Compile Data Set for Download or QSAR

Found 289 hits with Last Name = 'barlow' and Initial = 'jl'   

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))	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))	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))	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))	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))	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))	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))	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))	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))	BDBM50006185 (5-{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](C(C)C)C(=O)NCCN1CCOCC1 Show InChI InChI=1S/C43H72N4O8/c1-5-6-17-39(55-40(29-34-15-11-8-12-16-34)43(51)47-21-18-35(19-22-47)54-31-52-4)42(50)45-37(28-33-13-9-7-10-14-33)38(48)30-36(32(2)3)41(49)44-20-23-46-24-26-53-27-25-46/h8,11-12,15-16,32-33,35-40,48H,5-7,9-10,13-14,17-31H2,1-4H3,(H,44,49)(H,45,50)/t36-,37-,38-,39-,40-/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))	BDBM50006206 (5-{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](C(C)C)C(=O)NCCc1ccccn1 Show InChI InChI=1S/C44H68N4O7/c1-5-6-20-40(55-41(29-34-17-11-8-12-18-34)44(52)48-26-22-36(23-27-48)54-31-53-4)43(51)47-38(28-33-15-9-7-10-16-33)39(49)30-37(32(2)3)42(50)46-25-21-35-19-13-14-24-45-35/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,47,51)/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	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 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))	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	1.10	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro 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))	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	1.10	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))	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	1.10	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 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))	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	1.10	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description In vitro 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))	BDBM50036999 ((2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymeth...) 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](C(C)C)C(=O)NCCNc1nnc(N)[nH]1 Show InChI InChI=1S/C41H68N8O7/c1-5-6-17-35(56-36(25-30-15-11-8-12-16-30)39(53)49-22-18-31(19-23-49)55-27-54-4)38(52)45-33(24-29-13-9-7-10-14-29)34(50)26-32(28(2)3)37(51)43-20-21-44-41-46-40(42)47-48-41/h8,11-12,15-16,28-29,31-36,50H,5-7,9-10,13-14,17-27H2,1-4H3,(H,43,51)(H,45,52)(H4,42,44,46,47,48)/t32-,33-,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	1.10	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Tested in vitro for its ability to inhibit the human plasma renin at pH of 7.4				J Med Chem 37: 2991-3007 (1994) BindingDB Entry DOI: 10.7270/Q26H4GFS
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006148 (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)O[C@@H](Cc1ccccc1)C(=O)N1CCC(CC1)OCOC)C(C)C Show InChI InChI=1S/C41H69N3O7/c1-6-8-20-37(51-38(27-32-18-14-11-15-19-32)41(48)44-24-21-33(22-25-44)50-29-49-5)40(47)43-35(26-31-16-12-10-13-17-31)36(45)28-34(30(3)4)39(46)42-23-9-7-2/h11,14-15,18-19,30-31,33-38,45H,6-10,12-13,16-17,20-29H2,1-5H3,(H,42,46)(H,43,47)/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	1.20	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 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))	BDBM50006211 (CHEMBL49218 | {4-[2-(2-tert-Butoxycarbonylamino-3-...) Show SMILES