173725-24-1 , Undecyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranose,
正十一烷基-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:173725-24-1
C25H43NO9 / 501.61
MFCD08703973
正十一烷基-2-乙酰氨基-3,4,6-O-三乙酰基-2-脱氧-beta-D-吡喃葡萄糖苷,
Undecyl 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-beta-D-glucopyranoside, also known as Undecyl-GlcNAc-triacetate, is a chemical compound with potential applications in various fields of research and industry. This paper aims to provide an informative and engaging overview of the background, physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions of Undecyl-GlcNAc-triacetate.
Definition and Background
UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate is a synthetic molecule composed of a sugar and a lipid. It belongs to the class of glycolipids, which are compounds that contain both sugar and lipid components. Specifically, UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate is a tri-O-acetylated derivative of N-acetylglucosamine, which is a monosaccharide that is commonly found in glycoproteins and glycolipids.
Synthesis and Characterization
UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate can be synthesized using a variety of methods, including chemical synthesis and enzymatic synthesis. Chemical synthesis typically involves the acetylation of N-acetylglucosamine derivatives with acetyl chloride, followed by the addition of undecanol. Enzymatic synthesis typically involves the use of glycosyltransferases to catalyze the transfer of a sugar moiety onto a lipid acceptor.
Analytical Methods
There are several analytical methods that can be used to characterize and quantify UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate, including high-performance liquid chromatography (HPLC), nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry (MS), and infrared (IR) spectroscopy. These methods can be used to determine the purity of UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate, elucidate its chemical structure, and monitor its behavior in various contexts.
Biological Properties
UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate has been found to exhibit several biological properties that make it potentially useful for various applications. For example, it has been shown to be capable of modulating the behavior of immune cells, including dendritic cells and macrophages. It has also been shown to have antiviral properties, inhibiting the entry and replication of some viruses.
Toxicity and Safety in Scientific Experiments
Assessment of the toxicological profile of UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate is important to determine its safety in scientific experiments and potential applications. In vivo and in vitro studies have shown that UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate exhibits low toxicity and is well-tolerated in animal models when administered at moderate doses.
Applications in Scientific Experiments
UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate has potential applications in a variety of scientific experiments. For example, it can be used to probe the interactions between sugar-binding proteins and their ligands, elucidate the mechanisms of immune cell activation, and investigate the structure-function relationships of glycolipids.
Current State of Research
Current research on UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate is focused on elucidating its biological activities, optimizing its synthesis, and exploring its potential applications in various fields of research and industry.
Potential Implications in Various Fields of Research and Industry
UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate has potential implications in various fields of research and industry. For example, it can be used in the development of novel antiviral therapies, as well as in the design of novel biomaterials with improved properties.
Limitations and Future Directions
Despite its potential utility, UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate also has some limitations that must be addressed. For example, its low water solubility may limit its utility in certain contexts. Future research should focus on developing improved synthetic methods for UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate, as well as exploring its potential applications in a wider range of scientific and industrial contexts.
Future Directions
There are several future directions for research on UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate, including:
1. Developing improved methods for the synthesis of UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate, including the exploration of enzymatic synthesis.
2. Investigating the structural and functional properties of UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate in greater detail, using advanced analytical techniques.
3. Expanding the scope of UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate applications to include additional fields of research and industry.
4. Exploring the potential of UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate as a drug delivery agent, either alone or in combination with other molecules.
5. Optimizing the safety and toxicity profile of UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate in preclinical studies.
6. Investigating the potential of UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate to modulate the activity of other biochemical pathways, beyond those currently identified.
7. Developing UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate derivatives with improved solubility and other favorable properties.
Conclusion
UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate is a promising molecule with potential applications in various fields of research and industry. Its physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions have been reviewed in this paper. Further research is necessary to fully realize the potential of UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDEAc-triacetate.
CAS Number | 173725-24-1 |
Product Name | UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDE |
IUPAC Name | [(2R,3S,4R,5R,6R)-5-acetamido-3,4-diacetyloxy-6-undecoxyoxan-2-yl]methyl acetate |
Molecular Formula | C25H43NO9 |
Molecular Weight | 501.61 |
InChI | InChI=1S/C25H43NO9/c1-6-7-8-9-10-11-12-13-14-15-31-25-22(26-17(2)27)24(34-20(5)30)23(33-19(4)29)21(35-25)16-32-18(3)28/h21-25H,6-16H2,1-5H3,(H,26,27)/t21-,22-,23-,24-,25-/m1/s1 |
InChI Key | JGFIEQXFILUYQO-FXEFVXDJSA-N |
SMILES | CCCCCCCCCCCOC1C(C(C(C(O1)COC(=O)C)OC(=O)C)OC(=O)C)NC(=O)C |
CAS No: 173725-24-1 MDL No: MFCD08703973 Chemical Formula: C25H43NO9 Molecular Weight: 501.61 |
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