1487-52-1

Basic information

• Product Name: [S,(+)]-3-O-Benzyl-2-O-oleoyl-1-O-palmitoyl-L-glycerol
• Synonyms: [S,(+)]-3-O-Benzyl-2-O-oleoyl-1-O-palmitoyl-L-glycerol
• CAS NO: 1487-52-1
• Molecular Formula: C₄₄H₇₆O₅
• Molecular Weight: 0
• Mol File: 1487-52-1.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: [S,(+)]-3-O-Benzyl-2-O-oleoyl-1-O-palmitoyl-L-glycerol(CAS DataBase Reference)
• NIST Chemistry Reference: [S,(+)]-3-O-Benzyl-2-O-oleoyl-1-O-palmitoyl-L-glycerol(1487-52-1)
• EPA Substance Registry System: [S,(+)]-3-O-Benzyl-2-O-oleoyl-1-O-palmitoyl-L-glycerol(1487-52-1)

Safety Data

• Hazardous Substances Data: 1487-52-1(Hazardous Substances Data)

Usage

Description

[S,(+)]-3-O-Benzyl-2-O-oleoyl-1-O-palmitoyl-L-glycerol is a chemical compound with the molecular formula C31H54O5. It is a derivative of glycerol, consisting of a glycerol molecule with a benzyl group attached to the 3-oxygen, an oleoyl group attached to the 2-oxygen, and a palmitoyl group attached to the 1-oxygen. [S,(+)]-3-O-Benzyl-2-O-oleoyl-1-O-palmitoyl-L-glycerol is characterized by its unique structure and potential biological and pharmacological activities.

Uses

Used in Research and Pharmaceutical Settings:
[S,(+)]-3-O-Benzyl-2-O-oleoyl-1-O-palmitoyl-L-glycerol is used as a potential anti-inflammatory and anti-cancer agent for its potential biological and pharmacological activities. Its unique structure allows it to interact with various biological targets, making it a promising candidate for the development of new therapeutic strategies.
Used in Drug Delivery Applications:
In the field of drug delivery, [S,(+)]-3-O-Benzyl-2-O-oleoyl-1-O-palmitoyl-L-glycerol is used as a component in liposome and lipid nanoparticle formulations. Its incorporation into these delivery systems enhances the solubility, stability, and bioavailability of various drugs, leading to improved therapeutic outcomes.
Used in Lipid Chemistry:
As an important compound in the field of lipid chemistry, [S,(+)]-3-O-Benzyl-2-O-oleoyl-1-O-palmitoyl-L-glycerol contributes to the understanding of lipid structures and their interactions with biological systems. This knowledge can be applied to the design of novel lipid-based therapeutics and the development of targeted drug delivery systems.
Used in the Development of New Therapeutic Strategies:
The potential anti-inflammatory and anti-cancer activities of [S,(+)]-3-O-Benzyl-2-O-oleoyl-1-O-palmitoyl-L-glycerol make it a valuable compound in the development of new therapeutic strategies. Its unique structure and properties allow for the exploration of its interactions with various biological targets, which could lead to the discovery of novel treatments for a range of diseases and conditions.

Upstream product

• 56552-80-8 (R)-3-benzyloxy-1,2-propanediol 
• 16495-03-7 (S)-4-(benzyloxymethyl)-2,2-dimethyl-1,3-dioxolane 
• 100-39-0 benzyl bromide 
• 112-80-1 cis-Octadecenoic acid 
• 1487-50-9 1-O-hexadecanoyl-3-O-benzyl-sn-glycerol 

Downstream Products

• 6753-55-5 2-oleoyl-1-palmitoyl-sn-glycero-3-phosphocholine 
• 29541-66-0 1-O-palmitoyl-2-[(9z)-octadenoyl]-glycerol 

Relevant articles and documents

Synthesis of a small library of mixed-acid phospholipids from D-mannitol as a homochiral starting material

Synthesis of a series of mixed-acid phospholipids containing a polyunsaturated fatty acid using a newly protecting strategy are described. Thus, benzyl and methyl α-(2,4-dinitrophenyl)acetic acid which were respectively removed by BCl3 and 354 nm light are used as protecting groups.