CC(C)[C@H](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)NC(=O)OCCc1ccccn1 Show InChI InChI=1S/C42H61N7O7/c1-28(2)33(48-40(53)55-21-19-31-18-12-13-20-44-31)25-37(50)34(22-29-14-8-6-9-15-29)46-39(52)36(24-32-26-43-27-45-32)47-38(51)35(23-30-16-10-7-11-17-30)49-41(54)56-42(3,4)5/h7,10-13,16-18,20,26-29,33-37,50H,6,8-9,14-15,19,21-25H2,1-5H3,(H,43,45)(H,46,52)(H,47,51)(H,48,53)(H,49,54)/t33-,34-,35-,36-,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	1.30	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))	BDBM50006204 (5-{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](C(C)C)C(=O)NCCC[N+]1([O-])CCOCC1 Show InChI InChI=1S/C44H74N4O9/c1-5-6-18-40(57-41(30-35-16-11-8-12-17-35)44(52)47-22-19-36(20-23-47)56-32-54-4)43(51)46-38(29-34-14-9-7-10-15-34)39(49)31-37(33(2)3)42(50)45-21-13-24-48(53)25-27-55-28-26-48/h8,11-12,16-17,33-34,36-41,49H,5-7,9-10,13-15,18-32H2,1-4H3,(H,45,50)(H,46,51)/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	1.30	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))	BDBM50006176 (CHEMBL264194 | {4-[2-(2-tert-Butoxycarbonylamino-3...) Show SMILES CC(C)[C@H](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)NC(=O)OCCN1CCOCC1 Show InChI InChI=1S/C41H65N7O8/c1-28(2)32(46-39(52)55-21-18-48-16-19-54-20-17-48)25-36(49)33(22-29-12-8-6-9-13-29)44-38(51)35(24-31-26-42-27-43-31)45-37(50)34(23-30-14-10-7-11-15-30)47-40(53)56-41(3,4)5/h7,10-11,14-15,26-29,32-36,49H,6,8-9,12-13,16-25H2,1-5H3,(H,42,43)(H,44,51)(H,45,50)(H,46,52)(H,47,53)/t32-,33-,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	1.30	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))	BDBM50006208 (5-{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](C(C)C)C(=O)NCCCn1ccnc1 Show InChI InChI=1S/C43H69N5O7/c1-5-6-18-39(55-40(28-34-16-11-8-12-17-34)43(52)48-24-19-35(20-25-48)54-31-53-4)42(51)46-37(27-33-14-9-7-10-15-33)38(49)29-36(32(2)3)41(50)45-21-13-23-47-26-22-44-30-47/h8,11-12,16-17,22,26,30,32-33,35-40,49H,5-7,9-10,13-15,18-21,23-25,27-29,31H2,1-4H3,(H,45,50)(H,46,51)/t36-,37-,38-,39-,40-/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	1.30	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))	BDBM50006150 (2-[1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-...) Show SMILES COCOC1CCN(CC1)C(=O)[C@H](Cc1ccccc1)O[C@@H](C)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CC(C)C Show InChI InChI=1S/C33H54N2O7/c1-23(2)19-29(36)31(37)28(20-25-11-7-5-8-12-25)34-32(38)24(3)42-30(21-26-13-9-6-10-14-26)33(39)35-17-15-27(16-18-35)41-22-40-4/h6,9-10,13-14,23-25,27-31,36-37H,5,7-8,11-12,15-22H2,1-4H3,(H,34,38)/t24-,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	1.30	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))	BDBM50011228 ((R)-2-Benzyl-N-[(S)-1-[(1S,2R)-1-cyclohexylmethyl-...) Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H50N6O7/c1-2-40-22-30(48-35(40)46)32(43)28(18-25-11-7-4-8-12-25)38-34(45)29(20-27-21-36-23-37-27)39-33(44)26(17-24-9-5-3-6-10-24)19-31(42)41-13-15-47-16-14-41/h3,5-6,9-10,21,23,25-26,28-30,32,43H,2,4,7-8,11-20,22H2,1H3,(H,36,37)(H,38,45)(H,39,44)/t26-,28+,29+,30+,32-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.30	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046801 (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)CCn1ccnc1)Cc1ccccc1 Show InChI InChI=1S/C37H54N6O5S/c1-26(2)18-33(44)35(46)31(20-28-12-8-5-9-13-28)40-37(48)32(22-30-23-49-25-39-30)41-36(47)29(19-27-10-6-4-7-11-27)21-34(45)42(3)16-17-43-15-14-38-24-43/h4,6-7,10-11,14-15,23-26,28-29,31-33,35,44,46H,5,8-9,12-13,16-22H2,1-3H3,(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	1.30	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))	BDBM50036995 (1N-[3-methylamino(cyano imino)methylaminopropyl]-5...) 