Compile Data Set for Download or QSAR

Found 89 hits with Last Name = 'martin' and Initial = 'dl'   

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
Renin (Homo sapiens (Human))	BDBM50014078 (A-62198 | CHEMBL291591 | N-{(S)-1-[(S)-1-((1S,2R,3...) Show SMILES CC(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CN=[N+]=[N-] Show InChI InChI=1S/C30H44N8O5/c1-19(2)28(41)36-24(14-21-11-7-4-8-12-21)29(42)37-25(15-22-16-32-18-33-22)30(43)35-23(13-20-9-5-3-6-10-20)27(40)26(39)17-34-38-31/h4,7-8,11-12,16,18-20,23-27,39-40H,3,5-6,9-10,13-15,17H2,1-2H3,(H,32,33)(H,35,43)(H,36,41)(H,37,42)/t23-,24-,25-,26-,27+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.290	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014084 ((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOCOCCOC)Cc1ccccc1 Show InChI InChI=1S/C38H58N6O9/c1-4-44-24-33(53-38(44)49)35(46)31(20-28-13-9-6-10-14-28)41-37(48)32(22-30-23-39-25-40-30)42-36(47)29(19-27-11-7-5-8-12-27)21-34(45)43(2)15-16-51-26-52-18-17-50-3/h5,7-8,11-12,23,25,28-29,31-33,35,46H,4,6,9-10,13-22,24,26H2,1-3H3,(H,39,40)(H,41,48)(H,42,47)/t29-,31+,32+,33+,35-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.330	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014084 ((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOCOCCOC)Cc1ccccc1 Show InChI InChI=1S/C38H58N6O9/c1-4-44-24-33(53-38(44)49)35(46)31(20-28-13-9-6-10-14-28)41-37(48)32(22-30-23-39-25-40-30)42-36(47)29(19-27-11-7-5-8-12-27)21-34(45)43(2)15-16-51-26-52-18-17-50-3/h5,7-8,11-12,23,25,28-29,31-33,35,46H,4,6,9-10,13-22,24,26H2,1-3H3,(H,39,40)(H,41,48)(H,42,47)/t29-,31+,32+,33+,35-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.370	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014081 ((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOCOC)Cc1ccccc1 Show InChI InChI=1S/C36H54N6O8/c1-4-42-22-31(50-36(42)47)33(44)29(18-26-13-9-6-10-14-26)39-35(46)30(20-28-21-37-23-38-28)40-34(45)27(17-25-11-7-5-8-12-25)19-32(43)41(2)15-16-49-24-48-3/h5,7-8,11-12,21,23,26-27,29-31,33,44H,4,6,9-10,13-20,22,24H2,1-3H3,(H,37,38)(H,39,46)(H,40,45)/t27-,29+,30+,31+,33-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.490	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014084 ((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOCOCCOC)Cc1ccccc1 Show InChI InChI=1S/C38H58N6O9/c1-4-44-24-33(53-38(44)49)35(46)31(20-28-13-9-6-10-14-28)41-37(48)32(22-30-23-39-25-40-30)42-36(47)29(19-27-11-7-5-8-12-27)21-34(45)43(2)15-16-51-26-52-18-17-50-3/h5,7-8,11-12,23,25,28-29,31-33,35,46H,4,6,9-10,13-22,24,26H2,1-3H3,(H,39,40)(H,41,48)(H,42,47)/t29-,31+,32+,33+,35-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.570	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014073 ((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOC)Cc1ccccc1 Show InChI InChI=1S/C35H52N6O7/c1-4-41-22-30(48-35(41)46)32(43)28(18-25-13-9-6-10-14-25)38-34(45)29(20-27-21-36-23-37-27)39-33(44)26(17-24-11-7-5-8-12-24)19-31(42)40(2)15-16-47-3/h5,7-8,11-12,21,23,25-26,28-30,32,43H,4,6,9-10,13-20,22H2,1-3H3,(H,36,37)(H,38,45)(H,39,44)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.590	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011231 (2-Benzyl-N-{1-[1-cyclohexylmethyl-2-(3-ethyl-2-oxo...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H49N5O7S/c1-2-39-21-30(47-35(39)45)32(42)28(18-25-11-7-4-8-12-25)37-34(44)29(20-27-22-48-23-36-27)38-33(43)26(17-24-9-5-3-6-10-24)19-31(41)40-13-15-46-16-14-40/h3,5-6,9-10,22-23,25-26,28-30,32,42H,2,4,7-8,11-21H2,1H3,(H,37,44)(H,38,43)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.600	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Compound was evaluated for the inhibitory concentration against purified human renal renin at pH 6.5				J Med Chem 34: 469-71 (1991) BindingDB Entry DOI: 10.7270/Q2WD3ZH8
