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Compile Data Set for Download or QSAR

Found 33 hits Enz. Inhib. hit(s) with all data for entry = 50035883   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Renin


(Homo sapiens (Human))
BDBM50014078
PNG
(A-62198 | CHEMBL291591 | N-{(S)-1-[(S)-1-((1S,2R,3...)
Show SMILES CC(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CN=[N+]=[N-]
Show InChI InChI=1S/C30H44N8O5/c1-19(2)28(41)36-24(14-21-11-7-4-8-12-21)29(42)37-25(15-22-16-32-18-33-22)30(43)35-23(13-20-9-5-3-6-10-20)27(40)26(39)17-34-38-31/h4,7-8,11-12,16,18-20,23-27,39-40H,3,5-6,9-10,13-15,17H2,1-2H3,(H,32,33)(H,35,43)(H,36,41)(H,37,42)/t23-,24-,25-,26-,27+/m0/s1
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n/an/a 0.290n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014084
PNG
((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOCOCCOC)Cc1ccccc1
Show InChI InChI=1S/C38H58N6O9/c1-4-44-24-33(53-38(44)49)35(46)31(20-28-13-9-6-10-14-28)41-37(48)32(22-30-23-39-25-40-30)42-36(47)29(19-27-11-7-5-8-12-27)21-34(45)43(2)15-16-51-26-52-18-17-50-3/h5,7-8,11-12,23,25,28-29,31-33,35,46H,4,6,9-10,13-22,24,26H2,1-3H3,(H,39,40)(H,41,48)(H,42,47)/t29-,31+,32+,33+,35-/m1/s1
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n/an/a 0.330n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014084
PNG
((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOCOCCOC)Cc1ccccc1
Show InChI InChI=1S/C38H58N6O9/c1-4-44-24-33(53-38(44)49)35(46)31(20-28-13-9-6-10-14-28)41-37(48)32(22-30-23-39-25-40-30)42-36(47)29(19-27-11-7-5-8-12-27)21-34(45)43(2)15-16-51-26-52-18-17-50-3/h5,7-8,11-12,23,25,28-29,31-33,35,46H,4,6,9-10,13-22,24,26H2,1-3H3,(H,39,40)(H,41,48)(H,42,47)/t29-,31+,32+,33+,35-/m1/s1
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n/an/a 0.370n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014081
PNG
((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOCOC)Cc1ccccc1
Show InChI InChI=1S/C36H54N6O8/c1-4-42-22-31(50-36(42)47)33(44)29(18-26-13-9-6-10-14-26)39-35(46)30(20-28-21-37-23-38-28)40-34(45)27(17-25-11-7-5-8-12-25)19-32(43)41(2)15-16-49-24-48-3/h5,7-8,11-12,21,23,26-27,29-31,33,44H,4,6,9-10,13-20,22,24H2,1-3H3,(H,37,38)(H,39,46)(H,40,45)/t27-,29+,30+,31+,33-/m1/s1
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n/an/a 0.490n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014084
PNG
((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOCOCCOC)Cc1ccccc1
Show InChI InChI=1S/C38H58N6O9/c1-4-44-24-33(53-38(44)49)35(46)31(20-28-13-9-6-10-14-28)41-37(48)32(22-30-23-39-25-40-30)42-36(47)29(19-27-11-7-5-8-12-27)21-34(45)43(2)15-16-51-26-52-18-17-50-3/h5,7-8,11-12,23,25,28-29,31-33,35,46H,4,6,9-10,13-22,24,26H2,1-3H3,(H,39,40)(H,41,48)(H,42,47)/t29-,31+,32+,33+,35-/m1/s1
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n/an/a 0.570n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014073
PNG
((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOC)Cc1ccccc1
