Found 33 hits for monomerid = 7962 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Glutaminyl Cyclase
(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) | PDB MMDB
KEGG
UniProtKB/SwissProt
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| 2.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Probiodrug AG
| Assay Description QC activity was evaluated fluorometrically using Gln-AMC as substrate, and pyroglutamyl peptidase as the auxiliary enzyme. After conversion of Gln-AM... |
J Biol Chem 278: 49773-9 (2003)
Article DOI: 10.1074/jbc.M309077200 BindingDB Entry DOI: 10.7270/Q2513WDS |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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
UniProtKB/SwissProt
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| n/a | n/a | 28 | n/a | n/a | n/a | n/a | n/a | n/a |
CIBA-GEIGY Corporation
Curated by ChEMBL
| Assay Description Compound was evaluated in vitro for the inhibition of Thromboxane synthase using [14C]-arachidonic acid as radioligand |
J Med Chem 34: 1790-7 (1991)
BindingDB Entry DOI: 10.7270/Q2BR8R47 |
More data for this Ligand-Target Pair | |
Cytochrome P450 11B1
(Rattus norvegicus) | 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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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of 11 beta-hydroxylase from rat adrenal gland |
J Med Chem 29: 342-6 (1986)
BindingDB Entry DOI: 10.7270/Q2W66JSZ |
More data for this Ligand-Target Pair | |
Prostaglandin I2 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) | PDB MMDB
Reactome pathway KEGG
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of PGI-2 synthetase from porcine aorta |
J Med Chem 29: 342-6 (1986)
BindingDB Entry DOI: 10.7270/Q2W66JSZ |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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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| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of TXA2 synthetase from human platelets |
J Med Chem 29: 342-6 (1986)
BindingDB Entry DOI: 10.7270/Q2W66JSZ |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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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| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of thromboxane TXA2 synthetase from human platelets |
J Med Chem 29: 1643-50 (1986)
BindingDB Entry DOI: 10.7270/Q2C8289W |
More data for this Ligand-Target Pair | |
Prostaglandin I2 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) | PDB MMDB
Reactome pathway KEGG
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of porcine aorta prostacyclin PGI-2 synthetase |
J Med Chem 29: 1643-50 (1986)
BindingDB Entry DOI: 10.7270/Q2C8289W |
More data for this Ligand-Target Pair | |
Cytochrome P450 11B1
(Rattus norvegicus) | 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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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of rat adrenal 11-beta-hydroxylase |
J Med Chem 29: 1643-50 (1986)
BindingDB Entry DOI: 10.7270/Q2C8289W |
More data for this Ligand-Target Pair | |
Thromboxane-A synthase
(Rattus norvegicus) | 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) | Reactome pathway KEGG
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| n/a | n/a | 106 | n/a | n/a | n/a | n/a | n/a | n/a |
Sankyo Co., Ltd.
Curated by ChEMBL
| Assay Description Inhibition of thromboxane A2 synthetase |
J Med Chem 32: 1265-72 (1989)
BindingDB Entry DOI: 10.7270/Q2FF3RBV |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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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| n/a | n/a | 620 | n/a | n/a | n/a | n/a | n/a | n/a |
Sankyo Co., Ltd.
Curated by ChEMBL
| Assay Description Inhibition of platelet microsomal thromboxane A synthetase in humans |
J Med Chem 32: 1265-72 (1989)
BindingDB Entry DOI: 10.7270/Q2FF3RBV |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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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| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Research Center
Curated by ChEMBL
| Assay Description Inhibitory activity of the compound to inhibit Inophore-induced arachidonic acid metabolism (inhibition of TXB2 formation) in rat |
J Med Chem 32: 1842-60 (1989)
BindingDB Entry DOI: 10.7270/Q28W3C8B |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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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| 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 A2 synthetase |
J Med Chem 28: 1427-32 (1985)
BindingDB Entry DOI: 10.7270/Q2DJ5DN7 |
More data for this Ligand-Target Pair | |
Prostaglandin I2 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) | PDB MMDB
Reactome pathway KEGG
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of porcine aorta prostacyclin PGI-2 synthase |
J Med Chem 28: 1427-32 (1985)
BindingDB Entry DOI: 10.7270/Q2DJ5DN7 |
More data for this Ligand-Target Pair | |
Cytochrome P450 11B1
(Rattus norvegicus) | 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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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of rat adrenal 11-beta-hydroxylase |
J Med Chem 28: 1427-32 (1985)
BindingDB Entry DOI: 10.7270/Q2DJ5DN7 |
More data for this Ligand-Target Pair | |
Thromboxane-A synthase
(Rattus norvegicus) | 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) | Reactome pathway KEGG
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| n/a | n/a | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Compound was tested for inhibitory activity against thromboxane synthetase |
J Med Chem 29: 523-30 (1986)
BindingDB Entry DOI: 10.7270/Q27W6B6V |
More data for this Ligand-Target Pair | |
Bile salt export pump
(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) | PDB
UniProtKB/SwissProt
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| n/a | n/a | >1.00E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description Inhibition of human BSEP expressed in baculovirus transfected fall armyworm Sf21 cell membranes vesicles assessed as reduction in ATP-dependent [3H]-... |
Drug Metab Dispos 40: 2332-41 (2012)
Article DOI: 10.1124/dmd.112.047068 BindingDB Entry DOI: 10.7270/Q2ZP488M |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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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| n/a | n/a | 1.29E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Searle Research and Development
Curated by ChEMBL
| Assay Description Inhibition of Thromboxane B2 formation in collagen-stimulated human platelets in platelet rich plasma. |
J Med Chem 30: 1812-8 (1987)