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014079 ((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCO)Cc1ccccc1 Show InChI InChI=1S/C34H50N6O7/c1-3-40-21-29(47-34(40)46)31(43)27(17-24-12-8-5-9-13-24)37-33(45)28(19-26-20-35-22-36-26)38-32(44)25(16-23-10-6-4-7-11-23)18-30(42)39(2)14-15-41/h4,6-7,10-11,20,22,24-25,27-29,31,41,43H,3,5,8-9,12-19,21H2,1-2H3,(H,35,36)(H,37,45)(H,38,44)/t25-,27+,28+,29+,31-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.850	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011228 ((R)-2-Benzyl-N-[(S)-1-[(1S,2R)-1-cyclohexylmethyl-...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H50N6O7/c1-2-40-22-30(48-35(40)46)32(43)28(18-25-11-7-4-8-12-25)38-34(45)29(20-27-21-36-23-37-27)39-33(44)26(17-24-9-5-3-6-10-24)19-31(42)41-13-15-47-16-14-41/h3,5-6,9-10,21,23,25-26,28-30,32,43H,2,4,7-8,11-20,22H2,1H3,(H,36,37)(H,38,45)(H,39,44)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.990	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Compound was evaluated for the inhibitory concentration against purified human renal renin at pH 6.5				J Med Chem 34: 469-71 (1991) BindingDB Entry DOI: 10.7270/Q2WD3ZH8
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011228 ((R)-2-Benzyl-N-[(S)-1-[(1S,2R)-1-cyclohexylmethyl-...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H50N6O7/c1-2-40-22-30(48-35(40)46)32(43)28(18-25-11-7-4-8-12-25)38-34(45)29(20-27-21-36-23-37-27)39-33(44)26(17-24-9-5-3-6-10-24)19-31(42)41-13-15-47-16-14-41/h3,5-6,9-10,21,23,25-26,28-30,32,43H,2,4,7-8,11-20,22H2,1H3,(H,36,37)(H,38,45)(H,39,44)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.990	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011229 (2-Benzyl-N-[1-[1-cyclohexylmethyl-2-(3-ethyl-2-oxo...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1ccn[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H50N6O7/c1-2-40-23-30(48-35(40)46)32(43)28(20-25-11-7-4-8-12-25)37-34(45)29(22-27-13-14-36-39-27)38-33(44)26(19-24-9-5-3-6-10-24)21-31(42)41-15-17-47-18-16-41/h3,5-6,9-10,13-14,25-26,28-30,32,43H,2,4,7-8,11-12,15-23H2,1H3,(H,36,39)(H,37,45)(H,38,44)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.10	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Compound was evaluated for the inhibitory concentration against purified human renal renin at pH 6.5				J Med Chem 34: 469-71 (1991) BindingDB Entry DOI: 10.7270/Q2WD3ZH8
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014081 ((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOCOC)Cc1ccccc1 Show InChI InChI=1S/C36H54N6O8/c1-4-42-22-31(50-36(42)47)33(44)29(18-26-13-9-6-10-14-26)39-35(46)30(20-28-21-37-23-38-28)40-34(45)27(17-25-11-7-5-8-12-25)19-32(43)41(2)15-16-49-24-48-3/h5,7-8,11-12,21,23,26-27,29-31,33,44H,4,6,9-10,13-20,22,24H2,1-3H3,(H,37,38)(H,39,46)(H,40,45)/t27-,29+,30+,31+,33-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.10	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011228 ((R)-2-Benzyl-N-[(S)-1-[(1S,2R)-1-cyclohexylmethyl-...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H50N6O7/c1-2-40-22-30(48-35(40)46)32(43)28(18-25-11-7-4-8-12-25)38-34(45)29(20-27-21-36-23-37-27)39-33(44)26(17-24-9-5-3-6-10-24)19-31(42)41-13-15-47-16-14-41/h3,5-6,9-10,21,23,25-26,28-30,32,43H,2,4,7-8,11-20,22H2,1H3,(H,36,37)(H,38,45)(H,39,44)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.30	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Compound was evaluated for the inhibitory concentration against human plasma renin at pH 7.4				J Med Chem 34: 469-71 (1991) BindingDB Entry DOI: 10.7270/Q2WD3ZH8
