)P(O)(O)=C(N)C(C)C Show InChI InChI=1S/C11H25N2O2PS/c1-4-5-6-7-8-13-11(17)16(14,15)10(12)9(2)3/h9,14-15H,4-8,12H2,1-3H3,(H,13,17)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.18E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N				Bioorg Med Chem Lett 18: 3734-6 (2008) Article DOI: 10.1016/j.bmcl.2008.05.050 BindingDB Entry DOI: 10.7270/Q2H41R6T
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM50316034 (1-aminopentylphosphonic acid mono-(3,4-dimethylphe...) Show SMILES CCCCC(N)P(O)(=O)Oc1ccc(C)c(C)c1 Show InChI InChI=1S/C13H22NO3P/c1-4-5-6-13(14)18(15,16)17-12-8-7-10(2)11(3)9-12/h7-9,13H,4-6,14H2,1-3H3,(H,15,16)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N using Leu-AMC as substrate				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM50244109 (1-amino-2-methylpropyl(isobutylcarbamothioyl)phosp...) Show SMILES CC(C)CNC(=S)P(O)(O)=C(N)C(C)C Show InChI InChI=1S/C9H21N2O2PS/c1-6(2)5-11-9(15)14(12,13)8(10)7(3)4/h6-7,12-13H,5,10H2,1-4H3,(H,11,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N				Bioorg Med Chem Lett 18: 3734-6 (2008) Article DOI: 10.1016/j.bmcl.2008.05.050 BindingDB Entry DOI: 10.7270/Q2H41R6T
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM50316043 (1-amino-3-phenylpropylphosphonic acid mono-(4-t-bu...) Show SMILES CC(C)(C)c1ccc(OP(O)(=O)C(N)CCc2ccccc2)cc1 Show InChI InChI=1S/C19H26NO3P/c1-19(2,3)16-10-12-17(13-11-16)23-24(21,22)18(20)14-9-15-7-5-4-6-8-15/h4-8,10-13,18H,9,14,20H2,1-3H3,(H,21,22)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N using Leu-AMC as substrate				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair
Aminopeptidase N (Sus scrofa (Pig))	BDBM23971 ((2S)-2-[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanami...) Show SMILES CC(C)C[C@H](NC(=O)[C@@H](O)[C@H](N)Cc1ccccc1)C(O)=O Show InChI InChI=1S/C16H24N2O4/c1-10(2)8-13(16(21)22)18-15(20)14(19)12(17)9-11-6-4-3-5-7-11/h3-7,10,12-14,19H,8-9,17H2,1-2H3,(H,18,20)(H,21,22)/t12-,13+,14+/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroc£?aw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N				Bioorg Med Chem Lett 18: 3734-6 (2008) Article DOI: 10.1016/j.bmcl.2008.05.050 BindingDB Entry DOI: 10.7270/Q2H41R6T
					More data for this Ligand-Target Pair				3D Structure (crystal)
Aminopeptidase N (Sus scrofa (Pig))	BDBM23971 ((2S)-2-[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanami...) Show SMILES CC(C)C[C@H](NC(=O)[C@@H](O)[C@H](N)Cc1ccccc1)C(O)=O Show InChI InChI=1S/C16H24N2O4/c1-10(2)8-13(16(21)22)18-15(20)14(19)12(17)9-11-6-4-3-5-7-11/h3-7,10,12-14,19H,8-9,17H2,1-2H3,(H,18,20)(H,21,22)/t12-,13+,14+/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Wroclaw University of Technology Curated by ChEMBL					Assay Description Inhibition of pig kidney aminopeptidase N using Leu-AMC as substrate				Bioorg Med Chem 18: 2930-6 (2010) Article DOI: 10.1016/j.bmc.2010.02.056 BindingDB Entry DOI: 10.7270/Q2FN16C0
					More data for this Ligand-Target Pair				3D Structure (crystal)

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