Show InChI InChI=1S/C35H52N6O7/c1-4-41-22-30(48-35(41)46)32(43)28(18-25-13-9-6-10-14-25)38-34(45)29(20-27-21-36-23-37-27)39-33(44)26(17-24-11-7-5-8-12-24)19-31(42)40(2)15-16-47-3/h5,7-8,11-12,21,23,25-26,28-30,32,43H,4,6,9-10,13-20,22H2,1-3H3,(H,36,37)(H,38,45)(H,39,44)/t26-,28+,29+,30+,32-/m1/s1
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n/an/a 0.590n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014079
PNG
((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCO)Cc1ccccc1
Show InChI InChI=1S/C34H50N6O7/c1-3-40-21-29(47-34(40)46)31(43)27(17-24-12-8-5-9-13-24)37-33(45)28(19-26-20-35-22-36-26)38-32(44)25(16-23-10-6-4-7-11-23)18-30(42)39(2)14-15-41/h4,6-7,10-11,20,22,24-25,27-29,31,41,43H,3,5,8-9,12-19,21H2,1-2H3,(H,35,36)(H,37,45)(H,38,44)/t25-,27+,28+,29+,31-/m1/s1
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n/an/a 0.850n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50011228
PNG
((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
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n/an/a 0.990n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014081
PNG
((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOCOC)Cc1ccccc1
Show InChI InChI=1S/C36H54N6O8/c1-4-42-22-31(50-36(42)47)33(44)29(18-26-13-9-6-10-14-26)39-35(46)30(20-28-21-37-23-38-28)40-34(45)27(17-25-11-7-5-8-12-25)19-32(43)41(2)15-16-49-24-48-3/h5,7-8,11-12,21,23,26-27,29-31,33,44H,4,6,9-10,13-20,22,24H2,1-3H3,(H,37,38)(H,39,46)(H,40,45)/t27-,29+,30+,31+,33-/m1/s1
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n/an/a 1.10n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50011228
PNG
((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
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n/an/a 1.30n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014073
PNG
((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCOC)Cc1ccccc1
Show InChI InChI=1S/C35H52N6O7/c1-4-41-22-30(48-35(41)46)32(43)28(18-25-13-9-6-10-14-25)38-34(45)29(20-27-21-36-23-37-27)39-33(44)26(17-24-11-7-5-8-12-24)19-31(42)40(2)15-16-47-3/h5,7-8,11-12,21,23,25-26,28-30,32,43H,4,6,9-10,13-20,22H2,1-3H3,(H,36,37)(H,38,45)(H,39,44)/t26-,28+,29+,30+,32-/m1/s1
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n/an/a 1.5n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014071
PNG
((R)-2-Benzyl-4-[(3R,4S)-3,4-bis-(2-methoxy-ethoxym...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1C[C@@H](OCOCCOC)[C@H](C1)OCOCCOC)Cc1ccccc1
Show InChI InChI=1S/C43H66N6O12/c1-4-48-26-38(61-43(48)54)40(51)34(20-31-13-9-6-10-14-31)46-42(53)35(22-33-23-44-27-45-33)47-41(52)32(19-30-11-7-5-8-12-30)21-39(50)49-24-36(59-28-57-17-15-55-2)37(25-49)60-29-58-18-16-56-3/h5,7-8,11-12,23,27,31-32,34-38,40,51H,4,6,9-10,13-22,24-26,28-29H2,1-3H3,(H,44,45)(H,46,53)(H,47,52)/t32-,34+,35+,36-,37+,38+,40-/m1/s1
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n/an/a 1.60n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014085
PNG
((S)-N-[(S)-1-[(1S,2R)-1-Cyclohexylmethyl-2-((S)-3-...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N(C)CCOCOCCOC
