Found 131 hits with Last Name = 'iizuka' and Initial = 'k' 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)) | BDBM50012951
(4-Cyclohexyl-2-hydroxy-3-[3-(1H-imidazol-4-yl)-2-(...)Show SMILES CC(C)OC(=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1cccc2ccccc12 Show InChI InChI=1S/C38H51N5O7/c1-25(2)50-38(48)35(45)32(19-26-9-4-3-5-10-26)41-37(47)33(22-30-23-39-24-40-30)42-36(46)29(21-34(44)43-15-17-49-18-16-43)20-28-13-8-12-27-11-6-7-14-31(27)28/h6-8,11-14,23-26,29,32-33,35,45H,3-5,9-10,15-22H2,1-2H3,(H,39,40)(H,41,47)(H,42,46)/t29-,32-,33-,35?/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 2.40 | n/a | n/a | n/a | n/a | n/a | n/a |
Kissei Pharmaceutical Company, Ltd.
Curated by ChEMBL
| Assay Description
Tested for inhibition of renin from human |
J Med Chem 33: 2707-14 (1990)
BindingDB Entry DOI: 10.7270/Q2N29XJZ |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028756
(2-Methyl-3-(4-pyridin-3-ylmethyl-phenyl)-acrylic a...)Show InChI InChI=1S/C16H15NO2/c1-12(16(18)19)9-13-4-6-14(7-5-13)10-15-3-2-8-17-11-15/h2-9,11H,10H2,1H3,(H,18,19)/b12-9- | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against Thromboxane synthetase |
J Med Chem 24: 1149-55 (1982)
BindingDB Entry DOI: 10.7270/Q2FT8MMG |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028719
((2E)-3-[3-(1H-imidazol-1-ylmethyl)phenyl]-2-methyl...)Show InChI InChI=1S/C14H14N2O2/c1-11(14(17)18)7-12-3-2-4-13(8-12)9-16-6-5-15-10-16/h2-8,10H,9H2,1H3,(H,17,18)/b11-7+ | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028764
(3-(4-Imidazol-1-ylmethyl-phenyl)-2-methyl-acrylic ...)Show InChI InChI=1S/C14H14N2O2/c1-11(14(17)18)8-12-2-4-13(5-3-12)9-16-7-6-15-10-16/h2-8,10H,9H2,1H3,(H,17,18)/b11-8+ | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against Thromboxane synthetase |
J Med Chem 24: 1149-55 (1982)
BindingDB Entry DOI: 10.7270/Q2FT8MMG |
More data for this
Ligand-Target Pair | |
Renin
(Homo sapiens (Human)) | BDBM50012951
(4-Cyclohexyl-2-hydroxy-3-[3-(1H-imidazol-4-yl)-2-(...)Show SMILES CC(C)OC(=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1cccc2ccccc12 Show InChI InChI=1S/C38H51N5O7/c1-25(2)50-38(48)35(45)32(19-26-9-4-3-5-10-26)41-37(47)33(22-30-23-39-24-40-30)42-36(46)29(21-34(44)43-15-17-49-18-16-43)20-28-13-8-12-27-11-6-7-14-31(27)28/h6-8,11-14,23-26,29,32-33,35,45H,3-5,9-10,15-22H2,1-2H3,(H,39,40)(H,41,47)(H,42,46)/t29-,32-,33-,35?/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 4.70 | n/a | n/a | n/a | n/a | n/a | n/a |
Kissei Pharmaceutical Company, Ltd.
