Date published: 2026-5-24

1-800-457-3801

SCBT Portrait Logo
Seach Input

11(R)-HEDE

0.0(0)
Write a reviewAsk a question

Molecular Weight:
324.5
Molecular Formula:
C20H36O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

11(R)-HEDE, or 11(R)-hydroxyeicosatetraenoic acid, is a metabolite of arachidonic acid, primarily formed through the action of lipoxygenase enzymes, a pathway that is fundamental to the biosynthesis of various bioactive lipid mediators. This chemical plays a crucial role in the complex web of cellular signaling, particularly in the modulation of inflammation and immune responses at a molecular level. In research contexts, 11(R)-HEDE has been a focal point in studies exploring the dynamics of lipid mediator involvement in cellular processes. Its mechanism of action is centered around its interaction with specific receptors and enzymes that are pivotal in signaling pathways, influencing the production and function of other eicosanoids and cytokines. Researchers have utilized this compound to dissect the pathways through which cells respond to inflammatory stimuli, thereby contributing to a broader understanding of the regulation of inflammation at a cellular level. The study of 11(R)-HEDE also extends to its role in the resolution phase of inflammation, where it potentially aids in the cessation of inflammatory responses, thus ensuring that the process does not perpetuate damage to tissues. By examining the effects of 11(R)-HEDE in various cellular models, scientists aim to explain its complex roles within the network of lipid signaling.


11(R)-HEDE References

  1. A lipidomic screen of hyperglycemia-treated HRECs links 12/15-Lipoxygenase to microvascular dysfunction during diabetic retinopathy via NADPH oxidase.  |  Ibrahim, AS., et al. 2015. J Lipid Res. 56: 599-611. PMID: 25598081
  2. Interaction of 12/15-lipoxygenase with fatty acids alters the leukocyte kinetics leading to improved postmyocardial infarction healing.  |  Halade, GV., et al. 2017. Am J Physiol Heart Circ Physiol. 313: H89-H102. PMID: 28411230
  3. Influence of curing on the metabolite profile of water-boiled salted duck.  |  Li, C., et al. 2022. Food Chem. 397: 133752. PMID: 35917791
  4. Untargeted Metabolomic Analyses and Antilipidemic Effects of Citrus Physiological Premature Fruit Drop.  |  Wang, C., et al. 2024. Int J Mol Sci. 25: PMID: 38339154
  5. Translational Research in Acute Lung Injury and Pulmonary Fibrosis: Human lung fibroblasts produce proresolving peroxisome proliferator-activated receptor-γ ligands in a cyclooxygenase-2-dependent manner.  |  Lacy, Shannon H., et al. 2016. American Journal of Physiology-Lung Cellular and Molecular Physiology. 311.5: L855.
  6. Heart Failure: Novel Therapeutic Pathways Emerging from Basic Science: Interaction of 12/15-lipoxygenase with fatty acids alters the leukocyte kinetics leading to improved postmyocardial infarction healing.  |  Halade, Ganesh V., et al. 2017. American Journal of Physiology-Heart and Circulatory Physiology. 313.1: H89.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

11(R)-HEDE, 25 µg

sc-220582
25 µg
$135.00

11(R)-HEDE, 50 µg

sc-220582A
50 µg
$257.00