BindingDB Entry DOI: 10.7270/Q2ZP454K |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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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| n/a | n/a | 1.29E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Tested for inhibitory activity against intact human platelet TXA2 formation |
J Med Chem 30: 1588-95 (1987)
BindingDB Entry DOI: 10.7270/Q20R9NDV |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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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| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description In vitro inhibition of thromboxane synthase from human platelets. |
J Med Chem 29: 1637-43 (1986)
BindingDB Entry DOI: 10.7270/Q2WQ02S2 |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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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| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
ZENECA Pharmaceuticals
Curated by ChEMBL
| Assay Description In vitro inhibitory activity against human microsomal thromboxane synthase. |
J Med Chem 38: 1608-28 (1995)
BindingDB Entry DOI: 10.7270/Q2319TWW |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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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| n/a | n/a | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
University of the Saarland
Curated by ChEMBL
| Assay Description Inhibition of thromboxane synthase P450 TXA2 |
J Med Chem 43: 4437-45 (2000)
BindingDB Entry DOI: 10.7270/Q25H7FH3 |
More data for this Ligand-Target Pair | |
Thromboxane-A synthase
(Rattus norvegicus) | 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) | Reactome pathway KEGG
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| n/a | n/a | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Compound was tested for the inhibition of thromboxane formation (thromboxane synthetase) in platelets at a concentration of 10e-4 M |
J Med Chem 29: 816-9 (1986)
BindingDB Entry DOI: 10.7270/Q2H70GCD |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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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| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of human platelet thromboxane synthase (TXA2) was determined in human platelets |
J Med Chem 30: 185-93 (1987)
BindingDB Entry DOI: 10.7270/Q2222VBH |
More data for this Ligand-Target Pair | |
Thromboxane-A synthase
(Rattus norvegicus) | 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) | Reactome pathway KEGG
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| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
Medical Research Division of American Cyanamid Company
Curated by ChEMBL
| Assay Description Tested for inhibition of thromboxane synthetase from spontaneously hypertensive rats |
J Med Chem 30: 2277-83 (1988)
BindingDB Entry DOI: 10.7270/Q23T9HT6 |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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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| 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 A2 Synthase (P450 TxA2)
(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
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
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CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research UK
Curated by ChEMBL
| Assay Description Inhibition of Thromboxane A2 synthase after oral administration of 0.03 mmol/kg |
J Med Chem 33: 646-52 (1990)
BindingDB Entry DOI: 10.7270/Q25X29HP |
More data for this Ligand-Target Pair | |
Thromboxane-A synthase
(Rattus norvegicus) | 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) | Reactome pathway KEGG
UniProtKB/SwissProt
GoogleScholar AffyNet
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CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Farmitalia Carlo Erba
Curated by ChEMBL
| Assay Description In vitro inhibition of thromboxane B2 production in rat whole blood. |
J Med Chem 36: 2964-72 (1993)
BindingDB Entry DOI: 10.7270/Q22R3S9H |
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
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
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CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
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| PubMed
| n/a | n/a | 106 | n/a | n/a | n/a | n/a | n/a | n/a |
Sankyo Co., Ltd.
Curated by ChEMBL
| Assay Description Inhibition of platelet microsomal thromboxane A2 synthetase in rabbits |
J Med Chem 32: 1265-72 (1989)
BindingDB Entry DOI: 10.7270/Q2FF3RBV |
More data for this Ligand-Target Pair | |
Cyclooxygenase
(RAT) | 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) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of cyclooxygenase from RBL-1 cells. |
J Med Chem 29: 1643-50 (1986)
BindingDB Entry DOI: 10.7270/Q2C8289W |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase (cyclooxygenase)
(Ovis aries (Sheep)) | 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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
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CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of Prostaglandin G/H synthase from ram seminal vesicle microsomes |
J Med Chem 29: 342-6 (1986)
BindingDB Entry DOI: 10.7270/Q2W66JSZ |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase (cyclooxygenase)
(Ovis aries (Sheep)) | 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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
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CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of ram seminal vesicle Cyclooxygenase |
J Med Chem 28: 1427-32 (1985)
BindingDB Entry DOI: 10.7270/Q2DJ5DN7 |
More data for this Ligand-Target Pair | |
Thromboxane A2 Synthase (P450 TxA2)
(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
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
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CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
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| Article PubMed
| n/a | n/a | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universitat des Saarlandes
| Assay Description Thromboxane A2 synthase activity was assayed by measuring the fragmentation of prostaglandin H2 to form 12-hydroxy-5, 8,10-heptadecatrienoic acid and... |
J Med Chem 43: 1841-51 (2000)
Article DOI: 10.1021/jm991180u BindingDB Entry DOI: 10.7270/Q2D21VTH |
More data for this Ligand-Target Pair | |
Thromboxane-A synthase
(Rattus norvegicus) | 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) | Reactome pathway KEGG
UniProtKB/SwissProt
GoogleScholar AffyNet
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CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of thromboxane formation at a concentration of 10e -6 M. |
J Med Chem 30: 1036-40 (1987)
BindingDB Entry DOI: 10.7270/Q24F1PRV |
More data for this Ligand-Target Pair | |