Curated by ChEMBL
| Assay Description
Tested for inhibition of human plasma renin |
J Med Chem 33: 2707-14 (1990)
BindingDB Entry DOI: 10.7270/Q2N29XJZ |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028761
(2-Bromo-3-(4-pyridin-3-ylmethyl-phenyl)-acrylic ac...)Show InChI InChI=1S/C15H12BrNO2/c16-14(15(18)19)9-12-5-3-11(4-6-12)8-13-2-1-7-17-10-13/h1-7,9-10H,8H2,(H,18,19)/b14-9- | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against Thromboxane synthetase |
J Med Chem 24: 1149-55 (1982)
BindingDB Entry DOI: 10.7270/Q2FT8MMG |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028737
(4-(3-Imidazol-1-yl-propyl)-benzoic acid; hydrochlo...)Show InChI InChI=1S/C13H14N2O2/c16-13(17)12-5-3-11(4-6-12)2-1-8-15-9-7-14-10-15/h3-7,9-10H,1-2,8H2,(H,16,17) | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| PubMed
| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Renin
(Homo sapiens (Human)) | BDBM50012950
(2-Hydroxy-3-[3-(1H-imidazol-4-yl)-2-(4-morpholin-4...)Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1cccc2ccccc12)C(O)C(=O)OC(C)C Show InChI InChI=1S/C35H47N5O7/c1-22(2)16-29(32(42)35(45)47-23(3)4)38-34(44)30(19-27-20-36-21-37-27)39-33(43)26(18-31(41)40-12-14-46-15-13-40)17-25-10-7-9-24-8-5-6-11-28(24)25/h5-11,20-23,26,29-30,32,42H,12-19H2,1-4H3,(H,36,37)(H,38,44)(H,39,43)/t26-,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 | 6.20 | n/a | n/a | n/a | n/a | n/a | n/a |
Kissei Pharmaceutical Company, Ltd.
Curated by ChEMBL
| Assay Description
Tested for inhibition of human plasma renin |
J Med Chem 33: 2707-14 (1990)
BindingDB Entry DOI: 10.7270/Q2N29XJZ |
More data for this
Ligand-Target Pair | |
Renin
(Homo sapiens (Human)) | BDBM50012950
(2-Hydroxy-3-[3-(1H-imidazol-4-yl)-2-(4-morpholin-4...)Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1cccc2ccccc12)C(O)C(=O)OC(C)C Show InChI InChI=1S/C35H47N5O7/c1-22(2)16-29(32(42)35(45)47-23(3)4)38-34(44)30(19-27-20-36-21-37-27)39-33(43)26(18-31(41)40-12-14-46-15-13-40)17-25-10-7-9-24-8-5-6-11-28(24)25/h5-11,20-23,26,29-30,32,42H,12-19H2,1-4H3,(H,36,37)(H,38,44)(H,39,43)/t26-,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 | 6.70 | n/a | n/a | n/a | n/a | n/a | n/a |
Kissei Pharmaceutical Company, Ltd.
Curated by ChEMBL
| Assay Description
Tested for inhibition of renin from human |
J Med Chem 33: 2707-14 (1990)
BindingDB Entry DOI: 10.7270/Q2N29XJZ |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028752
(2-(4-Pyridin-3-ylmethyl-benzylidene)-butyric acid;...)Show InChI InChI=1S/C17H17NO2/c1-2-16(17(19)20)11-14-7-5-13(6-8-14)10-15-4-3-9-18-12-15/h3-9,11-12H,2,10H2,1H3,(H,19,20)/b16-11+ | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 7 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against Thromboxane synthetase |
J Med Chem 24: 1149-55 (1982)
BindingDB Entry DOI: 10.7270/Q2FT8MMG |
More data for this
Ligand-Target Pair | |
Renin
(Homo sapiens (Human)) | BDBM50022531