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011228 ((R)-2-Benzyl-N-[(S)-1-[(1S,2R)-1-cyclohexylmethyl-...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H50N6O7/c1-2-40-22-30(48-35(40)46)32(43)28(18-25-11-7-4-8-12-25)38-34(45)29(20-27-21-36-23-37-27)39-33(44)26(17-24-9-5-3-6-10-24)19-31(42)41-13-15-47-16-14-41/h3,5-6,9-10,21,23,25-26,28-30,32,43H,2,4,7-8,11-20,22H2,1H3,(H,36,37)(H,38,45)(H,39,44)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.30	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011228 ((R)-2-Benzyl-N-[(S)-1-[(1S,2R)-1-cyclohexylmethyl-...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H50N6O7/c1-2-40-22-30(48-35(40)46)32(43)28(18-25-11-7-4-8-12-25)38-34(45)29(20-27-21-36-23-37-27)39-33(44)26(17-24-9-5-3-6-10-24)19-31(42)41-13-15-47-16-14-41/h3,5-6,9-10,21,23,25-26,28-30,32,43H,2,4,7-8,11-20,22H2,1H3,(H,36,37)(H,38,45)(H,39,44)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.30	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014073 ((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOC)Cc1ccccc1 Show InChI InChI=1S/C35H52N6O7/c1-4-41-22-30(48-35(41)46)32(43)28(18-25-13-9-6-10-14-25)38-34(45)29(20-27-21-36-23-37-27)39-33(44)26(17-24-11-7-5-8-12-24)19-31(42)40(2)15-16-47-3/h5,7-8,11-12,21,23,25-26,28-30,32,43H,4,6,9-10,13-20,22H2,1-3H3,(H,36,37)(H,38,45)(H,39,44)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.5	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011227 (2-Benzyl-N-{1-[1-cyclohexylmethyl-2-(3-ethyl-2-oxo...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cccs1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C36H50N4O7S/c1-2-39-24-31(47-36(39)45)33(42)29(21-26-12-7-4-8-13-26)37-35(44)30(23-28-14-9-19-48-28)38-34(43)27(20-25-10-5-3-6-11-25)22-32(41)40-15-17-46-18-16-40/h3,5-6,9-11,14,19,26-27,29-31,33,42H,2,4,7-8,12-13,15-18,20-24H2,1H3,(H,37,44)(H,38,43)/t27-,29+,30+,31+,33-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.5	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Compound was evaluated for the inhibitory concentration against purified human renal renin at pH 6.5				J Med Chem 34: 469-71 (1991) BindingDB Entry DOI: 10.7270/Q2WD3ZH8
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022647 (2-Benzyl-N-[1-(1-cyclohexylmethyl-2,3-dihydroxy-5-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H53N5O6/c1-24(2)17-31(41)33(43)29(19-26-11-7-4-8-12-26)38-35(45)30(21-28-22-36-23-37-28)39-34(44)27(18-25-9-5-3-6-10-25)20-32(42)40-13-15-46-16-14-40/h3,5-6,9-10,22-24,26-27,29-31,33,41,43H,4,7-8,11-21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)/t27-,29+,30+,31+,33-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.60	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014071 ((R)-2-Benzyl-4-[(3R,4S)-3,4-bis-(2-methoxy-ethoxym...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1C[C@@H](OCOCCOC)[C@H](C1)OCOCCOC)Cc1ccccc1 Show InChI InChI=1S/C43H66N6O12/c1-4-48-26-38(61-43(48)54)40(51)34(20-31-13-9-6-10-14-31)46-42(53)35(22-33-23-44-27-45-33)47-41(52)32(19-30-11-7-5-8-12-30)21-39(50)49-24-36(59-28-57-17-15-55-2)37(25-49)60-29-58-18-16-56-3/h5,7-8,11-12,23,27,31-32,34-38,40,51H,4,6,9-10,13-22,24-26,28-29H2,1-3H3,(H,44,45)(H,46,53)(H,47,52)/t32-,34+,35+,36-,37+,38+,40-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.60	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014085 ((S)-N-[(S)-1-[(1S,2R)-1-Cyclohexylmethyl-2-((S)-3-...