Compile Data Set for Download or QSAR

Found 648 hits with Last Name = 'stein' and Initial = 'hh'   

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))	BDBM50046798 (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](Cc1ccccc1)CS(=O)(=O)N1CCN(C)CC1 |r| Show InChI InChI=1S/C35H55N5O6S2/c1-25(2)18-32(41)33(42)30(20-27-12-8-5-9-13-27)37-35(44)31(21-29-22-47-24-36-29)38-34(43)28(19-26-10-6-4-7-11-26)23-48(45,46)40-16-14-39(3)15-17-40/h4,6-7,10-11,22,24-25,27-28,30-33,41-42H,5,8-9,12-21,23H2,1-3H3,(H,37,44)(H,38,43)/t28-,30+,31+,32+,33-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	0.240	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro inhibitory concentration against monkey plasma renin at pH 7.4				J Med Chem 36: 460-7 (1993) BindingDB Entry DOI: 10.7270/Q2VT1R5C
					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	0.290	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022646 (CHEMBL307917 | Morpholine-4-carboxylic acid {1-[1-...) 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](CCc1ccccc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C35H54N6O6/c1-24(2)19-31(42)32(43)29(20-26-11-7-4-8-12-26)38-34(45)30(21-27-22-36-23-37-27)39-33(44)28(14-13-25-9-5-3-6-10-25)40-35(46)41-15-17-47-18-16-41/h3,5-6,9-10,22-24,26,28-32,42-43H,4,7-8,11-21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)(H,40,46)/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	0.300	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014049 (CHEMBL287953 | {1-[1-[1-Cyclohexylmethyl-2-hydroxy...) Show SMILES C[C@H]1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C34H49N5O7/c1-21-15-28(45-32(21)43)29(40)25(16-22-11-7-5-8-12-22)37-31(42)27(18-24-19-35-20-36-24)38-30(41)26(17-23-13-9-6-10-14-23)39-33(44)46-34(2,3)4/h6,9-10,13-14,19-22,25-29,40H,5,7-8,11-12,15-18H2,1-4H3,(H,35,36)(H,37,42)(H,38,41)(H,39,44)/t21-,25-,26-,27-,28-,29+/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	0.320	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro inhibition of human plasma renin.				J Med Chem 33: 1582-90 (1990) BindingDB Entry DOI: 10.7270/Q2NK3D0G
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022650 (CHEMBL75117 | Morpholine-4-carboxylic acid {1-[1-(...) 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](Cc1ccccc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C34H52N6O6/c1-23(2)17-30(41)31(42)27(18-24-9-5-3-6-10-24)37-33(44)29(20-26-21-35-22-36-26)38-32(43)28(19-25-11-7-4-8-12-25)39-34(45)40-13-15-46-16-14-40/h4,7-8,11-12,21-24,27-31,41-42H,3,5-6,9-10,13-20H2,1-2H3,(H,35,36)(H,37,44)(H,38,43)(H,39,45)/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	0.350	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					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	0.360	n/a	n/a	n/a	n/a	6.0	n/a
University of Texas Curated by ChEMBL					Assay Description In vitro inhibition of purified human renin at a pH of 6.0.				J Med Chem 35: 1710-21 (1992) BindingDB Entry DOI: 10.7270/Q2GT5M4C
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50280221 ((1S,2S,3R)-2-Phenyl-3-(propane-2-sulfonyl)-cyclopr...) Show SMILES CCCC[C@H](NC(=O)[C@@H]1[C@H]([C@H]1S(=O)(=O)C(C)C)c1ccccc1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CC(C)C Show InChI InChI=1S/C33H54N2O6S/c1-6-7-18-25(32(38)35-26(20-23-14-10-8-11-15-23)30(37)27(36)19-21(2)3)34-33(39)29-28(24-16-12-9-13-17-24)31(29)42(40,41)22(4)5/h9,12-13,16-17,21-23,25-31,36-37H,6-8,10-11,14-15,18-20H2,1-5H3,(H,34,39)(H,35,38)/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	Article	n/a	n/a	0.370	n/a	n/a	n/a	n/a	6.0	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of human plasma renin at PH 7.4				Bioorg Med Chem Lett 2: 1405-1410 (1992) Article DOI: 10.1016/S0960-894X(00)80522-3 BindingDB Entry DOI: 10.7270/Q2VD6ZBV
