Date published: 2026-5-24

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(±)14,15-DHET

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Alternate Names:
(±)14,15-dihydroxy-5Z,8Z,11Z-eicosatrienoic acid
Application:
(±)14,15-DHET is converts EETs into vicinal diols
Molecular Weight:
338.48
Molecular Formula:
C20H34O4
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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(±)14,15-DHET, also known as (±)14,15-dihydroxyeicosatrienoic acid, is a metabolite derived from the cytochrome P450 epoxygenase-mediated oxidation of arachidonic acid, specifically through the hydrolysis of 14,15-epoxyeicosatrienoic acid (14,15-EET) by soluble epoxide hydrolase (sEH). This compound plays a significant role in various biochemical pathways, especially in the modulation of signaling pathways related to cellular proliferation, angiogenesis, and inflammation. In research applications, (±)14,15-DHET serves as a marker and tool for understanding the intricate mechanisms of arachidonic acid metabolism and its implications in cellular function. Its role extends to the investigation of the endothelial response to physiological stimuli and the exploration of the broader implications of epoxyeicosatrienoic acids and their metabolites in cellular signaling and homeostasis. By studying (±)14,15-DHET, researchers gain valuable insights into the complex interplay between metabolic pathways and cellular responses, shedding light on the fundamental processes that underpin cellular health and disease states.


(±)14,15-DHET References

  1. Rapid, simultaneous quantitation of mono and dioxygenated metabolites of arachidonic acid in human CSF and rat brain.  |  Miller, TM., et al. 2009. J Chromatogr B Analyt Technol Biomed Life Sci. 877: 3991-4000. PMID: 19892608
  2. Stimulatory effects of arachidonic acid on myosin ATPase activity and contraction of smooth muscle via myosin motor domain.  |  Katayama, T., et al. 2010. Am J Physiol Heart Circ Physiol. 298: H505-14. PMID: 19933418
  3. Alterations in eicosanoid composition during embryonic development in the chorioallantoic membrane of the American alligator (Alligator mississippiensis) and domestic chicken (Gallus gallus).  |  Cantu, TM., et al. 2016. Gen Comp Endocrinol. 238: 78-87. PMID: 27401262
  4. A sensitive LC-MS/MS method for the quantification of regioisomers of epoxyeicosatrienoic and dihydroxyeicosatrienoic acids in human plasma during endothelial stimulation.  |  Duflot, T., et al. 2017. Anal Bioanal Chem. 409: 1845-1855. PMID: 27981341
  5. A sensitive and improved throughput UPLC-MS/MS quantitation method of total cytochrome P450 mediated arachidonic acid metabolites that can separate regio-isomers and cis/trans-EETs from human plasma.  |  Zeigler, M., et al. 2018. Chem Phys Lipids. 216: 162-170. PMID: 30201384
  6. Discovery and Optimization of Indoline-Based Compounds as Dual 5-LOX/sEH Inhibitors: In Vitro and In Vivo Anti-Inflammatory Characterization.  |  Cerqua, I., et al. 2022. J Med Chem. 65: 14456-14480. PMID: 36318728
  7. Multiplatform analyses reveal distinct drivers of systemic pathogenesis in adult versus pediatric severe acute COVID-19.  |  Druzak, S., et al. 2023. Nat Commun. 14: 1638. PMID: 37015925

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(±)14,15-DHET, 25 µg

sc-220605
25 µg
$159.00

(±)14,15-DHET, 50 µg

sc-220605A
50 µg
$296.00