Compile Data Set for Download or QSAR

Found 29 hits with Last Name = 'laubie' and Initial = 'm'   

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
Alpha-2A adrenergic receptor (Homo sapiens (Human))	BDBM50031306 (8-chlorospiro[1,2,3,4-tetrahydronaphthalene-2,4'-(...) Show SMILES NC1=NC2(CO1)CCc1cccc(Cl)c1C2 |t:1| Show InChI InChI=1S/C12H13ClN2O/c13-10-3-1-2-8-4-5-12(6-9(8)10)7-16-11(14)15-12/h1-3H,4-7H2,(H2,14,15)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2A adrenergic receptor in human platelets using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2A adrenergic receptor (Homo sapiens (Human))	BDBM50031324 (5',7'-dichlorospiro[4,5-dihydro-1H-imidazole-4,2'-...) Show SMILES Clc1cc(Cl)c2CCC3(CNC=N3)Cc2c1 |c:11| Show InChI InChI=1S/C12H12Cl2N2/c13-9-3-8-5-12(6-15-7-16-12)2-1-10(8)11(14)4-9/h3-4,7H,1-2,5-6H2,(H,15,16)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2A adrenergic receptor in human platelets using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2A adrenergic receptor (Homo sapiens (Human))	BDBM50031311 (7'-methylspiro[4,5-dihydro-1H-imidazole-4,2'-(1',2...) Show SMILES Cc1ccc2CCC3(CNC=N3)Cc2c1 |c:10| Show InChI InChI=1S/C13H16N2/c1-10-2-3-11-4-5-13(7-12(11)6-10)8-14-9-15-13/h2-3,6,9H,4-5,7-8H2,1H3,(H,14,15)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2A adrenergic receptor in human platelets using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2A adrenergic receptor (Homo sapiens (Human))	BDBM50031316 (5'-methoxyspiro[4,5-dihydro-1H-imidazole-4,2'-(1',...) Show SMILES COc1cccc2CC3(CNC=N3)CCc12 |c:11| Show InChI InChI=1S/C13H16N2O/c1-16-12-4-2-3-10-7-13(6-5-11(10)12)8-14-9-15-13/h2-4,9H,5-8H2,1H3,(H,14,15)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2A adrenergic receptor in human platelets using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2A adrenergic receptor (Homo sapiens (Human))	BDBM50031301 (8'-fluorospiro[4,5-dihydro-1H-imidazole-4,2'-(1',2...) Show SMILES Fc1cccc2CCC3(CNC=N3)Cc12 |c:11| Show InChI InChI=1S/C12H13FN2/c13-11-3-1-2-9-4-5-12(6-10(9)11)7-14-8-15-12/h1-3,8H,4-7H2,(H,14,15)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2A adrenergic receptor in human platelets using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2B adrenergic receptor (NEONATAL RAT)	BDBM50031306 (8-chlorospiro[1,2,3,4-tetrahydronaphthalene-2,4'-(...) Show SMILES NC1=NC2(CO1)CCc1cccc(Cl)c1C2 |t:1| Show InChI InChI=1S/C12H13ClN2O/c13-10-3-1-2-8-4-5-12(6-9(8)10)7-16-11(14)15-12/h1-3H,4-7H2,(H2,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2B adrenergic receptor in neonatal rat lung using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2A adrenergic receptor (Homo sapiens (Human))	BDBM50031319 (CHEMBL130853 | spiro[4,5-dihydro-1H-imidazole-4,2'...) Show SMILES C1NC=NC11CCc2ccccc2C1 |c:2| Show InChI InChI=1S/C12H14N2/c1-2-4-11-7-12(8-13-9-14-12)6-5-10(11)3-1/h1-4,9H,5-8H2,(H,13,14)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	34	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2A adrenergic receptor in human platelets using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2B adrenergic receptor (NEONATAL RAT)	BDBM50031311 (7'-methylspiro[4,5-dihydro-1H-imidazole-4,2'-(1',2...) Show SMILES Cc1ccc2CCC3(CNC=N3)Cc2c1 |c:10| Show InChI InChI=1S/C13H16N2/c1-10-2-3-11-4-5-13(7-12(11)6-10)8-14-9-15-13/h2-3,6,9H,4-5,7-8H2,1H3,(H,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	50	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2B adrenergic receptor in neonatal rat lung using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2A adrenergic receptor (Homo sapiens (Human))	BDBM50031308 (7'-methoxyspiro[4,5-dihydro-1H-imidazole-4,2'-(1',...) Show SMILES COc1ccc2CCC3(CNC=N3)Cc2c1 |c:11| Show InChI