850312P
Avanti
DOCPe
Avanti Research™ - A Croda Brand 850312P, powder
동의어(들):
2-((2,3-bis(oleoyloxy)propyl)dimethylammonio)ethyl ethyl phosphate
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모든 사진(2)
크기 선택
보기 변경
25 MG
₩275,674
About This Item
실험식(Hill 표기법):
C45H86NO8P
CAS Number:
Molecular Weight:
800.14
MDL number:
UNSPSC 코드:
51191904
NACRES:
NA.25
추천 제품
분석
>99% (TLC)
양식
powder
포장
pkg of 1 × 200 mg (850312P-200mg)
pkg of 1 × 25 mg (850312P-25mg)
제조업체/상표
Avanti Research™ - A Croda Brand 850312P
지질 유형
phospholipids
cardiolipins
배송 상태
dry ice
저장 온도
−20°C
SMILES string
[H]C(C[N+](C)(CCOP([O-])(OCC)=O)C)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCC/C=C\CCCCCCCC)=O
InChI
1S/C45H86NO8P/c1-6-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-44(47)51-42-43(41-46(4,5)39-40-53-55(49,50)52-8-3)54-45(48)38-36-34-32-30-28-26-24-22-20-18-16-14-12-10-7-2/h21-24,43H,6-20,25-42H2,1-5H3/b23-21-,24-22-
InChI key
WDTDXEZJIUAULM-SXAUZNKPSA-N
일반 설명
2-((2,3-bis(oleoyloxy)propyl)dimethylammonio)ethyl ethylphosphate (DOCPe) is a neutrally charged lipid.[1]
Inverse-phosphocholine lipids, a remix of a common phospholipid, contain headgroups with an inverted charge orientation relative to phosphocholine (PC) lipids. The iPC lipid headgroup has a quaternary amine adjacent to the bilayer interface and a phosphate that extends into the aqueous phase. Therefore iPC lipids afford a unique opportunity to investigate the biophysical and bioactivity-related ramifications of a charge inversion at the bilayer surface.
애플리케이션
DOCPe is suitable for liposomes preparation.[1]
포장
20 mL Clear Glass Screw Cap Vial (850312P-200mg)
5 mL Clear Glass Sealed Ampule (850312P-25mg)
법적 정보
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class Code
11 - Combustible Solids
가장 최신 버전 중 하나를 선택하세요:
Charge and Coordination Directed Liposome Fusion onto SiO2 and TiO2 Nanoparticles
Wang X, et al.
Langmuir, 35(5), 1672-1681 (2018)
Yibo Liu et al.
Langmuir : the ACS journal of surfaces and colloids, 34(32), 9337-9348 (2018-03-13)
Phospholipids are a major component of the cell membrane. In most natural phospholipids, the phosphate acts as a bridge, connecting the other portion of the polar headgroup with the hydrophobic tails. Such bridging phosphate is chemically quite inert. Synthetic lipids
Emily K Perttu et al.
Journal of the American Chemical Society, 134(10), 4485-4488 (2012-03-01)
Zwitterionic inverse-phosphocholine (iPC) lipids contain headgroups with an inverted charge orientation relative to phosphocholine (PC) lipids. The iPC lipid headgroup has a quaternary amine adjacent to the bilayer interface and a phosphate that extends into the aqueous phase. Neutral iPC
Feng Wang et al.
Journal of the American Chemical Society, 137(36), 11736-11742 (2015-08-25)
Zwitterionic phosphocholine (PC) lipids are highly biocompatible, representing a major component of the cell membrane. A simple mixing of PC liposomes and silica (SiO2) surface results in liposome fusion with the surface and formation of supported lipid bilayers. However, the
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