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50280229 ((1S,2S,3R)-2-Phenyl-3-(propane-2-sulfonyl)-cyclopr...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@@H]1[C@H]([C@H]1S(=O)(=O)C(C)C)c1ccccc1 Show InChI InChI=1S/C33H49N3O6S2/c1-20(2)15-27(37)30(38)25(16-22-11-7-5-8-12-22)35-32(39)26(17-24-18-43-19-34-24)36-33(40)29-28(23-13-9-6-10-14-23)31(29)44(41,42)21(3)4/h6,9-10,13-14,18-22,25-31,37-38H,5,7-8,11-12,15-17H2,1-4H3,(H,35,39)(H,36,40)/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	Article	n/a	n/a	0.380	n/a	n/a	n/a	n/a	6.0	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of purified human renin at PH 6.0				Bioorg Med Chem Lett 2: 1405-1410 (1992) Article DOI: 10.1016/S0960-894X(00)80522-3 BindingDB Entry DOI: 10.7270/Q2VD6ZBV
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014052 (CHEMBL445350 | {1-[1-(4-Azido-1-cyclohexylmethyl-2...) Show SMILES CC(C)(C)OC(=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/C31H46N8O6/c1-31(2,3)45-30(44)38-24(15-21-12-8-5-9-13-21)28(42)37-25(16-22-17-33-19-34-22)29(43)36-23(14-20-10-6-4-7-11-20)27(41)26(40)18-35-39-32/h5,8-9,12-13,17,19-20,23-27,40-41H,4,6-7,10-11,14-16,18H2,1-3H3,(H,33,34)(H,36,43)(H,37,42)(H,38,44)/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	0.400	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro inhibition of purified human renal renin.				J Med Chem 33: 1582-90 (1990) BindingDB Entry DOI: 10.7270/Q2NK3D0G
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022643 (4-Hydroxy-piperidine-1-carboxylic acid {1-[1-(1-cy...) 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](Cc1ccccc1)NC(=O)N1CCC(O)CC1 Show InChI InChI=1S/C35H54N6O6/c1-23(2)17-31(43)32(44)28(18-24-9-5-3-6-10-24)38-34(46)30(20-26-21-36-22-37-26)39-33(45)29(19-25-11-7-4-8-12-25)40-35(47)41-15-13-27(42)14-16-41/h4,7-8,11-12,21-24,27-32,42-44H,3,5-6,9-10,13-20H2,1-2H3,(H,36,37)(H,38,46)(H,39,45)(H,40,47)/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	0.420	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006125 (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(Cc1ccccc1)Cc1ccccc1 Show InChI InChI=1S/C36H49N3O4S/c1-25(2)18-33(40)34(41)31(21-28-16-10-5-11-17-28)38-36(43)32(22-30-23-44-24-37-30)39-35(42)29(19-26-12-6-3-7-13-26)20-27-14-8-4-9-15-27/h3-4,6-9,12-15,23-25,28-29,31-34,40-41H,5,10-11,16-22H2,1-2H3,(H,38,43)(H,39,42)/t31-,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	0.470	n/a	n/a	n/a	n/a	6.0	n/a
University of Texas Curated by ChEMBL					Assay Description In vitro inhibition of purified human renin at a pH of 6.0.				J Med Chem 35: 1710-21 (1992) BindingDB Entry DOI: 10.7270/Q2GT5M4C
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50280237 ((1S,2R,3S)-2-(2-Methoxymethoxy-ethanesulfonyl)-3-p...) Show SMILES COCOCCS(=O)(=O)[C@H]1[C@@H]([C@H]1c1ccccc1)C(=O)N[C@@H](Cc1cscn1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CC(C)C Show InChI InChI=1S/C34H51N3O8S2/c1-22(2)16-28(38)31(39)26(17-23-10-6-4-7-11-23)36-33(40)27(18-25-19-46-20-35-25)37-34(41)30-29(24-12-8-5-9-13-24)32(30)47(42,43)15-14-45-21-44-3/h5,8-9,12-13,19-20,22-23,26-32,38-39H,4,6-7,10-11,14-18,21H2,1-3H3,(H,36,40)(H,37,41)/t26-,27-,28-,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	Article	n/a	n/a	0.480	n/a	n/a	n/a	n/a	6.0	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of purified human renin at PH 6.0				Bioorg Med Chem Lett 2: 1405-1410 (1992) Article DOI: 10.1016/S0960-894X(00)80522-3 BindingDB Entry DOI: 10.7270/Q2VD6ZBV
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022649 (CHEMBL76458 | N-[1-(1-Cyclohexylmethyl-2,3-dihydro...) 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](Cc1ccccc1)NC(=O)N(C)C Show InChI InChI=1S/C32H50N6O5/c1-21(2)15-28(39)29(40)25(16-22-11-7-5-8-12-22)35-31(42)27(18-24-19-33-20-34-24)36-30(41)26(37-32(43)38(3)4)17-23-13-9-6-10-14-23/h6,9-10,13-14,19-22,25-29,39-40H,5,7-8,11-12,15-18H2,1-4H3,(H,33,34)(H,35,42)(H,36,41)(H,37,43)/t25-,26-,27-,28-,29+/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	0.5	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022645 (CHEMBL75510 | N-[1-(1-Cyclohexylmethyl-2,3-dihydro...) 