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N(C)CCOCOCCOC Show InChI InChI=1S/C38H59N7O10/c1-5-45-23-33(55-38(45)50)34(46)30(19-26-9-7-6-8-10-26)41-36(48)32(21-28-22-39-24-40-28)42-35(47)31(20-27-11-13-29(52-4)14-12-27)43-37(49)44(2)15-16-53-25-54-18-17-51-3/h11-14,22,24,26,30-34,46H,5-10,15-21,23,25H2,1-4H3,(H,39,40)(H,41,48)(H,42,47)(H,43,49)/t30-,31-,32-,33-,34+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.70	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014072 (CHEMBL58968 | N-[(S)-1-[(S)-1-[(1S,2R)-1-Cyclohexy...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)C(C)C Show InChI InChI=1S/C34H50N6O7/c1-5-40-19-29(47-34(40)45)30(41)26(15-22-9-7-6-8-10-22)37-33(44)28(17-24-18-35-20-36-24)39-32(43)27(38-31(42)21(2)3)16-23-11-13-25(46-4)14-12-23/h11-14,18,20-22,26-30,41H,5-10,15-17,19H2,1-4H3,(H,35,36)(H,37,44)(H,38,42)(H,39,43)/t26-,27-,28-,29-,30+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.70	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014079 ((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCO)Cc1ccccc1 Show InChI InChI=1S/C34H50N6O7/c1-3-40-21-29(47-34(40)46)31(43)27(17-24-12-8-5-9-13-24)37-33(45)28(19-26-20-35-22-36-26)38-32(44)25(16-23-10-6-4-7-11-23)18-30(42)39(2)14-15-41/h4,6-7,10-11,20,22,24-25,27-29,31,41,43H,3,5,8-9,12-19,21H2,1-2H3,(H,35,36)(H,37,45)(H,38,44)/t25-,27+,28+,29+,31-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.5	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014083 ((R)-2-Benzyl-4-((3R,4S)-3,4-bis-methoxymethoxy-pyr...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1C[C@@H](OCOC)[C@H](C1)OCOC)Cc1ccccc1 Show InChI InChI=1S/C39H58N6O10/c1-4-44-22-34(55-39(44)50)36(47)30(16-27-13-9-6-10-14-27)42-38(49)31(18-29-19-40-23-41-29)43-37(48)28(15-26-11-7-5-8-12-26)17-35(46)45-20-32(53-24-51-2)33(21-45)54-25-52-3/h5,7-8,11-12,19,23,27-28,30-34,36,47H,4,6,9-10,13-18,20-22,24-25H2,1-3H3,(H,40,41)(H,42,49)(H,43,48)/t28-,30+,31+,32-,33+,34+,36-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.70	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046785 (2-Benzyl-N-[1-(1-cyclohexylmethyl-2,3-dihydroxy-5-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1ccn[nH]1)NC(=O)[C@@H](CC(=O)N1CCN(C)CC1)Cc1ccccc1 Show InChI InChI=1S/C36H56N6O5/c1-25(2)20-32(43)34(45)30(22-27-12-8-5-9-13-27)38-36(47)31(24-29-14-15-37-40-29)39-35(46)28(21-26-10-6-4-7-11-26)23-33(44)42-18-16-41(3)17-19-42/h4,6-7,10-11,14-15,25,27-28,30-32,34,43,45H,5,8-9,12-13,16-24H2,1-3H3,(H,37,40)(H,38,47)(H,39,46)/t28-,30+,31+,32+,34-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.80	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014077 (CHEMBL61777 | Morpholine-4-carboxylic acid [(S)-1-...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C35H51N7O8/c1-3-41-21-30(50-35(41)47)31(43)27(17-23-7-5-4-6-8-23)38-33(45)29(19-25-20-36-22-37-25)39-32(44)28(18-24-9-11-26(48-2)12-10-24)40-34(46)42-13-15-49-16-14-42/h9-12,20,22-23,27-31,43H,3-8,13-19,21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)(H,40,46)/t27-,28-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.40	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046781 (2-Benzyl-N-[1-(1-cyclohexylmethyl-2,3-dihydroxy-5-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1ccn[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H53N5O6/c1-24(2)19-31(41)33(43)29(21-26-11-7-4-8-12-26)37-35(45)30(23-28-13-14-36-39-28)38-34(44)27(20-25-9-5-3-6-10-25)22-32(42)40-15-17-46-18-16-40/h3,5-6,9-10,13-14,24,26-27,29-31,33,41,43H,4,7-8,11-12,15-23H2,1-2H3,(H,36,39)(H,37,45)(H,38,44)/t27-,29+,30+,31+,33-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.5	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014080 ((S)-N-[(S)-1-[(1S,2R)-1-Cyclohexylmethyl-2-((S)-3-...