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](C(C)C)C(=O)NCCCNC(NC)=NC#N |w:54.57| Show InChI InChI=1S/C43H71N7O7/c1-6-7-19-38(57-39(27-33-17-12-9-13-18-33)42(54)50-24-20-34(21-25-50)56-30-55-5)41(53)49-36(26-32-15-10-8-11-16-32)37(51)28-35(31(2)3)40(52)46-22-14-23-47-43(45-4)48-29-44/h9,12-13,17-18,31-32,34-39,51H,6-8,10-11,14-16,19-28,30H2,1-5H3,(H,46,52)(H,49,53)(H2,45,47,48)/t35-,36-,37-,38-,39-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.30	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Tested in vitro for its ability to inhibit the human plasma renin at pH of 7.4				J Med Chem 37: 2991-3007 (1994) BindingDB Entry DOI: 10.7270/Q26H4GFS
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50036979 (1N-[3-cyanoimino(methylsulfanyl)methylaminopropyl]...) 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](C(C)C)C(=O)NCCCNC(SC)=NC#N |w:54.57| Show InChI InChI=1S/C43H70N6O7S/c1-6-7-19-38(56-39(27-33-17-12-9-13-18-33)42(53)49-24-20-34(21-25-49)55-30-54-4)41(52)48-36(26-32-15-10-8-11-16-32)37(50)28-35(31(2)3)40(51)45-22-14-23-46-43(57-5)47-29-44/h9,12-13,17-18,31-32,34-39,50H,6-8,10-11,14-16,19-28,30H2,1-5H3,(H,45,51)(H,46,47)(H,48,52)/t35-,36-,37-,38-,39-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.30	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Tested in vitro for its ability to inhibit the human plasma renin				J Med Chem 37: 2991-3007 (1994) BindingDB Entry DOI: 10.7270/Q26H4GFS
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006141 (2-[1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-...) Show SMILES CCC[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/C35H58N2O7/c1-5-12-31(34(40)36-29(22-26-13-8-6-9-14-26)33(39)30(38)21-25(2)3)44-32(23-27-15-10-7-11-16-27)35(41)37-19-17-28(18-20-37)43-24-42-4/h7,10-11,15-16,25-26,28-33,38-39H,5-6,8-9,12-14,17-24H2,1-4H3,(H,36,40)/t29-,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	1.40	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))	BDBM50006197 (5-{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](C(C)C)C(=O)NCCC[N+](C)(C)[O-] Show InChI InChI=1S/C42H72N4O8/c1-7-8-20-38(54-39(28-33-18-13-10-14-19-33)42(50)45-24-21-34(22-25-45)53-30-52-6)41(49)44-36(27-32-16-11-9-12-17-32)37(47)29-35(31(2)3)40(48)43-23-15-26-46(4,5)51/h10,13-14,18-19,31-32,34-39,47H,7-9,11-12,15-17,20-30H2,1-6H3,(H,43,48)(H,44,49)/t35-,36-,37-,38-,39-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.40	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))	BDBM50006195 ((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)OCCN1CCOCC1)C(C)C Show InChI InChI=1S/C43H72N4O9/c1-5-6-17-39(56-40(29-34-15-11-8-12-16-34)42(50)47-20-18-35(19-21-47)55-31-52-4)41(49)44-37(28-33-13-9-7-10-14-33)38(48)30-36(32(2)3)45-43(51)54-27-24-46-22-25-53-26-23-46/h8,11-12,15-16,32-33,35-40,48H,5-7,9-10,13-14,17-31H2,1-4H3,(H,44,49)(H,45,51)/t36-,37-,38-,39-,40-/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	1.40	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))	BDBM50006196 ((4-{2-[1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl...) Show SMILES CCCC[C@H](N[C@@H](Cc1ccccc1)C(=O)N1CCC(CC1)OCOC)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)C[C@H](NC(=O)OCCN(C)C)C(C)C Show InChI InChI=1S/C41H71N5O7/c1-7-8-19-34(42-37(27-32-17-13-10-14-18-32)40(49)46-22-20-33(21-23-46)53-29-51-6)39(48)43-36(26-31-15-11-9-12-16-31)38(47)28-35(30(2)3)44-41(50)52-25-24-45(4)5/h10,13-14,17-18,30-31,33-38,42,47H,7-9,11-12,15-16,19-29H2,1-6H3,(H,43,48)(H,44,50)/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	1.5	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))	BDBM50006184 ((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)OCCC)C(C)C Show InChI InChI=1S/C40H67N3O8/c1-6-8-19-36(51-37(26-31-17-13-10-14-18-31)39(46)43-22-20-32(21-23-43)50-28-48-5)38(45)41-34(25-30-15-11-9-12-16-30)35(44)27-33(29(3)4)42-40(47)49-24-7-2/h10,13-14,17-18,29-30,32-37,44H,6-9,11-12,15-16,19-28H2,1-5H3,(H,41,45)(H,42,47)/t33-,34-,35-,36-,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	1.5	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))	BDBM50006148 (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)O[C@@H](Cc1ccccc1)C(=O)N1CCC(CC1)OCOC)C(C)C Show InChI InChI=1S/C41H69N3O7/c1-6-8-20-37(51-38(27-32-18-14-11-15-19-32)41(48)44-24-21-33(22-25-44)50-29-49-5)40(47)43-35(26-31-16-12-10-13-17-31)36(45)28-34(30(3)4)39(46)42-23-9-7-2/h11,14-15,18-19,30-31,33-38,45H,6-10,12-13,16-17,20-29H2,1-5H3,(H,42,46)(H,43,47)/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	1.5	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))	BDBM50036977 (1N-[3-amino(cyanoimino)methylaminopropyl]-5-[1-[1-...) 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](C(C)C)C(=O)NCCCNC(N)=NC#N |w:53.56| Show InChI InChI=1S/C42H69N7O7/c1-5-6-18-37(56-38(26-32-16-11-8-12-17-32)41(53)49-23-19-33(20-24-49)55-29-54-4)40(52)48-35(25-31-14-9-7-10-15-31)36(50)27-34(30(2)3)39(51)45-21-13-22-46-42(44)47-28-43/h8,11-12,16-17,30-31,33-38,50H,5-7,9-10,13-15,18-27,29H2,1-4H3,(H,45,51)(H,48,52)(H3,44,46,47)/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	1.5	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Tested in vitro for its ability to inhibit the human plasma renin at pH of 7.4				J Med Chem 37: 2991-3007 (1994) BindingDB Entry DOI: 10.7270/Q26H4GFS
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50046806 (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](Cc1cscn1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CC(C)C Show InChI InChI=1S/C38H60N4O8S/c1-27(2)19-34(43)36(45)32(21-29-13-9-6-10-14-29)40-38(47)33(23-31-24-51-25-39-31)41-37(46)30(20-28-11-7-5-8-12-28)22-35(44)42(3)15-16-49-26-50-18-17-48-4/h5,7-8,11-12,24-25,27,29-30,32-34,36,43,45H,6,9-10,13-23,26H2,1-4H3,(H,40,47)(H,41,46)/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	1.60	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))	BDBM50046808 (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](Cn1cccn1)NC(=O)[C@@H](CC(=O)N(C)CCc1ccccn1)Cc1ccccc1 Show InChI InChI=1S/C39H56N6O5/c1-28(2)23-35(46)37(48)33(25-30-15-8-5-9-16-30)42-39(50)34(27-45-21-12-20-41-45)43-38(49)31(24-29-13-6-4-7-14-29)26-36(47)44(3)22-18-32-17-10-11-19-40-32/h4,6-7,10-14,17,19-21,28,30-31,33-35,37,46,48H,5,8-9,15-16,18,22-27H2,1-3H3,(H,42,50)(H,43,49)/t31-,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	1.60	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))	BDBM50022647 (2-Benzyl-N-[1-(1-cyclohexylmethyl-2,3-dihydroxy-5-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H53N5O6/c1-24(2)17-31(41)33(43)29(19-26-11-7-4-8-12-26)38-35(45)30(21-28-22-36-23-37-28)39-34(44)27(18-25-9-5-3-6-10-25)20-32(42)40-13-15-46-16-14-40/h3,5-6,9-10,22-24,26-27,29-31,33,41,43H,4,7-8,11-21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)/t27-,29+,30+,31+,33-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.60	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin at pH 7.4				J Med Chem 36: 449-59 (1993) BindingDB Entry DOI: 10.7270/Q20K27M6
