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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
化学文摘社编号:
分子量:
551.93
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.25
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assay

>99% (TLC)

form

powder

packaging

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

manufacturer/tradename

Avanti Research - A Croda Brand

lipid type

sphingolipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

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

General description

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。

Application

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

Biochem/physiol Actions

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。

Packaging

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)

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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全球贸易项目编号

货号GTIN
860517P-10MG04061835317608
860517P-25MG04061835317615
860517P-5MG04061835317622