Compile Data Set for Download or QSAR

Found 902 hits of ph data with Target = 'Renin'   

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))	BDBM50002966 (CHEMBL115430 | {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)NC(CC1CCCCC1)C(O)CC(=O)Nc1ccccc1 Show InChI InChI=1S/C37H50N6O6/c1-37(2,3)49-36(48)43-30(20-26-15-9-5-10-16-26)34(46)42-31(21-28-23-38-24-39-28)35(47)41-29(19-25-13-7-4-8-14-25)32(44)22-33(45)40-27-17-11-6-12-18-27/h5-6,9-12,15-18,23-25,29-32,44H,4,7-8,13-14,19-22H2,1-3H3,(H,38,39)(H,40,45)(H,41,47)(H,42,46)(H,43,48)/t29?,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	190	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002990 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSC[C@H](NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)COc1ccccn1 Show InChI InChI=1S/C34H49N5O6S/c1-46-23-28(32(41)37-27(20-24-10-4-2-5-11-24)29(40)22-44-31-14-8-9-17-36-31)38-33(42)30(21-25-12-6-3-7-13-25)45-34(43)39-18-15-26(35)16-19-39/h3,6-9,12-14,17,24,26-30,40H,2,4-5,10-11,15-16,18-23,35H2,1H3,(H,37,41)(H,38,42)/t27-,28-,29-,30-/m0/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	42	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002970 (4-[2-(2-tert-Butoxycarbonylamino-3-phenyl-propiony...) Show SMILES CC(C)OC(=O)CC(O)C(CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C34H51N5O7/c1-22(2)45-30(41)19-29(40)26(16-23-12-8-6-9-13-23)37-32(43)28(18-25-20-35-21-36-25)38-31(42)27(17-24-14-10-7-11-15-24)39-33(44)46-34(3,4)5/h7,10-11,14-15,20-23,26-29,40H,6,8-9,12-13,16-19H2,1-5H3,(H,35,36)(H,37,43)(H,38,42)(H,39,44)/t26?,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	175	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002972 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSC[C@H](NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)Cn1ccccc1=O Show InChI InChI=1S/C34H49N5O6S/c1-46-23-28(32(42)36-27(20-24-10-4-2-5-11-24)29(40)22-39-17-9-8-14-31(39)41)37-33(43)30(21-25-12-6-3-7-13-25)45-34(44)38-18-15-26(35)16-19-38/h3,6-9,12-14,17,24,26-30,40H,2,4-5,10-11,15-16,18-23,35H2,1H3,(H,36,42)(H,37,43)/t27-,28-,29-,30-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG MMDB PC cid PC sid PDB UniChem Similars	PubMed	n/a	n/a	41	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002974 (4-Amino-piperidine-1-carboxylic acid 1-[1-[1-cyclo...) Show SMILES NC1CCN(CC1)C(=O)O[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ccccn1 Show InChI InChI=1S/C37H51N7O5S/c38-28-14-18-44(19-15-28)37(48)49-33(22-27-11-5-2-6-12-27)36(47)43-31(23-29-24-39-25-41-29)35(46)42-30(21-26-9-3-1-4-10-26)32(45)16-20-50-34-13-7-8-17-40-34/h2,5-8,11-13,17,24-26,28,30-33,45H,1,3-4,9-10,14-16,18-23,38H2,(H,39,41)(H,42,46)(H,43,47)/t30-,31-,32-,33-/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	33	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002971 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CC(NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ccccn1 Show InChI InChI=1S/C34H49N5O5S/c1-24(37-33(42)30(23-26-12-6-3-7-13-26)44-34(43)39-19-15-27(35)16-20-39)32(41)38-28(22-25-10-4-2-5-11-25)29(40)17-21-45-31-14-8-9-18-36-31/h3,6-9,12-14,18,24-25,27-30,40H,2,4-5,10-11,15-17,19-23,35H2,1H3,(H,37,42)(H,38,41)/t24?,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	770	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002977 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSC[C@H](NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1nnc(C)s1 