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860724P

Avanti

N-24:0 Phytosphingosine

Avanti Research™ - A Croda Brand 860724P, powder

Synonym(e):

N-lignoceroyl-phytosphingosine (Saccharomyces Cerevisiae)

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About This Item

Empirische Formel (Hill-System):
C42H85NO4
CAS-Nummer:
34437-74-6
Molekulargewicht:
668.13
UNSPSC-Code:
12352211
NACRES:
NA.25

Form

powder

Verpackung

pkg of 1 × 10 mg (860724P-10mg)
pkg of 1 × 5 mg (860724P-5mg)

Hersteller/Markenname

Avanti Research™ - A Croda Brand 860724P

Lipid-Typ

sphingolipids

Versandbedingung

dry ice

Lagertemp.

−20°C

SMILES String

O[C@]([H])(CCCCCCCCCCCCCC)[C@](O)([H])[C@@]([H])(NC(CCCCCCCCCCCCCCCCCCCCCCC)=O)CO

Verwandte Kategorien

Allgemeine Beschreibung

N-24:0 Phytosphingosine or N-lignoceroyl-phytosphingosine belongs to the group of phytosphingosines. Phytosphingosine. It is widely found in membranes of fungi, plants, bacteria, marine organisms, and mammalian tissues.

Anwendung

N-24:0 Phytosphingosine has been used to study its influence on the organization and permeability barrier properties of model lipid membrane.

Biochem./physiol. Wirkung

Lipid membranes composed of N-24:0 phytosphingosine are highly permeable for ions, small and lipophilic molecules, than those based on non-hydroxy fatty acid ceramide[NS24].

Verpackung

5 mL Amber Glass Screw Cap Vial (860724P-10mg)
5 mL Amber Glass Screw Cap Vial (860724P-5mg)

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

Andrej Kováčik et al.
Biochimica et biophysica acta. Biomembranes, 1860(5), 1162-1170 (2018-02-07)
In this work, we studied model stratum corneum lipid mixtures composed of the hydroxylated skin ceramides N-lignoceroyl 6-hydroxysphingosine (Cer[NH]) and α-hydroxylignoceroyl phytosphingosine (Cer[AP]). Two model skin lipid mixtures of the composition Cer[NH] or Cer[AP], N-lignoceroyl sphingosine (Cer[NS]), lignoceric acid (C24:0)
Lukáš Opálka et al.
Langmuir : the ACS journal of surfaces and colloids, 32(48), 12894-12904 (2016-12-10)
Omega-O-acylceramides (acylCer), a subclass of sphingolipids with an ultralong N-acyl chain (from 20 to 38 carbons, most usually 30 and 32 carbons), are crucial components of the skin permeability barrier. AcylCer are involved in the formation of the long periodicity
Zheng Liu et al.
The Journal of organic chemistry, 75(13), 4356-4364 (2010-06-10)
An asymmetric synthesis of d-ribo-phytosphingosine (1) was achieved by utilizing the ProPhenol (12)-catalyzed alkynylation of unsaturated aldehyde 8 to afford allylic propargylic alcohol (S)-6 followed by asymmetric epoxidation and opening of propargylic epoxy alcohol anti-5 with NaN(3)/NH(4)Cl. Deprotection and reduction

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