Show InChI InChI=1S/C38H59N7O10/c1-5-45-23-33(55-38(45)50)34(46)30(19-26-9-7-6-8-10-26)41-36(48)32(21-28-22-39-24-40-28)42-35(47)31(20-27-11-13-29(52-4)14-12-27)43-37(49)44(2)15-16-53-25-54-18-17-51-3/h11-14,22,24,26,30-34,46H,5-10,15-21,23,25H2,1-4H3,(H,39,40)(H,41,48)(H,42,47)(H,43,49)/t30-,31-,32-,33-,34+/m0/s1
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n/an/a 1.70n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014072
PNG
(CHEMBL58968 | N-[(S)-1-[(S)-1-[(1S,2R)-1-Cyclohexy...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)C(C)C
Show InChI InChI=1S/C34H50N6O7/c1-5-40-19-29(47-34(40)45)30(41)26(15-22-9-7-6-8-10-22)37-33(44)28(17-24-18-35-20-36-24)39-32(43)27(38-31(42)21(2)3)16-23-11-13-25(46-4)14-12-23/h11-14,18,20-22,26-30,41H,5-10,15-17,19H2,1-4H3,(H,35,36)(H,37,44)(H,38,42)(H,39,43)/t26-,27-,28-,29-,30+/m0/s1
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n/an/a 1.70n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014079
PNG
((R)-2-Benzyl-N*1*-[(S)-1-[(1S,2R)-1-cyclohexylmeth...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N(C)CCO)Cc1ccccc1
Show InChI InChI=1S/C34H50N6O7/c1-3-40-21-29(47-34(40)46)31(43)27(17-24-12-8-5-9-13-24)37-33(45)28(19-26-20-35-22-36-26)38-32(44)25(16-23-10-6-4-7-11-23)18-30(42)39(2)14-15-41/h4,6-7,10-11,20,22,24-25,27-29,31,41,43H,3,5,8-9,12-19,21H2,1-2H3,(H,35,36)(H,37,45)(H,38,44)/t25-,27+,28+,29+,31-/m1/s1
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n/an/a 2.5n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014083
PNG
((R)-2-Benzyl-4-((3R,4S)-3,4-bis-methoxymethoxy-pyr...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1C[C@@H](OCOC)[C@H](C1)OCOC)Cc1ccccc1
Show InChI InChI=1S/C39H58N6O10/c1-4-44-22-34(55-39(44)50)36(47)30(16-27-13-9-6-10-14-27)42-38(49)31(18-29-19-40-23-41-29)43-37(48)28(15-26-11-7-5-8-12-26)17-35(46)45-20-32(53-24-51-2)33(21-45)54-25-52-3/h5,7-8,11-12,19,23,27-28,30-34,36,47H,4,6,9-10,13-18,20-22,24-25H2,1-3H3,(H,40,41)(H,42,49)(H,43,48)/t28-,30+,31+,32-,33+,34+,36-/m1/s1
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n/an/a 2.70n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014077
PNG
(CHEMBL61777 | Morpholine-4-carboxylic acid [(S)-1-...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1CCOCC1
Show InChI InChI=1S/C35H51N7O8/c1-3-41-21-30(50-35(41)47)31(43)27(17-23-7-5-4-6-8-23)38-33(45)29(19-25-20-36-22-37-25)39-32(44)28(18-24-9-11-26(48-2)12-10-24)40-34(46)42-13-15-49-16-14-42/h9-12,20,22-23,27-31,43H,3-8,13-19,21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)(H,40,46)/t27-,28-,29-,30-,31+/m0/s1
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n/an/a 3.40n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014080
PNG
((S)-N-[(S)-1-[(1S,2R)-1-Cyclohexylmethyl-2-((S)-3-...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N(C)CCOCOC