Show InChI InChI=1S/C33H50N6O5S3/c1-22-37-38-32(47-22)46-18-15-28(40)26(19-23-9-5-3-6-10-23)35-30(41)27(21-45-2)36-31(42)29(20-24-11-7-4-8-12-24)44-33(43)39-16-13-25(34)14-17-39/h4,7-8,11-12,23,25-29,40H,3,5-6,9-10,13-21,34H2,1-2H3,(H,35,41)(H,36,42)/t26-,27-,28-,29-/m0/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	16	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002978 (CHEMBL119893 | {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)NC(CC1CCCCC1)C(O)CCSc1ccccn1 Show InChI InChI=1S/C36H50N6O5S/c1-36(2,3)47-35(46)42-29(21-26-14-8-5-9-15-26)33(44)41-30(22-27-23-37-24-39-27)34(45)40-28(20-25-12-6-4-7-13-25)31(43)17-19-48-32-16-10-11-18-38-32/h5,8-11,14-16,18,23-25,28-31,43H,4,6-7,12-13,17,19-22H2,1-3H3,(H,37,39)(H,40,45)(H,41,44)(H,42,46)/t28?,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	130	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002982 (CHEMBL333707 | {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)NC(CC1CCCCC1)C(O)CCOc1ccccn1 Show InChI InChI=1S/C36H50N6O6/c1-36(2,3)48-35(46)42-29(21-26-14-8-5-9-15-26)33(44)41-30(22-27-23-37-24-39-27)34(45)40-28(20-25-12-6-4-7-13-25)31(43)17-19-47-32-16-10-11-18-38-32/h5,8-11,14-16,18,23-25,28-31,43H,4,6-7,12-13,17,19-22H2,1-3H3,(H,37,39)(H,40,45)(H,41,44)(H,42,46)/t28?,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	750	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002975 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CCCC(NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ccccn1 Show InChI InChI=1S/C36H53N5O5S/c1-2-11-29(39-35(44)32(25-27-14-7-4-8-15-27)46-36(45)41-21-17-28(37)18-22-41)34(43)40-30(24-26-12-5-3-6-13-26)31(42)19-23-47-33-16-9-10-20-38-33/h4,7-10,14-16,20,26,28-32,42H,2-3,5-6,11-13,17-19,21-25,37H2,1H3,(H,39,44)(H,40,43)/t29?,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	37	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002969 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSC[C@H](NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ncc(CO)n1C Show InChI InChI=1S/C35H54N6O6S2/c1-40-27(22-42)21-37-34(40)49-18-15-30(43)28(19-24-9-5-3-6-10-24)38-32(44)29(23-48-2)39-33(45)31(20-25-11-7-4-8-12-25)47-35(46)41-16-13-26(36)14-17-41/h4,7-8,11-12,21,24,26,28-31,42-43H,3,5-6,9-10,13-20,22-23,36H2,1-2H3,(H,38,44)(H,39,45)/t28-,29-,30-,31-/m0/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	2.60	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002984 (2-Benzyl-N-[1-[1-cyclohexylmethyl-2-hydroxy-4-(pyr...) Show SMILES CC(C)(C)S(=O)(=O)C[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ccccn1 Show InChI InChI=1S/C36H51N5O5S2/c1-36(2,3)48(45,46)24-28(20-26-12-6-4-7-13-26)34(43)41-31(22-29-23-37-25-39-29)35(44)40-30(21-27-14-8-5-9-15-27)32(42)17-19-47-33-16-10-11-18-38-33/h4,6-7,10-13,16,18,23,25,27-28,30-32,42H,5,8-9,14-15,17,19-22,24H2,1-3H3,(H,37,39)(H,40,44)(H,41,43)/t28-,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	3.60E+3	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair				3D Structure (docked)
