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
  • 3789-97-7 , 葡糖醛酰胺, D-Glucuronamide, CAS:3789-97-7
  • 3789-97-7 , 葡糖醛酰胺, D-Glucuronamide, CAS:3789-97-7
3789-97-7 , 葡糖醛酰胺, D-Glucuronamide, CAS:3789-97-73789-97-7 , 葡糖醛酰胺, D-Glucuronamide, CAS:3789-97-7

3789-97-7 , 葡糖醛酰胺, D-Glucuronamide, CAS:3789-97-7

3789-97-7 , 葡糖醛酰胺,
D-Glucuronamide,
CAS:3789-97-7
C6H11NO6 / 193.15
MFCD00006619

葡糖醛酰胺, D-Glucuronamide

Glucopyranuronamide is an emerging chemical compound with potential applications in various fields of scientific research and industrial production. This paper aims to provide an informative and engaging overview of this compound, including its definition, physical and chemical properties, synthesis and characterization methods, biological properties, toxicity and safety in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions.

Physical and Chemical Properties

Glucopyranuronamide is a solid that appears as white or colorless crystals. It has a melting point of 123-125°C and decomposes at higher temperatures. It is soluble in water and slightly soluble in organic solvents, such as methanol and ethanol. Glucopyranuronamide is stable under normal conditions, but it may decompose under acidic conditions.

Synthesis and Characterization

Glucopyranuronamide can be synthesized by reacting glucuronic acid with ammonia or an amine under mild reaction conditions. The reaction affords the corresponding glucuronamides, including glucopyranuronamide. The synthesis of glucopyranuronamide can be achieved by various methods, including thermal decomposition of glucuronic acid at 200°C, microwave-assisted synthesis, and solvent-free synthesis.

The characterization of glucopyranuronamide can be performed using various analytical techniques, including nuclear magnetic resonance (NMR) spectroscopy, infrared (IR) spectroscopy, and mass spectrometry (MS). NMR spectroscopy can provide information about the chemical structure and properties of a compound, including its molecular formula, functional groups, and molecular weight. IR spectroscopy can provide information about the functional groups and chemical bonding of a compound. MS can provide information about the mass and molecular weight of a compound.

Analytical Methods

Analytical methods can be used to detect and quantify glucopyranuronamide in various matrices, including biological fluids, environmental samples, and food products. The most commonly used methods for determining glucopyranuronamide are high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS). HPLC can separate and quantify glucopyranuronamide from complex matrices, including biological fluids and plant extracts. GC-MS can detect and quantify volatile derivatives of glucopyranuronamide in environmental samples and food products.

Biological Properties

Glucopyranuronamide exhibits various biological properties that make it a promising candidate for drug development and other applications. Glucopyranuronamide has been shown to possess antitumor, anti-inflammatory, and antioxidant activities. Glucopyranuronamide can also modulate the immune system and protect against oxidative damage.

Toxicity and Safety in Scientific Experiments

The toxicity and safety of glucopyranuronamide in scientific experiments depend on its concentration, administration route, and duration of exposure. In general, glucopyranuronamide has a low toxicity profile and is not associated with major adverse effects. However, high doses of glucopyranuronamide may cause gastrointestinal disturbances and liver damage. Therefore, it is important to carefully monitor the dose and duration of glucopyranuronamide in scientific experiments.

Applications in Scientific Experiments

Glucopyranuronamide has potential applications in various fields of scientific research, including drug discovery, agricultural science, and environmental science. Glucopyranuronamide can be used as a starting material for the synthesis of new drugs with antitumor, anti-inflammatory, and antioxidant activities. Glucopyranuronamide can also be used as a plant growth regulator and a soil conditioner in agricultural science. In environmental science, glucopyranuronamide can be used as a chelating agent for heavy metal ions and a stabilizer for radioactive waste.

Current State of Research

The current state of research on glucopyranuronamide is focused on its synthesis, characterization, and biological properties. Recent studies have shown that glucopyranuronamide possesses potent antitumor, anti-inflammatory, and antioxidant activities, and can modulate the immune system. The current state of research also shows that glucopyranuronamide can be synthesized by various methods, including microwave-assisted synthesis and solvent-free synthesis.

Potential Implications in Various Fields of Research and Industry

Glucopyranuronamide has potential implications in various fields of research and industry, including drug discovery, agricultural science, and environmental science. Glucopyranuronamide can be used as a starting material for the synthesis of new drugs with potent biological activities. Glucopyranuronamide can also be used as a plant growth regulator and a soil conditioner in agricultural science. In environmental science, glucopyranuronamide can be used as a chelating agent for heavy metal ions and a stabilizer for radioactive waste.

Limitations and Future Directions

Despite its potential applications, glucopyranuronamide has some limitations that need to be addressed in future research. First, the synthesis of glucopyranuronamide requires expensive starting materials, which may limit its commercial production. Second, the biological properties of glucopyranuronamide need to be further investigated to confirm its safety and efficacy. Third, the potential applications of glucopyranuronamide need to be validated in large-scale studies.

Future directions for the research on glucopyranuronamide include:

1. Development of new synthesis methods that are cost-effective and environmentally friendly.

2. Investigation of the mechanisms of action of glucopyranuronamide in biological systems.

3. Exploration of the potential applications of glucopyranuronamide in other fields of research and industry, such as biotechnology, materials science, and energy production.

4. Optimization of the formulation and delivery of glucopyranuronamide for various applications.

5. Development of new analytical methods for the detection and quantification of glucopyranuronamide in complex matrices.

Conclusion

Glucopyranuronamide is an emerging chemical compound that has potential applications in various fields of scientific research and industry. Glucopyranuronamide can be synthesized by various methods and characterized using various analytical techniques. Glucopyranuronamide exhibits potent biological properties and has low toxicity and safety profiles in scientific experiments. Glucopyranuronamide has potential implications in drug discovery, agricultural science, and environmental science. Future research on glucopyranuronamide should focus on addressing its limitations and exploring its potential applications in other fields of research and industry.

D-Glucuronamide is a kinetic model system for the glycosylation reaction, which is an important step in the biosynthesis of complex oligosaccharides and polysaccharides. It has been shown to be an amide analog that can be acetylated with acetic anhydride in a reaction mechanism that involves nucleophilic attack by the amino group of D-glucuronamide on the electrophilic carbonyl carbon of acetic anhydride. The second-order rate constants for this reaction were determined to be 2.3×10 M-1s-1 at pH 7 and 25°C. NMR spectra showed that the product was not a simple amide but rather a glycopolymer with a distribution of different sugar residues, including D-glucose, D-galactose, and D-mannose.

CAS Number

3789-97-7

Product Name

Glucopyranuronamide

IUPAC Name

(2S,3S,4S,5R)-3,4,5,6-tetrahydroxyoxane-2-carboxamide

Molecular Formula

C6H11NO6

Molecular Weight

193.15 g/mol

InChI

InChI=1S/C6H11NO6/c7-5(11)4-2(9)1(8)3(10)6(12)13-4/h1-4,6,8-10,12H,(H2,7,11)/t1-,2-,3+,4-,6?/m0/s1

InChI Key

VOIFKEWOFUNPBN-AQKNRBDQSA-N

SMILES

C1(C(C(OC(C1O)O)C(=O)N)O)O

Canonical SMILES

C1(C(C(OC(C1O)O)C(=O)N)O)O

Isomeric SMILES

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


CAS No: 3789-97-7 MDL No: MFCD00006619 Chemical Formula: C6H11NO6 Molecular Weight: 193.15

在线询价

用手机扫描二维码关闭
二维码