(±) 11 (12) -EET

CAT:
804-HY-130494-01
Size:
25 μg (312.04 μM x 250 μL in Ethanol)
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
(±) 11 (12) -EET - image 1

(±) 11 (12) -EET

  • 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].
  • Product Name Alternative :

    11,12-EET
  • UNSPSC :

    12352005
  • Target :

    NOD-like Receptor (NLR)
  • Type :

    Reference compound
  • Related Pathways :

    Immunology/Inflammation
  • Applications :

    COVID-19-immunoregulation
  • Field of Research :

    Inflammation/Immunology; Cardiovascular Disease
  • Assay Protocol :

    https://www.medchemexpress.com/racemic-11-12-eet.html
  • Concentration :

    312.04 μM * 250 μL in Ethanol
  • Purity :

    98.30
  • Solubility :

    10 mM in DMSO
  • Smiles :

    CCCCC/C=C\C[C@H]1O[C@H]1C/C=C\C/C=C\CCCC(O)=O
  • Molecular Formula :

    C20H32O3
  • Molecular Weight :

    320.47
  • References & Citations :

    [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.
  • Shipping Conditions :

    Blue Ice
  • Storage Conditions :

    Solution, -20°C, 2 years
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    No Development Reported
  • Isoform :

    NLRP3
  • CAS Number :

    [87173-81-7]

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