Date published: 2026-5-25

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5(R)-HETE (CAS 61641-47-2)

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Application:
5(R)-HETE is a potent chemotactic agent found in S. solidissima
CAS Number:
61641-47-2
Molecular Weight:
320.5
Molecular Formula:
C20H32O3
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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5(R)-HETE, identified by the CAS number 61641-47-2, is a specific enantiomer of hydroxyeicosatetraenoic acid (HETE), a metabolite derived from the oxidation of arachidonic acid primarily through the action of the 5-lipoxygenase enzyme. This particular compound is characterized by the presence of a hydroxyl group at the fifth carbon in the R configuration, distinguishing it from other isomers with different spatial arrangements. In scientific research, 5(R)-HETE is extensively studied for its role as a lipid mediator that influences various cellular signaling pathways. This compound has been shown to be involved in the modulation of intracellular calcium levels, which is crucial for activating several signaling cascades within cells. Additionally, 5(R)-HETE interacts with specific receptors that facilitate cellular responses to oxidative stress and modulate the behavior of immune cells. Research involving 5(R)-HETE is critical for understanding the complex interactions and regulatory mechanisms within lipid signaling networks that influence cellular adaptation and responses to physiological stimuli. By studying this molecule, researchers aim to decipher the nuanced roles of lipid mediators in signaling processes, contributing to a broader understanding of cellular dynamics and homeostasis in various biological contexts.


5(R)-HETE (CAS 61641-47-2) References

  1. Metabolism of 5(S)-hydroxy-6,8,11,14-eicosatetraenoic acid and other 5(S)-hydroxyeicosanoids by a specific dehydrogenase in human polymorphonuclear leukocytes.  |  Powell, WS., et al. 1992. J Biol Chem. 267: 19233-41. PMID: 1326548
  2. Baking reduces prostaglandin, resolvin, and hydroxy-fatty acid content of farm-raised Atlantic salmon (Salmo salar).  |  Raatz, SK., et al. 2011. J Agric Food Chem. 59: 11278-86. PMID: 21919483
  3. Biomarkers for personalizing omega-3 fatty acid dosing.  |  Jiang, Y., et al. 2014. Cancer Prev Res (Phila). 7: 1011-22. PMID: 25139294
  4. Effects of fish oil supplementation on prostaglandins in normal and tumor colon tissue: modulation by the lipogenic phenotype of colon tumors.  |  Djuric, Z., et al. 2017. J Nutr Biochem. 46: 90-99. PMID: 28486173
  5. Analysis of HETEs in human whole blood by chiral UHPLC-ECAPCI/HRMS.  |  Mazaleuskaya, LL., et al. 2018. J Lipid Res. 59: 564-575. PMID: 29301865
  6. Chiral lipidomics of monoepoxy and monohydroxy metabolites derived from long-chain polyunsaturated fatty acids.  |  Blum, M., et al. 2019. J Lipid Res. 60: 135-148. PMID: 30409844
  7. LC-MS profiling-based non-targeted secondary metabolite screening for deciphering cosmeceutical potential of Malaysian algae.  |  Lim, MW., et al. 2023. J Cosmet Dermatol. 22: 2810-2815. PMID: 37313630
  8. 5-Hydroxyeicosatetraenoic acid (HETE)-induced neutrophil transcellular migration is dependent upon enantiomeric structure.  |  Bittleman, DB. and Casale, TB. 1995. Am J Respir Cell Mol Biol. 12: 260-7. PMID: 7873191
  9. Metabolism of 5(S)-hydroxyeicosanoids by a specific dehydrogenase in human neutrophils.  |  Powell, WS., et al. 1993. J Lipid Mediat. 6: 361-8. PMID: 8395251
  10. Discovery of 5R-lipoxygenase activity in oocytes of the surf clam, Spisula solidissima.  |  Hada, T., et al. 1997. Biochim Biophys Acta. 1346: 109-19. PMID: 9219894
  11. Stereospecific synthesis of 5S-HETE, 5R-HETE and their transformation to 5 (±) HPETE  |  Zamboni, R. and Rokach, J. 1983. Tetrahedron Letters. 24(10): 999-1002.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

5(R)-HETE, 25 µg

sc-205148
25 µg
$112.00

5(R)-HETE, 50 µg

sc-205148A
50 µg
$214.00