((+)2-Hydroxy-3-[3-(1H-imidazol-4-yl)-2-(4-morpholi...)Show SMILES CC(C)CC(NC(=O)C(Cc1cnc[nH]1)NC(=O)C(CC(=O)N1CCOCC1)Cc1cccc2ccccc12)C(O)C(=O)OC(C)C Show InChI InChI=1S/C35H47N5O7/c1-22(2)16-29(32(42)35(45)47-23(3)4)38-34(44)30(19-27-20-36-21-37-27)39-33(43)26(18-31(41)40-12-14-46-15-13-40)17-25-10-7-9-24-8-5-6-11-28(24)25/h5-11,20-23,26,29-30,32,42H,12-19H2,1-4H3,(H,36,37)(H,38,44)(H,39,43) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 7.80 | n/a | n/a | n/a | n/a | n/a | n/a |
Kissei Pharmaceutical Co., Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory concentration was measured against plasma renin from human |
J Med Chem 31: 701-4 (1988)
BindingDB Entry DOI: 10.7270/Q26H4GDB |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028709
(8-Imidazol-1-yl-2,2-dimethyl-oct-6-ynoic acid; hyd...)Show InChI InChI=1S/C13H18N2O2/c1-13(2,12(16)17)7-5-3-4-6-9-15-10-8-14-11-15/h8,10-11H,3,5,7,9H2,1-2H3,(H,16,17) | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
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| n/a | n/a | 9 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028767
(3-(4-Pyridin-3-ylmethyl-phenyl)-acrylic acid; hydr...)Show InChI InChI=1S/C15H13NO2/c17-15(18)8-7-12-3-5-13(6-4-12)10-14-2-1-9-16-11-14/h1-9,11H,10H2,(H,17,18)/b8-7+ | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
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| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against Thromboxane synthetase |
J Med Chem 24: 1149-55 (1982)
BindingDB Entry DOI: 10.7270/Q2FT8MMG |
More data for this
Ligand-Target Pair | |
Cathepsin D
(Bos taurus) | BDBM912
((3S,4S)-3-hydroxy-4-[(2S)-2-[(3S,4S)-3-hydroxy-6-m...)Show SMILES CC(C)C[C@H](NC(=O)[C@H](C)NC(=O)C[C@H](O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)CC(C)C)C(C)C)C(C)C)[C@@H](O)CC(O)=O |r| Show InChI InChI=1S/C34H63N5O9/c1-17(2)12-23(37-33(47)31(21(9)10)39-34(48)30(20(7)8)38-27(42)14-19(5)6)25(40)15-28(43)35-22(11)32(46)36-24(13-18(3)4)26(41)16-29(44)45/h17-26,30-31,40-41H,12-16H2,1-11H3,(H,35,43)(H,36,46)(H,37,47)(H,38,42)(H,39,48)(H,44,45)/t22-,23-,24-,25-,26-,30-,31-/m0/s1 | PDB
MMDB
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B.MOAD
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CHEMBL
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| MMDB
PubMed
| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
Kissei Pharmaceutical Company, Ltd.
Curated by ChEMBL
| Assay Description
Tested for inhibition of Cathepsin D from bovine |
J Med Chem 33: 2707-14 (1990)
BindingDB Entry DOI: 10.7270/Q2N29XJZ |
More data for this
Ligand-Target Pair | |
Renin
(Homo sapiens (Human)) | BDBM50022525
(2-Hydroxy-3-[3-(1H-imidazol-4-yl)-2-(4-morpholin-4...)Show SMILES COC(=O)C(O)C(CC(C)C)NC(=O)C(Cc1cnc[nH]1)NC(=O)C(CC(=O)N1CCOCC1)Cc1cccc2ccccc12 Show InChI InChI=1S/C33H43N5O7/c1-21(2)15-27(30(40)33(43)44-3)36-32(42)28(18-25-19-34-20-35-25)37-31(41)24(17-29(39)38-11-13-45-14-12-38)16-23-9-6-8-22-7-4-5-10-26(22)23/h4-10,19-21,24,27-28,30,40H,11-18H2,1-3H3,(H,34,35)(H,36,42)(H,37,41) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
Kissei Pharmaceutical Co., Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory concentration against human renin |
J Med Chem 31: 701-4 (1988)
