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Merck
CN

840009C

Avanti

PAF (from Heart PC)

Avanti Research - A Croda Brand

别名:

1-alkyl-2-acetoyl-sn-glycero-3-phosphocholine

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关于此项目

化学文摘社编号:
UNSPSC代码:
12352211
NACRES:
NA.25
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产品名称

PAF (from Heart PC), Avanti Research - A Croda Brand 840009C

方案

>99% (TLC)

表单

liquid

包装

pkg of 1 × 1 mL (840009C-5mg)

制造商/商品名称

Avanti Research - A Croda Brand 840009C

浓度

5 mg/mL (840009C-5mg)

脂质类型

lipid extracts
phosphoglycerides

运输

dry ice

储存温度

−20°C

InChI

1S/C12H26NO7P/c1-6-17-9-12(20-11(2)14)10-19-21(15,16)18-8-7-13(3,4)5/h12H,6-10H2,1-5H3/t12-/m1/s1

InChI key

OLGKYSVSAKLUHK-GFCCVEGCSA-N

一般描述

Platelet-activating factor (PAF; 1-O-alkyl-2-acetyl-sn-glycero-3-phosphocholine), an endogenous phospholipid is synthesized by several cells. PAF is a phosphatidylcholine derivative.

生化/生理作用

Platelet-activating factor (PAF; 1-O-alkyl-2-acetyl-sn-glycero-3-phosphocholine) is linked with arterial thrombosis, endotoxic shock, acute inflammation and acute allergic disease. It acts as a mediator of pathogenesis of ulcerative colitis and Crohn′s disease in human colon. It also participates in platelet activation and inflammation.

包装

5 mL Clear Glass Sealed Ampule (840009C-5mg)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

象形图

Skull and crossbonesHealth hazard

警示用语:

Danger

危险分类

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

靶器官

Central nervous system

储存分类代码

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

闪点(°F)

does not flash

闪点(°C)

does not flash

法规信息

危险化学品
易制毒化学品(2类)
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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PAFAH Ib phospholipase A2 subunits have distinct roles in maintaining Golgi structure and function
Bechler ME and Brown WJ
Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids, 1831(3), 595-601 (2013)
Thromboxane A2-mediated Cl- secretion induced by platelet-activating factor in isolated rat colon
Suzuki T, et al.
European Journal of Pharmacology, 400(2-3), 297-303 (2000)

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