Merck
CN
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文件

870202O

Avanti

18:1 PDP PE

Avanti Polar Lipids 870202O

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别名:
1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-[3-(2-pyridyldithio)propionate] (sodium salt)
经验公式（希尔记法）:
C49H84N2O9PNaS2
CAS号:
474944-13-3
分子量:
963.29
NACRES:
NA.25

形式

liquid

包装

pkg of 1 × 25 mg (870202O-25mg)

manufacturer/tradename

Avanti Polar Lipids 870202O

运输

dry ice

储存温度

−20°C

SMILES string

[H][C@@](COP([O-])(OCCNC(CCSSC1=CC=CC=N1)=O)=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCC/C=C\CCCCCCCC)=O.[Na+]

InChI

1S/C49H85N2O9PS2.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-36-48(53)57-43-45(60-49(54)37-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2)44-59-61(55,56)58-41-40-50-46(52)38-42-62-63-47-35-33-34-39-51-47;/h17-20,33-35,39,45H,3-16,21-32,36-38,40-44H2,1-2H3,(H,50,52)(H,55,56);/q;+1/p-1/b19-17-,20-18-;/t45-;/m1./s1

InChI key

LFMWVVNPVNIPJG-JQRYTBKHSA-M

一般描述

18:1 PDP PE, also referred as 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-[3-(2-pyridyldithio)propionate], is a head group modified functionalized lipid. Functionalized lipids mainly act as reporter molecules.

应用

18:1 PDP PE may be used in the preparation of hydrophobized disulfide-linked oligodeoxyribonucleotide (ODN). It may also be used in the preparation of liposomes.

包装

5 mL Clear Glass Sealed Ampule (870202O-25mg)

储存分类代码

10 - Combustible liquids

WGK

WGK 3

分析证书(COA)

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示例

T1503
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705578-5MG-PW

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1000309185

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Wanlop Weecharangsan et al.
Anticancer research, 30(1), 31-37 (2010-02-13)
Disulfide-linked oligodeoxyribonucleotide (ODN) liposomes were formulated and evaluated for the delivery of antisense ODN G3139 in KB human oral carcinoma cells. Liposomes composed of 1,2-di-(9Z-octadecenoyl)-3-trimethylammo-nium-propane (DOTAP)/egg phosphatidylcholine/alpha-tocopheryl polyethylene glycol 1000 succinate were incorporated with hydrophobized disulfide-linked ODN. Disulfide-linked ODN liposomes
Pathways for modulating exosome lipids identified by high-density lipoprotein-like nanoparticle binding to scavenger receptor type B-1
Angeloni NL, et al.
Scientific Reports, 6(1) (2016)
Laura Wayteck et al.
Biomaterials, 77, 243-254 (2015-11-26)
Following intravenous injection of anti-cancer nanomedicines, many barriers need to be overcome en route to the tumor. Cell-mediated delivery of nanoparticles (NPs) is promising in terms of overcoming several of these barriers based on the tumoritropic migratory properties of particular
Pathways for modulating exosome lipids identified by high-density lipoprotein-like nanoparticle binding to scavenger receptor type B-1
Angeloni NL, et al.
Scientific reports, 6(1) (2016)
Disulfide-linked liposomes: effective delivery vehicle for Bcl-2 antisense oligodeoxyribonucleotide G3139
Weecharangsan W, et al.
Anticancer Research, 30(1), 31-37 (2010)
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