Date published: 2026-2-1

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2-Linoleoyl-1-palmitoyl-sn-glycero-3-phosphoethanolamine (CAS 13206-00-3)

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Alternate Names:
3-sn-Phosphatidylethanolamine; 2-linoleoyl-1-palmitoyl; L-α-Phosphatidylethanolamine
CAS Number:
13206-00-3
Molecular Weight:
715.98
Molecular Formula:
C39H74NO8P
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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2-Linoleoyl-1-palmitoyl-sn-glycero-3-phosphoethanolamine, a phospholipid with a specific fatty acid composition, has been extensively studied in various scientific research applications due to its unique chemical properties and biological activities. Researchers have employed this compound to investigate its mechanisms of action in plant biology, biochemistry, and molecular biology. Specifically, studies have shown that this phospholipid can modulate the activity of enzymes involved in plant cell signaling, such as phospholipase D and phosphatidylinositol-specific phospholipase C, and regulate the expression of genes involved in plant stress responses. Additionally, this compound has been used as a model system to study the mechanisms of plant cell membrane biogenesis, including the role of phospholipid metabolism and protein-protein interactions. Furthermore, 2-Linoleoyl-1-palmitoyl-sn-glycero-3-phosphoethanolamine has been used in the study of plant-pathogen interactions, enabling researchers to investigate the mechanisms of disease resistance and develop novel strategies for disease control. In particular, this compound has been used as a substrate in enzymatic assays to study the activity of enzymes involved in phospholipid metabolism, providing insights into the regulation of plant membrane lipid synthesis and degradation. Overall, the scientific research applications of this phospholipid have contributed significantly to our understanding of plant biology, biochemistry, and molecular biology.


2-Linoleoyl-1-palmitoyl-sn-glycero-3-phosphoethanolamine (CAS 13206-00-3) References

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  2. Identification of 1-palmitoyl-2-linoleoyl-phosphatidylethanolamine modifications under oxidative stress conditions by LC-MS/MS.  |  Domingues, MR., et al. 2009. Biomed Chromatogr. 23: 588-601. PMID: 19277956
  3. Commonalities in Metabolic Reprogramming between Tobacco Use and Oral Cancer.  |  Rushing, BR., et al. 2022. Int J Environ Res Public Health. 19: PMID: 36011897
  4. Metabolomics and Proteomics Characterizing Hepatic Reactions to Dietary Linseed Oil in Duck.  |  Zhang, Y., et al. 2022. Int J Mol Sci. 23: PMID: 36555340
  5. The Combination of Bioinformatics Analysis and Untargeted Metabolomics Reveals Potential Biomarkers and Key Metabolic Pathways in Asthma.  |  Huang, F., et al. 2022. Metabolites. 13: PMID: 36676950
  6. Integration of proteome and metabolome profiling to reveal heat stress response and tolerance mechanisms of Serratia sp. AXJ-M for the bioremediation of papermaking black liquor.  |  An, X., et al. 2023. J Hazard Mater. 450: 131092. PMID: 36857821
  7. Exogenous Melatonin Enhances the Low Phosphorus Tolerance of Barley Roots of Different Genotypes.  |  Ma, Z., et al. 2023. Cells. 12: PMID: 37408231
  8. The Implications in Meat Quality and Nutrition by Comparing the Metabolites of Pectoral Muscle between Adult Indigenous Chickens and Commercial Laying Hens.  |  Yin, L., et al. 2023. Metabolites. 13: PMID: 37512547
  9. Integrated Mechanism of Immune Response Modulation by Arctium Lappa L. Fructans Based on Microbiome and Metabolomics Technologies.  |  Li, L., et al. 2024. J Agric Food Chem. 72: 10981-10994. PMID: 38691768
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Linoleoyl-1-palmitoyl-sn-glycero-3-phosphoethanolamine, 25 mg

sc-209207
25 mg
$220.00