Date published: 2026-6-7

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13(S)-HOTrE(γ) (CAS 74784-20-6)

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Application:
13(S)-HOTrE(γ) is the 15-LO product of γ-linolenic acid
CAS Number:
74784-20-6
Purity:
≥98%
Molecular Weight:
294.4
Molecular Formula:
C18H30O3
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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13(S)-HOTrE(γ), with the CAS number 74784-20-6, is a specific enantiomer of hydroxyoctadecatrienoic acid, distinguished by its S-configuration and the gamma (γ) designation. This compound is a hydroxylated form of linolenic acid, a process typically mediated by lipoxygenases, a class of enzymes that introduce molecular oxygen into polyunsaturated fatty acids. As a research chemical, 13(S)-HOTrE(γ) is extensively used to study the biochemical pathways involved in lipid metabolism and the regulatory mechanisms of fatty acids in cellular processes. The specific actions of this molecule include the modulation of signaling pathways that regulate inflammation, cell proliferation, and apoptosis. It operates primarily through its interaction with various cellular receptors, such as peroxisome proliferator-activated receptors (PPARs), which play a critical role in lipid signaling and metabolism. This interaction often results in changes to gene expression patterns that influence cellular behavior. In biochemical and cellular biology research, 13(S)-HOTrE(γ) is instrumental in elucidating the roles of hydroxylated fatty acids in maintaining cellular homeostasis and responding to physiological stresses. By studying this molecule, researchers gain insights into the complex dynamics of lipid signaling in health and the response mechanisms to oxidative stress, providing a deeper understanding of the pathways that govern cell function and adaptation.


13(S)-HOTrE(γ) (CAS 74784-20-6) References

  1. Kinetic and structural investigations into the allosteric and pH effect on the substrate specificity of human epithelial 15-lipoxygenase-2.  |  Joshi, N., et al. 2013. Biochemistry. 52: 8026-35. PMID: 24171444
  2. Oxylipin concentration, but not fatty acid composition, is altered in human donor milk pasteurised using both thermal and non-thermal techniques.  |  Pitino, MA., et al. 2019. Br J Nutr. 122: 47-55. PMID: 31006410
  3. Metabolomics Profiles Associated with the Treatment of Zuojin Pill on Patients with Chronic Nonatrophic Gastritis.  |  Ma, X., et al. 2022. Front Pharmacol. 13: 898680. PMID: 35899115
  4. Inhibitory Investigations of Acyl-CoA Derivatives against Human Lipoxygenase Isozymes.  |  Tran, M., et al. 2023. Int J Mol Sci. 24: PMID: 37446119
  5. The association of eicosanoids and eicosanoid-related metabolites with pulmonary hypertension.  |  McNeill, JN., et al. 2023. Eur Respir J. 62: PMID: 37857430
  6. Plasma oxylipin profile of postpartum dairy cows categorized into different systemic inflammatory grades in the first week after parturition.  |  Grantz, JM., et al. 2024. JDS Commun. 5: 155-160. PMID: 38482129
  7. Highly efficient oxidation of plant oils to C18 trihydroxy fatty acids by Escherichia coli co-expressing lipoxygenase and epoxide hydrolase  |  Jin Lee, et al. 2022. Green Chem. 24: 2062-2072.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

13(S)-HOTrE(γ), 25 µg

sc-205007
25 µg
$45.00

13(S)-HOTrE(γ), 100 µg

sc-205007A
100 µg
$165.00