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840857C

Avanti

16:0-18:1 PA

1-palmitoyl-2-oleoyl-sn-glycero-3-phosphate (sodium salt), chloroform

Synonyme(s) :

1-hexadecanoyl-2--(9Z-octadecenoyl)-sn-glycero-3-phosphate (sodium salt); POPA; PA(16:0/18:1(9Z)); 110616

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About This Item

Formule empirique (notation de Hill):
C37H70O8PNa
Numéro CAS:
169437-35-8
Poids moléculaire :
696.91
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.25

Pureté

>99% (TLC)

Forme

liquid

Conditionnement

pkg of 1 × 2.5 mL (840857C-25mg)
pkg of 2 × 4 mL (840857C-200mg)
pkg of 5 × 4 mL (840857C-500mg)

Fabricant/nom de marque

Avanti Research™ - A Croda Brand 840857C

Concentration

10 mg/mL (840857C-25mg)
25 mg/mL (840857C-200mg)
25 mg/mL (840857C-500mg)

Type de lipide

phospholipids
cardiolipins

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

[H][C@@](COP([O-])(O)=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O.[Na+]

InChI

1S/C37H71O8P.Na/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-37(39)45-35(34-44-46(40,41)42)33-43-36(38)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2;/h17-18,35H,3-16,19-34H2,1-2H3,(H2,40,41,42);/q;+1/p-1/b18-17-;/t35-;/m1./s1

Clé InChI

PPYXMAJBOKWTQX-RYRMQHSSSA-M

Description générale

16:0-18:1 PA (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphate (sodium salt)/POPA) has eight oxygen atoms and one hydroxyl hydrogen atom. POPA is an anionic lipid.

Application

16:0-18:1 PA (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphate (sodium salt)) has been used to study its effects on the monogalactosyldiacylglycerol (MGDG) synthase activity of chloroplast envelope and in liposome Pull-Down Assay with the C2-like domain of SEIPIN.

Actions biochimiques/physiologiques

Phosphatidic acid (PA) serves as a precursor for phosphatidylcholine or phosphatidylserine. It is involved in influencing the membrane curvature and signaling.

Conditionnement

5 mL Clear Glass Sealed Ampule (840857C-200mg)
5 mL Clear Glass Sealed Ampule (840857C-25mg)
5 mL Clear Glass Sealed Ampule (840857C-500mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Souvent commandé avec ce produit

Réf. du produit
Description
Tarif

Pictogrammes

Skull and crossbonesHealth hazard
GHS06,GHS08

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)

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".

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Consulter la Bibliothèque de documents

Allison Dickey et al.
Biophysical journal, 95(6), 2636-2646 (2008-06-03)
To better understand bilayer property dependency on lipid electrostatics and headgroup size, we use atomistic molecular dynamics simulations to study negatively charged and neutral lipid membranes. We compare the negatively charged phosphatidic acid (PA), which at physiological pH and salt
Renhong Yan et al.
Developmental cell, 47(2), 248-256 (2018-10-09)
The biogenesis of lipid droplets (LDs) and the development of adipocytes are two key aspects of mammalian fat storage. SEIPIN, an integral membrane protein of the endoplasmic reticulum (ER), plays a critical role in both LD formation and adipogenesis. The
R J Perrin et al.
The Journal of biological chemistry, 275(44), 34393-34398 (2000-08-23)
alpha-Synuclein has been centrally implicated in neurodegenerative disease, and a normal function in developmental synaptic plasticity has been suggested by studies in songbirds. A variety of observations suggest the protein partitions between membrane and cytosol, a behavior apparently conferred by
Bixia Zhang et al.
Plant physiology (2020-04-26)
Cinnamate 4-hydroxylase (C4H, CYP73A) is a cytochrome P450 monooxygenase associated externally with endoplasmic reticulum of plant cells. The enzyme uses NADPH-cytochrome P450 reductase (CPR) as a donor of electrons and hydroxylates cinnamic acid to form 4-coumaric acid in phenylpropanoid metabolism.
Nadezhda Y Davydova et al.
The Biochemical journal, 476(23), 3661-3685 (2019-11-22)
In this study, we investigate the ability of ethanol-inducible CYP2E1 to interact with other cytochrome P450 species and affect the metabolism of their substrates. As a model system, we used CYP2E1-enriched human liver microsomes (HLM) obtained by the incorporation of
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