BindingDB Entry DOI: 10.7270/Q26H4GDB |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50017896
((E)-3-(4-Imidazol-1-ylmethyl-phenyl)-acrylic acid ...)Show InChI InChI=1S/C13H12N2O2/c16-13(17)6-5-11-1-3-12(4-2-11)9-15-8-7-14-10-15/h1-8,10H,9H2,(H,16,17)/b6-5+ | KEGG
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| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028762
(2-Methyl-3-(5-pyridin-3-ylmethyl-thiophen-2-yl)-ac...)Show InChI InChI=1S/C14H13NO2S/c1-10(14(16)17)7-12-4-5-13(18-12)8-11-3-2-6-15-9-11/h2-7,9H,8H2,1H3,(H,16,17)/b10-7+ | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
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| CHEMBL
PC cid
PC sid
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Similars
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| n/a | n/a | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against Thromboxane synthetase |
J Med Chem 24: 1149-55 (1982)
BindingDB Entry DOI: 10.7270/Q2FT8MMG |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM7962
(4-(2-Imidazol-1-yl-ethoxy)-benzoic acid; hydrochlo...)Show InChI InChI=1S/C12H12N2O3/c15-12(16)10-1-3-11(4-2-10)17-8-7-14-6-5-13-9-14/h1-6,9H,7-8H2,(H,15,16) | KEGG
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CHEMBL
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| n/a | n/a | 14 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028734
(8-Imidazol-1-yl-oct-2-enoic acid | CHEMBL14771)Show InChI InChI=1S/C11H16N2O2/c14-11(15)6-4-2-1-3-5-8-13-9-7-12-10-13/h4,6-7,9-10H,1-3,5,8H2,(H,14,15)/b6-4- | KEGG
UniProtKB/SwissProt
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antibodypedia
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AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
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| n/a | n/a | 16 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028713
(8-Imidazol-1-yl-2-methylene-octanoic acid; hydroch...)Show InChI InChI=1S/C12H18N2O2/c1-11(12(15)16)6-4-2-3-5-8-14-9-7-13-10-14/h7,9-10H,1-6,8H2,(H,15,16) | KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
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| n/a | n/a | 16 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Pepsin A
(Porcine) | BDBM912
((3S,4S)-3-hydroxy-4-[(2S)-2-[(3S,4S)-3-hydroxy-6-m...)Show SMILES CC(C)C[C@H](NC(=O)[C@H](C)NC(=O)C[C@H](O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)CC(C)C)C(C)C)C(C)C)[C@@H](O)CC(O)=O |r| Show InChI InChI=1S/C34H63N5O9/c1-17(2)12-23(37-33(47)31(21(9)10)39-34(48)30(20(7)8)38-27(42)14-19(5)6)25(40)15-28(43)35-22(11)32(46)36-24(13-18(3)4)26(41)16-29(44)45/h17-26,30-31,40-41H,12-16H2,1-11H3,(H,35,43)(H,36,46)(H,37,47)(H,38,42)(H,39,48)(H,44,45)/t22-,23-,24-,25-,26-,30-,31-/m0/s1 | PDB
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Kissei Pharmaceutical Company, Ltd.
Curated by ChEMBL
| Assay Description
Tested for inhibition of pepsin from porcine |
J Med Chem 33: 2707-14 (1990)
BindingDB Entry DOI: 10.7270/Q2N29XJZ |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028760
