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重要文件

868584P

Avanti

16:0-d31 SM

Avanti Research - A Croda Brand 868584P, powder

同義詞:

N-棕榈酰-d31-D-赤型-鞘氨醇磷酸胆碱

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About This Item

經驗公式(希爾表示法):
C39H48N2O6PD31
CAS號碼:
分子量::
734.22
MDL號碼:
分類程式碼代碼:
12352211
NACRES:
NA.25

形狀

powder

包裝

pkg of 1 × 1 mg (868584P-1mg)
pkg of 1 × 5 mg (868584P-5mg)

製造商/商標名

Avanti Research - A Croda Brand 868584P

運輸包裝

dry ice

儲存溫度

−20°C

SMILES 字串

[H][C@](/C=C/CCCCCCCCCCCCC)(O)[C@@]([H])(NC(C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])=O)COP([O-]

一般說明

16:0-d31 Sm或 N-棕榈酰-d31-D-赤型鞘氨醇磷酰胆碱是氘标记的 N-棕榈酰鞘氨醇(SM)。 N-棕榈酰-SM是鞘磷脂,含由 N-连接的16个C原子酰基链。 鞘磷脂存在于哺乳动物细胞膜外小叶。是神经元和脂质双层的重要结构成分。

應用

16:0-d31 Sm或 N-棕榈酰-d31-D-赤型-鞘氨醇磷酰胆碱可用作质谱法中的内标,定量生物样品中的脂质。

包裝

5 mL棕色玻璃螺旋盖样品瓶((868584P-1mg)
5 mL棕色玻璃螺旋盖样品瓶((868584P-5mg)

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

儲存類別代碼

11 - Combustible Solids


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分析證明 (COA)

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Structure and lipid interaction of N-palmitoylsphingomyelin in bilayer membranes as revealed by 2H-NMR spectroscopy
Mehnert T, et al.
Biophysical Journal, 90(3), 939-946 (2006)
J Peter Slotte
Biochimica et biophysica acta, 1858(2), 304-310 (2015-12-15)
Sphingomyelin is an important constituent of mammalian cell membranes. Its molecular structure is N-acyl-D-erythro-sphingosylphosphorylcholine. The N-acyls in sphingomyelin often contain 16-24 carbons that are mostly saturated chains; however, the monounsaturated 24:1(Δ15c) acyl chain is also common. In addition to the
Nadine Beckmann et al.
International journal of molecular sciences, 20(24) (2019-12-15)
Farber disease is a rare lysosomal storage disorder resulting from acid ceramidase deficiency and subsequent ceramide accumulation. No treatments for Farber disease are clinically available, and affected patients have a severely shortened lifespan. We have recently reported a novel acid
Kotaro Hama et al.
Journal of lipid research, 61(4), 523-536 (2020-02-23)
X-linked adrenoleukodystrophy (X-ALD) is an inherited disorder caused by deleterious mutations in the ABCD1 gene. The ABCD1 protein transports very long-chain FAs (VLCFAs) from the cytosol into the peroxisome where the VLCFAs are degraded through β-oxidation. ABCD1 dysfunction leads to

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