欢迎光临~北京凯森莱科技有限公司
语言选择: 中文版 ∷  英文版
  • 6082-04-8 ,甲基-2-乙酰氨基-2-脱氧-a-D-葡萄糖苷, CAS:6082-04-8
6082-04-8 ,甲基-2-乙酰氨基-2-脱氧-a-D-葡萄糖苷, CAS:6082-04-8

6082-04-8 ,甲基-2-乙酰氨基-2-脱氧-a-D-葡萄糖苷, CAS:6082-04-8

6082-04-8 ,甲基-2-乙酰氨基-2-脱氧-a-D-葡萄糖苷,
Methyl 2-acetamido-2-deoxy-a-D-glucopyranoside,
CAS:6082-04-8
C9H17NO6 / 235.23
MFCD00056076

Methyl 2-acetamido-2-deoxy-a-D-glucopyranoside

甲基-2-乙酰氨基-2-脱氧-a-D-葡萄糖苷

Methyl 2-acetamido-2-deoxy-alpha-D-glucopyranoside (MAG) is a glycosylation inhibitor that has various applications in scientific research. This article provides an overview of the definition, background, properties, synthesis, characterization, analytical methods, biological properties, and toxicity and safety in scientific experiments of MAG. It also discusses the potential implications of MAG in various fields of research and industry, the current state of research, limitations, and future directions.

Definition and Background

MAG is a monosaccharide, which is a type of simple sugar that consists of a single saccharide unit. MAG belongs to the class of N-acetylglucosamine (GlcNAc) derivatives, which are important building blocks in the biosynthesis of complex polysaccharides such as chitin and peptidoglycan. MAG is also a potent inhibitor of glycosylation, a post-translational modification process that involves the addition of sugar chains to proteins and lipids.

Physical and Chemical Properties

MAG is a white solid powder that is soluble in water. Its melting point is 200-201 °C, and its molecular weight is 235.23 g/mol. MAG has a chemical formula of C9H17NO6, and its structure consists of a glucose ring that is attached to an N-acetyl group and an amide group.

Synthesis and Characterization

MAG can be synthesized through various methods, including chemical synthesis, enzymatic synthesis, and chemoenzymatic synthesis. Chemical synthesis involves the reaction of GlcNAc with methyl acetate under acidic conditions to produce MAG. Enzymatic synthesis involves the use of enzymes such as GlcNAc-2-epimerase and N-acetylglucosamine-2-epimerase to convert GlcNAc to MAG. Chemoenzymatic synthesis combines both chemical and enzymatic methods to produce MAG.

Analytical Methods

Various analytical methods such as High-performance liquid chromatography (HPLC), nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry can be used to characterize MAG. HPLC separates and quantifies the different compounds in the solution, while NMR and mass spectrometry identify the molecular structure and molecular weight of MAG.

Biological Properties

MAG has various biological properties, including antiviral, antibacterial, and antifungal activities. For example, MAG inhibits the replication of human immunodeficiency virus (HIV) by interfering with glycosylation of virus envelope glycoprotein. In addition, MAG also inhibits the growth of bacteria such as Streptococcus pneumoniae, Staphylococcus aureus, and Escherichia coli.

Toxicity and Safety in Scientific Experiments

MAG is considered a safe compound for scientific experiments, as it has low toxicity in both in vitro and in vivo models. However, as with any chemical compound, proper handling and disposal procedures should be followed to ensure safety.

Applications in Scientific Experiments

MAG has various applications in scientific experiments, particularly in the study of glycosylation. MAG can be used to inhibit the glycosylation of specific proteins, which can lead to the identification of the functions of glycoproteins in various biological processes. MAG has also been used as a tool to study the mechanisms of glycoprotein synthesis and the effects of glycosylation on protein structure and function.

Current State of Research

Currently, research on MAG is focused on exploring its potential applications in various fields of research and industry. Recent studies have shown that MAG has potential as an antiviral agent, and it has been suggested that it could be used in the development of vaccines against viral infections.

Potential Implications in Various Fields of Research and Industry

MAG has various potential implications in various fields of research and industry, including medicine, biotechnology, and materials science. In medicine, MAG could be used as a potential antiviral agent and in the development of vaccines. In biotechnology, MAG can be used to study the structure and function of glycoproteins, which play critical roles in cellular processes. In materials science, MAG can be used in the synthesis of chitinous materials, which have various applications in biodegradable plastics and wound healing.

Limitations and Future Directions

One limitation of MAG is its low solubility in organic solvents, which can restrict its use in some applications. Future directions for research on MAG include developing new methods for synthesis and purification, exploring its potential as an antiviral agent, and investigating its use in the synthesis of chitinous materials with improved properties such as biodegradability and mechanical strength.

In conclusion, MAG is a glycosylation inhibitor that has various applications in scientific research. It has antiviral, antibacterial, and antifungal activities and can be used to study the structure and function of glycoproteins. Further research is needed to explore its potential in various fields of research and industry, and to overcome limitations such as low solubility.

CAS Number

6082-04-8

Product Name

Methyl 2-acetamido-2-deoxy-alpha-D-glucopyranoside

IUPAC Name

N-[4,5-dihydroxy-6-(hydroxymethyl)-2-methoxyoxan-3-yl]acetamide

Molecular Formula

C9H17NO6

Molecular Weight

235.23 g/mol

InChI

InChI=1S/C9H17NO6/c1-4(12)10-6-8(14)7(13)5(3-11)16-9(6)15-2/h5-9,11,13-14H,3H2,1-2H3,(H,10,12)

InChI Key

ZEVOCXOZYFLVKN-OKNNCHMLSA-N

SMILES

CC(=O)NC1C(C(C(OC1OC)CO)O)O

Synonyms

Methyl 2-(Acetylamino)-2-deoxy-α-D-glucopyranoside; Methyl N-Acetyl-α-D-glucosaminide; Methyl N-Acetyl-α-glucosaminide; NSC 77914; α-Methyl N-Acetylglucosaminide;GlcNAc1-α-OMe;

Canonical SMILES

CC(=O)NC1C(C(C(OC1OC)CO)O)O

Isomeric SMILES

CC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@@H]1OC)CO)O)O

CAS No: 6082-04-8 Synonyms: GlcNAc-a-OMeMethyl N-acetyl-a-D-glucosamine MDL No: MFCD00056076 Chemical Formula: C9H17NO6 Molecular Weight: 235.23

在线询价

用手机扫描二维码关闭
二维码