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50036989 ((2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymeth...) 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](C(C)C)C(=O)NCCCNc1nnc(N)[nH]1 Show InChI InChI=1S/C42H70N8O7/c1-5-6-18-36(57-37(26-31-16-11-8-12-17-31)40(54)50-23-19-32(20-24-50)56-28-55-4)39(53)46-34(25-30-14-9-7-10-15-30)35(51)27-33(29(2)3)38(52)44-21-13-22-45-42-47-41(43)48-49-42/h8,11-12,16-17,29-30,32-37,51H,5-7,9-10,13-15,18-28H2,1-4H3,(H,44,52)(H,46,53)(H4,43,45,47,48,49)/t33-,34-,35-,36-,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	1.70	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Tested in vitro for its ability to inhibit the human plasma renin at pH of 7.4				J Med Chem 37: 2991-3007 (1994) BindingDB Entry DOI: 10.7270/Q26H4GFS
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006207 (CHEMBL301395 | {4-[2-(2-tert-Butoxycarbonylamino-3...) Show SMILES CCCOC(=O)N[C@@H](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)C(C)C Show InChI InChI=1S/C38H60N6O7/c1-7-18-50-36(48)43-29(25(2)3)22-33(45)30(19-26-14-10-8-11-15-26)41-35(47)32(21-28-23-39-24-40-28)42-34(46)31(20-27-16-12-9-13-17-27)44-37(49)51-38(4,5)6/h9,12-13,16-17,23-26,29-33,45H,7-8,10-11,14-15,18-22H2,1-6H3,(H,39,40)(H,41,47)(H,42,46)(H,43,48)(H,44,49)/t29-,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	1.70	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))	BDBM50036974 (1N-[2-amino(cyanoimino)methylaminoethyl]-5-[1-[1-b...) 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](C(C)C)C(=O)NCCNC(N)=NC#N |w:52.55| Show InChI InChI=1S/C41H67N7O7/c1-5-6-17-36(55-37(25-31-15-11-8-12-16-31)40(52)48-22-18-32(19-23-48)54-28-53-4)39(51)47-34(24-30-13-9-7-10-14-30)35(49)26-33(29(2)3)38(50)44-20-21-45-41(43)46-27-42/h8,11-12,15-16,29-30,32-37,49H,5-7,9-10,13-14,17-26,28H2,1-4H3,(H,44,50)(H,47,51)(H3,43,45,46)/t33-,34-,35-,36-,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	1.80	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Tested in vitro for its ability to inhibit the human plasma renin at pH of 7.4				J Med Chem 37: 2991-3007 (1994) BindingDB Entry DOI: 10.7270/Q26H4GFS
					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	1.80	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				3D Structure (docked)
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))	BDBM50046805 (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)N(C)CCc1ccccn1 Show InChI InChI=1S/C38H55N5O6S2/c1-27(2)20-35(44)36(45)33(22-29-14-8-5-9-15-29)41-38(47)34(23-32-24-50-26-40-32)42-37(46)30(21-28-12-6-4-7-13-28)25-51(48,49)43(3)19-17-31-16-10-11-18-39-31/h4,6-7,10-13,16,18,24,26-27,29-30,33-36,44-45H,5,8-9,14-15,17,19-23,25H2,1-3H3,(H,41,47)(H,42,46)/t30-,33+,34+,35+,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	1.80	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))	BDBM50006200 ((4-{2-[1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl...) Show SMILES CCCC[C@H](N[C@@H](Cc1ccccc1)C(=O)N1CCC(CC1)OCOC)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)C[C@H](NC(=O)OCCN1CCOCC1)C(C)C Show InChI InChI=1S/C43H73N5O8/c1-5-6-17-36(44-39(29-34-15-11-8-12-16-34)42(51)48-20-18-35(19-21-48)56-31-53-4)41(50)45-38(28-33-13-9-7-10-14-33)40(49)30-37(32(2)3)46-43(52)55-27-24-47-22-25-54-26-23-47/h8,11-12,15-16,32-33,35-40,44,49H,5-7,9-10,13-14,17-31H2,1-4H3,(H,45,50)(H,46,52)/t36-,37-,38-,39-,40-/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 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))	BDBM50037007 ((2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymeth...) 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](C(C)C)C(=O)NCCCNC(N)=O Show InChI InChI=1S/C41H69N5O8/c1-5-6-18-36(54-37(26-31-16-11-8-12-17-31)40(50)46-23-19-32(20-24-46)53-28-52-4)39(49)45-34(25-30-14-9-7-10-15-30)35(47)27-33(29(2)3)38(48)43-21-13-22-44-41(42)51/h8,11-12,16-17,29-30,32-37,47H,5-7,9-10,13-15,18-28H2,1-4H3,(H,43,48)(H,45,49)(H3,42,44,51)/t33-,34-,35-,36-,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	2	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Tested in vitro for its ability to inhibit the human plasma renin at pH of 7.4				J Med Chem 37: 2991-3007 (1994) BindingDB Entry DOI: 10.7270/Q26H4GFS
