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Merck
CN

860724P

Avanti

N-24：0植物鞘氨醇

Avanti Research™ - A Croda Brand

别名:

N-木香油基-植物鞘氨醇（酿酒酵母）

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关于此项目

经验公式（希尔记法）:
C42H85NO4
化学文摘社编号:
34437-74-6
分子量:
668.13
MDL number:
MFCD08703058
UNSPSC Code:
12352211
NACRES:
NA.25

主要文件

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产品名称

N-24：0植物鞘氨醇, Avanti Research™ - A Croda Brand 860724P, powder

InChI

1S/C42H85NO4/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-25-27-29-31-33-35-37-41(46)43-39(38-44)42(47)40(45)36-34-32-30-28-26-16-14-12-10-8-6-4-2/h39-40,42,44-45,47H,3-38H2,1-2H3,(H,43,46)/t39-,40+,42-/m0/s1

InChI key

ZESJDNWGTANZCC-LFVSMIGWSA-N

SMILES string

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

assay

>99% (TLC)

form

powder

packaging

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

manufacturer/tradename

Avanti Research™ - A Croda Brand 860724P

lipid type

sphingolipids

shipped in

dry ice

storage temp.

−20°C

相关类别

Application

N-24:0 植物鞘氨醇已用于研究其对模型脂质膜组织和透性障特性的影响。

Biochem/physiol Actions

相较于非羟基脂肪酸神经酰胺[NS24]，由N-24:0植物鞘氨醇组成的脂质膜对离子、亲脂小分子具有很高的渗透性。

General description

N-24:0植物鞘氨醇或N-木香油基-植物鞘氨醇属于植物鞘氨醇基。植物鞘氨醇。它广泛存在于真菌、植物、细菌、海洋生物和哺乳动物组织的膜中。

Packaging

5 mL棕色玻璃螺旋盖小瓶（860724P-10mg）
5 mL棕色玻璃螺旋盖小瓶（860724P-5mg）

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

存储类别

11 - Combustible Solids

wgk

WGK 3

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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