(3-(3-Methyl-4-pyridin-3-ylmethyl-phenyl)-but-2-eno...)Show InChI InChI=1S/C17H17NO2/c1-12-8-15(13(2)9-17(19)20)5-6-16(12)10-14-4-3-7-18-11-14/h3-9,11H,10H2,1-2H3,(H,19,20)/b13-9+ | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against Thromboxane synthetase |
J Med Chem 24: 1149-55 (1982)
BindingDB Entry DOI: 10.7270/Q2FT8MMG |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028772
(2-Methyl-3-(4-pyridin-3-ylmethyl-phenyl)-propionic...)Show InChI InChI=1S/C16H17NO2/c1-12(16(18)19)9-13-4-6-14(7-5-13)10-15-3-2-8-17-11-15/h2-8,11-12H,9-10H2,1H3,(H,18,19) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against Thromboxane synthetase |
J Med Chem 24: 1149-55 (1982)
BindingDB Entry DOI: 10.7270/Q2FT8MMG |
More data for this
Ligand-Target Pair | |
Renin
(Homo sapiens (Human)) | BDBM50022526
((-)2-Hydroxy-3-{3-(1H-imidazol-4-yl)-2-[3-naphthal...)Show SMILES COC(=O)C(O)C(CC(C)C)NC(=O)C(Cc1cnc[nH]1)NC(=O)C(CC(=O)NCCc1ccccc1)Cc1cccc2ccccc12 Show InChI InChI=1S/C37H45N5O6/c1-24(2)18-31(34(44)37(47)48-3)41-36(46)32(21-29-22-38-23-40-29)42-35(45)28(19-27-14-9-13-26-12-7-8-15-30(26)27)20-33(43)39-17-16-25-10-5-4-6-11-25/h4-15,22-24,28,31-32,34,44H,16-21H2,1-3H3,(H,38,40)(H,39,43)(H,41,46)(H,42,45) | PDB
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Kissei Pharmaceutical Co., Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory concentration was measured against plasma renin from dog |
J Med Chem 31: 701-4 (1988)
BindingDB Entry DOI: 10.7270/Q26H4GDB |
More data for this
Ligand-Target Pair | |
Renin
(Homo sapiens (Human)) | BDBM50022529
(2-Hydroxy-3-[3-(1H-imidazol-4-yl)-2-(2-naphthalen-...)Show SMILES COC(=O)C(O)C(CC(C)C)NC(=O)C(Cc1cnc[nH]1)NC(=O)C(CC(=O)N1CCCCC1)Cc1cccc2ccccc12 Show InChI InChI=1S/C34H45N5O6/c1-22(2)16-28(31(41)34(44)45-3)37-33(43)29(19-26-20-35-21-36-26)38-32(42)25(18-30(40)39-14-7-4-8-15-39)17-24-12-9-11-23-10-5-6-13-27(23)24/h5-6,9-13,20-22,25,28-29,31,41H,4,7-8,14-19H2,1-3H3,(H,35,36)(H,37,43)(H,38,42) | PDB
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Kissei Pharmaceutical Co., Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory concentration was measured against plasma renin from dog |
J Med Chem 31: 701-4 (1988)
BindingDB Entry DOI: 10.7270/Q26H4GDB |
More data for this
Ligand-Target Pair | |
Renin
(Homo sapiens (Human)) | BDBM50022530
(3-[2-(3-Dimethylcarbamoyl-2-naphthalen-1-ylmethyl-...)Show SMILES COC(=O)C(O)C(CC(C)C)NC(=O)C(Cc1cnc[nH]1)NC(=O)C(CC(=O)N(C)C)Cc1cccc2ccccc12 Show InChI InChI=1S/C31H41N5O6/c1-19(2)13-25(28(38)31(41)42-5)34-30(40)26(16-23-17-32-18-33-23)35-29(39)22(15-27(37)36(3)4)14-21-11-8-10-20-9-6-7-12-24(20)21/h6-12,17-19,22,25-26,28,38H,13-16H2,1-5H3,(H,32,33)(H,34,40)(H,35,39) | PDB
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Kissei Pharmaceutical Co., Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory concentration was measured against plasma renin from dog |
J Med Chem 31: 701-4 (1988)
BindingDB Entry DOI: 10.7270/Q26H4GDB |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028735
(2-Chloro-8-imidazol-1-yl-octanoic acid; hydrochlor...)Show InChI InChI=1S/C11H17ClN2O2/c12-10(11(15)16)5-3-1-2-4-7-14-8-6-13-9-14/h6,8-10H,1-5,7H2,(H,15,16) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028758
