Compile Data Set for Download or QSAR

Found 27 hits with Last Name = 'padova' and Initial = 'g'   

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
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021311 (1-(2-Benzoylsulfanyl-cyclopentanecarbonyl)-pyrroli...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCC[C@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C18H21NO4S/c20-16(19-11-5-9-14(19)17(21)22)13-8-4-10-15(13)24-18(23)12-6-2-1-3-7-12/h1-3,6-7,13-15H,4-5,8-11H2,(H,21,22)/t13-,14+,15-/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	580	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM21642 ((2S)-1-[(2S)-2-methyl-3-sulfanylpropanoyl]pyrrolid...) Show SMILES C[C@H](CS)C(=O)N1CCC[C@H]1C(O)=O Show InChI InChI=1S/C9H15NO3S/c1-6(5-14)8(11)10-4-2-3-7(10)9(12)13/h6-7,14H,2-5H2,1H3,(H,12,13)/t6-,7+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	590	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021303 (1-(2-Mercapto-cyclopentanecarbonyl)-pyrrolidine-2-...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCC[C@H]1S Show InChI InChI=1S/C11H17NO3S/c13-10(7-3-1-5-9(7)16)12-6-2-4-8(12)11(14)15/h7-9,16H,1-6H2,(H,14,15)/t7-,8+,9-/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.11E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021312 (1-(2-Mercapto-cyclobutanecarbonyl)-pyrrolidine-2-c...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CC[C@H]1S Show InChI InChI=1S/C10H15NO3S/c12-9(6-3-4-8(6)15)11-5-1-2-7(11)10(13)14/h6-8,15H,1-5H2,(H,13,14)/t6-,7+,8-/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.26E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021308 (1-(2-Mercapto-cyclopentanecarbonyl)-pyrrolidine-2-...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)C1CCCC1S Show InChI InChI=1S/C11H17NO3S/c13-10(7-3-1-5-9(7)16)12-6-2-4-8(12)11(14)15/h7-9,16H,1-6H2,(H,14,15)/t7?,8-,9?/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.64E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021306 (1-(2-Benzoylsulfanyl-cyclobutanecarbonyl)-pyrrolid...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CC[C@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C17H19NO4S/c19-15(18-10-4-7-13(18)16(20)21)12-8-9-14(12)23-17(22)11-5-2-1-3-6-11/h1-3,5-6,12-14H,4,7-10H2,(H,20,21)/t12-,13+,14-/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021317 (1-(2-Mercapto-cyclohexanecarbonyl)-pyrrolidine-2-c...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)C1CCCCC1S Show InChI InChI=1S/C12H19NO3S/c14-11(8-4-1-2-6-10(8)17)13-7-3-5-9(13)12(15)16/h8-10,17H,1-7H2,(H,15,16)/t8?,9-,10?/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.14E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021314 (1-(2-Mercapto-cyclobutanecarbonyl)-pyrrolidine-2-c...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)[C@H]1CC[C@@H]1S Show InChI InChI=1S/C10H15NO3S/c12-9(6-3-4-8(6)15)11-5-1-2-7(11)10(13)14/h6-8,15H,1-5H2,(H,13,14)/t6-,7-,8-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.27E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021297 (1-(2-Mercapto-cyclopentanecarbonyl)-pyrrolidine-2-...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCC[C@@H]1S Show InChI InChI=1S/C11H17NO3S/c13-10(7-3-1-5-9(7)16)12-6-2-4-8(12)11(14)15/h7-9,16H,1-6H2,(H,14,15)/t7-,8+,9+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.95E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021319 (1-(2-Mercapto-cyclopentanecarbonyl)-pyrrolidine-2-...