2954-46-3 Usage
Uses
Used in Membrane Biophysics and Biochemistry Research:
Dilauroylphosphatidylserine is used as a model lipid for studying the structure, dynamics, and interactions of biological membranes. Its similarity to natural phospholipids allows researchers to gain insights into the fundamental properties of cell membranes and their role in various biological processes.
Used in Drug Delivery Systems:
Dilauroylphosphatidylserine is used as a component in drug delivery systems, particularly in the formation of liposomes. Its ability to form stable vesicles and compatibility with other phospholipids and lipids makes it an ideal candidate for encapsulating and delivering therapeutic agents to target cells and tissues.
Used in Liposome Research:
Dilauroylphosphatidylserine is used as a key ingredient in the development of liposomes for various applications, including drug delivery, vaccine development, and gene therapy. Its properties contribute to the stability and functionality of liposomal formulations, enhancing their potential in medical and biotechnological applications.
Used in Biotechnology and Pharmaceutical Research:
Dilauroylphosphatidylserine plays an important role in advancing our understanding of membrane structure and function, as well as its potential applications in biotechnology and pharmaceutical research. Its unique properties and versatility make it a valuable tool for studying and manipulating biological membranes in various experimental settings.
Check Digit Verification of cas no
The CAS Registry Mumber 2954-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,5 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2954-46:
(6*2)+(5*9)+(4*5)+(3*4)+(2*4)+(1*6)=103
103 % 10 = 3
So 2954-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C30H58NO10P/c1-3-5-7-9-11-13-15-17-19-21-28(32)38-23-26(24-39-42(36,37)40-25-27(31)30(34)35)41-29(33)22-20-18-16-14-12-10-8-6-4-2/h26-27H,3-25,31H2,1-2H3,(H,34,35)(H,36,37)/t26?,27-/m0/s1
2954-46-3Relevant academic research and scientific papers
Preparation method of 1,2-di-fatty acyl-sn-glycerol-3-phosphatidylserine
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Paragraph 0077; 0094-0098, (2021/06/22)
The invention provides a preparation method of 1,2-bis (fatty acyl)-sn-glycerol-3-phosphatidylserine. The method comprises the following steps: enabling (S)-glyceryl acetonide, bis(diisopropyl amino)(trichloroethoxy) phosphine and N-Troc-serine benzyl ester to react and oxidize to obtain 1,2-O-isopropylidene-glycerol-3-phosphoryl-N-Troc-serine benzyl ester; carrying out hydrolysis reaction on the 1,2-O-isopropylidene-glycerol-3-phosphoryl-N-Troc-serine benzyl ester to obtain 2,3-dihydroxy propyl-1-phosphoryl-N-Troc-serine benzyl ester; enabling 2,3-dihydroxypropyl-1-phosphoryl-N-Troc-serine benzyl ester and fatty acid to be subjected to a condensation reaction to obtain 1,2-difatty acyl-sn-glycerol-3-phosphoryl-N-Troc-serine benzyl ester; carrying out hydrogenation reaction on the 1,2-di-fatty acyl-sn-glycerol-3-phosphoryl-N-Troc-serine benzyl ester to obtain 1,2-di-fatty acyl-sn-glycerol-3-phosphoryl-N-Troc-serine; and carrying out a deprotection reaction on the 1,2-difatty acyl-sn-glycerol-3-phosphoryl-N-Troc-serine to obtain the 1, 2-difatty acyl-sn-glycerol-3-phosphatidylserine.