(2-Methyl-3-[4-(1-pyridin-3-yl-ethyl)-phenyl]-acryl...)Show InChI InChI=1S/C17H17NO2/c1-12(17(19)20)10-14-5-7-15(8-6-14)13(2)16-4-3-9-18-11-16/h3-11,13H,1-2H3,(H,19,20)/b12-10+ | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against Thromboxane synthetase |
J Med Chem 24: 1149-55 (1982)
BindingDB Entry DOI: 10.7270/Q2FT8MMG |
More data for this
Ligand-Target Pair | |
Renin
(Homo sapiens (Human)) | BDBM50022530
(3-[2-(3-Dimethylcarbamoyl-2-naphthalen-1-ylmethyl-...)Show SMILES COC(=O)C(O)C(CC(C)C)NC(=O)C(Cc1cnc[nH]1)NC(=O)C(CC(=O)N(C)C)Cc1cccc2ccccc12 Show InChI InChI=1S/C31H41N5O6/c1-19(2)13-25(28(38)31(41)42-5)34-30(40)26(16-23-17-32-18-33-23)35-29(39)22(15-27(37)36(3)4)14-21-11-8-10-20-9-6-7-12-24(20)21/h6-12,17-19,22,25-26,28,38H,13-16H2,1-5H3,(H,32,33)(H,34,40)(H,35,39) | PDB
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Kissei Pharmaceutical Co., Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory concentration was measured against plasma renin from human |
J Med Chem 31: 701-4 (1988)
BindingDB Entry DOI: 10.7270/Q26H4GDB |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028707
(2-(4-Imidazol-1-ylmethyl-phenoxy)-2-methyl-propion...)Show InChI InChI=1S/C14H16N2O3/c1-14(2,13(17)18)19-12-5-3-11(4-6-12)9-16-8-7-15-10-16/h3-8,10H,9H2,1-2H3,(H,17,18) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Renin
(Homo sapiens (Human)) | BDBM50022531
((+)2-Hydroxy-3-[3-(1H-imidazol-4-yl)-2-(4-morpholi...)Show SMILES CC(C)CC(NC(=O)C(Cc1cnc[nH]1)NC(=O)C(CC(=O)N1CCOCC1)Cc1cccc2ccccc12)C(O)C(=O)OC(C)C Show InChI InChI=1S/C35H47N5O7/c1-22(2)16-29(32(42)35(45)47-23(3)4)38-34(44)30(19-27-20-36-21-37-27)39-33(43)26(18-31(41)40-12-14-46-15-13-40)17-25-10-7-9-24-8-5-6-11-28(24)25/h5-11,20-23,26,29-30,32,42H,12-19H2,1-4H3,(H,36,37)(H,38,44)(H,39,43) | PDB
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Kissei Pharmaceutical Co., Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory concentration was measured against plasma renin from dog |
J Med Chem 31: 701-4 (1988)
BindingDB Entry DOI: 10.7270/Q26H4GDB |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028724
(8-Imidazol-1-yl-2,2-dimethyl-octanoic acid; hydroc...)Show InChI InChI=1S/C13H22N2O2/c1-13(2,12(16)17)7-5-3-4-6-9-15-10-8-14-11-15/h8,10-11H,3-7,9H2,1-2H3,(H,16,17) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028741
(8-Imidazol-1-yl-oct-6-ynoic acid; hydrochloride | ...)Show InChI InChI=1S/C11H14N2O2/c14-11(15)6-4-2-1-3-5-8-13-9-7-12-10-13/h7,9-10H,1-2,4,6,8H2,(H,14,15) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028742
(8-Imidazol-1-yl-2-methyl-octanoic acid; hydrochlor...)Show InChI InChI=1S/C12H20N2O2/c1-11(12(15)16)6-4-2-3-5-8-14-9-7-13-10-14/h7,9-11H,2-6,8H2,1H3,(H,15,16) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028720
(3-(3-Imidazol-1-ylmethyl-phenyl)-acrylic acid; hyd...)Show InChI InChI=1S/C13H12N2O2/c16-13(17)5-4-11-2-1-3-12(8-11)9-15-7-6-14-10-15/h1-8,10H,9H2,(H,16,17)/b5-4+ | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM92497
