Identification | Back Directory | [Name]
(+/-)8,9-EET | [CAS]
81246-85-7 | [Synonyms]
8,9-EET 8(9)-EPETRE (+/-)8,9-EET (+/-)8,9-EET (+/-)8(9)-EPETRE 8,9-epoxyeicosatrienoicacid (+)8,9-Epoxyeicosa-8z,11z,14z trienoic acid (+/-)8,9-EPOXYEICOSA-5Z,11Z,14Z-TRIENOIC ACID (+/-)8(9)-EPOXY-5Z,11Z,14Z-EICOSATRIENOIC ACID (+/-)-8,9-Epoxyeicosa-5Z,11Z,14Z-trienoic Acid (5Z,8S,9R,11Z,14Z)-8,9-Epoxy-5,11,14-icosatrienoic acid 5-Heptenoic acid, 7-[3-(2,5-undecadien-1-yl)-2-oxiranyl]- (Z)-7-[3-[(2Z,5Z)-undeca-2,5-dienyl]oxiran-2-yl]hept-5-enoic acid (Z)-7-[(2S,3R)-3-[(2Z,5Z)-2,5-Undecadienyl]oxiranyl]-5-heptenoic acid (±)-8,9-Epoxyeicosa-5Z,11Z,14Z-trienoic acid (8,9-epoxyeicosatrienoic acid) | [Molecular Formula]
C20H32O3 | [MDL Number]
MFCD00065840 | [MOL File]
81246-85-7.mol | [Molecular Weight]
320.47 |
Chemical Properties | Back Directory | [Boiling point ]
456.2±20.0 °C(Predicted) | [density ]
0.983±0.06 g/cm3(Predicted) | [storage temp. ]
−20°C | [solubility ]
DMF: 50 mg/ml DMSO: 50 mg/ml Ethanol: 50 mg/mlPBS pH 7.2: 1 mg/ml | [pka]
4.77±0.10(Predicted) |
Hazard Information | Back Directory | [Uses]
(+/-)8,9-Epoxyeicosa-5Z,11Z,14Z-trienoic acid is a glucagon inducer in pancreatic islets. | [References]
[1] N. CHACOS . Novel epoxides formed during the liver cytochrome P-450 oxidation of arachidonic acid[J]. Biochemical and biophysical research communications, 1982, 104 3: Pages 916-922. DOI: 10.1016/0006-291x(82)91336-5 [2] E. OLIW J O F Guengerich. Oxygenation of arachidonic acid by hepatic monooxygenases. Isolation and metabolism of four epoxide intermediates.[J]. The Journal of Biological Chemistry, 1982, 109 1: 3771-3781. DOI: 10.1016/s0021-9258(18)34848-8 [3] JI Y. ZHANG . Regiospecific and enantioselective metabolism of 8,9-epoxyeicosatrienoic acid by cyclooxygenase[J]. Biochemical and biophysical research communications, 1992, 183 1: Pages 138-143. DOI: 10.1016/0006-291x(92)91619-2 [4] JONAS BYSTROM. Endogenous epoxygenases are modulators of monocyte/macrophage activity.[J]. PLoS ONE, 2011: e26591. DOI: 10.1371/journal.pone.0026591 [5] AMY A RAND. Cyclooxygenase-derived proangiogenic metabolites of epoxyeicosatrienoic acids.[J]. Proceedings of the National Academy of Sciences of the United States of America, 2017, 114 17: 4370-4375. DOI: 10.1073/pnas.1616893114 [6] T KATOH. Glomerular stereospecific synthesis and hemodynamic actions of 8,9-epoxyeicosatrienoic acid in rat kidney.[J]. American Journal of Physiology, 1991, 261 4 Pt 2: F578-86. DOI: 10.1152/ajprenal.1991.261.4.f578 [7] FADUMO A. ISSE . Quantification of Epoxyeicosatrienoic acids Enantiomers: The development of reliable and practical liquid chromatography mass Spectrometry assay[J]. Journal of Chromatography B, 2024, 1247: Article 124346. DOI: 10.1016/j.jchromb.2024.124346 [8] ZONGYUAN WU, FANG WEI* Analytical Strategy for Oxylipin Annotation by Combining Chemical Derivatization-Based Retention Index Algorithm and Feature Tandem Mass Spectrometric Fragmentation as a Biomarker Discovery Tool[J]. Analytical Chemistry, 2023, 95 43: 15933-15942. DOI: 10.1021/acs.analchem.3c02789 [9] ANDREI KORNILOV. Revising the structure of a new eicosanoid from human platelets to 8,9-11,12-diepoxy-13-hydroxyeicosadienoic acid.[J]. The Journal of Biological Chemistry, 2019, 294 23: 9225-9238. DOI: 10.1074/jbc.ra119.008915 [10] REUT LEVI-ROSENZVIG . 5,6-δ-DHTL, a stable metabolite of arachidonic acid, is a potential EDHF that mediates microvascular dilation[J]. Free Radical Biology and Medicine, 2017, 103: Pages 87-94. DOI: 10.1016/j.freeradbiomed.2016.12.022 |
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