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850697C

Avanti

06:0 PE

1,2-dihexanoyl-sn-glycero-3-phosphoethanolamine, chloroform

Synonyme(s) :

PE(6:0/6:0)

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About This Item

Formule empirique (notation de Hill):
C17H34NO8P
Numéro CAS:
Poids moléculaire :
411.43
Code UNSPSC :
51191904
Nomenclature NACRES :
NA.25

Pureté

>99% (TLC)

Forme

liquid

Conditionnement

pkg of 1 × 2.5 mL (850697C-25mg)

Fabricant/nom de marque

Avanti Research - A Croda Brand 850697C

Concentration

10 mg/mL (850697C-25mg)

Type de lipide

phospholipids
cardiolipins

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

[H][C@@](COP([O-])(OCC[NH3+])=O)(OC(CCCCC)=O)COC(CCCCC)=O

Description générale

06:0 PE (1,2-dihexanoyl-sn-glycero-3-phosphoethanolamine/DHPE) is a phosphoethanolamine (PE) molecule which carries short acyl chains. It is an ethanolamine-type substrate and a water-soluble phospholipid.

Application

06:0 PE (1,2-dihexanoyl-sn-glycero-3-phosphoethanolamine/DHPE) may be used:
  • as a substrate for glycerophosphoethanolamine ethanolaminephosphodiesterase (GPE-EP) in specificity studies as a phosphoethanolamine (PE) standard in liquid chromatographic analysis of milk phospholipids
  • as a phospholipid substrate to study the kinetic parameters for the glucose transporter type 4 (Glu4) mutants
  • as calibration standard in hydrophilic interaction liquid chromatography (HILIC) and ion mobility (IM)

Actions biochimiques/physiologiques

Phosphoethanolamine (PE) is known to possess antitumor activity and inhibitory effects on tumor progression in vivo. It also exhibits antiproliferative and proapoptotic effects. It acts as a precursor of phosphatidylcholine and phosphatidylethanolamine.

Conditionnement

5 mL Clear Glass Sealed Ampule (850697C-25mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Pictogrammes

Skull and crossbonesHealth hazard

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

Organes cibles

Central nervous system, Liver,Kidney

Classe de danger pour l'eau (WGK)

WGK 3


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Theoretical Study of Phosphoethanolamine: A Synthetic Anticancer Agent with Broad Antitumor Activity
Lorenzo VP, et al.
Journal of Chemistry (2020)
S F Martin et al.
Biochemistry, 39(12), 3410-3415 (2000-03-22)
The phosphatidylcholine-preferring phospholipase C from Bacillus cereus (PLC(Bc)) is a 28.5 kDa enzyme with three zinc ions in its active site. The roles that a number of amino acid residues play as zinc ligands and in binding and catalysis have
Lipidomics by HILIC-Ion Mobility-Mass Spectrometry
Ion Mobility-Mass Spectrometry, 119-132 (2020)
Peter Fagan et al.
Journal of chromatography. A, 1054(1-2), 241-249 (2004-11-24)
Two methods have been developed for the analysis of bovine milk phospholipid (PL) classes by NP-HPLC with evaporative light scattering detection. In the first method, a PVA-Sil guard column was used for the rapid determination of the major milk PL
Shingo Mineta et al.
Journal of bioscience and bioengineering, 119(2), 123-130 (2014-08-20)
Streptomyces sanglieri extracellularly produces a glycerophosphoethanolamine ethanolaminephosphodiesterase (GPE-EP). The gene encoding the enzyme was found to consist of a 2124-bp ORF, which codes for an N-terminal 48 residue signal peptide required for secretion and a 660 amino acid mature protein

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