(CHEMBL542051 | Omega-imidazolyl octanoic acid)Show InChI InChI=1S/C11H18N2O2/c14-11(15)6-4-2-1-3-5-8-13-9-7-12-10-13/h7,9-10H,1-6,8H2,(H,14,15) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM92497
(CHEMBL542051 | Omega-imidazolyl octanoic acid)Show InChI InChI=1S/C11H18N2O2/c14-11(15)6-4-2-1-3-5-8-13-9-7-12-10-13/h7,9-10H,1-6,8H2,(H,14,15) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against Thromboxane synthetase |
J Med Chem 24: 1149-55 (1982)
BindingDB Entry DOI: 10.7270/Q2FT8MMG |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028743
(8-Imidazol-1-yl-2-phenyl-octanoic acid; hydrochlor...)Show InChI InChI=1S/C17H22N2O2/c20-17(21)16(15-8-4-3-5-9-15)10-6-1-2-7-12-19-13-11-18-14-19/h3-5,8-9,11,13-14,16H,1-2,6-7,10,12H2,(H,20,21) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028727
(2-(4-Imidazol-1-ylmethyl-phenoxy)-propionic acid; ...)Show InChI InChI=1S/C13H14N2O3/c1-10(13(16)17)18-12-4-2-11(3-5-12)8-15-7-6-14-9-15/h2-7,9-10H,8H2,1H3,(H,16,17) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028714
(7-Imidazol-1-yl-heptanoic acid; hydrochloride | CH...)Show InChI InChI=1S/C10H16N2O2/c13-10(14)5-3-1-2-4-7-12-8-6-11-9-12/h6,8-9H,1-5,7H2,(H,13,14) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028714
(7-Imidazol-1-yl-heptanoic acid; hydrochloride | CH...)Show InChI InChI=1S/C10H16N2O2/c13-10(14)5-3-1-2-4-7-12-8-6-11-9-12/h6,8-9H,1-5,7H2,(H,13,14) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against Thromboxane synthetase |
J Med Chem 24: 1149-55 (1982)
BindingDB Entry DOI: 10.7270/Q2FT8MMG |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50025106
(CHEMBL42341 | CHEMBL544900 | [4-(2H-Imidazol-1-ylm...)Show InChI InChI=1S/C12H12N2O3/c15-12(16)8-17-11-3-1-10(2-4-11)7-14-6-5-13-9-14/h1-6,9H,7-8H2,(H,15,16) | KEGG
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TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028722
(8-Imidazol-1-yl-octa-2,4-dienoic acid; hydrochlori...)Show InChI InChI=1S/C11H14N2O2/c14-11(15)6-4-2-1-3-5-8-13-9-7-12-10-13/h1-2,4,6-7,9-10H,3,5,8H2,(H,14,15)/b2-1+,6-4+ | KEGG
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| CHEMBL
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| n/a | n/a | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Renin
(Homo sapiens (Human)) | BDBM50022529
(2-Hydroxy-3-[3-(1H-imidazol-4-yl)-2-(2-naphthalen-...)Show SMILES COC(=O)C(O)C(CC(C)C)NC(=O)C(Cc1cnc[nH]1)NC(=O)C(CC(=O)N1CCCCC1)Cc1cccc2ccccc12 Show InChI InChI=1S/C34H45N5O6/c1-22(2)16-28(31(41)34(44)45-3)37-33(43)29(19-26-20-35-21-36-26)38-32(42)25(18-30(40)39-14-7-4-8-15-39)17-24-12-9-11-23-10-5-6-13-27(23)24/h5-6,9-13,20-22,25,28-29,31,41H,4,7-8,14-19H2,1-3H3,(H,35,36)(H,37,43)(H,38,42) | PDB
MMDB
Reactome pathway
KEGG
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Kissei Pharmaceutical Co., Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory concentration was measured against plasma renin from human |
J Med Chem 31: 701-4 (1988)
BindingDB Entry DOI: 10.7270/Q26H4GDB |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028718
