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Merck

840505C

Avanti

18:0-20:4 PG

1-stearoyl-2-arachidonoyl-sn-glycero-3-phospho-(1′-rac-glycerol) (sodium salt), chloroform

别名:

1-octadecanoyl-2-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phospho-(1′racglycerol) (sodium salt); SAPG; PG(18:0/20:4(5Z,8Z,11Z,14Z)); 110653

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About This Item

经验公式(希尔记法):
C44H78O10PNa
分子量:
821.05
分類程式碼代碼:
51191904
NACRES:
NA.25

化驗

>99% (TLC)

形狀

liquid

包裝

pkg of 1 × 2.5 mL (840505C-25mg)

製造商/商標名

Avanti Research - A Croda Brand 840505C

濃度

10 mg/mL (840505C-25mg)

脂質類型

phospholipids
cardiolipins

運輸包裝

dry ice

儲存溫度

−20°C

SMILES 字串

[Na+].[P](=O)([O-])(OC[C@H](OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC)COC(=O)CCCCCCCCCCCCCCCCC)OCC(O)CO

InChI

1S/C44H79O10P.Na/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-30-32-34-36-44(48)54-42(40-53-55(49,50)52-38-41(46)37-45)39-51-43(47)35-33-31-29-27-25-23-21-18-16-14-12-10-8-6-4-2;/h11,13,17,19,22,24,28,30,41-42,45-46H,3-10,12,14-16,18,20-21,23,25-27,29,31-40H2,1-2H3,(H,49,50);/q;+1/p-1/b13-11-,19-17-,24-22-,30-28-;/t41?,42-;/m1./s1

InChI 密鑰

XLHSHRIGGNFBGF-PYXSUFCTSA-M

一般說明

18:0-20:4 PG or 1-stearoyl-2-arachidonoyl-sn-glycero-3-phospho-(1′-rac-glycerol) is a sodium salt of glycerophospholipid, with substitution of stearic acid, arachidonic acid and phospho-rac-(1-glycerol) at the sn-1, sn-2 and sn-3 positions respectively, in the glycerol backbone.

應用

18:0-20:4 PG or 1-stearoyl-2-arachidonoyl-sn-glycero-3-phospho-(1′-rac-glycerol) (sodium salt) has been used as a standard in liquid chromatography tandem mass spectrometry (LC?MS/MS) method for lipid quantification.

包裝

5 mL Clear Glass Sealed Ampule (840505C-25mg)

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

象形圖

Skull and crossbonesHealth hazard

訊號詞

Danger

危險分類

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

標靶器官

Central nervous system

水污染物質分類(WGK)

WGK 3


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Max Scherer et al.
Analytical chemistry, 82(21), 8794-8799 (2010-10-16)
Cardiolipin (CL) and bis(monoacylglycero)phosphate (BMP) are unique lipid structures with important biological roles for mitochondrial integrity and endolysosomal degradation, respectively. They are synthesized from common precursors, phosphatidylglycerol (PG) and phosphatidic acid (PA). Here we present a rapid method for the

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