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCC[C@@H]1S Show InChI InChI=1S/C11H17NO3S/c13-10(7-3-1-5-9(7)16)12-6-2-4-8(12)11(14)15/h7-9,16H,1-6H2,(H,14,15)/t7-,8-,9-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.43E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021299 (1-(2-Benzoylsulfanyl-cyclopentanecarbonyl)-pyrroli...) Show SMILES CC(C)(C)OC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCC[C@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C22H29NO4S/c1-22(2,3)27-20(25)17-12-8-14-23(17)19(24)16-11-7-13-18(16)28-21(26)15-9-5-4-6-10-15/h4-6,9-10,16-18H,7-8,11-14H2,1-3H3/t16-,17-,18+/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.24E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021307 (1-(2-Benzoylsulfanyl-cyclopentanecarbonyl)-pyrroli...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCC[C@@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C18H21NO4S/c20-16(19-11-5-9-14(19)17(21)22)13-8-4-10-15(13)24-18(23)12-6-2-1-3-7-12/h1-3,6-7,13-15H,4-5,8-11H2,(H,21,22)/t13-,14+,15+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.44E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021305 (1-(2-Benzoylsulfanyl-cyclopentanecarbonyl)-pyrroli...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCC[C@@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C18H21NO4S/c20-16(19-11-5-9-14(19)17(21)22)13-8-4-10-15(13)24-18(23)12-6-2-1-3-7-12/h1-3,6-7,13-15H,4-5,8-11H2,(H,21,22)/t13-,14-,15-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.44E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021301 (1-(2-Mercapto-cyclopentanecarbonyl)-pyrrolidine-2-...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCC[C@H]1S Show InChI InChI=1S/C11H17NO3S/c13-10(7-3-1-5-9(7)16)12-6-2-4-8(12)11(14)15/h7-9,16H,1-6H2,(H,14,15)/t7-,8-,9+/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.06E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021310 (1-(2-Mercapto-3,3-dimethyl-cyclopentanecarbonyl)-p...) Show SMILES CC1(C)CC[C@H]([C@@H]1S)C(=O)N1CCC[C@H]1C(O)=O Show InChI InChI=1S/C13H21NO3S/c1-13(2)6-5-8(10(13)18)11(15)14-7-3-4-9(14)12(16)17/h8-10,18H,3-7H2,1-2H3,(H,16,17)/t8-,9+,10+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.15E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021309 (1-(2-Benzoylsulfanyl-3,3-dimethyl-cyclopentanecarb...) Show SMILES CC(C)(C)OC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCC(C)(C)[C@@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C24H33NO4S/c1-23(2,3)29-21(27)18-12-9-15-25(18)20(26)17-13-14-24(4,5)19(17)30-22(28)16-10-7-6-8-11-16/h6-8,10-11,17-19H,9,12-15H2,1-5H3/t17-,18+,19-/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021304 (1-(2-Benzoylsulfanyl-cyclopentanecarbonyl)-pyrroli...) Show SMILES CC(C)(C)OC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCC[C@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C22H29NO4S/c1-22(2,3)27-20(25)17-12-8-14-23(17)19(24)16-11-7-13-18(16)28-21(26)15-9-5-4-6-10-15/h4-6,9-10,16-18H,7-8,11-14H2,1-3H3/t16-,17+,18-/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021313 (1-(2-Benzoylsulfanyl-cyclobutanecarbonyl)-pyrrolid...) Show SMILES CC(C)(C)OC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CC[C@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C21H27NO4S/c1-21(2,3)26-19(24)16-10-7-13-22(16)18(23)15-11-12-17(15)27-20(25)14-8-5-4-6-9-14/h4-6,8-9,15-17H,7,10-13H2,1-3H3/t15-,16+,17-/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021302 (1-(2-Benzoylsulfanyl-cyclobutanecarbonyl)-pyrrolid...