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描述
1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine
化驗
>99% (TLC)
形狀
powder
包裝
pkg of 1 × 1 g (850757P-1g)
pkg of 2 × 100 mg (850757P-200mg)
pkg of 5 × 100 mg (850757P-500mg)
pkg of 1 × 25 mg (850757P-25mg)
製造商／商標名
Avanti Research™ - A Croda Brand
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 已用于制备大单层膜囊泡 (LUV)。 也用于制备双偏振干涉法 (DPI) 的脂质体。
包裝
5 mL 透明玻璃密封安瓿 (850757P-200 mg)
5 mL 透明玻璃密封安瓿 (850757P-25 mg)
5 mL 透明玻璃密封安瓿 (850757P-500 mg)
60 mL 琥珀色广口螺旋盖玻璃瓶 (850757P-1g)
法律資訊
Avanti Research is a trademark of Avanti Polar Lipids, LLC
也與該產品經常一起購買
产品编号
说明
价格
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
The use of liprotides to stabilize and transport hydrophobic molecules
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Biochemistry, 54(31), 4815-4823 (2015)
Using protein-fatty acid complexes to improve vitamin D stability
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Journal of Dairy Science, 99(10), 7755-7767 (2016)
Mariya Chavarha et al.
Langmuir : the ACS journal of surfaces and colloids, 28(48), 16596-16604 (2012-11-13)
Prior studies have shown that the biological mixture of the two hydrophobic surfactant proteins, SP-B and SP-C, produces faster adsorption of the surfactant lipids to an air/water interface, and that they induce 1-palmitoyl-2-oleoyl phosphatidylethanolamine (POPE) to form inverse bicontinuous cubic
Examination of the Interaction between a Membrane Active Peptide and Artificial Bilayers by Dual Polarisation Interferometry
Payne JAE, et al.
Bio-protocol, 7(1), e2087-e2087 (2017)
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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