Show InChI InChI=1S/C36H55N7O9/c1-5-43-21-31(52-36(43)48)32(44)28(17-24-9-7-6-8-10-24)39-34(46)30(19-26-20-37-22-38-26)40-33(45)29(18-25-11-13-27(50-4)14-12-25)41-35(47)42(2)15-16-51-23-49-3/h11-14,20,22,24,28-32,44H,5-10,15-19,21,23H2,1-4H3,(H,37,38)(H,39,46)(H,40,45)(H,41,47)/t28-,29-,30-,31-,32+/m0/s1
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n/an/a 4.60n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014075
PNG
((3R,4S)-3,4-Dihydroxy-pyrrolidine-1-carboxylic aci...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1C[C@H](O)[C@H](O)C1
Show InChI InChI=1S/C35H51N7O9/c1-3-41-19-30(51-35(41)49)31(45)25(13-21-7-5-4-6-8-21)38-33(47)27(15-23-16-36-20-37-23)39-32(46)26(14-22-9-11-24(50-2)12-10-22)40-34(48)42-17-28(43)29(44)18-42/h9-12,16,20-21,25-31,43-45H,3-8,13-15,17-19H2,1-2H3,(H,36,37)(H,38,47)(H,39,46)(H,40,48)/t25-,26-,27-,28-,29+,30-,31+/m0/s1
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n/an/a 6.90n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014071
PNG
((R)-2-Benzyl-4-[(3R,4S)-3,4-bis-(2-methoxy-ethoxym...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1C[C@@H](OCOCCOC)[C@H](C1)OCOCCOC)Cc1ccccc1
Show InChI InChI=1S/C43H66N6O12/c1-4-48-26-38(61-43(48)54)40(51)34(20-31-13-9-6-10-14-31)46-42(53)35(22-33-23-44-27-45-33)47-41(52)32(19-30-11-7-5-8-12-30)21-39(50)49-24-36(59-28-57-17-15-55-2)37(25-49)60-29-58-18-16-56-3/h5,7-8,11-12,23,27,31-32,34-38,40,51H,4,6,9-10,13-22,24-26,28-29H2,1-3H3,(H,44,45)(H,46,53)(H,47,52)/t32-,34+,35+,36-,37+,38+,40-/m1/s1
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n/an/a 7.30n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014082
PNG
((S)-N-[(S)-1-[(1S,2R)-1-Cyclohexylmethyl-2-((S)-3-...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N(C)CC(O)CO
Show InChI InChI=1S/C35H53N7O9/c1-4-42-19-30(51-35(42)49)31(45)27(14-22-8-6-5-7-9-22)38-33(47)29(16-24-17-36-21-37-24)39-32(46)28(15-23-10-12-26(50-3)13-11-23)40-34(48)41(2)18-25(44)20-43/h10-13,17,21-22,25,27-31,43-45H,4-9,14-16,18-20H2,1-3H3,(H,36,37)(H,38,47)(H,39,46)(H,40,48)/t25?,27-,28-,29-,30-,31+/m0/s1
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n/an/a 7.90n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014076
PNG
((3R,4S)-3,4-Bis-(2-methoxy-ethoxymethoxy)-pyrrolid...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1C[C@@H](OCOCCOC)[C@H](C1)OCOCCOC
Show InChI InChI=1S/C43H67N7O13/c1-5-49-25-38(63-43(49)55)39(51)33(19-29-9-7-6-8-10-29)46-41(53)35(21-31-22-44-26-45-31)47-40(52)34(20-30-11-13-32(58-4)14-12-30)48-42(54)50-23-36(61-27-59-17-15-56-2)37(24-50)62-28-60-18-16-57-3/h11-14,22,26,29,33-39,51H,5-10,15-21,23-25,27-28H2,1-4H3,(H,44,45)(H,46,53)(H,47,52)(H,48,54)/t33-,34-,35-,36-,37+,38-,39+/m0/s1
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n/an/a 8.5n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014075
PNG
((3R,4S)-3,4-Dihydroxy-pyrrolidine-1-carboxylic aci...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1C[C@H](O)[C@H](O)C1
Show InChI InChI=1S/C35H51N7O9/c1-3-41-19-30(51-35(41)49)31(45)25(13-21-7-5-4-6-8-21)38-33(47)27(15-23-16-36-20-37-23)39-32(46)26(14-22-9-11-24(50-2)12-10-22)40-34(48)42-17-28(43)29(44)18-42/h9-12,16,20-21,25-31,43-45H,3-8,13-15,17-19H2,1-2H3,(H,36,37)(H,38,47)(H,39,46)(H,40,48)/t25-,26-,27-,28-,29+,30-,31+/m0/s1