Renin (Homo sapiens (Human))	BDBM50002986 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSCCC(NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ccccn1 Show InChI InChI=1S/C36H53N5O5S2/c1-47-22-17-29(39-35(44)32(25-27-12-6-3-7-13-27)46-36(45)41-20-15-28(37)16-21-41)34(43)40-30(24-26-10-4-2-5-11-26)31(42)18-23-48-33-14-8-9-19-38-33/h3,6-9,12-14,19,26,28-32,42H,2,4-5,10-11,15-18,20-25,37H2,1H3,(H,39,44)(H,40,43)/t29?,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	140	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002980 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CCCCC(NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ccccn1 Show InChI InChI=1S/C37H55N5O5S/c1-2-3-16-30(40-36(45)33(26-28-14-8-5-9-15-28)47-37(46)42-22-18-29(38)19-23-42)35(44)41-31(25-27-12-6-4-7-13-27)32(43)20-24-48-34-17-10-11-21-39-34/h5,8-11,14-15,17,21,27,29-33,43H,2-4,6-7,12-13,16,18-20,22-26,38H2,1H3,(H,40,45)(H,41,44)/t30?,31-,32-,33-/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	58	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002988 (CHEMBL118172 | Morpholine-4-carboxylic acid 1-[1-[...) Show SMILES O[C@@H](CCSc1ccccn1)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCOCC1 Show InChI InChI=1S/C36H48N6O6S/c43-31(14-20-49-33-13-7-8-15-38-33)29(21-26-9-3-1-4-10-26)40-34(44)30(23-28-24-37-25-39-28)41-35(45)32(22-27-11-5-2-6-12-27)48-36(46)42-16-18-47-19-17-42/h2,5-8,11-13,15,24-26,29-32,43H,1,3-4,9-10,14,16-23H2,(H,37,39)(H,40,44)(H,41,45)/t29-,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	250	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002979 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSC[C@H](NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1nnnn1C Show InChI InChI=1S/C32H50N8O5S2/c1-39-31(36-37-38-39)47-18-15-27(41)25(19-22-9-5-3-6-10-22)34-29(42)26(21-46-2)35-30(43)28(20-23-11-7-4-8-12-23)45-32(44)40-16-13-24(33)14-17-40/h4,7-8,11-12,22,24-28,41H,3,5-6,9-10,13-21,33H2,1-2H3,(H,34,42)(H,35,43)/t25-,26-,27-,28-/m0/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	34	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002987 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSC[C@H](NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ncccn1 Show InChI InChI=1S/C34H50N6O5S2/c1-46-23-28(39-32(43)30(22-25-11-6-3-7-12-25)45-34(44)40-18-13-26(35)14-19-40)31(42)38-27(21-24-9-4-2-5-10-24)29(41)15-20-47-33-36-16-8-17-37-33/h3,6-8,11-12,16-17,24,26-30,41H,2,4-5,9-10,13-15,18-23,35H2,1H3,(H,38,42)(H,39,43)/t27-,28-,29-,30-/m0/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	41	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002981 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSC[C@H](NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)Cn1ccc(=O)cc1 Show InChI InChI=1S/C34H49N5O6S/c1-46-23-29(32(42)36-28(20-24-8-4-2-5-9-24)30(41)22-38-16-14-27(40)15-17-38)37-33(43)31(21-25-10-6-3-7-11-25)45-34(44)39-18-12-26(35)13-19-39/h3,6-7,10-11,14-17,24,26,28-31,41H,2,4-5,8-9,12-13,18-23,35H2,1H3,(H,36,42)(H,37,43)/t28-,29-,30-,31-/m0/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	4.40E+3	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002991 (4-tert-Butoxycarbonylamino-piperidine-1-carboxylic...) Show SMILES CC(C)(C)OC(=O)NC1CCN(CC1)C(=O)O[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ccccn1 Show InChI InChI=1S/C42H59N7O7S/c1-42(2,3)56-40(53)46-31-17-21-49(22-18-31)41(54)55-36(25-30-14-8-5-9-15-30)39(52)48-34(26-32-27-43-28-45-32)38(51)47-33(24-29-12-6-4-7-13-29)35(50)19-23-57-37-16-10-11-20-44-37/h5,8-11,14-16,20,27-29,31,33-36,50H,4,6-7,12-13,17-19,21-26H2,1-3H3,(H,43,45)(H,46,53)(H,47,51)(H,48,52)/t33-,34-,35-,36-/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	230	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002993 (CHEMBL334319 | {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)NC(CC1CCCCC1)C(O)CSc1ccccn1 