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](Cc1ccccc1)NC(=O)N(C)CCO Show InChI InChI=1S/C33H52N6O6/c1-22(2)16-29(41)30(42)26(17-23-10-6-4-7-11-23)36-32(44)28(19-25-20-34-21-35-25)37-31(43)27(18-24-12-8-5-9-13-24)38-33(45)39(3)14-15-40/h5,8-9,12-13,20-23,26-30,40-42H,4,6-7,10-11,14-19H2,1-3H3,(H,34,35)(H,36,44)(H,37,43)(H,38,45)/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	0.550	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022651 (CHEMBL306274 | Morpholine-4-carboxylic acid {1-[1-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)C(Cc1ccccc1)=NC(=O)N1CCOCC1 |w:37.40| Show InChI InChI=1S/C34H50N6O6/c1-23(2)17-30(41)31(42)27(18-24-9-5-3-6-10-24)37-33(44)29(20-26-21-35-22-36-26)38-32(43)28(19-25-11-7-4-8-12-25)39-34(45)40-13-15-46-16-14-40/h4,7-8,11-12,21-24,27,29-31,41-42H,3,5-6,9-10,13-20H2,1-2H3,(H,35,36)(H,37,44)(H,38,43)/t27-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	0.580	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50280235 ((1S,2S,3R)-2-Phenyl-3-(propane-2-sulfonyl)-cyclopr...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1[C@H]([C@H]1S(=O)(=O)C(C)C)c1ccccc1 Show InChI InChI=1S/C33H54N2O6S/c1-20(2)17-26(32(38)34-25(19-23-13-9-7-10-14-23)30(37)27(36)18-21(3)4)35-33(39)29-28(24-15-11-8-12-16-24)31(29)42(40,41)22(5)6/h8,11-12,15-16,20-23,25-31,36-37H,7,9-10,13-14,17-19H2,1-6H3,(H,34,38)(H,35,39)/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	Article	n/a	n/a	0.590	n/a	n/a	n/a	n/a	6.0	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of purified human renin at PH 6.0				Bioorg Med Chem Lett 2: 1405-1410 (1992) Article DOI: 10.1016/S0960-894X(00)80522-3 BindingDB Entry DOI: 10.7270/Q2VD6ZBV
					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))	BDBM50280224 ((1S,2R,3S)-2-Methanesulfonyl-3-phenyl-cyclopropane...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@@H]1[C@H]([C@H]1S(C)(=O)=O)c1ccccc1 Show InChI InChI=1S/C31H45N3O6S2/c1-19(2)14-25(35)28(36)23(15-20-10-6-4-7-11-20)33-30(37)24(16-22-17-41-18-32-22)34-31(38)27-26(29(27)42(3,39)40)21-12-8-5-9-13-21/h5,8-9,12-13,17-20,23-29,35-36H,4,6-7,10-11,14-16H2,1-3H3,(H,33,37)(H,34,38)/t23-,24-,25-,26+,27+,28+,29+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.630	n/a	n/a	n/a	n/a	6.0	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of purified human renin at PH 6.0				Bioorg Med Chem Lett 2: 1405-1410 (1992) Article DOI: 10.1016/S0960-894X(00)80522-3 BindingDB Entry DOI: 10.7270/Q2VD6ZBV
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014059 (CHEMBL38954 | {1-[1-[1-Cyclohexylmethyl-2-(3-ethyl...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C34H50N6O7/c1-5-40-20-28(46-33(40)45)29(41)25(16-22-12-8-6-9-13-22)37-31(43)27(18-24-19-35-21-36-24)38-30(42)26(17-23-14-10-7-11-15-23)39-32(44)47-34(2,3)4/h7,10-11,14-15,19,21-22,25-29,41H,5-6,8-9,12-13,16-18,20H2,1-4H3,(H,35,36)(H,37,43)(H,38,42)(H,39,44)/t25-,26-,27-,28-,29+/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	0.630	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro inhibition of human plasma renin.				J Med Chem 33: 1582-90 (1990) BindingDB Entry DOI: 10.7270/Q2NK3D0G
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50280222 ((1S,2R,3S)-2-Ethenesulfonyl-3-phenyl-cyclopropanec...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@@H]1[C@H]([C@H]1S(=O)(=O)C=C)c1ccccc1 Show InChI InChI=1S/C32H45N3O6S2/c1-4-43(40,41)30-27(22-13-9-6-10-14-22)28(30)32(39)35-25(17-23-18-42-19-33-23)31(38)34-24(16-21-11-7-5-8-12-21)29(37)26(36)15-20(2)3/h4,6,9-10,13-14,18-21,24-30,36-37H,1,5,7-8,11-12,15-17H2,2-3H3,(H,34,38)(H,35,39)/t24-,25-,26-,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	Article	n/a	n/a	0.630	n/a	n/a	n/a	n/a	6.0	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of purified human renin at PH 6.0				Bioorg Med Chem Lett 2: 1405-1410 (1992) Article DOI: 10.1016/S0960-894X(00)80522-3 BindingDB Entry DOI: 10.7270/Q2VD6ZBV
