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32899-41-5, 3-Palmitoyl-sn-glycerol, CAS:32899-41-5

32899-41-5,
3-Palmitoyl-sn-glycerol,
CAS:32899-41-5
MFCD00066457
C19H38O4 / 330.5

L-alpha-甘油棕榈酸酯, 3-棕榈酰-sn-甘油, 3-Palmitoyl-sn-glycerol

3-Palmitoyl-sn-glycerol is a fatty acid that is synthesized in the body from 3-hydroxyacyl coenzyme A. It aids in the synthesis of glycerides and phospholipids, which are important for cellular membranes. 3-Palmitoyl-sn-glycerol has been shown to have a hypoglycemic effect on diabetic patients, which may be due to its ability to reduce hepatic glucose production and increase insulin sensitivity. This compound also plays an important role in energy metabolism by providing the substrate for beta oxidation and ketogenesis. 3-Palmitoyl-sn-glycerol is used as a supplement for people with metabolic disorders, such as obesity and diabetes mellitus type II. It can be found in ganoderma lucidum, which has been shown to have antiinflammatory properties.

3-palmitoyl-sn-glycerol is a 3-acyl-sn-glycerol in which the acyl group is specified as palmitoyl (hexadecanoyl). It has a role as a metabolite. It is a 3-acyl-sn-glycerol and a 1-monopalmitoylglycerol. It is an enantiomer of a 1-hexadecanoyl-sn-glycerol.

1-Hexadecanoyl-sn-glycerol, also known as mono-1-palmitoyl-rac-glycerol (MPG), is a naturally occurring glyceride molecule that is found in various biological systems, including mammalian tissues, milk, and vegetation. MPG’s purpose in biological systems is not fully understood; however, many researchers speculate that this molecule has a role in the regulation of metabolism, energy storage, cell signaling, inflammation, and apoptosis. In recent years, there has been a growing interest in the properties and potential applications of MPG in various fields of research and industry.

Synthesis and Characterization:

MPG can be synthesized through several methods, including chemical synthesis, enzymatic synthesis, and extraction from natural sources. The most commonly used synthesis method involves esterification of palmitic acid with glycerol in the presence of an acid catalyst. Characterization of MPG can be done through various analytical methods, including gas chromatography, mass spectrometry, infrared spectroscopy, and nuclear magnetic resonance spectroscopy.

Analytical Methods:

The most commonly used analytical methods for detecting and quantifying MPG include high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS). These methods allow for the detection and quantification of MPG in various biological matrices, including blood, milk, and tissues.

Biological Properties:

MPG has been shown to exhibit various biological properties, including anti-inflammatory, anti-cancer, anti-oxidant, and immunomodulatory effects. It has been suggested that MPG may have potential therapeutic applications in various diseases, including cancer, Alzheimer’s disease, and cardiovascular disease.

Toxicity and Safety in Scientific Experiments:

Studies conducted on MPG in animal models have shown that there are no significant toxic effects or adverse reactions associated with this molecule. However, data on the safety of MPG in humans is limited, and further research is needed to establish its safety for human consumption.

Applications in Scientific Experiments:

MPG has been widely used in scientific experiments as a model lipid molecule for investigating lipid metabolism, bioenergetics, and signaling. It has also been used as a component in the development of liposomal drug delivery systems for targeted drug delivery.

Current State of Research:

Current research on MPG is focused on elucidating its biological functions and potential therapeutic applications. There is also a growing interest in the development of MPG-based liposomal drug delivery systems and other applications in the biotechnology and food industries.

Potential Implications in Various Fields of Research and Industry:

MPG exhibits various beneficial properties that may have potential implications in various fields of research and industry. In the pharmaceutical industry, MPG may be used as a component in drug delivery systems, or as a potential treatment for various diseases. In the food industry, MPG may be used as an emulsifier, stabilizer, and texturizer. In the biotechnology industry, MPG may be used in the development of biofuels, biosensors, and other biotechnological applications.

Limitations and Future Directions:

MPG’s potential applications are limited by several factors, including its low solubility in water and limited availability from natural sources. Future research is needed to overcome these limitations and establish the safety and efficacy of MPG-based drug delivery systems and other applications in various fields of research and industry. Some possible future directions include developing new synthesis methods for increasing MPG’s availability, improving its water solubility, and exploring its potential in advanced biotechnological applications, such as bioelectrochemistry and biosensors.

CAS Number32899-41-5
Product Name1-Hexadecanoyl-sn-glycerol
IUPAC Name[(2S)-2,3-dihydroxypropyl] hexadecanoate
Molecular FormulaC₁₉H₃₈O₄
Molecular Weight330.5 g/mol
InChIInChI=1S/C19H38O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19(22)23-17-18(21)16-20/h18,20-21H,2-17H2,1H3/t18-/m0/s1
InChI KeyQHZLMUACJMDIAE-GOSISDBHSA-N
SMILESCCCCCCCCCCCCCCCC(=O)OCC(CO)O
Synonyms1-glyceryl hexadecanoate, 1-monohexadecanoyl-rac-glycerol, 1-monohexadecanoylglycerol, 1-monopalmitin, palmitoyl glycerol, palmitoyl glycerol, (+,-)-isomer, palmitoyl glycerol, hexadecanoic-1-(14)C-labeled cpd, (R)-isomer, rac-1(3)-palmitoyl glycerol
Canonical SMILESCCCCCCCCCCCCCCCC(=O)OCC(CO)O
Isomeric SMILESCCCCCCCCCCCCCCCC(=O)OC[C@@H](CO)O


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