Accéder au contenu
Merck
Toutes les photos(1)

Key Documents

LM1104

Avanti

17:0-14:1 PE

Avanti Research - A Croda Brand

Synonyme(s) :

1-heptadecanoyl-2-(9Z-tetradecenoyl)-sn-glycero-3-phosphoethanolamine

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme


About This Item

Formule empirique (notation de Hill):
C36H70NO8P
Numéro CAS:
Poids moléculaire :
675.92
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.25

Forme

methanol solution

Conditionnement

pkg of 1 × 1 mL (LM1104-1EA)

Fabricant/nom de marque

Avanti Research - A Croda Brand

Concentration

~10 μg/mL (Refer to C of A for lot specific concentration.)

Application(s)

lipidomics
metabolomics

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

[H][C@@](COP([O-])(OCC[NH3+])=O)(OC(CCCCCCC/C=C\CCCC)=O)COC(CCCCCCCCCCCCCCCC)=O

Description générale

Phosphoethanolamine (PE) acts as a parent compound for phosphatidylcholine and phosphatidylethanolamine synthesis.

Application

17:0-14:1 PE or 1-heptadecanoyl-2-(9Z-tetradecenoyl)-sn-glycero-3-phosphoethanolamine has been used as an internal standard:
  • for lipid quantification using liquid chromatography-mass spectrometry (LC-MS)
  • for the detection of lipids by tandem mass spectrometry (MS/MS) (related to lipidome analyses)
  • in lipid extraction using MTBE protocol

Actions biochimiques/physiologiques

Phosphoethanolamine (PE) is known to show extensive antitumor action and prevents tumor proliferation, in vivo. Synthetic PE inhibits lung metastasis.

Conditionnement

2 mL Amber Glass Sealed Ampule (LM1104-1EA)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Pictogrammes

FlameSkull and crossbonesHealth hazard

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Organes cibles

Eyes

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

49.5 °F - closed cup

Point d'éclair (°C)

9.7 °C - closed cup


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Mathieu Frechin et al.
Nature, 523(7558), 88-91 (2015-05-27)
Cells sense the context in which they grow to adapt their phenotype and allow multicellular patterning by mechanisms of autocrine and paracrine signalling. However, patterns also form in cell populations exposed to the same signalling molecules and substratum, which often
Cell-intrinsic adaptation of lipid composition to local crowding drives social behaviour
Frechin M. et al.
Nature, 523(7558), 88-91 (2015)
Kallol Gupta et al.
Nature protocols, 13(5), 1106-1120 (2018-04-28)
With the recent success in determining membrane protein structures, further detailed understanding of the identity and function of the bound lipidome is essential. Using an approach that combines high-energy native mass spectrometry (HE-nMS) and solution-phase lipid profiling, this protocol can
A K Ferreira et al.
British journal of cancer, 109(11), 2819-2828 (2013-11-10)
We recently showed that synthetic phosphoethanolamine reduces tumour growth and inhibits lung metastasis in vivo. Here, we investigated its anti-leukaemia effects using acute promyelocytic leukaemia (APL) as a model. Cytotoxic effects of Pho-s on leukaemia cells were evaluated by MTT
Ursula Loizides-Mangold et al.
Journal of lipid research, 53(8), 1522-1534 (2012-05-26)
Glycosylphosphatidylinositol (GPI) anchor biosynthesis takes place in the endoplasmic reticulum (ER). After protein attachment, the GPI anchor is transported to the Golgi where it undergoes fatty acid remodeling. The ER exit of GPI-anchored proteins is controlled by glycan remodeling and

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique