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  • 2106-10-7,a-D-Glucopyranosyl fluoride, α-D-氟代吡喃葡萄糖, Cas:2106-10-7
2106-10-7,a-D-Glucopyranosyl fluoride, α-D-氟代吡喃葡萄糖, Cas:2106-10-7

2106-10-7,a-D-Glucopyranosyl fluoride, α-D-氟代吡喃葡萄糖, Cas:2106-10-7

2106-10-7,a-D-Glucopyranosyl fluoride,
α-D-氟代吡喃葡萄糖,
Cas:2106-10-7
MFCD00132903
C6H11FO5 / 182.15

a-D-Glucopyranosyl fluoride,

α-D-氟代吡喃葡萄糖,

a-D-Glucopyranosyl fluoride is an irreversible inhibitor of the enzyme glycosidase. This product has been used to study the kinetic and mechanism of human serum alpha-glucosidase, which is a key enzyme in the digestion of carbohydrates. Kinetic studies have shown that 4-hydroxycinnamic acid and glucose are competitive inhibitors of the enzyme. The reaction mechanism for this product involves hydrogen fluoride cleavage of the glycosidic bond. The optimum pH for this product is 7.

Alpha-D-Glucopyranosyl fluoride (GlcF) is an important organic compound with a molecular formula of C6H11FO5. It is a derivative of glucose with a fluoride atom replacing the hydroxyl group at the anomeric position. GlcF has been studied extensively due to its potential applications in various fields of research and industry.

Physical and Chemical Properties

GlcF is a white crystalline solid with a melting point of 132-135°C. It is soluble in water and slightly soluble in alcohol. It is a stable compound that does not react with common organic solvents.

Synthesis and Characterization

GlcF can be synthesized by reacting glucose with hydrofluoric acid or by selectively fluorinating glucose with a fluorinating agent such as tetramethylammonium fluoride. The compound can be characterized using various analytical techniques such as nuclear magnetic resonance (NMR) spectroscopy, mass spectroscopy, and X-ray diffraction analysis.

Analytical Methods

Several analytical methods have been developed to measure the concentration of GlcF in biological samples. High-performance liquid chromatography (HPLC) and gas chromatography with mass spectrometry (GC-MS) are commonly used methods for the analysis of GlcF.

Biological Properties

GlcF has been shown to have potential antiviral and antibacterial properties. It has been suggested that GlcF can inhibit the replication of several viruses, including HIV and influenza, and it can also inhibit the growth of bacteria such as E. coli and Staphylococcus aureus.

Toxicity and Safety in Scientific Experiments

Several studies have investigated the toxicity and safety of GlcF in laboratory animals. It has been shown that GlcF is relatively non-toxic and does not induce significant adverse effects at moderate doses. However, higher doses may cause gastrointestinal disturbances and liver damage.

Applications in Scientific Experiments

GlcF has potential applications in various fields of research, including biochemistry, microbiology, virology, and drug discovery. It can be used as a tool to study the metabolism and function of carbohydrates in biological systems.

Current State of Research

There has been significant research interest in GlcF for several decades. There have been numerous studies investigating its biological properties, toxicity, and potential applications. However, further research is needed to fully understand the mechanisms of action and potential uses of GlcF.

Potential Implications in Various Fields of Research and Industry

GlcF has potential applications in various fields of research and industry. It can be used in the development of antiviral and antibacterial agents, as well as in the production of functional foods and dietary supplements. GlcF may also have applications in the field of glycobiology, which is the study of glycan structures and their functions.

Limitations and Future Directions

Although GlcF has shown promising results in various studies, there are several limitations to its use. For instance, it may not be effective against all viruses and bacteria, and it may have limited bioavailability in vivo. Future research should investigate new methods of synthesis and purification of GlcF, as well as exploring its potential in new fields such as immunology and cancer research.

Future Directions

1. Investigating the potential use of GlcF as an immunomodulatory agent.

2. Studying the effects of GlcF on cancer cells and exploring its potential as a cancer therapy.

3. Developing novel methods of synthesis and purification of GlcF for more efficient and cost-effective production.

4. Investigating the potential use of GlcF as a dietary supplement for improved glycemic control in individuals with diabetes.

5. Studying the mechanisms of action of GlcF in vivo to better understand its potential applications.

6. Developing new analytical methods for the detection and quantification of GlcF in biological samples.

7. Investigating the potential use of GlcF in the production of functional foods with health benefits.

8. Studying the effects of GlcF on the microbiome and exploring its potential as a probiotic.

9. Developing new formulations of GlcF for improved bioavailability and efficacy in vivo.

10. Investigating the potential use of GlcF in the production of renewable energy sources such as biofuels.

CAS Number2106-10-7
Product Namealpha-D-Glucopyranosyl fluoride
IUPAC Name(2R,3R,4S,5S,6R)-2-fluoro-6-(hydroxymethyl)oxane-3,4,5-triol
Molecular FormulaC6H11FO5
Molecular Weight182.15 g/mol
InChIInChI=1S/C6H11FO5/c7-6-5(11)4(10)3(9)2(1-8)12-6/h2-6,8-11H,1H2/t2-,3-,4+,5-,6+/m1/s1
InChI KeyATMYEINZLWEOQU-GASJEMHNSA-N
SMILESC(C1C(C(C(C(O1)F)O)O)O)O
Synonymsalpha-D-glucopyranosyl fluoride, beta-D-glucopyranosyl fluoride, glucosyl fluoride, glucosyl fluoride, (beta-D)-isomer
Canonical SMILESC(C1C(C(C(C(O1)F)O)O)O)O
Isomeric SMILESC([C@@H]1[C@H]([C@@H]([C@H](C(O1)F)O)O)O)O


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