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N(C)CCOCOC Show InChI InChI=1S/C36H55N7O9/c1-5-43-21-31(52-36(43)48)32(44)28(17-24-9-7-6-8-10-24)39-34(46)30(19-26-20-37-22-38-26)40-33(45)29(18-25-11-13-27(50-4)14-12-25)41-35(47)42(2)15-16-51-23-49-3/h11-14,20,22,24,28-32,44H,5-10,15-19,21,23H2,1-4H3,(H,37,38)(H,39,46)(H,40,45)(H,41,47)/t28-,29-,30-,31-,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4.60	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046786 (2-Benzyl-N-[1-(1-cyclohexylmethyl-2,3-dihydroxy-5-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCN(C)CC1)Cc1ccccc1 Show InChI InChI=1S/C36H56N6O5/c1-25(2)18-32(43)34(45)30(20-27-12-8-5-9-13-27)39-36(47)31(22-29-23-37-24-38-29)40-35(46)28(19-26-10-6-4-7-11-26)21-33(44)42-16-14-41(3)15-17-42/h4,6-7,10-11,23-25,27-28,30-32,34,43,45H,5,8-9,12-22H2,1-3H3,(H,37,38)(H,39,47)(H,40,46)/t28-,30+,31+,32+,34-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.40	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014075 ((3R,4S)-3,4-Dihydroxy-pyrrolidine-1-carboxylic aci...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1C[C@H](O)[C@H](O)C1 Show InChI InChI=1S/C35H51N7O9/c1-3-41-19-30(51-35(41)49)31(45)25(13-21-7-5-4-6-8-21)38-33(47)27(15-23-16-36-20-37-23)39-32(46)26(14-22-9-11-24(50-2)12-10-22)40-34(48)42-17-28(43)29(44)18-42/h9-12,16,20-21,25-31,43-45H,3-8,13-15,17-19H2,1-2H3,(H,36,37)(H,38,47)(H,39,46)(H,40,48)/t25-,26-,27-,28-,29+,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	6.90	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014071 ((R)-2-Benzyl-4-[(3R,4S)-3,4-bis-(2-methoxy-ethoxym...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1C[C@@H](OCOCCOC)[C@H](C1)OCOCCOC)Cc1ccccc1 Show InChI InChI=1S/C43H66N6O12/c1-4-48-26-38(61-43(48)54)40(51)34(20-31-13-9-6-10-14-31)46-42(53)35(22-33-23-44-27-45-33)47-41(52)32(19-30-11-7-5-8-12-30)21-39(50)49-24-36(59-28-57-17-15-55-2)37(25-49)60-29-58-18-16-56-3/h5,7-8,11-12,23,27,31-32,34-38,40,51H,4,6,9-10,13-22,24-26,28-29H2,1-3H3,(H,44,45)(H,46,53)(H,47,52)/t32-,34+,35+,36-,37+,38+,40-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.30	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011230 (2-Benzyl-N-[1-[1-cyclohexylmethyl-2-(3-ethyl-2-oxo...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cn(C)cn1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C36H52N6O7/c1-3-41-23-31(49-36(41)47)33(44)29(19-26-12-8-5-9-13-26)38-35(46)30(21-28-22-40(2)24-37-28)39-34(45)27(18-25-10-6-4-7-11-25)20-32(43)42-14-16-48-17-15-42/h4,6-7,10-11,22,24,26-27,29-31,33,44H,3,5,8-9,12-21,23H2,1-2H3,(H,38,46)(H,39,45)/t27-,29+,30+,31+,33-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.40	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Compound was evaluated for the inhibitory concentration against purified human renal renin at pH 6.5				J Med Chem 34: 469-71 (1991) BindingDB Entry DOI: 10.7270/Q2WD3ZH8
