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重要文件

850757C

Avanti

磷脂酰乙醇胺(16:0-18:1 PE)

Avanti Research - A Croda Brand

同義詞:

1-十六酰-2-(9Z-十八烯酰)-sn-甘油-3-磷酸乙醇胺;POPE;PE(16:0/18:1(9Z));110637

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About This Item

經驗公式(希爾表示法):
C39H76NO8P
CAS號碼:
分子量::
718.00
分類程式碼代碼:
51191904
NACRES:
NA.25

描述

1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine, chloroform

化驗

>99% (TLC)

形狀

liquid

包裝

pkg of 1 × 2.5 mL (850757C-25mg)
pkg of 2 × 20 mL (850757C-1g)
pkg of 2 × 4 mL (850757C-200mg)
pkg of 5 × 4 mL (850757C-500mg)

製造商/商標名

Avanti Research - A Croda Brand

濃度

10 mg/mL (850757C-25mg)
25 mg/mL (850757C-1g)
25 mg/mL (850757C-200mg)
25 mg/mL (850757C-500mg)

脂質類型

cardiolipins
phospholipids

運輸包裝

dry ice

儲存溫度

−20°C

SMILES 字串

[H][C@@](COP([O-])(OCC[NH3+])=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O

InChI

1S/C39H76NO8P/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-39(42)48-37(36-47-49(43,44)46-34-33-40)35-45-38(41)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h17-18,37H,3-16,19-36,40H2,1-2H3,(H,43,44)/b18-17-

InChI 密鑰

FHQVHHIBKUMWTI-ZCXUNETKSA-N

應用

16:0-18:1 PE(磷脂酰乙醇胺)作为合成脂质已用于制备脂质体。

包裝

30 mL带螺旋盖的琥珀色窄口玻璃瓶(850757C-1g)
5 mL透明玻璃密封安瓿(850757C-200mg)
5 mL透明玻璃密封安瓿(850757C-25mg)
5 mL透明玻璃密封安瓿(850757C-500mg)

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 - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

標靶器官

Central nervous system, Liver,Kidney

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。

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存取文件庫

Ionization Properties of Phospholipids Determined by Zeta Potential Measurements
Sathappa M and Alder NN
Bio-protocol, 6(22) (2016)
Mitochondria: Practical Protocols (2018)
Tânia Silva et al.
Langmuir : the ACS journal of surfaces and colloids, 34(5), 2158-2170 (2018-01-07)
An understanding of the mechanism of action of antimicrobial peptides is fundamental to the development of new and more active antibiotics. In the present work, we use a wide range of techniques (SANS, SAXD, DSC, ITC, CD, and confocal and
Sónia Troeira Henriques et al.
Journal of the American Chemical Society, 141(51), 20460-20469 (2019-11-26)
Peptides with pharmaceutical activities are attractive drug leads, and knowledge of their mode-of-action is essential for translation into the clinic. Comparison of native and enantiomeric peptides has long been used as a powerful approach to discriminate membrane- or receptor-mediated modes-of-action
Charles G Cranfield et al.
Langmuir : the ACS journal of surfaces and colloids, 33(26), 6630-6637 (2017-06-14)
Cyclotides are cyclic disulfide-rich peptides that are chemically and thermally stable and possess pharmaceutical and insecticidal properties. The activities reported for cyclotides correlate with their ability to target phosphatidylethanolamine (PE)-phospholipids and disrupt cell membranes. However, the mechanism by which this

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