Date published: 2026-4-20

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tetranor-12(R)-HETE (CAS 135271-51-1)

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Alternate Names:
8(R)-HHxTrE
Application:
tetranor-12(R)-HETE is an oxidation metabolite of 12(R)-HETE
CAS Number:
135271-51-1
Molecular Weight:
266.4
Molecular Formula:
C16H26O3
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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Tetranor-12(R)-HETE, registered under CAS number 135271-51-1, represents a metabolically processed form of 12(R)-HETE, characterized by the removal of four carbon atoms from the carboxylic end of the parent molecule. This transformation results in a shortened lipid mediator that retains the hydroxyl group at the twelfth carbon in the R configuration. Tetranor-12(R)-HETE is particularly notable for its role in modulating intracellular signaling pathways that influence cellular responses to oxidative stress and environmental changes. In biochemical research, this compound is utilized to study the finer aspects of lipid metabolism and its impact on cell signaling dynamics. The specific actions of tetranor-12(R)-HETE include the modulation of enzymatic activities and the interaction with specific lipid receptors, which are crucial for understanding the regulation of cellular processes such as inflammation, cell migration, and apoptosis. Research involving tetranor-12(R)-HETE provides valuable insights into the complex pathways by which lipid mediators influence cellular behavior, shedding light on the mechanisms by which cells maintain homeostasis and adapt to physiological challenges. This understanding is vital for advancing the knowledge of cellular biochemistry and the complex network of signaling molecules that orchestrate cellular function and response.


tetranor-12(R)-HETE (CAS 135271-51-1) References

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  2. Metabolism of 12(R)-hydroxy-5,8,10,14-eicosatetraenoic acid (12(R)-HETE) in corneal tissues: formation of novel metabolites.  |  Nishimura, M., et al. 1991. Arch Biochem Biophys. 290: 326-35. PMID: 1929401
  3. Target lipidomics approach to reveal the resolution of inflammation induced by Chinese medicine combination in Liu-Shen-Wan against realgar overexposure to rats.  |  Wang, J., et al. 2020. J Ethnopharmacol. 249: 112171. PMID: 31442622
  4. The Regulation Network of Glycerolipid Metabolism as Coregulators of Immunotherapy-Related Myocarditis.  |  Yang, X., et al. 2023. Cardiovasc Ther. 2023: 8774971. PMID: 37388276
  5. Therapeutic effects and mechanisms of Inonotus hispidus extract and active monomer compounds in a rat mammary gland hyperplasia model.  |  Han, C. and Bao, H. 2024. J Ethnopharmacol. 319: 117274. PMID: 37797875
  6. A concise synthesis of (R)-hydroxy-E, Z-diene fatty acids: preparation of 12 (R)-hete, tetranor-12 (R)-hete, and 13 (R)-hode.  |  Lumin, Sun, et al. 1991. Tetrahedron letters. 32.21: 2315-2318.
  7. Untargeted metabolomics analysis in drug-naïve patients with severe obsessive–compulsive disorder.  |  Li, Zheqin, et al. 2023. Frontiers in Neuroscience. 17: 1148971.
  8. Metabolomics revealed that toxic cyanobacteria stress reduced the flavor quality of Bellamya aeruginosa.  |  Huang, Yuqi, et al. 2024. Frontiers in Sustainable Food Systems. 8: 1379140.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

tetranor-12(R)-HETE, 25 µg

sc-205520
25 µg
$204.00

tetranor-12(R)-HETE, 100 µg

sc-205520A
100 µg
$555.00