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n/an/a 8.70n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014077
PNG
(CHEMBL61777 | Morpholine-4-carboxylic acid [(S)-1-...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1CCOCC1
Show InChI InChI=1S/C35H51N7O8/c1-3-41-21-30(50-35(41)47)31(43)27(17-23-7-5-4-6-8-23)38-33(45)29(19-25-20-36-22-37-25)39-32(44)28(18-24-9-11-26(48-2)12-10-24)40-34(46)42-13-15-49-16-14-42/h9-12,20,22-23,27-31,43H,3-8,13-19,21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)(H,40,46)/t27-,28-,29-,30-,31+/m0/s1
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n/an/a 9.60n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014072
PNG
(CHEMBL58968 | N-[(S)-1-[(S)-1-[(1S,2R)-1-Cyclohexy...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)C(C)C
Show InChI InChI=1S/C34H50N6O7/c1-5-40-19-29(47-34(40)45)30(41)26(15-22-9-7-6-8-10-22)37-33(44)28(17-24-18-35-20-36-24)39-32(43)27(38-31(42)21(2)3)16-23-11-13-25(46-4)14-12-23/h11-14,18,20-22,26-30,41H,5-10,15-17,19H2,1-4H3,(H,35,36)(H,37,44)(H,38,42)(H,39,43)/t26-,27-,28-,29-,30+/m0/s1
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n/an/a 9.90n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014083
PNG
((R)-2-Benzyl-4-((3R,4S)-3,4-bis-methoxymethoxy-pyr...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1C[C@@H](OCOC)[C@H](C1)OCOC)Cc1ccccc1
Show InChI InChI=1S/C39H58N6O10/c1-4-44-22-34(55-39(44)50)36(47)30(16-27-13-9-6-10-14-27)42-38(49)31(18-29-19-40-23-41-29)43-37(48)28(15-26-11-7-5-8-12-26)17-35(46)45-20-32(53-24-51-2)33(21-45)54-25-52-3/h5,7-8,11-12,19,23,27-28,30-34,36,47H,4,6,9-10,13-18,20-22,24-25H2,1-3H3,(H,40,41)(H,42,49)(H,43,48)/t28-,30+,31+,32-,33+,34+,36-/m1/s1
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n/an/a 11n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014074
PNG
((3R,4S)-3,4-Bis-methoxymethoxy-pyrrolidine-1-carbo...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1C[C@@H](OCOC)[C@H](C1)OCOC
Show InChI InChI=1S/C39H59N7O11/c1-5-45-21-34(57-39(45)51)35(47)29(15-25-9-7-6-8-10-25)42-37(49)31(17-27-18-40-22-41-27)43-36(48)30(16-26-11-13-28(54-4)14-12-26)44-38(50)46-19-32(55-23-52-2)33(20-46)56-24-53-3/h11-14,18,22,25,29-35,47H,5-10,15-17,19-21,23-24H2,1-4H3,(H,40,41)(H,42,49)(H,43,48)(H,44,50)/t29-,30-,31-,32-,33+,34-,35+/m0/s1
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n/an/a 12n/an/an/an/a6.5n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014085
PNG
((S)-N-[(S)-1-[(1S,2R)-1-Cyclohexylmethyl-2-((S)-3-...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N(C)CCOCOCCOC
Show InChI InChI=1S/C38H59N7O10/c1-5-45-23-33(55-38(45)50)34(46)30(19-26-9-7-6-8-10-26)41-36(48)32(21-28-22-39-24-40-28)42-35(47)31(20-27-11-13-29(52-4)14-12-27)43-37(49)44(2)15-16-53-25-54-18-17-51-3/h11-14,22,24,26,30-34,46H,5-10,15-21,23,25H2,1-4H3,(H,39,40)(H,41,48)(H,42,47)(H,43,49)/t30-,31-,32-,33-,34+/m0/s1