InChI=1S/C13H16N2O/c1-16-12-3-2-10-4-5-13(7-11(10)6-12)8-14-9-15-13/h2-3,6,9H,4-5,7-8H2,1H3,(H,14,15)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	51	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2A adrenergic receptor in human platelets using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2A adrenergic receptor (Homo sapiens (Human))	BDBM50031330 (8'-methoxyspiro[4,5-dihydro-1H-imidazole-4,2'-(1',...) Show SMILES COc1cccc2CCC3(CNC=N3)Cc12 |c:12| Show InChI InChI=1S/C13H16N2O/c1-16-12-4-2-3-10-5-6-13(7-11(10)12)8-14-9-15-13/h2-4,9H,5-8H2,1H3,(H,14,15)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	51	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2A adrenergic receptor in human platelets using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2A adrenergic receptor (Homo sapiens (Human))	BDBM50031326 (6'-methoxyspiro[4,5-dihydro-1H-imidazole-4,2'-(1',...) Show SMILES COc1ccc2CC3(CNC=N3)CCc2c1 |c:10| Show InChI InChI=1S/C13H16N2O/c1-16-12-3-2-11-7-13(8-14-9-15-13)5-4-10(11)6-12/h2-3,6,9H,4-5,7-8H2,1H3,(H,14,15)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	87	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2A adrenergic receptor in human platelets using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2B adrenergic receptor (NEONATAL RAT)	BDBM50031324 (5',7'-dichlorospiro[4,5-dihydro-1H-imidazole-4,2'-...) Show SMILES Clc1cc(Cl)c2CCC3(CNC=N3)Cc2c1 |c:11| Show InChI InChI=1S/C12H12Cl2N2/c13-9-3-8-5-12(6-15-7-16-12)2-1-10(8)11(14)4-9/h3-4,7H,1-2,5-6H2,(H,15,16)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	95	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2B adrenergic receptor in neonatal rat lung using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2B adrenergic receptor (NEONATAL RAT)	BDBM50031330 (8'-methoxyspiro[4,5-dihydro-1H-imidazole-4,2'-(1',...) Show SMILES COc1cccc2CCC3(CNC=N3)Cc12 |c:12| Show InChI InChI=1S/C13H16N2O/c1-16-12-4-2-3-10-5-6-13(7-11(10)12)8-14-9-15-13/h2-4,9H,5-8H2,1H3,(H,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	99	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2B adrenergic receptor in neonatal rat lung using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2B adrenergic receptor (NEONATAL RAT)	BDBM50031308 (7'-methoxyspiro[4,5-dihydro-1H-imidazole-4,2'-(1',...) Show SMILES COc1ccc2CCC3(CNC=N3)Cc2c1 |c:11| Show InChI InChI=1S/C13H16N2O/c1-16-12-3-2-10-4-5-13(7-11(10)6-12)8-14-9-15-13/h2-3,6,9H,4-5,7-8H2,1H3,(H,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	99	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2B adrenergic receptor in neonatal rat lung using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2B adrenergic receptor (NEONATAL RAT)	BDBM50031301 (8'-fluorospiro[4,5-dihydro-1H-imidazole-4,2'-(1',2...) Show SMILES Fc1cccc2CCC3(CNC=N3)Cc12 |c:11| Show InChI InChI=1S/C12H13FN2/c13-11-3-1-2-9-4-5-12(6-10(9)11)7-14-8-15-12/h1-3,8H,4-7H2,(H,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	152	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2B adrenergic receptor in neonatal rat lung using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2B adrenergic receptor (NEONATAL RAT)	BDBM50031316 (5'-methoxyspiro[4,5-dihydro-1H-imidazole-4,2'-(1',...) Show SMILES COc1cccc2CC3(CNC=N3)CCc12 |c:11| Show InChI InChI=1S/C13H16N2O/c1-16-12-4-2-3-10-7-13(6-5-11(10)12)8-14-9-15-13/h2-4,9H,5-8H2,1H3,(H,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	159	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2B adrenergic receptor in neonatal rat lung using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2B adrenergic receptor (NEONATAL RAT)	BDBM50027067 ((2-Chloro-5-trifluoromethyl-phenyl)-(4,5-dihydro-1...) Show SMILES FC(F)(F)c1ccc(Cl)c(c1)\[#7]=[#6]-1/[#7]-[#6]-[#6]-[#7]-1 Show InChI