Show InChI InChI=1S/C35H48N6O5S/c1-35(2,3)46-34(45)41-28(19-25-14-8-5-9-15-25)32(43)40-29(20-26-21-36-23-38-26)33(44)39-27(18-24-12-6-4-7-13-24)30(42)22-47-31-16-10-11-17-37-31/h5,8-11,14-17,21,23-24,27-30,42H,4,6-7,12-13,18-20,22H2,1-3H3,(H,36,38)(H,39,44)(H,40,43)(H,41,45)/t27?,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	150	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002992 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSC[C@H](NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CSc1nnc[nH]1 Show InChI InChI=1S/C31H47N7O5S2/c1-44-18-25(28(40)35-24(16-21-8-4-2-5-9-21)26(39)19-45-30-33-20-34-37-30)36-29(41)27(17-22-10-6-3-7-11-22)43-31(42)38-14-12-23(32)13-15-38/h3,6-7,10-11,20-21,23-27,39H,2,4-5,8-9,12-19,32H2,1H3,(H,35,40)(H,36,41)(H,33,34,37)/t24-,25-,26-,27-/m0/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	16	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002976 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSC[C@H](NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)COc1ccncc1 Show InChI InChI=1S/C34H49N5O6S/c1-46-23-29(32(41)37-28(20-24-8-4-2-5-9-24)30(40)22-44-27-12-16-36-17-13-27)38-33(42)31(21-25-10-6-3-7-11-25)45-34(43)39-18-14-26(35)15-19-39/h3,6-7,10-13,16-17,24,26,28-31,40H,2,4-5,8-9,14-15,18-23,35H2,1H3,(H,37,41)(H,38,42)/t28-,29-,30-,31-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG MMDB PC cid PC sid PDB UniChem Similars	PubMed	n/a	n/a	56	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002989 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSCC(NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ccccn1 Show InChI InChI=1S/C35H51N5O5S2/c1-46-24-29(39-34(43)31(23-26-12-6-3-7-13-26)45-35(44)40-19-15-27(36)16-20-40)33(42)38-28(22-25-10-4-2-5-11-25)30(41)17-21-47-32-14-8-9-18-37-32/h3,6-9,12-14,18,25,27-31,41H,2,4-5,10-11,15-17,19-24,36H2,1H3,(H,38,42)(H,39,43)/t28-,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	9.30	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002973 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSC[C@H](NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ccncc1 Show InChI InChI=1S/C35H51N5O5S2/c1-46-24-30(39-34(43)32(23-26-10-6-3-7-11-26)45-35(44)40-19-14-27(36)15-20-40)33(42)38-29(22-25-8-4-2-5-9-25)31(41)16-21-47-28-12-17-37-18-13-28/h3,6-7,10-13,17-18,25,27,29-32,41H,2,4-5,8-9,14-16,19-24,36H2,1H3,(H,38,42)(H,39,43)/t29-,30-,31-,32-/m0/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	53	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002967 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSC[C@H](NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CSc1ccccn1 Show InChI InChI=1S/C34H49N5O5S2/c1-45-22-28(32(41)37-27(20-24-10-4-2-5-11-24)29(40)23-46-31-14-8-9-17-36-31)38-33(42)30(21-25-12-6-3-7-13-25)44-34(43)39-18-15-26(35)16-19-39/h3,6-9,12-14,17,24,26-30,40H,2,4-5,10-11,15-16,18-23,35H2,1H3,(H,37,41)(H,38,42)/t27-,28-,29-,30-/m0/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	8.5	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002985 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CSC[C@H](NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1nccs1 Show InChI InChI=1S/C33H49N5O5S3/c1-44-22-27(30(40)36-26(20-23-8-4-2-5-9-23)28(39)14-18-45-32-35-15-19-46-32)37-31(41)29(21-24-10-6-3-7-11-24)43-33(42)38-16-12-25(34)13-17-38/h3,6-7,10-11,15,19,23,25-29,39H,2,4-5,8-9,12-14,16-18,20-22,34H2,1H3,(H,36,40)(H,37,41)/t26-,27-,28-,29-/m0/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	