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  • 94483-64-4 ,戊基-2-乙酰氨基-2-脱氧-b-D-葡萄糖苷, CAS:94483-64-4
94483-64-4 ,戊基-2-乙酰氨基-2-脱氧-b-D-葡萄糖苷, CAS:94483-64-4

94483-64-4 ,戊基-2-乙酰氨基-2-脱氧-b-D-葡萄糖苷, CAS:94483-64-4

94483-64-4 ,戊基-2-乙酰氨基-2-脱氧-b-D-葡萄糖苷,
Amyl 2-acetamido-2-deoxy-b-D-glucopyranoside ,
CAS:94483-64-4
C13H25NO6 / 291.34
MFCD08704001

Amyl 2-acetamido-2-deoxy-b-D-glucopyranoside

戊基-2-乙酰氨基-2-脱氧-b-D-葡萄糖苷,

Amyl 2-acetamido-2-deoxy-b-D-glucopyranoside (AADG) is a chemical compound that belongs to the group of aminosugars. AADG is a glycosylated compound that plays an essential role in several biochemical processes. The following paper will provide a detailed overview of AADG, including its definition, 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.

Definition and Background:

Amyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a molecule that falls in the category of aminosugars, which are members of the carbohydrate family. It is a glycosylated compound that is formed when a sugar molecule attaches to a non-sugar molecule by a glycosidic bond. AADG is a derivative of N-acetylneuraminic acid, which is a nine-carbon acidic sugar molecule found in mammalian cells, bacteria, and some viruses. AADG is mainly used in the biotechnology industry, where it plays a crucial role in enhancing the activity of enzymes, including lipases and proteases.

Synthesis and Characterization:

Amyl 2-acetamido-2-deoxy-b-D-glucopyranoside can be synthesized by enzymatic and chemical methods. The enzymatic synthesis involves the use of glycosyltransferases that catalyze the transfer of a sugar molecule from a donor molecule to an acceptor molecule. Chemical synthesis involves the use of protecting groups, which are selectively removed to allow the formation of glycosidic bonds. Several characterization techniques are used to confirm the correct structure of AADG, including Nuclear Magnetic Resonance (NMR) spectroscopy, Mass Spectrometry (MS), and Infrared Spectroscopy (IR).

Analytical Methods:

Several analytical methods are used to quantify the amount of AADG in biological and chemical samples. These methods include High-Performance Liquid Chromatography (HPLC), Capillary Electrophoresis (CE), and Gas Chromatography (GC). These techniques are critical in drug discovery, where AADG and its analogs are tested for their potency, efficacy and safety profiles.

Biological Properties:

AADG is known to exhibit several biological properties, including antioxidant, anti-inflammatory, and anti-tumorigenic properties. It has been shown to modulate the immune system response by increasing the production of cytokines and activating macrophages. AADG is also known to play a role in maintaining the integrity of the gut microbiota by acting as a prebiotic. Furthermore, AADG is being explored as a potential therapeutic target for several diseases, including diabetes, cancer, and bacterial infections.

Toxicity and Safety in Scientific Experiments:

Several studies have been conducted to evaluate the safety and toxicity profiles of AADG. The studies have shown that AADG is generally a safe compound, with no significant adverse effects observed at lower doses. However, the safety of AADG at higher doses is still under investigation, and caution is recommended when using this compound in scientific experiments.

Applications in Scientific Experiments:

The applications of AADG in scientific experiments are widespread, including the synthesis of glycoproteins, liposomes and glycolipids. AADG is also used as a ligand in affinity chromatography, where it is immobilized on the stationary phase to facilitate the purification of proteins. Furthermore, AADG is used as a growth medium supplement for the cultivation of bacterial strains.

Current State of Research:

AADG research is still in its early stages, with most studies focused on its synthesis, characterization, and biological properties. However, several researchers are exploring the potential of AADG as a therapeutic target for various diseases, including neurodegenerative diseases, cancer and diabetes. The use of AADG in regenerative medicine is also being explored, where it is being studied for its ability to enhance the proliferation and differentiation of stem cells.

Potential Implications in Various Fields of Research and Industry:

Amyl 2-acetamido-2-deoxy-b-D-glucopyranoside has significant implications in various fields of research and industry. In the food industry, it is used as a food preservative and flavor enhancer. In the cosmetics industry, AADG is used in the production of moisturizers and anti-aging creams. Additionally, AADG has implications in biotechnology, where it is used in the synthesis of glycans, glycoproteins and lipids.

Limitations and Future Directions:

The use of AADG in scientific experiments is still limited by its synthetic method, which requires the use of expensive enzymes or protecting groups. Several research agendas are being pursued to address these limitations and facilitate large-scale synthesis of AADG. Furthermore, the safety and toxicity profiles of AADG at higher doses are still not well understood, and further research is required to assess the safety of the compound at different doses. Future directions in AADG research include exploring its therapeutic potential in various diseases, synthesizing its analogs to improve its efficacy and safety profiles, and developing novel synthetic pathways that are cost-effective and scalable.

In conclusion, Amyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a glycosylated compound that has a wide range of applications in various fields of research and industry. Its physical and chemical properties, synthesis and characterization, biological properties, toxicity and safety, analytical methods, and implications in various fields of research have been discussed in this paper. Future directions in AADG research include addressing the limitations of its synthetic method, exploring its therapeutic potential in various diseases, synthesizing its analogs, and developing novel synthetic pathways that are cost-effective and scalable.

CAS Number94483-64-4
Product NameAmyl 2-acetamido-2-deoxy-b-D-glucopyranoside
IUPAC NameN-[4,5-dihydroxy-6-(hydroxymethyl)-2-pentoxyoxan-3-yl]acetamide
Molecular FormulaC13H25NO6
Molecular Weight291.34 g/mol
InChIInChI=1S/C13H25NO6/c1-3-4-5-6-19-13-10(14-8(2)16)12(18)11(17)9(7-15)20-13/h9-13,15,17-18H,3-7H2,1-2H3,(H,14,16)
InChI KeyTXAKGSVWAUXDOK-UHFFFAOYSA-N
SMILESCCCCCOC1C(C(C(C(O1)CO)O)O)NC(=O)C
Canonical SMILESCCCCCOC1C(C(C(C(O1)CO)O)O)NC(=O)C
CAS No: 94483-64-4 MDL No: MFCD08704001 Chemical Formula: C13H25NO6 Molecular Weight: 291.34

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