InChI=1S/C10H9ClF3N3/c11-7-2-1-6(10(12,13)14)5-8(7)17-9-15-3-4-16-9/h1-2,5H,3-4H2,(H2,15,16,17)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	179	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2B adrenergic receptor in neonatal rat lung using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2B adrenergic receptor (NEONATAL RAT)	BDBM50031319 (CHEMBL130853 | spiro[4,5-dihydro-1H-imidazole-4,2'...) Show SMILES C1NC=NC11CCc2ccccc2C1 |c:2| Show InChI InChI=1S/C12H14N2/c1-2-4-11-7-12(8-13-9-14-12)6-5-10(11)3-1/h1-4,9H,5-8H2,(H,13,14)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	275	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2B adrenergic receptor in neonatal rat lung using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2B adrenergic receptor (NEONATAL RAT)	BDBM50031326 (6'-methoxyspiro[4,5-dihydro-1H-imidazole-4,2'-(1',...) Show SMILES COc1ccc2CC3(CNC=N3)CCc2c1 |c:10| Show InChI InChI=1S/C13H16N2O/c1-16-12-3-2-11-7-13(8-14-9-15-13)5-4-10(11)6-12/h2-3,6,9H,4-5,7-8H2,1H3,(H,14,15)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2B adrenergic receptor in neonatal rat lung using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Alpha-2A adrenergic receptor (Homo sapiens (Human))	BDBM50027067 ((2-Chloro-5-trifluoromethyl-phenyl)-(4,5-dihydro-1...) Show SMILES FC(F)(F)c1ccc(Cl)c(c1)\[#7]=[#6]-1/[#7]-[#6]-[#6]-[#7]-1 Show InChI InChI=1S/C10H9ClF3N3/c11-7-2-1-6(10(12,13)14)5-8(7)17-9-15-3-4-16-9/h1-2,5H,3-4H2,(H2,15,16,17)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	1.56E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Recherches Servier Curated by ChEMBL					Assay Description Binding affinity towards Alpha-2A adrenergic receptor in human platelets using [3H]-RX-821002 as radioligand				J Med Chem 38: 4056-69 (1995) BindingDB Entry DOI: 10.7270/Q2DV1HXN
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50367254 (ENALAPRILAT) Show SMILES C[C@H](N[C@@H](CCc1ccccc1)C(O)=O)C(=O)N1CCC[C@H]1C(O)=O |r| Show InChI InChI=1S/C18H24N2O5/c1-12(16(21)20-11-5-8-15(20)18(24)25)19-14(17(22)23)10-9-13-6-3-2-4-7-13/h2-4,6-7,12,14-15,19H,5,8-11H2,1H3,(H,22,23)(H,24,25)/t12-,14-,15-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase MCE KEGG MMDB PC cid PC sid PDB UniChem Similars	PubMed	n/a	n/a	1.20	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Chimie des Substances Naturelles Curated by ChEMBL					Assay Description In vitro activity against angiotensin I converting enzyme especially against Hip-His-Leu residues				J Med Chem 34: 663-9 (1991) BindingDB Entry DOI: 10.7270/Q21V5FKF
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50011365 (1-[2-(1-Carboxy-butylamino)-propionyl]-octahydro-i...) Show SMILES CCCC(N[C@@H](C)C(=O)N1C2CCCCC2CC1C(O)=O)C(O)=O Show InChI InChI=1S/C17H28N2O5/c1-3-6-12(16(21)22)18-10(2)15(20)19-13-8-5-4-7-11(13)9-14(19)17(23)24/h10-14,18H,3-9H2,1-2H3,(H,21,22)(H,23,24)/t10-,11?,12?,13?,14?/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.5	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Chimie des Substances Naturelles Curated by ChEMBL					Assay Description In vitro activity against angiotensin I converting enzyme especially against Hip-His-Leu residues				J Med Chem 34: 663-9 (1991) BindingDB Entry DOI: 10.7270/Q21V5FKF
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50011362 (1-(3-Mercapto-2-methyl-propionyl)-pyrrolidine-2-ca...) Show SMILES C[C@@H](CS)C(=O)N1CCCC1C(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?/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.5	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Chimie des Substances Naturelles Curated by ChEMBL					Assay Description In vitro activity against angiotensin I converting enzyme especially against Hip-His-Leu residues				J Med Chem 34: 663-9 (1991) BindingDB Entry DOI: 10.7270/Q21V5FKF