5	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002994 (2-Benzyl-N-[1-[1-cyclohexylmethyl-2-hydroxy-4-(pyr...) Show SMILES CC(C)(C)S(=O)(=O)C[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ccccn1 Show InChI InChI=1S/C36H51N5O5S2/c1-36(2,3)48(45,46)24-28(20-26-12-6-4-7-13-26)34(43)41-31(22-29-23-37-25-39-29)35(44)40-30(21-27-14-8-5-9-15-27)32(42)17-19-47-33-16-10-11-18-38-33/h4,6-7,10-13,16,18,23,25,27-28,30-32,42H,5,8-9,14-15,17,19-22,24H2,1-3H3,(H,37,39)(H,40,44)(H,41,43)/t28-,30+,31+,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	46	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair				3D Structure (docked)
Renin (Homo sapiens (Human))	BDBM50002995 (CHEMBL327068 | {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)NC(CC1CCCCC1)C(O)COc1ccccn1 Show InChI InChI=1S/C35H48N6O6/c1-35(2,3)47-34(45)41-28(19-25-14-8-5-9-15-25)32(43)40-29(20-26-21-36-23-38-26)33(44)39-27(18-24-12-6-4-7-13-24)30(42)22-46-31-16-10-11-17-37-31/h5,8-11,14-17,21,23-24,27-30,42H,4,6-7,12-13,18-20,22H2,1-3H3,(H,36,38)(H,39,44)(H,40,43)(H,41,45)/t27?,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	140	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002983 (4-Amino-piperidine-1-carboxylic acid 1-{1-[1-cyclo...) Show SMILES CC(C)CC(NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCC(N)CC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CCSc1ccccn1 Show InChI InChI=1S/C37H55N5O5S/c1-26(2)23-31(41-36(45)33(25-28-13-7-4-8-14-28)47-37(46)42-20-16-29(38)17-21-42)35(44)40-30(24-27-11-5-3-6-12-27)32(43)18-22-48-34-15-9-10-19-39-34/h4,7-10,13-15,19,26-27,29-33,43H,3,5-6,11-12,16-18,20-25,38H2,1-2H3,(H,40,44)(H,41,45)/t30-,31?,32-,33-/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	130	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50002968 (CHEMBL117799 | {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)NC(CC1CCCCC1)C(O)CCCSc1ccccn1 Show InChI InChI=1S/C37H52N6O5S/c1-37(2,3)48-36(47)43-30(22-27-15-8-5-9-16-27)34(45)42-31(23-28-24-38-25-40-28)35(46)41-29(21-26-13-6-4-7-14-26)32(44)17-12-20-49-33-18-10-11-19-39-33/h5,8-11,15-16,18-19,24-26,29-32,44H,4,6-7,12-14,17,20-23H2,1-3H3,(H,38,40)(H,41,46)(H,42,45)(H,43,47)/t29?,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	310	n/a	n/a	n/a	n/a	5.5	n/a
E. Merck Darmstadt Curated by ChEMBL					Assay Description In vitro inhibitory activity against human plasma renin at pH 5.5 for suppression of angiotensin I formation.				J Med Chem 35: 3525-36 (1992) BindingDB Entry DOI: 10.7270/Q2DB80S4
					More data for this Ligand-Target Pair
Renin (Rattus norvegicus)	BDBM50405191 (CHEMBL269752) Show SMILES CC[C@](C)(N)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)NC(CC(C)C)C(O)CC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(N)=O Show InChI InChI=1S/C54H77N13O9/c1-7-54(6,56)53(76)66-43(26-37-29-58-31-60-37)52(75)67-20-14-19-44(67)51(74)65-41(24-35-17-12-9-13-18-35)49(72)64-42(25-36-28-57-30-59-36)50(73)62-38(21-32(2)3)45(68)27-46(69)61-40(22-33(4)5)48(71)63-39(47(55)70)23-34-15-10-8-11-16-34/h8-13,15-18,28-33,38-45,68H,7,14,19-27,56H2,1-6H3,(H2,55,70)(H,57,59)(H,58,60)(H,61,69)(H,62,73)(H,63,71)(H,64,72)(H,65,74)(H,66,76)/t38?,39-,40-,41-,42-,43-,44-,45?,54-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	115	n/a	n/a	n/a	n/a	n/a	n/a	6.0	n/a
TBA Curated by ChEMBL					Assay Description The compound was tested for inhibition of rat plasma renin at pH of 6.0.				J Med Chem 28: 1779-90 (1986) BindingDB Entry DOI: 10.7270/Q2FJ2HC2
					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))	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))	BDBM50280236 ((1S,2R,3S)-2-Benzenesulfonyl-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(=O)(=O)c1ccccc1)c1ccccc1 Show InChI InChI=1S/C36H47N3O6S2/c1-23(2)18-30(40)33(41)28(19-24-12-6-3-7-13-24)38-35(42)29(20-26-21-46-22-37-26)39-36(43)32-31(25-14-8-4-9-15-25)34(32)47(44,45)27-16-10-5-11-17-27/h4-5,8-11,14-17,21-24,28-34,40-41H,3,6-7,12-13,18-20H2,1-2H3,(H,38,42)(H,39,43)/t28-,29-,30-,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	Article	n/a	n/a	1.20	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))	BDBM50280228 ((1R,2R,3S)-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	7	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))	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))	BDBM50280238 ((1R,2R,3S)-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](Cn1ccnc1)NC(=O)[C@H]1[C@@H]([C@@H]1S(=O)(=O)C(C)C)c1ccccc1 Show InChI InChI=1S/C33H50N4O6S/c1-21(2)17-27(38)30(39)25(18-23-11-7-5-8-12-23)35-32(40)26(19-37-16-15-34-20-37)36-33(41)29-28(24-13-9-6-10-14-24)31(29)44(42,43)22(3)4/h6,9-10,13-16,20-23,25-31,38-39H,5,7-8,11-12,17-19H2,1-4H3,(H,35,40)(H,36,41)/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	2.5	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))	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))	BDBM50006119 (2-Ethyl-3-(morpholine-4-carbonyl)-cyclopropanecarb...) Show SMILES CC[C@H]1[C@H]([C@@H]1C(=O)N1CCOCC1)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/C31H50N4O6S/c1-4-22-26(27(22)31(40)35-10-12-41-13-11-35)30(39)34-24(16-21-17-42-18-32-21)29(38)33-23(15-20-8-6-5-7-9-20)28(37)25(36)14-19(2)3/h17-20,22-28,36-37H,4-16H2,1-3H3,(H,33,38)(H,34,39)/t22-,23-,24-,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	16	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))	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))	BDBM50006124 (2-Ethyl-3-(morpholine-4-carbonyl)-cyclopropanecarb...) Show SMILES CC[C@@H]1[C@H]([C@@H]1C(=O)N1CCOCC1)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/C31H50N4O6S/c1-4-22-26(27(22)31(40)35-10-12-41-13-11-35)30(39)34-24(16-21-17-42-18-32-21)29(38)33-23(15-20-8-6-5-7-9-20)28(37)25(36)14-19(2)3/h17-20,22-28,36-37H,4-16H2,1-3H3,(H,33,38)(H,34,39)/t22-,23+,24+,25+,26-,27-,28-/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	10	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))	BDBM50006134 (2-Benzyl-3-(morpholine-4-carbonyl)-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](Cc2ccccc2)[C@@H]1C(=O)N1CCOCC1 Show InChI InChI=1S/C36H52N4O6S/c1-23(2)17-30(41)33(42)28(19-25-11-7-4-8-12-25)38-34(43)29(20-26-21-47-22-37-26)39-35(44)31-27(18-24-9-5-3-6-10-24)32(31)36(45)40-13-15-46-16-14-40/h3,5-6,9-10,21-23,25,27-33,41-42H,4,7-8,11-20H2,1-2H3,(H,38,43)(H,39,44)/t27-,28-,29-,30-,31-,32-,33+/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	10	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))	BDBM50006160 (2-(1-Benzyl-2-morpholin-4-yl-2-oxo-ethylamino)-N-(...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)C(C)N[C@@H](Cc1ccccc1)C(=O)N1CCOCC1 Show InChI InChI=1S/C30H49N3O5/c1-21(2)18-27(34)28(35)25(19-23-10-6-4-7-11-23)32-29(36)22(3)31-26(20-24-12-8-5-9-13-24)30(37)33-14-16-38-17-15-33/h5,8-9,12-13,21-23,25-28,31,34-35H,4,6-7,10-11,14-20H2,1-3H3,(H,32,36)/t22?,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	85	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
