850706P

16:1 PE

1,2-dipalmitoleoyl-sn-glycero-3-phosphoethanolamine, powder

• Synonyme(s) : 1,2-di-(9Z-hexadecenoyl)-sn-glycero-3-phosphoethanolamine; PE(16:1(9Z)/16:1(9Z))
• Formule empirique (notation de Hill): C₃₇H₇₀NO₈P
• Numéro CAS: 61599-23-3
• Poids moléculaire : 687.93
• Code UNSPSC : 51191904
• Nomenclature NACRES : NA.25

Propriétés

• Pureté: >99% (TLC)
• Forme: powder
• Conditionnement: pkg of 2 × 100 mg (850706P-200mg); pkg of 1 × 25 mg (850706P-25mg)
• Fabricant/nom de marque: Avanti Research^™ - A Croda Brand 850706P
• Type de lipide: cardiolipins; phospholipids
• Conditions d'expédition: dry ice
• Température de stockage: −20°C
• Chaîne SMILES: [H][C@@](COP([O-])(OCC[NH3+])=O)(OC(CCCCCCC/C=C\CCCCCC)=O)COC(CCCCCCC/C=C\CCCCCC)=O

Description

Description générale

Phosphatidylethanolamine is an aminophospholipid, which is found in eukaryotic and prokaryotic cells. It is one of the most abundant glycerophospholipids in biological membranes. Phosphatidylethanolamine is found in nervous tissue.

Application

16:1 PE has been used to assess the linearity of response of lipid classes. It has also been used as an internal standard for the determination of plasmenyl-PC and plasmenyl-PE of human heart mitochondria using a Bligh -Dyer extraction method.

Actions biochimiques/physiologiques

Phosphatidylethanolamine forms pure lipid structures. It maintains membrane fluidity in eukaryotic cells. Phosphatidylethanolamine plays a critical role in autophagy, cell division and protein folding. It acts as a precursor for the synthesis of various protein modifications. Phosphatidylethanolamine functions as an intermediate for the synthesis of glycerophospholipid classes.

Conditionnement

5 mL Clear Glass Sealed Ampule (850706P-200mg)

5 mL Clear Glass Sealed Ampule (850706P-25mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids