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來源證明/COA

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860467P

Avanti

N-C16-desoxymethylsphingosine

Name: N-C16-desoxymethylsphingosine
Brand: AVANTI

Avanti Polar Lipids 860467P, powder

同義詞:

N-palmitoyl-1-desoxymethylsphingosine (m17:1/16:0)

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About This Item

經驗公式（希爾表示法）:

C₃₃H₆₅NO₂

CAS號碼:

1246298-57-6

分子量：:

507.87

分類程式碼代碼:

12352211

NACRES:

NA.25

形狀

powder

包裝

pkg of 1 × 1 mg (860467P-1mg)
pkg of 1 × 5 mg (860467P-5mg)

製造商／商標名

Avanti Polar Lipids 860467P

脂質類型

sphingolipids
bioactive lipids

運輸包裝

dry ice

儲存溫度

−20°C

SMILES 字串

[H][C@](/C=C/CCCCCCCCCCCCC)(O)CNC(CCCCCCCCCCCCCCC)=O

一般說明

Desoxymethylsphingosine is an atypical deoxy-sphingoid base.

應用

N-C16-desoxymethylsphingosine or N-palmitoyl-1-desoxymethylsphingosine (m17:1/16:0) has been used as a standard in the quantitation of atypical sphingoid bases in biological samples by reverse-phase liquid chromatography coupled to electrospray ionization tandem mass spectrometry (LC-MS/MS).

包裝

5 mL Amber Glass Screw Cap Vial (860467P-1mg)

5 mL Amber Glass Screw Cap Vial (860467P-5mg)

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

分析證明 (COA)

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Simultaneous quantification of lyso-neutral glycosphingolipids and neutral glycosphingolipids by N-acetylation with [3H]acetic anhydride.

Jacques Bodennec et al.

Journal of lipid research, 44(7), 1413-1419 (2003-05-06)

We describe a new method that permits quantification in the pmol to nmol range of three lyso-neutral glycosphingolipids (lyso-n-GSLs), glucosylsphingosine (GlcSph), galactosylsphingosine (GalSph), and lactosylsphingosine, in the same sample as neutral glycosphingolipids (n-GSLs). Lyso-n-GSLs and n-GSLs are initially obtained from

Analysis of 1-Deoxysphingoid Bases and Their N-Acyl Metabolites and Exploration of Their Occurrence in Some Food Materials.

Junliang Wan et al.

Journal of agricultural and food chemistry, 67(46), 12953-12961 (2019-10-23)

Most common sphingolipids are comprised of "typical" sphingoid bases (sphinganine, sphingosine, and structurally related compounds) and are produced via the condensation of l-serine with a fatty acyl-CoA by serine palmitoyltransferase. Some organisms, including mammals, also produce "atypical" sphingoid bases that

Biodiversity of sphingoid bases ("sphingosines") and related amino alcohols.

Sarah T Pruett et al.

Journal of lipid research, 49(8), 1621-1639 (2008-05-24)

"Sphingosin" was first described by J. L. W. Thudichum in 1884 and structurally characterized as 2S,3R,4E-2-aminooctadec-4-ene-1,3-diol in 1947 by Herb Carter, who also proposed the designation of "lipides derived from sphingosine as sphingolipides." This category of amino alcohols is now

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