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Key Documents

860724P

Avanti

N-24:0 Phytosphingosine

Avanti Research - A Croda Brand 860724P, powder

동의어(들):

N-lignoceroyl-phytosphingosine (Saccharomyces Cerevisiae)

로그인조직 및 계약 가격 보기


About This Item

실험식(Hill 표기법):
C42H85NO4
CAS Number:
Molecular Weight:
668.13
UNSPSC 코드:
12352211
NACRES:
NA.25

형태

powder

포장

pkg of 1 × 10 mg (860724P-10mg)
pkg of 1 × 5 mg (860724P-5mg)

제조업체/상표

Avanti Research - A Croda Brand 860724P

지질 유형

sphingolipids

배송 상태

dry ice

저장 온도

−20°C

SMILES string

O[C@]([H])(CCCCCCCCCCCCCC)[C@](O)([H])[C@@]([H])(NC(CCCCCCCCCCCCCCCCCCCCCCC)=O)CO

일반 설명

N-24:0 Phytosphingosine or N-lignoceroyl-phytosphingosine belongs to the group of phytosphingosines. Phytosphingosine. It is widely found in membranes of fungi, plants, bacteria, marine organisms, and mammalian tissues.

애플리케이션

N-24:0 Phytosphingosine has been used to study its influence on the organization and permeability barrier properties of model lipid membrane.

생화학적/생리학적 작용

Lipid membranes composed of N-24:0 phytosphingosine are highly permeable for ions, small and lipophilic molecules, than those based on non-hydroxy fatty acid ceramide[NS24].

포장

5 mL Amber Glass Screw Cap Vial (860724P-10mg)
5 mL Amber Glass Screw Cap Vial (860724P-5mg)

법적 정보

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 3


시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

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문서 라이브러리 방문

Andrej Kováčik et al.
Biochimica et biophysica acta. Biomembranes, 1860(5), 1162-1170 (2018-02-07)
In this work, we studied model stratum corneum lipid mixtures composed of the hydroxylated skin ceramides N-lignoceroyl 6-hydroxysphingosine (Cer[NH]) and α-hydroxylignoceroyl phytosphingosine (Cer[AP]). Two model skin lipid mixtures of the composition Cer[NH] or Cer[AP], N-lignoceroyl sphingosine (Cer[NS]), lignoceric acid (C24:0)
Lukáš Opálka et al.
Langmuir : the ACS journal of surfaces and colloids, 32(48), 12894-12904 (2016-12-10)
Omega-O-acylceramides (acylCer), a subclass of sphingolipids with an ultralong N-acyl chain (from 20 to 38 carbons, most usually 30 and 32 carbons), are crucial components of the skin permeability barrier. AcylCer are involved in the formation of the long periodicity
Zheng Liu et al.
The Journal of organic chemistry, 75(13), 4356-4364 (2010-06-10)
An asymmetric synthesis of d-ribo-phytosphingosine (1) was achieved by utilizing the ProPhenol (12)-catalyzed alkynylation of unsaturated aldehyde 8 to afford allylic propargylic alcohol (S)-6 followed by asymmetric epoxidation and opening of propargylic epoxy alcohol anti-5 with NaN(3)/NH(4)Cl. Deprotection and reduction

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