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011230 (2-Benzyl-N-[1-[1-cyclohexylmethyl-2-(3-ethyl-2-oxo...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cn(C)cn1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C36H52N6O7/c1-3-41-23-31(49-36(41)47)33(44)29(19-26-12-8-5-9-13-26)38-35(46)30(21-28-22-40(2)24-37-28)39-34(45)27(18-25-10-6-4-7-11-25)20-32(43)42-14-16-48-17-15-42/h4,6-7,10-11,22,24,26-27,29-31,33,44H,3,5,8-9,12-21,23H2,1-2H3,(H,38,46)(H,39,45)/t27-,29+,30+,31+,33-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.40	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Compound was evaluated for the inhibitory concentration against human plasma renin at pH 7.4				J Med Chem 34: 469-71 (1991) BindingDB Entry DOI: 10.7270/Q2WD3ZH8
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014082 ((S)-N-[(S)-1-[(1S,2R)-1-Cyclohexylmethyl-2-((S)-3-...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N(C)CC(O)CO Show InChI InChI=1S/C35H53N7O9/c1-4-42-19-30(51-35(42)49)31(45)27(14-22-8-6-5-7-9-22)38-33(47)29(16-24-17-36-21-37-24)39-32(46)28(15-23-10-12-26(50-3)13-11-23)40-34(48)41(2)18-25(44)20-43/h10-13,17,21-22,25,27-31,43-45H,4-9,14-16,18-20H2,1-3H3,(H,36,37)(H,38,47)(H,39,46)(H,40,48)/t25?,27-,28-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.90	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011231 (2-Benzyl-N-{1-[1-cyclohexylmethyl-2-(3-ethyl-2-oxo...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H49N5O7S/c1-2-39-21-30(47-35(39)45)32(42)28(18-25-11-7-4-8-12-25)37-34(44)29(20-27-22-48-23-36-27)38-33(43)26(17-24-9-5-3-6-10-24)19-31(41)40-13-15-46-16-14-40/h3,5-6,9-10,22-23,25-26,28-30,32,42H,2,4,7-8,11-21H2,1H3,(H,37,44)(H,38,43)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.10	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Compound was evaluated for the inhibitory concentration against human plasma renin at pH 7.4				J Med Chem 34: 469-71 (1991) BindingDB Entry DOI: 10.7270/Q2WD3ZH8
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011231 (2-Benzyl-N-{1-[1-cyclohexylmethyl-2-(3-ethyl-2-oxo...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H49N5O7S/c1-2-39-21-30(47-35(39)45)32(42)28(18-25-11-7-4-8-12-25)37-34(44)29(20-27-22-48-23-36-27)38-33(43)26(17-24-9-5-3-6-10-24)19-31(41)40-13-15-46-16-14-40/h3,5-6,9-10,22-23,25-26,28-30,32,42H,2,4,7-8,11-21H2,1H3,(H,37,44)(H,38,43)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.10	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006122 (2-Benzyl-N-[1-(1-cyclohexylmethyl-2,3-dihydroxy-5-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H52N4O6S/c1-24(2)17-31(40)33(42)29(19-26-11-7-4-8-12-26)37-35(44)30(21-28-22-46-23-36-28)38-34(43)27(18-25-9-5-3-6-10-25)20-32(41)39-13-15-45-16-14-39/h3,5-6,9-10,22-24,26-27,29-31,33,40,42H,4,7-8,11-21H2,1-2H3,(H,37,44)(H,38,43)/t27-,29+,30+,31+,33-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.30	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014076 ((3R,4S)-3,4-Bis-(2-methoxy-ethoxymethoxy)-pyrrolid...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1C[C@@H](OCOCCOC)[C@H](C1)OCOCCOC Show InChI InChI=1S/C43H67N7O13/c1-5-49-25-38(63-43(49)55)39(51)33(19-29-9-7-6-8-10-29)46-41(53)35(21-31-22-44-26-45-31)47-40(52)34(20-30-11-13-32(58-4)14-12-30)48-42(54)50-23-36(61-27-59-17-15-56-2)37(24-50)62-28-60-18-16-57-3/h11-14,22,26,29,33-39,51H,5-10,15-21,23-25,27-28H2,1-4H3,(H,44,45)(H,46,53)(H,47,52)(H,48,54)/t33-,34-,35-,36-,37+,38-,39+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.5	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014075 ((3R,4S)-3,4-Dihydroxy-pyrrolidine-1-carboxylic aci...