Renin (Homo sapiens (Human))	BDBM50006146 (2-[1-(1-Cyclohexylmethyl-2,3-dihydroxy-5-methyl-he...) Show SMILES CCOC(=O)C(CCc1ccccc1)N[C@@H](CC(C)C)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CC(C)C Show InChI InChI=1S/C32H54N2O5/c1-6-39-32(38)26(18-17-24-13-9-7-10-14-24)33-28(19-22(2)3)31(37)34-27(21-25-15-11-8-12-16-25)30(36)29(35)20-23(4)5/h7,9-10,13-14,22-23,25-30,33,35-36H,6,8,11-12,15-21H2,1-5H3,(H,34,37)/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	160	n/a	n/a	n/a	n/a	6.0	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))	BDBM50006158 (2-[1-(1-Cyclohexylmethyl-2,3-dihydroxy-5-methyl-he...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)C(CC(C)C)N[C@@H](CCc1ccccc1)C(=O)OC(C)(C)C Show InChI InChI=1S/C34H58N2O5/c1-23(2)20-29(35-27(33(40)41-34(5,6)7)19-18-25-14-10-8-11-15-25)32(39)36-28(22-26-16-12-9-13-17-26)31(38)30(37)21-24(3)4/h8,10-11,14-15,23-24,26-31,35,37-38H,9,12-13,16-22H2,1-7H3,(H,36,39)/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	1.00E+3	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
Renin (Homo sapiens (Human))	BDBM50006142 (2-(1-Benzyl-2-morpholin-4-yl-2-oxo-ethylamino)-hex...) Show SMILES CCCC[C@H](N[C@@H](Cc1ccccc1)C(=O)N1CCOCC1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CC(C)C Show InChI InChI=1S/C33H55N3O5/c1-4-5-16-27(34-29(23-26-14-10-7-11-15-26)33(40)36-17-19-41-20-18-36)32(39)35-28(22-25-12-8-6-9-13-25)31(38)30(37)21-24(2)3/h7,10-11,14-15,24-25,27-31,34,37-38H,4-6,8-9,12-13,16-23H2,1-3H3,(H,35,39)/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	13	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 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))	BDBM50006161 (2-[1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-...) Show SMILES CCCC[C@H](N[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/C36H61N3O6/c1-5-6-17-30(35(42)38-31(23-27-13-9-7-10-14-27)34(41)33(40)22-26(2)3)37-32(24-28-15-11-8-12-16-28)36(43)39-20-18-29(19-21-39)45-25-44-4/h8,11-12,15-16,26-27,29-34,37,40-41H,5-7,9-10,13-14,17-25H2,1-4H3,(H,38,42)/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	3.90	n/a	n/a	n/a	n/a	6.0	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))	BDBM50006174 (2-[1-Benzyl-2-(4-methoxymethylsulfanyl-piperidin-1...) Show SMILES CCCC[C@H](O[C@@H](Cc1ccccc1)C(=O)N1CCC(CC1)SCOC)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CC(C)C Show InChI InChI=1S/C36H60N2O6S/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)44-33(24-28-15-11-8-12-16-28)36(42)38-20-18-29(19-21-38)45-25-43-4/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	1.80	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
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 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
Renin (Homo sapiens (Human))	BDBM50006163 (2-[1-(1-Cyclohexylmethyl-2,3-dihydroxy-5-methyl-he...) Show SMILES CCOC(=O)C(CCc1ccccc1)N[C@@H](C)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CC(C)C Show InChI InChI=1S/C29H48N2O5/c1-5-36-29(35)24(17-16-22-12-8-6-9-13-22)30-21(4)28(34)31-25(19-23-14-10-7-11-15-23)27(33)26(32)18-20(2)3/h6,8-9,12-13,20-21,23-27,30,32-33H,5,7,10-11,14-19H2,1-4H3,(H,31,34)/t21-,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	150	n/a	n/a	n/a	n/a	6.0	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

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