(8-Imidazol-1-yl-octa-6,7-dienoic acid; hydrochlori...)Show SMILES OC(=O)CCCCC=C=Cn1ccnc1 |(18.93,-1.35,;17.59,-.58,;17.59,.97,;16.27,-1.37,;14.91,-.6,;13.59,-1.37,;12.25,-.63,;10.91,-1.4,;9.57,-.63,;8.25,.15,;6.92,.92,;5.41,.53,;4.59,1.83,;5.57,3.03,;7.01,2.47,)| Show InChI InChI=1S/C11H14N2O2/c14-11(15)6-4-2-1-3-5-8-13-9-7-12-10-13/h3,7-10H,1-2,4,6H2,(H,14,15) | KEGG
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| n/a | n/a | 42 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028729
(8-Imidazol-1-yl-oct-2-ynoic acid; hydrochloride | ...)Show InChI InChI=1S/C11H14N2O2/c14-11(15)6-4-2-1-3-5-8-13-9-7-12-10-13/h7,9-10H,1-3,5,8H2,(H,14,15) | KEGG
UniProtKB/SwissProt
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| CHEMBL
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| n/a | n/a | 42 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028703
(4-(3-Imidazol-1-yl-propenyl)-benzoic acid; hydroch...)Show InChI InChI=1S/C13H12N2O2/c16-13(17)12-5-3-11(4-6-12)2-1-8-15-9-7-14-10-15/h1-7,9-10H,8H2,(H,16,17)/b2-1+ | KEGG
UniProtKB/SwissProt
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| CHEMBL
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| n/a | n/a | 44 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028745
(1-(6-Imidazol-1-yl-hexyl)-cyclohexanecarboxylic ac...)Show InChI InChI=1S/C16H26N2O2/c19-15(20)16(9-5-3-6-10-16)8-4-1-2-7-12-18-13-11-17-14-18/h11,13-14H,1-10,12H2,(H,19,20) | KEGG
UniProtKB/SwissProt
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| n/a | n/a | 46 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against human thromboxane synthetase |
J Med Chem 24: 1139-48 (1982)
BindingDB Entry DOI: 10.7270/Q2KK9CB6 |
More data for this
Ligand-Target Pair | |
Thromboxane-A synthase
(Homo sapiens (Human)) | BDBM50028774
(3-(5-Pyridin-3-ylmethyl-thiophen-2-yl)-acrylic aci...)Show InChI InChI=1S/C13H11NO2S/c15-13(16)6-5-11-3-4-12(17-11)8-10-2-1-7-14-9-10/h1-7,9H,8H2,(H,15,16)/b6-5+ | KEGG
UniProtKB/SwissProt
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| CHEMBL
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| n/a | n/a | 47 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibitory activity against Thromboxane synthetase |
J Med Chem 24: 1149-55 (1982)
BindingDB Entry DOI: 10.7270/Q2FT8MMG |
More data for this
Ligand-Target Pair | |
Renin
(Homo sapiens (Human)) | BDBM50022525
(2-Hydroxy-3-[3-(1H-imidazol-4-yl)-2-(4-morpholin-4...)Show SMILES COC(=O)C(O)C(CC(C)C)NC(=O)C(Cc1cnc[nH]1)NC(=O)C(CC(=O)N1CCOCC1)Cc1cccc2ccccc12 Show InChI InChI=1S/C33H43N5O7/c1-21(2)15-27(30(40)33(43)44-3)36-32(42)28(18-25-19-34-20-35-25)37-31(41)24(17-29(39)38-11-13-45-14-12-38)16-23-9-6-8-22-7-4-5-10-26(22)23/h4-10,19-21,24,27-28,30,40H,11-18H2,1-3H3,(H,34,35)(H,36,42)(H,37,41) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
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| n/a | n/a | 52 | n/a | n/a | n/a | n/a | n/a | n/a |
Kissei Pharmaceutical Co., Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory concentration against human renin |
J Med Chem 31: 701-4 (1988)
BindingDB Entry DOI: 10.7270/Q26H4GDB |
More data for this
Ligand-Target Pair | |
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