860724P
Avanti
N-24：0植物鞘氨醇
Avanti Research™ - A Croda Brand
别名:
N-木香油基-植物鞘氨醇（酿酒酵母）
Product Name
N-24：0植物鞘氨醇, Avanti Research™ - A Croda Brand 860724P, powder
表单
powder
包装
pkg of 1 × 10 mg (860724P-10mg)
pkg of 1 × 5 mg (860724P-5mg)
制造商/商品名称
Avanti Research™ - A Croda Brand 860724P
脂质类型
sphingolipids
运输
dry ice
储存温度
−20°C
SMILES字符串
O[C@]([H])(CCCCCCCCCCCCCC)[C@](O)([H])[C@@]([H])(NC(CCCCCCCCCCCCCCCCCCCCCCC)=O)CO
InChI
1S/C42H85NO4/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-25-27-29-31-33-35-37-41(46)43-39(38-44)42(47)40(45)36-34-32-30-28-26-16-14-12-10-8-6-4-2/h39-40,42,44-45,47H,3-38H2,1-2H3,(H,43,46)/t39-,40+,42-/m0/s1
InChI key
ZESJDNWGTANZCC-LFVSMIGWSA-N
一般描述
N-24:0植物鞘氨醇或N-木香油基-植物鞘氨醇属于植物鞘氨醇基。植物鞘氨醇。它广泛存在于真菌、植物、细菌、海洋生物和哺乳动物组织的膜中。
应用
N-24:0 植物鞘氨醇已用于研究其对模型脂质膜组织和透性障特性的影响。
生化/生理作用
相较于非羟基脂肪酸神经酰胺[NS24]，由N-24:0植物鞘氨醇组成的脂质膜对离子、亲脂小分子具有很高的渗透性。
包装
5 mL棕色玻璃螺旋盖小瓶（860724P-10mg）
5 mL棕色玻璃螺旋盖小瓶（860724P-5mg）
法律信息
Avanti Research is a trademark of Avanti Polar Lipids, LLC
储存分类代码
11 - Combustible Solids
WGK
WGK 3
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
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持