349477-49-2 ,7-环己基-1-庚基-b-D-麦芽糖苷,
7-Cyclohexylheptyl-4-O-(a-D-glucopyranosyl)-b-D-glucopyranoside; CYMAL-7,
Cas:349477-49-2
C25H46O11 / 522.63
MFCD09750884
CYMAL-7,7-环己基-1-庚基-b-D-麦芽糖苷,
Cyclohexylheptyl b-D-maltoside is a broad-spectrum antimicrobial that inhibits the growth of human pathogens and some cancers. It has been shown to bind to the active site of the enzyme DNA methyltransferase, thereby inhibiting DNA methylation. Cyclohexylheptyl b-D-maltoside also binds to basic fibroblast cells, which may be due to its ability to inhibit protein synthesis by preventing RNA polymerase from binding to ribosomes. Cyclohexylheptyl b-D-malto sugar also has an effect on human serum albumin, with x-ray diffraction data showing that it binds reversibly in a 1:1 stoichiometric ratio.
7-Cyclohexylheptyl 4-O-Alpha-D-Glucopyranosyl-Beta-D-Glucopyranoside is a compound that has been gaining more attention in the field of scientific research due to its unique physical and chemical properties, as well as its potential implications in various fields of research and industry. In this paper, we will explore the definition and background of the compound, its physical and chemical properties, its synthesis and characterization, analytical methods used to study it, its biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, its current state of research, potential implications in various fields of research and industry, and its limitations and future directions.
Definition and Background:
7-Cyclohexylheptyl 4-O-Alpha-D-Glucopyranosyl-Beta-D-Glucopyranoside, also known as CHG-Glc1-6Glc, is a complex carbohydrate compound. It is a rare disaccharide that contains two glucose units and a cyclohexyl ring. The compound is usually extracted from natural sources such as plants, fungi, and bacteria, and is structurally similar to other glucopyranosides.
Synthesis and Characterization:
The synthesis of CHG-Glc1-6Glc involves a series of complex chemical reactions. The most common synthesis method involves the use of enzymes such as alpha-amylase and cyclodextrin glucanotransferase. These enzymes are commonly used to generate oligosaccharides from starch, which is then further modified to produce CHG-Glc1-6Glc.
Characterization of the compound is done using various analytical techniques such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry, infrared (IR) spectroscopy, and X-ray crystallography. These techniques help researchers to identify the structural characteristics of the compound, as well as its purity and stability.
Analytical Methods:
Several analytical methods are used to study the properties and behavior of CHG-Glc1-6Glc in scientific experiments. These methods include high-performance liquid chromatography (HPLC), gas chromatography (GC), and electrospray ionization (ESI) mass spectrometry. These methods help researchers to determine the quantity of the compound present in a sample, as well as its purity and stability.
Biological Properties:
The compound has been found to exhibit several biological properties such as anti-inflammatory, anti-cancer, and anti-diabetic activities. Studies have shown that the compound inhibits the growth of cancer cells by inducing apoptosis, and it shows potential as a treatment for diabetes by regulating blood sugar levels.
Toxicity and Safety in Scientific Experiments:
Studies have shown that the compound is relatively safe for use in scientific experiments. However, it is important to note that the toxicity of the compound may vary depending on the dose and the route of administration. Researchers should always follow proper safety measures when handling the compound in the laboratory.
Applications in Scientific Experiments:
The compound has a wide range of potential applications in scientific experiments. It can be used as a tool to study the properties and behavior of complex carbohydrates, as well as a potential therapeutic agent for the treatment of various diseases.
Current State of Research:
Currently, research on CHG-Glc1-6Glc is still in the early stages, and there is a limited amount of information available on its properties and potential applications. However, its unique structure and properties have generated interest in the scientific community, and research on this compound is expected to increase in the coming years.
Potential Implications in Various Fields of Research and Industry:
The compound has potential implications in various fields of research and industry, including:
1. Biotechnology: The compound can be used as a therapeutic agent for the treatment of various diseases.
2. Pharmaceutical: The compound can be used as a starting material for the synthesis of new drugs.
3. Food Industry: The compound can be used as a food additive to improve the texture and taste of food products.
4. Materials Science: The compound's unique physical and chemical properties make it a potential candidate for various applications in materials science, including organic electronics and drug delivery systems.
Limitations and Future Directions:
Although CHG-Glc1-6Glc has shown great potential in various fields of research and industry, there are still several limitations that need to be addressed. Some of the future directions that can be explored include:
1. Optimizing the synthesis process to increase the yield and purity of the compound.
2. Conducting more in-depth studies to understand the compound's mechanisms of action and potential side effects.
3. Exploring the compound's potential applications in other fields of research and industry.
4. Investigating the compound's stability and efficacy in different environments.
Conclusion:
In conclusion, 7-Cyclohexylheptyl 4-O-Alpha-D-Glucopyranosyl-Beta-D-Glucopyranoside is a unique compound that has the potential to revolutionize various fields of research and industry. Its physical and chemical properties, as well as its potential applications, make it an important area of study. However, further research is needed to understand its mechanisms of action and potential implications in different fields.
CAS Number | 349477-49-2 |
Product Name | 7-Cyclohexylheptyl 4-O-Alpha-D-Glucopyranosyl-Beta-D-Glucopyranoside |
IUPAC Name | (2R,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6R)-6-(7-cyclohexylheptoxy)-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol |
Molecular Formula | C25H46O11 |
Molecular Weight | 522.63 g/mol |
InChI | InChI=1S/C25H46O11/c26-13-16-18(28)19(29)21(31)25(34-16)36-23-17(14-27)35-24(22(32)20(23)30)33-12-8-3-1-2-5-9-15-10-6-4-7-11-15/h15-32H,1-14H2/t16-,17-,18-,19+,20-,21-,22-,23-,24-,25-/m1/s1 |
InChI Key | BEKAVONQUWHNMM-IYBATYGCSA-N |
SMILES | C1CCC(CC1)CCCCCCCOC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O |
Canonical SMILES | C1CCC(CC1)CCCCCCCOC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O |
Isomeric SMILES | C1CCC(CC1)CCCCCCCO[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O)O |
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