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)[C@H]1CC[C@@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C17H19NO4S/c19-15(18-10-4-7-13(18)16(20)21)12-8-9-14(12)23-17(22)11-5-2-1-3-6-11/h1-3,5-6,12-14H,4,7-10H2,(H,20,21)/t12-,13-,14-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021315 (1-(2-Benzoylsulfanyl-3,3-dimethyl-cyclopentanecarb...) Show SMILES CC(C)(C)OC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCC(C)(C)[C@@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C24H33NO4S/c1-23(2,3)29-21(27)18-12-9-15-25(18)20(26)17-13-14-24(4,5)19(17)30-22(28)16-10-7-6-8-11-16/h6-8,10-11,17-19H,9,12-15H2,1-5H3/t17-,18-,19+/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021321 (1-(2-Benzoylsulfanyl-3,3-dimethyl-cyclopentanecarb...) Show SMILES CC1(C)CC[C@@H]([C@H]1SC(=O)c1ccccc1)C(=O)N1CCC[C@H]1C(O)=O Show InChI InChI=1S/C20H25NO4S/c1-20(2)11-10-14(17(22)21-12-6-9-15(21)18(23)24)16(20)26-19(25)13-7-4-3-5-8-13/h3-5,7-8,14-16H,6,9-12H2,1-2H3,(H,23,24)/t14-,15-,16+/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021298 (1-(2-Benzoylsulfanyl-cyclopentanecarbonyl)-pyrroli...) Show SMILES CC(C)(C)OC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCC[C@@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C22H29NO4S/c1-22(2,3)27-20(25)17-12-8-14-23(17)19(24)16-11-7-13-18(16)28-21(26)15-9-5-4-6-10-15/h4-6,9-10,16-18H,7-8,11-14H2,1-3H3/t16-,17+,18+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021316 (1-(2-Benzoylsulfanyl-cyclobutanecarbonyl)-pyrrolid...) Show SMILES CC(C)(C)OC(=O)[C@@H]1CCCN1C(=O)[C@H]1CC[C@@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C21H27NO4S/c1-21(2,3)26-19(24)16-10-7-13-22(16)18(23)15-11-12-17(15)27-20(25)14-8-5-4-6-9-14/h4-6,8-9,15-17H,7,10-13H2,1-3H3/t15-,16-,17-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021318 (1-(2-Mercapto-3,3-dimethyl-cyclopentanecarbonyl)-p...) Show SMILES CC1(C)CC[C@@H]([C@H]1S)C(=O)N1CCC[C@H]1C(O)=O Show InChI InChI=1S/C13H21NO3S/c1-13(2)6-5-8(10(13)18)11(15)14-7-3-4-9(14)12(16)17/h8-10,18H,3-7H2,1-2H3,(H,16,17)/t8-,9-,10+/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021320 (1-(2-Benzoylsulfanyl-3,3-dimethyl-cyclopentanecarb...) Show SMILES CC1(C)CC[C@H]([C@H]1SC(=O)c1ccccc1)C(=O)N1CCC[C@H]1C(O)=O Show InChI InChI=1S/C20H25NO4S/c1-20(2)11-10-14(17(22)21-12-6-9-15(21)18(23)24)16(20)26-19(25)13-7-4-3-5-8-13/h3-5,7-8,14-16H,6,9-12H2,1-2H3,(H,23,24)/t14-,15+,16-/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021296 (1-(2-Benzoylsulfanyl-cyclopentanecarbonyl)-pyrroli...) Show SMILES OC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCC[C@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C18H21NO4S/c20-16(19-11-5-9-14(19)17(21)22)13-8-4-10-15(13)24-18(23)12-6-2-1-3-7-12/h1-3,6-7,13-15H,4-5,8-11H2,(H,21,22)/t13-,14-,15+/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50021300 (1-(2-Benzoylsulfanyl-cyclopentanecarbonyl)-pyrroli...) Show SMILES CC(C)(C)OC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCC[C@@H]1SC(=O)c1ccccc1 Show InChI InChI=1S/C22H29NO4S/c1-22(2,3)27-20(25)17-12-8-14-23(17)19(24)16-11-7-13-18(16)28-21(26)15-9-5-4-6-10-15/h4-6,9-10,16-18H,7-8,11-14H2,1-3H3/t16-,17-,18-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against Angiotensin I converting enzyme				J Med Chem 29: 411-7 (1986) BindingDB Entry DOI: 10.7270/Q218372M
					More data for this Ligand-Target Pair