Date published: 2026-5-1

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8(R)-HETE (CAS 105500-09-2)

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Application:
8(R)-HETE is formed from the lipoxygenation of arachidonic acid
CAS Number:
105500-09-2
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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8(R)-HETE, bearing the CAS number 105500-09-2, represents a specific enantiomer of 8-hydroxyeicosatetraenoic acid, a metabolite derived from the lipoxygenase-mediated oxidation of arachidonic acid. This particular isomer is characterized by the positional and stereo-specific placement of a hydroxyl group on the eighth carbon in the R configuration. As an active lipid mediator, 8(R)-HETE plays a crucial role in the regulation of various intracellular signaling pathways that influence cellular functions such as migration, adhesion, and the modulation of inflammatory mediator synthesis. In research settings, 8(R)-HETE is valued for its utility in elucidating the mechanisms through which oxygenated derivatives of essential fatty acids influence cell signaling. Its interaction with specific receptors and signaling proteins allows researchers to probe the dynamics of lipid signaling in cellular communication and response mechanisms. Studies involving 8(R)-HETE have provided significant insights into the complex roles of lipid mediators in the regulation of cellular environments, particularly in understanding how cells react to and manage oxidative stress and other signaling disruptions. This research contributes broadly to the field of cell biology, offering deeper understanding of the nuanced regulatory roles that such lipid mediators play in maintaining cellular homeostasis.


8(R)-HETE (CAS 105500-09-2) References

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  3. 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
  4. Stereospecific induction of starfish oocyte maturation by (8R)-hydroxyeicosatetraenoic acid.  |  Meijer, L., et al. 1986. J Biol Chem. 261: 17040-7. PMID: 3097019
  5. Multi-Omics Analysis Reveals the Systematic Relationship Between Oral Homeostasis and Chronic Sleep Deprivation in Rats.  |  Chen, P., et al. 2022. Front Immunol. 13: 847132. PMID: 35432311
  6. Global Metabolomics of Fireflies (Coleoptera: Lampyridae) Explore Metabolic Adaptation to Fresh Water in Insects.  |  Yang, L., et al. 2022. Insects. 13: PMID: 36135524
  7. Time course of western diet (WD) induced nonalcoholic steatohepatitis (NASH) in female and male Ldlr-/- mice.  |  Spooner, MH., et al. 2023. PLoS One. 18: e0292432. PMID: 37819925
  8. Non-targeted metabolomics analysis of metabolite changes in two quinoa genotypes under drought stress.  |  Zhu, X., et al. 2023. BMC Plant Biol. 23: 503. PMID: 37858063
  9. Possible involvement of arachidonic acid and eicosanoids in metamorphic events in Hydractinia echinata (Coelenterata; Hydrozoa).  |  Leitz, T., et al. 1994. J Exp Zool. 269: 422-31. PMID: 8057074
  10. Hypolipidemic drugs, polyunsaturated fatty acids, and eicosanoids are ligands for peroxisome proliferator-activated receptors alpha and delta.  |  Forman, BM., et al. 1997. Proc Natl Acad Sci U S A. 94: 4312-7. PMID: 9113986
  11. Fatty acids and eicosanoids regulate gene expression through direct interactions with peroxisome proliferator-activated receptors alpha and gamma.  |  Kliewer, SA., et al. 1997. Proc Natl Acad Sci U S A. 94: 4318-23. PMID: 9113987

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

8(R)-HETE, 25 µg

sc-205180
25 µg
$140.00

8(R)-HETE, 50 µg

sc-205180A
50 µg
$266.00