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n/an/a 14n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50006202
PNG
(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
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n/an/a 14n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014076
PNG
((3R,4S)-3,4-Bis-(2-methoxy-ethoxymethoxy)-pyrrolid...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1C[C@@H](OCOCCOC)[C@H](C1)OCOCCOC
Show InChI InChI=1S/C43H67N7O13/c1-5-49-25-38(63-43(49)55)39(51)33(19-29-9-7-6-8-10-29)46-41(53)35(21-31-22-44-26-45-31)47-40(52)34(20-30-11-13-32(58-4)14-12-30)48-42(54)50-23-36(61-27-59-17-15-56-2)37(24-50)62-28-60-18-16-57-3/h11-14,22,26,29,33-39,51H,5-10,15-21,23-25,27-28H2,1-4H3,(H,44,45)(H,46,53)(H,47,52)(H,48,54)/t33-,34-,35-,36-,37+,38-,39+/m0/s1
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n/an/a 26n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014080
PNG
((S)-N-[(S)-1-[(1S,2R)-1-Cyclohexylmethyl-2-((S)-3-...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N(C)CCOCOC
Show InChI InChI=1S/C36H55N7O9/c1-5-43-21-31(52-36(43)48)32(44)28(17-24-9-7-6-8-10-24)39-34(46)30(19-26-20-37-22-38-26)40-33(45)29(18-25-11-13-27(50-4)14-12-25)41-35(47)42(2)15-16-51-23-49-3/h11-14,20,22,24,28-32,44H,5-10,15-19,21,23H2,1-4H3,(H,37,38)(H,39,46)(H,40,45)(H,41,47)/t28-,29-,30-,31-,32+/m0/s1
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n/an/a 27n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against purified human renal renin at pH 6.5


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014082
PNG
((S)-N-[(S)-1-[(1S,2R)-1-Cyclohexylmethyl-2-((S)-3-...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N(C)CC(O)CO
Show InChI InChI=1S/C35H53N7O9/c1-4-42-19-30(51-35(42)49)31(45)27(14-22-8-6-5-7-9-22)38-33(47)29(16-24-17-36-21-37-24)39-32(46)28(15-23-10-12-26(50-3)13-11-23)40-34(48)41(2)18-25(44)20-43/h10-13,17,21-22,25,27-31,43-45H,4-9,14-16,18-20H2,1-3H3,(H,36,37)(H,38,47)(H,39,46)(H,40,48)/t25?,27-,28-,29-,30-,31+/m0/s1
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n/an/a 46n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50014074
PNG
((3R,4S)-3,4-Bis-methoxymethoxy-pyrrolidine-1-carbo...)
Show SMILES CCN1C[C@H](OC1=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)N1C[C@@H](OCOC)[C@H](C1)OCOC
Show InChI InChI=1S/C39H59N7O11/c1-5-45-21-34(57-39(45)51)35(47)29(15-25-9-7-6-8-10-25)42-37(49)31(17-27-18-40-22-41-27)43-36(48)30(16-26-11-13-28(54-4)14-12-26)44-38(50)46-19-32(55-23-52-2)33(20-46)56-24-53-3/h11-14,18,22,25,29-35,47H,5-10,15-17,19-21,23-24H2,1-4H3,(H,40,41)(H,42,49)(H,43,48)(H,44,50)/t29-,30-,31-,32-,33+,34-,35+/m0/s1
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n/an/a 59n/an/an/an/a7.4n/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against human plasma renin at pH 7.4


J Med Chem 33: 1962-9 (1990)


BindingDB Entry DOI: 10.7270/Q2KW5GN2
More data for this
Ligand-Target Pair