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022644 (CHEMBL73712 | Piperazine-1-carboxylic acid {1-[1-(...) 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](Cc1ccccc1)NC(=O)N1CCNCC1 Show InChI InChI=1S/C34H53N7O5/c1-23(2)17-30(42)31(43)27(18-24-9-5-3-6-10-24)38-33(45)29(20-26-21-36-22-37-26)39-32(44)28(19-25-11-7-4-8-12-25)40-34(46)41-15-13-35-14-16-41/h4,7-8,11-12,21-24,27-31,35,42-43H,3,5-6,9-10,13-20H2,1-2H3,(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	0.650	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022643 (4-Hydroxy-piperidine-1-carboxylic acid {1-[1-(1-cy...) 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](Cc1ccccc1)NC(=O)N1CCC(O)CC1 Show InChI InChI=1S/C35H54N6O6/c1-23(2)17-31(43)32(44)28(18-24-9-5-3-6-10-24)38-34(46)30(20-26-21-36-22-37-26)39-33(45)29(19-25-11-7-4-8-12-25)40-35(47)41-15-13-27(42)14-16-41/h4,7-8,11-12,21-24,27-32,42-44H,3,5-6,9-10,13-20H2,1-2H3,(H,36,37)(H,38,46)(H,39,45)(H,40,47)/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	0.680	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50280227 ((1S,2R,3S)-2-(2-Morpholin-4-yl-2-oxo-ethyl)-3-phen...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@H]1[C@H](CC(=O)N2CCOCC2)[C@@H]1c1ccccc1 Show InChI InChI=1S/C36H52N4O6S/c1-23(2)17-30(41)34(43)28(18-24-9-5-3-6-10-24)38-35(44)29(19-26-21-47-22-37-26)39-36(45)33-27(32(33)25-11-7-4-8-12-25)20-31(42)40-13-15-46-16-14-40/h4,7-8,11-12,21-24,27-30,32-34,41,43H,3,5-6,9-10,13-20H2,1-2H3,(H,38,44)(H,39,45)/t27-,28+,29+,30+,32+,33+,34-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.700	n/a	n/a	n/a	n/a	6.0	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of purified human renin at PH 6.0				Bioorg Med Chem Lett 2: 1405-1410 (1992) Article DOI: 10.1016/S0960-894X(00)80522-3 BindingDB Entry DOI: 10.7270/Q2VD6ZBV
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014060 (CHEMBL288346 | {1-[1-{1-Cyclohexylmethyl-2-hydroxy...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H]1CN(CCO)C(=O)O1 Show InChI InChI=1S/C34H50N6O8/c1-34(2,3)48-32(45)39-26(17-23-12-8-5-9-13-23)30(43)38-27(18-24-19-35-21-36-24)31(44)37-25(16-22-10-6-4-7-11-22)29(42)28-20-40(14-15-41)33(46)47-28/h5,8-9,12-13,19,21-22,25-29,41-42H,4,6-7,10-11,14-18,20H2,1-3H3,(H,35,36)(H,37,44)(H,38,43)(H,39,45)/t25-,26-,27-,28-,29+/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	0.700	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro inhibition of purified human renal renin.				J Med Chem 33: 1582-90 (1990) BindingDB Entry DOI: 10.7270/Q2NK3D0G
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006138 (2-(Morpholine-4-carbonyl)-3-phenyl-cyclopropanecar...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@H]1[C@@H]([C@@H]1c1ccccc1)C(=O)N1CCOCC1 Show InChI InChI=1S/C35H50N4O6S/c1-22(2)17-28(40)32(41)26(18-23-9-5-3-6-10-23)37-33(42)27(19-25-20-46-21-36-25)38-34(43)30-29(24-11-7-4-8-12-24)31(30)35(44)39-13-15-45-16-14-39/h4,7-8,11-12,20-23,26-32,40-41H,3,5-6,9-10,13-19H2,1-2H3,(H,37,42)(H,38,43)/t26-,27-,28-,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	0.700	n/a	n/a	n/a	n/a	6.0	n/a
University of Texas Curated by ChEMBL					Assay Description In vitro potency against human plasma renin at pH 7.4				J Med Chem 35: 1710-21 (1992) BindingDB Entry DOI: 10.7270/Q2GT5M4C
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50405479 (CHEMBL2028988) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](NC(O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OC(C)(C)C)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(O)=O |r| Show InChI InChI=1S/C54H80N14O11/c1-10-32(6)44(50(74)64-41(52(76)77)23-36-26-57-29-60-36)67-49(73)43(31(4)5)66-47(71)37(19-30(2)3)61-46(70)39(21-34-24-55-27-58-34)62-45(69)38(20-33-15-12-11-13-16-33)63-48(72)42-17-14-18-68(42)51(75)40(22-35-25-56-28-59-35)65-53(78)79-54(7,8)9/h11-13,15-16,24-32,37-44,47,66,71H,10,14,17-23H2,1-9H3,(H,55,58)(H,56,59)(H,57,60)(H,61,70)(H,62,69)(H,63,72)(H,64,74)(H,65,78)(H,67,73)(H,76,77)/t32-,37-,38-,39-,40-,41-,42-,43-,44-,47?