Date published: 2025-10-14

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(±)14,15-DiHETE

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Alternate Names:
(±)14,15-Dihydroxy-Eicosa-5,8,11,17-Tetraenoic Acid
Application:
(±)14,15-DiHETE is an ω-3 fatty acid metabolite of eicosapentaenoic acid
Molecular Weight:
336.47
Molecular Formula:
C20H32O4
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-DiHETE, designated by its CAS registry number, is a dihydroxy derivative of eicosatetraenoic acid (EET), an eicosanoid, which plays a critical role in the study of cellular signaling and lipid metabolism. This compound is particularly noted for its involvement in the enzymatic pathways where it is formed by the epoxidation of arachidonic acid followed by hydration. The presence of hydroxyl groups at the 14th and 15th positions significantly modifies its interaction with various cell membrane components and signaling receptors. In research settings, (±)14,15-DiHETE has been used to explore the regulation of intracellular signaling pathways associated with the regulation of vascular tone, platelet aggregation, and inflammation. The compound′s ability to act at the cellular level, influencing the dynamics of calcium ion channels and other signaling molecules, makes it a valuable tool in physiological studies. Researchers have employed (±)14,15-DiHETE to understand more about the complex interplay between different lipid mediators in the cell and their roles in cellular communication processes. These studies shed light on the broader implications of lipid signaling in maintaining cellular homeostasis and responding to environmental changes, providing insights into fundamental biological processes.


(±)14,15-DiHETE References

  1. Urinary excretion of diols derived from eicosapentaenoic acid during n-3 fatty acid ingestion by man.  |  Knapp, HR., et al. 1991. Prostaglandins. 42: 47-54. PMID: 1771239
  2. Oxidation of 5,8,11,14,17-eicosapentaenoic acid by hepatic and renal microsomes.  |  Van Rollins, M., et al. 1988. Biochim Biophys Acta. 966: 133-49. PMID: 2839239
  3. Oxidation of docosahexaenoic acid by rat liver microsomes.  |  VanRollins, M., et al. 1984. J Biol Chem. 259: 5776-83. PMID: 6232277
  4. High-performance liquid chromatography-thermospray mass spectrometry of epoxy polyunsaturated fatty acids and epoxyhydroxy polyunsaturated fatty acids from an incubation mixture of rat tissue homogenate.  |  Yamane, M., et al. 1994. J Chromatogr. 652: 123-36. PMID: 8006098

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(±)14,15-DiHETE, 25 µg

sc-220606
25 µg
$114.00

(±)14,15-DiHETE, 50 µg

sc-220606A
50 µg
$162.00