Date published: 2025-10-14

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5(S),12(S)-DiHETE (CAS 73151-67-4)

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Alternate Names:
(5S,12S)-Dihydroxy-(6E,8E,10E,14Z)-eicosatetraenoic acid; 5,12-Di-HETE
Application:
5(S),12(S)-DiHETE is a compound that acts as a potent eicosanoid lipid mediator
CAS Number:
73151-67-4
Purity:
≥98%
Molecular Weight:
336.47
Molecular Formula:
C20H32O4
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(S),12(S)-DiHETE is a compound that acts as a potent eicosanoid lipid mediator. Leukotrienes comprise a family of endogenous metabolites of certain fatty acids and are related to thromboxanes and prostaglandins. They are potent eicosanoid lipid mediators that play numerous roles in inflammation, immunological functions and maintaining biological homeostasis. Leukotrienes possess a conjugated triene structure which gives them their name. They are generally isolated from leukocytes and primarily act through specific G protein-coupled receptors. 5(S),12(S)-DiHETE (6-trans-12-epi-LTB4) is synthesized via nonenzymatic hydrolysis of LTA4 (sc-201039) and by myeloperoxidase-dependent metabolism of cysteinyl leukotrienes. See 5-Lipoxygenase Pathway for structure


5(S),12(S)-DiHETE (CAS 73151-67-4) References

  1. Cutaneous inflammation: effects of hydroxy acids and eicosanoid pathway inhibitors on vascular permeability.  |  Waldman, JS., et al. 1989. J Invest Dermatol. 92: 112-6. PMID: 2491876
  2. The effect of selected arachidonic acid metabolites on natural killer cell activity.  |  Field, WE., et al. 1988. Prostaglandins. 36: 411-9. PMID: 3148962
  3. Role of Human 15-Lipoxygenase-2 in the Biosynthesis of the Lipoxin Intermediate, 5S,15S-diHpETE, Implicated with the Altered Positional Specificity of Human 15-Lipoxygenase-1.  |  Perry, SC., et al. 2020. Biochemistry. 59: 4118-4130. PMID: 33048542
  4. Subgingival Microbiome and Specialized Pro-Resolving Lipid Mediator Pathway Profiles Are Correlated in Periodontal Inflammation.  |  Lee, CT., et al. 2021. Front Immunol. 12: 691216. PMID: 34177951
  5. Plasma oxidative lipidomics reveals signatures for sepsis-associated acute kidney injury.  |  Zhou, L., et al. 2023. Clin Chim Acta. 551: 117616. PMID: 37884118
  6. Metabolism of arachidonic acid in polymorphonuclear leukocytes. Structural analysis of novel hydroxylated compounds.  |  Borgeat, P. and Samuelsson, B. 1979. J Biol Chem. 254: 7865-9. PMID: 468794
  7. Studies on the mechanism of formation of the 5S, 12S-dihydroxy-6,8,10,14(E,Z,E,Z)-icosatetraenoic acid in leukocytes.  |  Borgeat, P., et al. 1982. Prostaglandins. 23: 713-24. PMID: 6289381
  8. The myeloperoxidase-dependent metabolism of leukotrienes C4, D4, and E4 to 6-trans-leukotriene B4 diastereoisomers and the subclass-specific S-diastereoisomeric sulfoxides.  |  Lee, CW., et al. 1983. J Biol Chem. 258: 15004-10. PMID: 6317683
  9. Formation and effects of leukotrienes and lipoxins in human bone marrow.  |  Lindgren, JA., et al. 1993. J Lipid Mediat. 6: 313-20. PMID: 8357990
  10. Stimulation of human myelopoiesis by leukotrienes B4 and C4: interactions with granulocyte-macrophage colony-stimulating factor.  |  Stenke, L., et al. 1993. Blood. 81: 352-6. PMID: 8380723

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

5(S),12(S)-DiHETE, 25 µg

sc-200426
25 µg
$446.00

5(S),12(S)-DiHETE, 50 µg

sc-200426A
50 µg
$772.00