/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	0.700	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition against human plasma renin				J Med Chem 30: 1729-37 (1987) BindingDB Entry DOI: 10.7270/Q2MK6BW4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014048 (CHEMBL41303 | {1-[1-[1-Cyclohexylmethyl-2-hydroxy-...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H]1CC(=C)C(=O)O1 Show InChI InChI=1S/C34H47N5O7/c1-21-15-28(45-32(21)43)29(40)25(16-22-11-7-5-8-12-22)37-31(42)27(18-24-19-35-20-36-24)38-30(41)26(17-23-13-9-6-10-14-23)39-33(44)46-34(2,3)4/h6,9-10,13-14,19-20,22,25-29,40H,1,5,7-8,11-12,15-18H2,2-4H3,(H,35,36)(H,37,42)(H,38,41)(H,39,44)/t25-,26-,27-,28-,29+/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	0.710	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro inhibition of purified human renal renin.				J Med Chem 33: 1582-90 (1990) BindingDB Entry DOI: 10.7270/Q2NK3D0G
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046799 (2-Benzyl-N*1*-[1-(1-cyclohexylmethyl-2,3-dihydroxy...) 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)N(C)CCn1cccn1)Cc1ccccc1 Show InChI InChI=1S/C37H54N6O5S/c1-26(2)19-33(44)35(46)31(21-28-13-8-5-9-14-28)40-37(48)32(23-30-24-49-25-38-30)41-36(47)29(20-27-11-6-4-7-12-27)22-34(45)42(3)17-18-43-16-10-15-39-43/h4,6-7,10-12,15-16,24-26,28-29,31-33,35,44,46H,5,8-9,13-14,17-23H2,1-3H3,(H,40,48)(H,41,47)/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	0.720	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory concentration against human plasma renin at pH 7.4				J Med Chem 36: 460-7 (1993) BindingDB Entry DOI: 10.7270/Q2VT1R5C
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046794 (2-Benzyl-N*1*-[1-(1-cyclohexylmethyl-2,3-dihydroxy...) 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)N(C)CCc1ccccn1)Cc1ccccc1 Show InChI InChI=1S/C39H55N5O5S/c1-27(2)20-35(45)37(47)33(22-29-14-8-5-9-15-29)42-39(49)34(24-32-25-50-26-41-32)43-38(48)30(21-28-12-6-4-7-13-28)23-36(46)44(3)19-17-31-16-10-11-18-40-31/h4,6-7,10-13,16,18,25-27,29-30,33-35,37,45,47H,5,8-9,14-15,17,19-24H2,1-3H3,(H,42,49)(H,43,48)/t30-,33+,34+,35+,37-/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	0.760	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro inhibitory concentration against monkey plasma renin at pH 7.4				J Med Chem 36: 460-7 (1993) BindingDB Entry DOI: 10.7270/Q2VT1R5C
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022653 (CHEMBL309345 | Morpholine-4-carboxylic acid [1-[1-...) Show SMILES COc1ccc(C[C@H](NC(=O)N2CCOCC2)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/C35H54N6O7/c1-23(2)17-31(42)32(43)28(18-24-7-5-4-6-8-24)38-34(45)30(20-26-21-36-22-37-26)39-33(44)29(19-25-9-11-27(47-3)12-10-25)40-35(46)41-13-15-48-16-14-41/h9-12,21-24,28-32,42-43H,4-8,13-20H2,1-3H3,(H,36,37)(H,38,45)(H,39,44)(H,40,46)/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	0.760	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50280219 (3-Benzenesulfonyl-2-benzyl-N-[(S)-1-((1S,2R,3S)-1-...) Show SMILES CO[C@@H](CC(C)C)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)C(Cc1ccccc1)CS(=O)(=O)c1ccccc1 Show InChI InChI=1S/C37H51N3O6S2/c1-26(2)19-34(46-3)35(41)32(21-28-15-9-5-10-16-28)39-37(43)33(22-30-23-47-25-38-30)40-36(42)29(20-27-13-7-4-8-14-27)24-48(44,45)31-17-11-6-12-18-31/h4,6-8,11-14,17-18,23,25-26,28-29,32-35,41H,5,9-10,15-16,19-22,24H2,1-3H3,(H,39,43)(H,40,42)/t29?,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	Article	n/a	n/a	0.770	n/a	n/a	n/a	n/a	6.0	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of purified human renin at PH 6.0				Bioorg Med Chem Lett 2: 1405-1410 (1992) Article DOI: 10.1016/S0960-894X(00)80522-3 BindingDB Entry DOI: 10.7270/Q2VD6ZBV