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006179 ((2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymeth...) Show SMILES CCCC[C@H](N[C@@H](Cc1ccccc1)C(=O)N1CCC(CC1)OCOC)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)C[C@@H](C(C)C)C(=O)NCCCn1ccnc1 Show InChI InChI=1S/C43H70N6O6/c1-5-6-18-37(46-39(28-34-16-11-8-12-17-34)43(53)49-24-19-35(20-25-49)55-31-54-4)42(52)47-38(27-33-14-9-7-10-15-33)40(50)29-36(32(2)3)41(51)45-21-13-23-48-26-22-44-30-48/h8,11-12,16-17,22,26,30,32-33,35-40,46,50H,5-7,9-10,13-15,18-21,23-25,27-29,31H2,1-4H3,(H,45,51)(H,47,52)/t36-,37-,38-,39-,40-/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	2	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))	BDBM50006192 (5-{2-[1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)...) Show SMILES CCCC[C@H](N[C@@H](Cc1ccccc1)C(=O)N1CCC(CC1)OCOC)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)C[C@@H](C(C)C)C(=O)NCCCN(C)C Show InChI InChI=1S/C42H73N5O6/c1-7-8-20-36(44-38(28-33-18-13-10-14-19-33)42(51)47-25-21-34(22-26-47)53-30-52-6)41(50)45-37(27-32-16-11-9-12-17-32)39(48)29-35(31(2)3)40(49)43-23-15-24-46(4)5/h10,13-14,18-19,31-32,34-39,44,48H,7-9,11-12,15-17,20-30H2,1-6H3,(H,43,49)(H,45,50)/t35-,36-,37-,38-,39-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.10	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				3D Structure (docked)
Renin (Homo sapiens (Human))	BDBM50036985 ((2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymeth...) 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](C(C)C)C(=O)NCCNC(N)=S Show InChI InChI=1S/C40H67N5O7S/c1-5-6-17-35(52-36(25-30-15-11-8-12-16-30)39(49)45-22-18-31(19-23-45)51-27-50-4)38(48)44-33(24-29-13-9-7-10-14-29)34(46)26-32(28(2)3)37(47)42-20-21-43-40(41)53/h8,11-12,15-16,28-29,31-36,46H,5-7,9-10,13-14,17-27H2,1-4H3,(H,42,47)(H,44,48)(H3,41,43,53)/t32-,33-,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	2.20	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Tested in vitro for its ability to inhibit the human plasma renin at pH of 7.4				J Med Chem 37: 2991-3007 (1994) BindingDB Entry DOI: 10.7270/Q26H4GFS
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50006183 ((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)OCc1ccccc1)C(C)C Show InChI InChI=1S/C44H67N3O8/c1-5-6-22-40(55-41(28-34-18-12-8-13-19-34)43(50)47-25-23-36(24-26-47)54-31-52-4)42(49)45-38(27-33-16-10-7-11-17-33)39(48)29-37(32(2)3)46-44(51)53-30-35-20-14-9-15-21-35/h8-9,12-15,18-21,32-33,36-41,48H,5-7,10-11,16-17,22-31H2,1-4H3,(H,45,49)(H,46,51)/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	2.20	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))	BDBM50006202 (3-Amino-N-[1-[1-(1-cyclohexylmethyl-2,3-dihydroxy-...) Show SMILES COc1ccc(C[C@H](NC(=O)CC(C)(C)N)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N[C@@H](CC2CCCCC2)[C@@H](O)[C@@H](O)CC(C)C)cc1 Show InChI InChI=1S/C35H56N6O6/c1-22(2)15-30(42)32(44)27(16-23-9-7-6-8-10-23)40-34(46)29(18-25-20-37-21-38-25)41-33(45)28(39-31(43)19-35(3,4)36)17-24-11-13-26(47-5)14-12-24/h11-14,20-23,27-30,32,42,44H,6-10,15-19,36H2,1-5H3,(H,37,38)(H,39,43)(H,40,46)(H,41,45)/t27-,28-,29-,30-,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.30	n/a	n/a	n/a	n/a	7.7	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against renin in monkey plasma at pH 7.7				J Med Chem 35: 1735-46 (1992) BindingDB Entry DOI: 10.7270/Q27943MQ
					More data for this Ligand-Target Pair

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