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50011361 (1-[2-(1-Carboxy-butylamino)-acetyl]-octahydro-indo...) Show SMILES CCC[C@H](NCC(=O)N1C2CCCCC2C[C@H]1C(O)=O)C(O)=O |r| Show InChI InChI=1S/C16H26N2O5/c1-2-5-11(15(20)21)17-9-14(19)18-12-7-4-3-6-10(12)8-13(18)16(22)23/h10-13,17H,2-9H2,1H3,(H,20,21)(H,22,23)/t10?,11-,12?,13-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.90	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Chimie des Substances Naturelles Curated by ChEMBL					Assay Description In vitro activity against angiotensin I converting enzyme especially against Hip-His-Leu residues				J Med Chem 34: 663-9 (1991) BindingDB Entry DOI: 10.7270/Q21V5FKF
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50011367 (1-(3-Mercapto-2-methyl-propionyl)-pyrrolidine-2-ca...) Show SMILES C[C@H](CS)C(=O)N1CCCC1C(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 MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MMDB PC cid PC sid PDB UniChem Similars	PubMed	n/a	n/a	23	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Chimie des Substances Naturelles Curated by ChEMBL					Assay Description In vitro activity against angiotensin I converting enzyme especially against Hip-His-Leu residues				J Med Chem 34: 663-9 (1991) BindingDB Entry DOI: 10.7270/Q21V5FKF
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50011366 ((S)1-(3-Mercapto-propionyl)-pyrrolidine-2-carboxyl...) Show SMILES OC(=O)C1CCCN1C(=O)CCS Show InChI InChI=1S/C8H13NO3S/c10-7(3-5-13)9-4-1-2-6(9)8(11)12/h6,13H,1-5H2,(H,11,12)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Chimie des Substances Naturelles Curated by ChEMBL					Assay Description In vitro activity against angiotensin I converting enzyme especially against Hip-His-Leu residues				J Med Chem 34: 663-9 (1991) BindingDB Entry DOI: 10.7270/Q21V5FKF
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50011364 (1-[2-(1-Carboxy-3-phenyl-propylamino)-acetyl]-pyrr...) Show SMILES OC(=O)[C@H](CCc1ccccc1)NCC(=O)N1CCC[C@H]1C(O)=O |r| Show InChI InChI=1S/C17H22N2O5/c20-15(19-10-4-7-14(19)17(23)24)11-18-13(16(21)22)9-8-12-5-2-1-3-6-12/h1-3,5-6,13-14,18H,4,7-11H2,(H,21,22)(H,23,24)/t13-,14-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	230	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Chimie des Substances Naturelles Curated by ChEMBL					Assay Description In vitro activity against angiotensin I converting enzyme especially against Hip-His-Leu residues				J Med Chem 34: 663-9 (1991) BindingDB Entry DOI: 10.7270/Q21V5FKF
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50011363 (1-[2-(1-Carboxy-butylamino)-propionyl]-octahydro-i...) Show SMILES CCCC(N[C@H](C)C(=O)N1C2CCCCC2CC1C(O)=O)C(O)=O Show InChI InChI=1S/C17H28N2O5/c1-3-6-12(16(21)22)18-10(2)15(20)19-13-8-5-4-7-11(13)9-14(19)17(23)24/h10-14,18H,3-9H2,1-2H3,(H,21,22)(H,23,24)/t10-,11?,12?,13?,14?/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Chimie des Substances Naturelles Curated by ChEMBL					Assay Description In vitro activity against angiotensin I converting enzyme especially against Hip-His-Leu residues				J Med Chem 34: 663-9 (1991) BindingDB Entry DOI: 10.7270/Q21V5FKF
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50011359 (1-[2-(1-Carboxy-3-phenyl-propylamino)-propionyl]-p...) Show SMILES C[C@@H](NC(CCc1ccccc1)C(O)=O)C(=O)N1CCCC1C(O)=O Show InChI InChI=1S/C18H24N2O5/c1-12(16(21)20-11-5-8-15(20)18(24)25)19-14(17(22)23)10-9-13-6-3-2-4-7-13/h2-4,6-7,12,14-15,19H,5,8-11H2,1H3,(H,22,23)(H,24,25)/t12-,14?,15?/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Chimie des Substances Naturelles Curated by ChEMBL					Assay Description In vitro activity against angiotensin I converting enzyme especially against Hip-His-Leu residues				J Med Chem 34: 663-9 (1991) BindingDB Entry DOI: 10.7270/Q21V5FKF
					More data for this Ligand-Target Pair