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50280231 ((1S,2R,3R)-2-Cyclohexyl-3-(propane-2-sulfonyl)-cyc...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@@H]1[C@H]([C@H]1S(=O)(=O)C(C)C)C1CCCCC1 Show InChI InChI=1S/C33H55N3O6S2/c1-20(2)15-27(37)30(38)25(16-22-11-7-5-8-12-22)35-32(39)26(17-24-18-43-19-34-24)36-33(40)29-28(23-13-9-6-10-14-23)31(29)44(41,42)21(3)4/h18-23,25-31,37-38H,5-17H2,1-4H3,(H,35,39)(H,36,40)/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	Article	n/a	n/a	0.790	n/a	n/a	n/a	n/a	6.0	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of purified human renin at PH 6.0				Bioorg Med Chem Lett 2: 1405-1410 (1992) Article DOI: 10.1016/S0960-894X(00)80522-3 BindingDB Entry DOI: 10.7270/Q2VD6ZBV
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022641 (2-Benzylidene-N-[1-(1-cyclohexylmethyl-2,3-dihydro...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)C(CC(=O)N1CCOCC1)=Cc1ccccc1 |w:39.42| Show InChI InChI=1S/C35H51N5O6/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/h3,5-6,9-10,18,22-24,26,29-31,33,41,43H,4,7-8,11-17,19-21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)/t29-,30-,31-,33+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	0.790	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046802 (2-Benzyl-N*1*-[1-(1-cyclohexylmethyl-2,3-dihydroxy...) Show SMILES COCCOCOCCN(C)C(=O)C[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CC(C)C Show InChI InChI=1S/C38H61N5O8/c1-27(2)19-34(44)36(46)32(21-29-13-9-6-10-14-29)41-38(48)33(23-31-24-39-25-40-31)42-37(47)30(20-28-11-7-5-8-12-28)22-35(45)43(3)15-16-50-26-51-18-17-49-4/h5,7-8,11-12,24-25,27,29-30,32-34,36,44,46H,6,9-10,13-23,26H2,1-4H3,(H,39,40)(H,41,48)(H,42,47)/t30-,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	0.800	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory concentration against human plasma renin at pH 7.4				J Med Chem 36: 460-7 (1993) BindingDB Entry DOI: 10.7270/Q2VT1R5C
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50405497 (CHEMBL2115482) Show SMILES CC(C)CNC(=O)[C@](O)(CCl)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C37H57ClN6O7/c1-24(2)20-40-34(48)37(50,22-38)19-31(45)28(16-25-12-8-6-9-13-25)42-33(47)30(18-27-21-39-23-41-27)43-32(46)29(17-26-14-10-7-11-15-26)44-35(49)51-36(3,4)5/h7,10-11,14-15,21,23-25,28-31,45,50H,6,8-9,12-13,16-20,22H2,1-5H3,(H,39,41)(H,40,48)(H,42,47)(H,43,46)(H,44,49)/t28-,29-,30-,31-,37+/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	0.800	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human renin				J Med Chem 30: 1978-83 (1987) BindingDB Entry DOI: 10.7270/Q27943N5
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022654 (CHEMBL265485 | Morpholine-4-carboxylic acid 1-[1-(...) 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](Cc1ccccc1)OC(=O)N1CCOCC1 Show InChI InChI=1S/C34H51N5O7/c1-23(2)17-29(40)31(41)27(18-24-9-5-3-6-10-24)37-32(42)28(20-26-21-35-22-36-26)38-33(43)30(19-25-11-7-4-8-12-25)46-34(44)39-13-15-45-16-14-39/h4,7-8,11-12,21-24,27-31,40-41H,3,5-6,9-10,13-20H2,1-2H3,(H,35,36)(H,37,42)(H,38,43)/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	0.820	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014053 (CHEMBL416429 | {1-[1-[1-Cyclohexylmethyl-2-hydroxy...) Show SMILES CC(C)N1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C35H52N6O7/c1-22(2)41-20-29(47-34(41)46)30(42)26(16-23-12-8-6-9-13-23)38-32(44)28(18-25-19-36-21-37-25)39-31(43)27(17-24-14-10-7-11-15-24)40-33(45)48-35(3,4)5/h7,10-11,14-15,19,21-23,26-30,42H,6,8-9,12-13,16-18,20H2,1-5H3,(H,36,37)(H,38,44)(H,39,43)(H,40,45)/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	0.840	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro inhibition of purified human renal renin.				J Med Chem 33: 1582-90 (1990) BindingDB Entry DOI: 10.7270/Q2NK3D0G
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046796 ((S)-N-[(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-di...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@H](Cc1ccccc1)CS(=O)(=O)C(C)(C)C Show InChI InChI=1S/C34H53N3O6S2/c1-23(2)16-30(38)31(39)28(18-25-14-10-7-11-15-25)36-33(41)29(19-27-20-44-22-35-27)37-32(40)26(17-24-12-8-6-9-13-24)21-45(42,43)34(3,4)5/h6,8-9,12-13,20,22-23,25-26,28-31,38-39H,7,10-11,14-19,21H2,1-5H3,(H,36,41)(H,37,40)/t26-,28+,29+,30+,31-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.870	n/a	n/a	n/a	n/a	7.4	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of human plasma renin at PH 7.4				Bioorg Med Chem Lett 2: 1405-1410 (1992) Article DOI: 10.1016/S0960-894X(00)80522-3 BindingDB Entry DOI: 10.7270/Q2VD6ZBV
