Date published: 2025-10-13

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1-Palmitoyl-sn-glycero-3-phosphoethanolamine (CAS 53862-35-4)

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Alternate Names:
1-Palmitoyl-sn-glycero-3-phosphoethanolamine is also known as 16:0 LPE.
Application:
1-Palmitoyl-sn-glycero-3-phosphoethanolamine is a naturally occurring lysophospholipid that inhibits the growth of L. donovani promastigotes.
CAS Number:
53862-35-4
Molecular Weight:
453.6
Molecular Formula:
C21H44NO7P
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

1-Palmitoyl-sn-glycero-3-phosphoethanolamine (P-PEtn) is a naturally occurring lysophospholipid that inhibits the growth of L. donovani promastigotes. 1-Palmitoyl-sn-glycero-3-phosphoethanolamine is involved in signal transduction, cell membrane remodeling, and lipid metabolism. It is also a precursor for the synthesis of other phospholipids and is involved in the formation of various membrane-associated proteins. In the quanitfication of saturated lysophosphoethanolamines, 1-Palmitoyl-sn-glycero-3-phosphoethanolamine may be used as an internal standard. It has been used to degranulate human eosinophils.


1-Palmitoyl-sn-glycero-3-phosphoethanolamine (CAS 53862-35-4) References

  1. Purification and characterization of secretory phospholipase B, lysophospholipase and lysophospholipase/transacylase from a virulent strain of the pathogenic fungus Cryptococcus neoformans.  |  Chen, SC., et al. 2000. Biochem J. 347: 431-9. PMID: 10749672
  2. Effects of lipid composition on the membrane activity and lipid phase behaviour of Vibrio sp. DSM14379 cells grown at various NaCl concentrations.  |  Danevcic, T., et al. 2005. Biochim Biophys Acta. 1712: 1-8. PMID: 15878424
  3. Development and validation of a UHPLC-ESI-MS/MS method for the simultaneous quantification of mammal lysophosphatidylcholines and lysophosphatidylethanolamines in serum.  |  Suárez-García, S., et al. 2017. J Chromatogr B Analyt Technol Biomed Life Sci. 1055-1056: 86-97. PMID: 28445851
  4. Phospholipids and UDP-glucuronosyltransferase. Structure/function relationships.  |  Zakim, D., et al. 1988. J Biol Chem. 263: 5164-9. PMID: 3128536
  5. A Lipidomic Analysis of Leaves of Esca-Affected Grapevine Suggests a Role for Galactolipids in the Defense Response and Appearance of Foliar Symptoms.  |  Goufo, P. and Cortez, I. 2020. Biology (Basel). 9: PMID: 32899845
  6. Cocultivation of Anaerobic Fungi with Rumen Bacteria Establishes an Antagonistic Relationship.  |  Swift, CL., et al. 2021. mBio. 12: e0144221. PMID: 34399620

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Palmitoyl-sn-glycero-3-phosphoethanolamine, 5 mg

sc-208685
5 mg
$61.00

1-Palmitoyl-sn-glycero-3-phosphoethanolamine, 25 mg

sc-208685A
25 mg
$186.00