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1C[C@H](O)[C@H](O)C1 Show InChI InChI=1S/C35H51N7O9/c1-3-41-19-30(51-35(41)49)31(45)25(13-21-7-5-4-6-8-21)38-33(47)27(15-23-16-36-20-37-23)39-32(46)26(14-22-9-11-24(50-2)12-10-22)40-34(48)42-17-28(43)29(44)18-42/h9-12,16,20-21,25-31,43-45H,3-8,13-15,17-19H2,1-2H3,(H,36,37)(H,38,47)(H,39,46)(H,40,48)/t25-,26-,27-,28-,29+,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.70	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014077 (CHEMBL61777 | Morpholine-4-carboxylic acid [(S)-1-...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C35H51N7O8/c1-3-41-21-30(50-35(41)47)31(43)27(17-23-7-5-4-6-8-23)38-33(45)29(19-25-20-36-22-37-25)39-32(44)28(18-24-9-11-26(48-2)12-10-24)40-34(46)42-13-15-49-16-14-42/h9-12,20,22-23,27-31,43H,3-8,13-19,21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)(H,40,46)/t27-,28-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	9.60	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014072 (CHEMBL58968 | N-[(S)-1-[(S)-1-[(1S,2R)-1-Cyclohexy...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)C(C)C Show InChI InChI=1S/C34H50N6O7/c1-5-40-19-29(47-34(40)45)30(41)26(15-22-9-7-6-8-10-22)37-33(44)28(17-24-18-35-20-36-24)39-32(43)27(38-31(42)21(2)3)16-23-11-13-25(46-4)14-12-23/h11-14,18,20-22,26-30,41H,5-10,15-17,19H2,1-4H3,(H,35,36)(H,37,44)(H,38,42)(H,39,43)/t26-,27-,28-,29-,30+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	9.90	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046782 (CHEMBL341744 | N-[2-Azido-1-(1-cyclohexylmethyl-2,...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](CN=[N+]=[N-])NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C32H50N6O6/c1-22(2)17-28(39)30(41)26(19-24-11-7-4-8-12-24)35-32(43)27(21-34-37-33)36-31(42)25(18-23-9-5-3-6-10-23)20-29(40)38-13-15-44-16-14-38/h3,5-6,9-10,22,24-28,30,39,41H,4,7-8,11-21H2,1-2H3,(H,35,43)(H,36,42)/t25-,26+,27+,28+,30-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014083 ((R)-2-Benzyl-4-((3R,4S)-3,4-bis-methoxymethoxy-pyr...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1C[C@@H](OCOC)[C@H](C1)OCOC)Cc1ccccc1 Show InChI InChI=1S/C39H58N6O10/c1-4-44-22-34(55-39(44)50)36(47)30(16-27-13-9-6-10-14-27)42-38(49)31(18-29-19-40-23-41-29)43-37(48)28(15-26-11-7-5-8-12-26)17-35(46)45-20-32(53-24-51-2)33(21-45)54-25-52-3/h5,7-8,11-12,19,23,27-28,30-34,36,47H,4,6,9-10,13-18,20-22,24-25H2,1-3H3,(H,40,41)(H,42,49)(H,43,48)/t28-,30+,31+,32-,33+,34+,36-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014074 ((3R,4S)-3,4-Bis-methoxymethoxy-pyrrolidine-1-carbo...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1C[C@@H](OCOC)[C@H](C1)OCOC Show InChI InChI=1S/C39H59N7O11/c1-5-45-21-34(57-39(45)51)35(47)29(15-25-9-7-6-8-10-25)42-37(49)31(17-27-18-40-22-41-27)43-36(48)30(16-26-11-13-28(54-4)14-12-26)44-38(50)46-19-32(55-23-52-2)33(20-46)56-24-53-3/h11-14,18,22,25,29-35,47H,5-10,15-17,19-21,23-24H2,1-4H3,(H,40,41)(H,42,49)(H,43,48)(H,44,50)/t29-,30-,31-,32-,33+,34-,35+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	12	n/a	n/a	n/a	n/a	6.5	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against purified human renal renin at pH 6.5				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014085 ((S)-N-[(S)-1-[(1S,2R)-1-Cyclohexylmethyl-2-((S)-3-...