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046796 ((S)-N-[(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-di...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cscn1)NC(=O)[C@H](Cc1ccccc1)CS(=O)(=O)C(C)(C)C Show InChI InChI=1S/C34H53N3O6S2/c1-23(2)16-30(38)31(39)28(18-25-14-10-7-11-15-25)36-33(41)29(19-27-20-44-22-35-27)37-32(40)26(17-24-12-8-6-9-13-24)21-45(42,43)34(3,4)5/h6,8-9,12-13,20,22-23,25-26,28-31,38-39H,7,10-11,14-19,21H2,1-5H3,(H,36,41)(H,37,40)/t26-,28+,29+,30+,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	0.870	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory concentration against human plasma renin at pH 7.4				J Med Chem 36: 460-7 (1993) BindingDB Entry DOI: 10.7270/Q2VT1R5C
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022650 (CHEMBL75117 | Morpholine-4-carboxylic acid {1-[1-(...) 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](Cc1ccccc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C34H52N6O6/c1-23(2)17-30(41)31(42)27(18-24-9-5-3-6-10-24)37-33(44)29(20-26-21-35-22-36-26)38-32(43)28(19-25-11-7-4-8-12-25)39-34(45)40-13-15-46-16-14-40/h4,7-8,11-12,21-24,27-31,41-42H,3,5-6,9-10,13-20H2,1-2H3,(H,35,36)(H,37,44)(H,38,43)(H,39,45)/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	0.890	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014063 (CHEMBL290215 | {1-[1-[1-Cyclohexylmethyl-2-(4,4-di...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H]1CC(C)(C)C(=O)O1 Show InChI InChI=1S/C35H51N5O7/c1-34(2,3)47-33(45)40-26(17-23-14-10-7-11-15-23)30(42)39-27(18-24-20-36-21-37-24)31(43)38-25(16-22-12-8-6-9-13-22)29(41)28-19-35(4,5)32(44)46-28/h7,10-11,14-15,20-22,25-29,41H,6,8-9,12-13,16-19H2,1-5H3,(H,36,37)(H,38,43)(H,39,42)(H,40,45)/t25-,26-,27-,28-,29+/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	0.890	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro inhibition of purified human renal renin.				J Med Chem 33: 1582-90 (1990) BindingDB Entry DOI: 10.7270/Q2NK3D0G
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006189 ((4-{2-[1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl...) Show SMILES CCCC[C@H](O[C@@H](Cc1ccccc1)C(=O)N1CCC(CC1)OCOC)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)C[C@H](NC(=O)OCCc1ccccn1)C(C)C Show InChI InChI=1S/C44H68N4O8/c1-5-6-20-40(56-41(29-34-17-11-8-12-18-34)43(51)48-25-21-36(22-26-48)55-31-53-4)42(50)46-38(28-33-15-9-7-10-16-33)39(49)30-37(32(2)3)47-44(52)54-27-23-35-19-13-14-24-45-35/h8,11-14,17-19,24,32-33,36-41,49H,5-7,9-10,15-16,20-23,25-31H2,1-4H3,(H,46,50)(H,47,52)/t37-,38-,39-,40-,41-/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	0.900	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro activity against human renin (pH 6.0)				J Med Chem 35: 1735-46 (1992) BindingDB Entry DOI: 10.7270/Q27943MQ
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006157 (5-{2-[1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)...) Show SMILES CCCCNC(=O)[C@@H](C[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](CCCC)N[C@@H](Cc1ccccc1)C(=O)N1CCC(CC1)OCOC)C(C)C Show InChI InChI=1S/C41H70N4O6/c1-6-8-20-35(43-37(27-32-18-14-11-15-19-32)41(49)45-24-21-33(22-25-45)51-29-50-5)40(48)44-36(26-31-16-12-10-13-17-31)38(46)28-34(30(3)4)39(47)42-23-9-7-2/h11,14-15,18-19,30-31,33-38,43,46H,6-10,12-13,16-17,20-29H2,1-5H3,(H,42,47)(H,44,48)/t34-,35-,36-,37-,38-/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	0.900	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro potency against plasma renin at a pH of 7.4				J Med Chem 35: 1722-34 (1992) BindingDB Entry DOI: 10.7270/Q2C24VCH
					More data for this Ligand-Target Pair				3D Structure (docked)
