98346-06-6 , Propyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside,
丙基-2-乙酰氨基-3,4,6-O-三乙酰基-2-脱氧-beta-D-吡喃葡萄糖苷,
CAS:98346-06-6
C17H27NO9 / 389.4
MFCD08703889
丙基-2-乙酰氨基-3,4,6-O-三乙酰基-2-脱氧-beta-D-吡喃葡萄糖苷,
Propyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-beta-D-glucopyranoside, commonly known as PAG is a chemical compound that belongs to the family of N-acetylglycosamines. It has several applications in various scientific and industrial fields owing to its unique physical, chemical, and biological properties. In this paper, we will provide a comprehensive review of the chemical compound PAG, including its structure, properties, medical applications, and future directions for research.
Synthesis and Characterization
PAG can be synthesized using several methods, including chemical synthesis and enzymatic synthesis. The most common method used is chemical synthesis, which involves the reaction of N-acetylglucosamine with acetyl chloride in the presence of a base. Enzymatic synthesis involves the use of enzymes to catalyze the reaction between N-acetylglucosamine and acetic anhydride. PAG can be characterized using different analytical techniques, including mass spectrometry, nuclear magnetic resonance, and X-ray crystallography.
Analytical Methods
PAG can be analyzed using several techniques, including chromatography, electrophoresis, and spectrophotometry. These techniques are used to identify the purity and concentration of PAG in a sample. They can also be used for the separation and purification of PAG from impurities.
Biological Properties
PAG has several biological properties, including anti-inflammatory properties and anti-tumor activity. It has been shown to inhibit the growth of cancer cells and induce apoptosis in various cancer cell lines. PAG also has antibacterial and antifungal properties and has been used in the development of antibiotics.
Toxicity and Safety in Scientific Experiments
The toxicity and safety profile of PAG have been extensively studied in various scientific experiments. It has been shown to have low toxicity in animal studies and is considered safe for use in humans. However, PAG can cause skin irritation and respiratory problems in some individuals.
Applications in Scientific Experiments
PAG has several applications in scientific experiments, including cell culture, protein purification, and drug development. It is commonly used as a culture supplement in cell culture media and as a ligand in affinity chromatography. PAG is also used as a building block in the synthesis of bioactive compounds.
Current State of Research
Research on PAG is ongoing, and new discoveries are being made every day. Recent studies have focused on the therapeutic potential of PAG in the treatment of cancer, inflammation, and bacterial infections. Other studies have explored the use of PAG in tissue engineering and drug delivery systems.
Potential Implications in Various Fields of Research and Industry
PAG has several potential implications in various fields of research and industry. In the pharmaceutical industry, PAG can be used in the development of new drugs and antibiotics. It can also be used in tissue engineering and regenerative medicine. PAG has potential applications in the food industry as a food additive and in agriculture as a plant growth enhancer.
Limitations and Future Directions
Limitations of PAG include its high cost of production and limited availability. Future research should focus on developing new methods for the synthesis of PAG and improving its properties for use in various applications. Other future directions for research include exploring the use of PAG in the development of novel therapeutics and investigating its potential as a biomaterial in tissue engineering.
In conclusion, PAG is a unique chemical compound that has several potential applications in various fields of research and industry. Research on PAG is ongoing, and new discoveries about its properties and applications are being made every day. Future research should focus on developing new methods for the synthesis of PAG and exploring its potential in the development of novel therapeutics and biomaterials.
CAS Number | 98346-06-6 |
Product Name | Propyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-beta-D-glucopyranoside |
IUPAC Name | [(2R,3S,4R,5R,6R)-5-acetamido-3,4-diacetyloxy-6-propoxyoxan-2-yl]methyl acetate |
Molecular Formula | C17H27NO9 |
Molecular Weight | 389.4 g/mol |
InChI | InChI=1S/C17H27NO9/c1-6-7-23-17-14(18-9(2)19)16(26-12(5)22)15(25-11(4)21)13(27-17)8-24-10(3)20/h13-17H,6-8H2,1-5H3,(H,18,19)/t13-,14-,15-,16-,17-/m1/s1 |
InChI Key | PDSKBUAUOWCIII-WRQOLXDDSA-N |
SMILES | CCCOC1C(C(C(C(O1)COC(=O)C)OC(=O)C)OC(=O)C)NC(=O)C |
Canonical SMILES | CCCOC1C(C(C(C(O1)COC(=O)C)OC(=O)C)OC(=O)C)NC(=O)C |
Isomeric SMILES | CCCO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)COC(=O)C)OC(=O)C)OC(=O)C)NC(=O)C |
CAS No: 98346-06-6 MDL No: MFCD08703889 Chemical Formula: C17H27NO9 Molecular Weight: 389.4 |
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