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N(C)CCOCOCCOC Show InChI InChI=1S/C38H59N7O10/c1-5-45-23-33(55-38(45)50)34(46)30(19-26-9-7-6-8-10-26)41-36(48)32(21-28-22-39-24-40-28)42-35(47)31(20-27-11-13-29(52-4)14-12-27)43-37(49)44(2)15-16-53-25-54-18-17-51-3/h11-14,22,24,26,30-34,46H,5-10,15-21,23,25H2,1-4H3,(H,39,40)(H,41,48)(H,42,47)(H,43,49)/t30-,31-,32-,33-,34+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006202 (3-Amino-N-[1-[1-(1-cyclohexylmethyl-2,3-dihydroxy-...) Show SMILES COc1ccc(C[C@H](NC(=O)CC(C)(C)N)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N[C@@H](CC2CCCCC2)[C@@H](O)[C@@H](O)CC(C)C)cc1 Show InChI InChI=1S/C35H56N6O6/c1-22(2)15-30(42)32(44)27(16-23-9-7-6-8-10-23)40-34(46)29(18-25-20-37-21-38-25)41-33(45)28(39-31(43)19-35(3,4)36)17-24-11-13-26(47-5)14-12-24/h11-14,20-23,27-30,32,42,44H,6-10,15-19,36H2,1-5H3,(H,37,38)(H,39,43)(H,40,46)(H,41,45)/t27-,28-,29-,30-,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006202 (3-Amino-N-[1-[1-(1-cyclohexylmethyl-2,3-dihydroxy-...) Show SMILES COc1ccc(C[C@H](NC(=O)CC(C)(C)N)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N[C@@H](CC2CCCCC2)[C@@H](O)[C@@H](O)CC(C)C)cc1 Show InChI InChI=1S/C35H56N6O6/c1-22(2)15-30(42)32(44)27(16-23-9-7-6-8-10-23)40-34(46)29(18-25-20-37-21-38-25)41-33(45)28(39-31(43)19-35(3,4)36)17-24-11-13-26(47-5)14-12-24/h11-14,20-23,27-30,32,42,44H,6-10,15-19,36H2,1-5H3,(H,37,38)(H,39,43)(H,40,46)(H,41,45)/t27-,28-,29-,30-,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human plasma renin at pH 7.4				J Med Chem 33: 1962-9 (1990) BindingDB Entry DOI: 10.7270/Q2KW5GN2
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046773 (3-Amino-N-[1-[1-[1-cyclohexylmethyl-2-(3-ethyl-2-o...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)CC(C)(C)N Show InChI InChI=1S/C35H53N7O7/c1-5-42-20-29(49-34(42)47)31(44)26(15-22-9-7-6-8-10-22)40-33(46)28(17-24-19-37-21-38-24)41-32(45)27(39-30(43)18-35(2,3)36)16-23-11-13-25(48-4)14-12-23/h11-14,19,21-22,26-29,31,44H,5-10,15-18,20,36H2,1-4H3,(H,37,38)(H,39,43)(H,40,46)(H,41,45)/t26-,27-,28-,29-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046774 (2-Benzyl-N-[1-(1-cyclohexylmethyl-2,3-dihydroxy-5-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cn1cccn1)NC(=O)[C@@H](CC(=O)N1CCN(C)CC1)Cc1ccccc1 Show InChI InChI=1S/C36H56N6O5/c1-26(2)21-32(43)34(45)30(23-28-13-8-5-9-14-28)38-36(47)31(25-42-16-10-15-37-42)39-35(46)29(22-27-11-6-4-7-12-27)24-33(44)41-19-17-40(3)18-20-41/h4,6-7,10-12,15-16,26,28-32,34,43,45H,5,8-9,13-14,17-25H2,1-3H3,(H,38,47)(H,39,46)/t29-,30+,31+,32+,34-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	18	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046776 (2-Benzyl-N-[1-(1-cyclohexylmethyl-2,3-dihydroxy-5-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@@H](CC(=O)N1CCN(C)CC1)Cc1ccccc1 Show InChI InChI=1S/C36H55N5O5S/c1-25(2)18-32(42)34(44)30(20-27-12-8-5-9-13-27)38-36(46)31(22-29-23-47-24-37-29)39-35(45)28(19-26-10-6-4-7-11-26)21-33(43)41-16-14-40(3)15-17-41/h4,6-7,10-11,23-25,27-28,30-32,34,42,44H,5,8-9,12-22H2,1-3H3,(H,38,46)(H,39,45)/t28-,30+,31+,32+,34-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	18	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50011229 (2-Benzyl-N-[1-[1-cyclohexylmethyl-2-(3-ethyl-2-oxo...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1ccn[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H50N6O7/c1-2-40-23-30(48-35(40)46)32(43)28(20-25-11-7-4-8-12-25)37-34(45)29(22-27-13-14-36-39-27)38-33(44)26(19-24-9-5-3-6-10-24)21-31(42)41-15-17-47-18-16-41/h3,5-6,9-10,13-14,25-26,28-30,32,43H,2,4,7-8,11-12,15-23H2,1H3,(H,36,39)(H,37,45)(H,38,44)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	21	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Compound was evaluated for the inhibitory concentration against human plasma renin at pH 7.4				J Med Chem 34: 469-71 (1991) BindingDB Entry DOI: 10.7270/Q2WD3ZH8
					More data for this Ligand-Target Pair

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