Renin (Homo sapiens (Human))	BDBM50014054 ((5R){1-[1-[1-Cyclohexylmethyl-2-hydroxy-2-(3-metho...) Show SMILES CON1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C33H48N6O8/c1-33(2,3)47-31(43)38-25(16-22-13-9-6-10-14-22)29(41)37-26(17-23-18-34-20-35-23)30(42)36-24(15-21-11-7-5-8-12-21)28(40)27-19-39(45-4)32(44)46-27/h6,9-10,13-14,18,20-21,24-28,40H,5,7-8,11-12,15-17,19H2,1-4H3,(H,34,35)(H,36,42)(H,37,41)(H,38,43)/t24-,25-,26-,27-,28+/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	0.900	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro inhibition of purified human renal renin.				J Med Chem 33: 1582-90 (1990) BindingDB Entry DOI: 10.7270/Q2NK3D0G
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006147 (2-[1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-...) Show SMILES CC[C@H](O[C@@H](Cc1ccccc1)C(=O)N1CCC(CC1)OCOC)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CC(C)C Show InChI InChI=1S/C34H56N2O7/c1-5-30(33(39)35-28(21-25-12-8-6-9-13-25)32(38)29(37)20-24(2)3)43-31(22-26-14-10-7-11-15-26)34(40)36-18-16-27(17-19-36)42-23-41-4/h7,10-11,14-15,24-25,27-32,37-38H,5-6,8-9,12-13,16-23H2,1-4H3,(H,35,39)/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	0.900	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro potency against purified renin at a pH of 6.0.				J Med Chem 35: 1722-34 (1992) BindingDB Entry DOI: 10.7270/Q2C24VCH
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022642 (CHEMBL74765 | Morpholine-4-carboxylic acid (1-{[1-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)N(C)C(=O)[C@H](Cc1ccccc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C35H54N6O6/c1-24(2)18-31(42)32(43)28(19-25-10-6-4-7-11-25)38-33(44)30(21-27-22-36-23-37-27)40(3)34(45)29(20-26-12-8-5-9-13-26)39-35(46)41-14-16-47-17-15-41/h5,8-9,12-13,22-25,28-32,42-43H,4,6-7,10-11,14-21H2,1-3H3,(H,36,37)(H,38,44)(H,39,46)/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	0.940	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022645 (CHEMBL75510 | N-[1-(1-Cyclohexylmethyl-2,3-dihydro...) 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](Cc1ccccc1)NC(=O)N(C)CCO Show InChI InChI=1S/C33H52N6O6/c1-22(2)16-29(41)30(42)26(17-23-10-6-4-7-11-23)36-32(44)28(19-25-20-34-21-35-25)37-31(43)27(18-24-12-8-5-9-13-24)38-33(45)39(3)14-15-40/h5,8-9,12-13,20-23,26-30,40-42H,4,6-7,10-11,14-19H2,1-3H3,(H,34,35)(H,36,44)(H,37,43)(H,38,45)/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	0.980	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					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))	BDBM50006152 (2-[1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-...) Show SMILES CCCC[C@H](O[C@@H](Cc1ccccc1)C(=O)N1CCC(CC1)OCOC)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CC(C)C Show InChI InChI=1S/C36H60N2O7/c1-5-6-17-32(35(41)37-30(23-27-13-9-7-10-14-27)34(40)31(39)22-26(2)3)45-33(24-28-15-11-8-12-16-28)36(42)38-20-18-29(19-21-38)44-25-43-4/h8,11-12,15-16,26-27,29-34,39-40H,5-7,9-10,13-14,17-25H2,1-4H3,(H,37,41)/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	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro potency against human plasma renin at a pH of 7.4				J Med Chem 35: 1735-46 (1992) BindingDB Entry DOI: 10.7270/Q27943MQ
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50014056 (CHEMBL290605 | {1-[1-[1-Cyclohexylmethyl-2-hydroxy...) Show SMILES CCCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C35H52N6O7/c1-5-16-41-21-29(47-34(41)46)30(42)26(17-23-12-8-6-9-13-23)38-32(44)28(19-25-20-36-22-37-25)39-31(43)27(18-24-14-10-7-11-15-24)40-33(45)48-35(2,3)4/h7,10-11,14-15,20,22-23,26-30,42H,5-6,8-9,12-13,16-19,21H2,1-4H3,(H,36,37)(H,38,44)(H,39,43)(H,40,45)/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	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro inhibition of human plasma renin.				J Med Chem 33: 1582-90 (1990) BindingDB Entry DOI: 10.7270/Q2NK3D0G
					More data for this Ligand-Target Pair

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