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850325P

Avanti

10:0 PC

1,2-didecanoyl-sn-glycero-3-phosphocholine, powder

Synonyme(s) :

1,2-dicapryl-sn-glycero-3-phosphocholine; PC(10:0/10:0)

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About This Item

Formule empirique (notation de Hill):
C28H56NO8P
Numéro CAS:
Poids moléculaire :
565.72
Numéro MDL:
Code UNSPSC :
51191904
Nomenclature NACRES :
NA.25

Essai

>99% (TLC)

Forme

powder

Conditionnement

pkg of 1 × 200 mg (850325P-200mg)
pkg of 1 × 25 mg (850325P-25mg)

Fabricant/nom de marque

Avanti Research - A Croda Brand 850325P

Type de lipide

cardiolipins
phospholipids

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

[O-]P(OCC[N+](C)(C)C)(OC[C@]([H])(OC(CCCCCCCCC)=O)COC(CCCCCCCCC)=O)=O

InChI

1S/C28H56NO8P/c1-6-8-10-12-14-16-18-20-27(30)34-24-26(25-36-38(32,33)35-23-22-29(3,4)5)37-28(31)21-19-17-15-13-11-9-7-2/h26H,6-25H2,1-5H3

Clé InChI

MLKLDGSYMHFAOC-UHFFFAOYSA-N

Description générale

10:0 PC (DDPC/1,2-didecanoyl-sn-glycero-3-phosphocholine) is a zwitterionic and shorter-acyl chain phospholipid.
The list of Phosphatidylcholine products offered by Avanti is designed to provide compounds having a variety of physical properties. Products available include short chain (C3-C8 are water soluble and hygroscopic), saturated, multi-unsaturated and mixed acid PC′s. All of the products are purified by HPLC, and special precautions are taken to protect the products for oxidization and hydrolysis.

Application

10:0 PC (DDPC/1,2-didecanoyl-sn-glycero-3-phosphocholine) may be used:
  • as an internal standard to measure lipid metabolites for metabolic profiling using hydrophilic interaction liquid chromatography (HILIC)
  • to prepare lipid bilayer to reconstitute Vpu (membrane protein) and for biophysical studies
  • to prepare phospholipid membrane to study lipid-induced conformation of a 27-residue Cry4Ba-α7 peptide

Actions biochimiques/physiologiques

High or low level of phosphatidylcholine (PC) can affect energy metabolism in several organelles.

Conditionnement

20 mL Clear Glass Screw Cap Vial (850325P-200mg)
5 mL Clear Glass Sealed Ampule (850325P-25mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Lot/Batch Number

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Les clients ont également consulté

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Sang Ho Park et al.
Journal of molecular biology, 350(2), 310-318 (2005-06-07)
In order to investigate the compensation mechanism of a trans-membrane helix in response to hydrophobic mismatch, the tilt and rotation angles of the trans-membrane helix of Vpu aligned in lipid bilayers of various thickness were determined using orientation-dependent frequencies obtained
Kasorn Tiewsiri et al.
Archives of biochemistry and biophysics, 482(1-2), 17-24 (2008-12-24)
Helix 7 in the Cry4Ba-pore-forming domain contains conserved Tyr(249) and Phe(264) that are crucially involved in mosquito-larvicidal activity. We have now characterized lipid-induced conformation of a 27-residue Cry4Ba-alpha7 peptide in phospholipid membranes using ATR-FTIR and hydrogen/deuterium (H(+)/D(+)) exchange experiments. ATR-FTIR
Jelske N van der Veen et al.
Biochimica et biophysica acta. Biomembranes, 1859(9 Pt B), 1558-1572 (2017-04-16)
Phosphatidylcholine (PC) and phosphatidylethanolamine (PE) are the most abundant phospholipids in all mammalian cell membranes. In the 1950s, Eugene Kennedy and co-workers performed groundbreaking research that established the general outline of many of the pathways of phospholipid biosynthesis. In recent
Chun-Cheih Chao et al.
Cell, 179(7), 1483-1498 (2019-12-10)
Metabolism has been shown to control peripheral immunity, but little is known about its role in central nervous system (CNS) inflammation. Through a combination of proteomic, metabolomic, transcriptomic, and perturbation studies, we found that sphingolipid metabolism in astrocytes triggers the

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