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Merck
CN

860517P

Avanti

C17 神经酰胺 (d18:1/17:0)

Avanti Research - A Croda Brand

别名:

N-十七酰-D-赤-鞘氨醇

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关于此项目

经验公式(希尔记法):
C35H69NO3
CAS Number:
分子量:
551.93
MDL编号:
UNSPSC代码:
12352211
NACRES:
NA.25
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表单

powder

包装

pkg of 1 × 10 mg (860517P-10mg)
pkg of 1 × 25 mg (860517P-25mg)
pkg of 1 × 5 mg (860517P-5mg)

制造商/商品名称

Avanti Research - A Croda Brand

脂质类型

sphingolipids

运输

dry ice

储存温度

−20°C

SMILES字符串

OC[C@]([H])(NC(CCCCCCCCCCCCCCCC)=O)[C@]([H])(O)/C=C/CCCCCCCCCCCCC

InChI

1S/C35H69NO3/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-35(39)36-33(32-37)34(38)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h28,30,33-34,37-38H,3-27,29,31-32H2,1-2H3,(H,36,39)/b30-28+/t33-,34+/m0/s1

InChI key

ICWGMOFDULMCFL-QKSCFGQVSA-N

一般描述

甲酰胺合成可通过以下两种方法进行介导:通过鞘氨醇或鞘氨醇水解的挽救途径;或通过二氢神经酰胺形成的从头途径。在结构上,神经酰胺具有鞘氨醇碱基,即通过酰胺键与脂肪酸连接的长链氨基醇。

应用

C17神经酰胺(d18:1/17:0)已被用于:
  • 通过色谱与负离子电喷雾电离串联质谱联用定量测定心肌神经酰胺的内标物,
  • 作为串联质谱(MS/MS)的内标物
  • 作为鞘磷脂合酶2的底物

生化/生理作用

神经酰胺在调节各种细胞过程(如衰老和凋亡)中起关键作用。它们直接参与皮肤细胞的增殖和分化并调节皮肤屏障功能。基于神经酰胺的类似物是潜在的抗肿瘤药,被视为抑癌脂质。

包装

5 mL 棕色螺旋盖玻璃瓶l (860517P-10mg)
5 mL 棕色螺旋盖玻璃瓶l (860517P-25mg)
5 mL 棕色螺旋盖玻璃瓶l (860517P-5mg)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

储存分类代码

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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