(11S,12R)-EET

Modify Date: 2024-01-11 00:16:16

(11S,12R)-EET Structure
(11S,12R)-EET structure
Common Name (11S,12R)-EET
CAS Number 123931-40-8 Molecular Weight 320.466
Density 1.0±0.1 g/cm3 Boiling Point 461.8±33.0 °C at 760 mmHg
Molecular Formula C20H32O3 Melting Point N/A
MSDS USA Flash Point 154.6±18.9 °C
Symbol GHS02 GHS07
GHS02, GHS07
Signal Word Danger

 Use of (11S,12R)-EET


(±)11(12)-EET is a NLRP3 inflammasome inhibitor. (±)11(12)-EET can be used for the research of anti-inflammatory, angiogenic and cardioprotective[1][2][3][4][6].

 Names

Name 11,12-Epoxy-(5Z,8Z,14Z)-eicosatrienoic acid
Synonym More Synonyms

 (11S,12R)-EET Biological Activity

Description (±)11(12)-EET is a NLRP3 inflammasome inhibitor. (±)11(12)-EET can be used for the research of anti-inflammatory, angiogenic and cardioprotective[1][2][3][4][6].
Related Catalog
Target

NLRP3 inflammasome

In Vitro (±)11(12)-EET (5 μM; 10 mimutes; macrophages) depresses NLRP3 protein expression, dramatically decreases the expression of pro-IL-1β in cells and the supernatant and reduces the intracellular ROS[1]. Western Blot Analysis[1] Cell Line: Macrophages Concentration: 5 μM Incubation Time: 10 mimutes Result: Depresses NLRP3 protein expression. Immunofluorescence[1] Cell Line: Macrophages Concentration: 5 μM Incubation Time: 10 mimutes Result: Reduced the intracellular ROS.
In Vivo (±)11(12)-EET increases adhesion of isolated peripheral blood leukocytes in a chamber coated with P-selectin and ICAM-1 in 50 µg/kg[5].
References

[1]. Luo XQ, et al. Epoxyeicosatrienoic acids inhibit the activation of NLRP3 inflammasome in murine macrophages. J Cell Physiol. 2020;235(12):9910-9921.

[2]. Chacos N, et al. Novel epoxides formed during the liver cytochrome P-450 oxidation of arachidonic acid. Biochem Biophys Res Commun. 1982;104(3):916-922.

[3]. Oliw EH, et al. Oxygenation of arachidonic acid by hepatic monooxygenases. Isolation and metabolism of four epoxide intermediates. J Biol Chem. 1982;257(7):3771-3781.

[4]. Capdevila JH, et al. Cytochrome P450 and arachidonic acid bioactivation. Molecular and functional properties of the arachidonate monooxygenase. J Lipid Res. 2000;41(2):163-181.

[5]. Wang Z, et al. Arachidonic acid inhibits basolateral K channels in the cortical collecting duct via cytochrome P-450 epoxygenase-dependent metabolic pathways. Am J Physiol Renal Physiol. 2008;294(6):F1441-F1447.

[6]. Spector AA. Arachidonic acid cytochrome P450 epoxygenase pathway. J Lipid Res. 2009;50 Suppl(Suppl):S52-S56.

 Chemical & Physical Properties

Density 1.0±0.1 g/cm3
Boiling Point 461.8±33.0 °C at 760 mmHg
Molecular Formula C20H32O3
Molecular Weight 320.466
Flash Point 154.6±18.9 °C
Exact Mass 320.235138
PSA 49.83000
LogP 6.30
Vapour Pressure 0.0±2.4 mmHg at 25°C
Index of Refraction 1.501

 Safety Information

Symbol GHS02 GHS07
GHS02, GHS07
Signal Word Danger
Hazard Statements H225-H319
Precautionary Statements P210-P280-P305 + P351 + P338-P337 + P313-P403 + P235
RIDADR UN1170 - class 3 - PG 2 - Ethanol, solution

 Articles15

More Articles
Protective effects of n-6 fatty acids-enriched diet on intestinal ischaemia/reperfusion injury involve lipoxin A4 and its receptor.

Br. J. Pharmacol. 172(3) , 910-23, (2015)

Long-term intake of dietary fatty acids is known to predispose to chronic inflammation, but their effects on acute intestinal ischaemia/reperfusion (I/R) injury is unknown. The aim of this study was t...

Cyp2c44 epoxygenase in the collecting duct is essential for the high K+ intake-induced antihypertensive effect.

Am. J. Physiol. Renal Physiol. 307(4) , F453-60, (2014)

Cytochrome P-450, family 2, subfamily c, polypeptide 44 (Cyp2c44) epoxygenase metabolizes arachidonic acid (AA) to epoxyeicosatrienoic acids (EETs) in kidney and vascular tissues. In the present study...

UHPLC-MS/MS analysis of arachidonic acid and 10 of its major cytochrome P450 metabolites as free acids in rat livers: effects of hepatic ischemia.

J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 964 , 153-63, (2014)

The cytochrome P450 metabolites of arachidonic acid (AA) are mostly present in tissues, such as the liver, as bound to phospholipids, with only a small fraction available as free acids. The purpose of...

 Synonyms

5,8-Decadienoic acid, 10-[(2S,3R)-3-[(2Z)-2-octen-1-yl]oxiranyl]-, (5Z,8Z)-
(5Z,8Z)-10-{(2S,3R)-3-[(2Z)-2-Octen-1-yl]-2-oxiranyl}-5,8-decadienoic acid
(11S,12R)-EET
(5Z,8Z)-10-{(2S,3R)-3-[(2Z)-oct-2-en-1-yl]oxiran-2-yl}deca-5,8-dienoic acid
(5Z,8Z)-10-{(2S,3R)-3-[(2Z)-2-Octen-1-yl]-2-oxiranyl}-5,8-decadie noic acid
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