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  • 13639-50-4 ,1,2,3,4,6-五-O-乙酰基-1-硫代 β-D-吡喃葡萄糖, CAS:13639-50-4
13639-50-4 ,1,2,3,4,6-五-O-乙酰基-1-硫代 β-D-吡喃葡萄糖, CAS:13639-50-4

13639-50-4 ,1,2,3,4,6-五-O-乙酰基-1-硫代 β-D-吡喃葡萄糖, CAS:13639-50-4

13639-50-4 , Penta-O-acetyl-1-thio-b-D
glucopyranoside,
1,2,3,4,6-五-O-乙酰基-1-硫代 β-D-吡喃葡萄糖,
CAS:13639-50-4
C16H22O10S / 406.405

Penta-O-acetyl-1-thio-b-D glucopyranoside

1,2,3,4,6-五-O-乙酰基-1-硫代 β-D-吡喃葡萄糖,

1-Thio-beta-D-glucose pentaacetate is a member of the thio-sugar family with potential applications in various fields of research and industry. This compound is synthesized from glucose and thioacetic acid and has a unique structure that confers certain properties that are useful in biological and chemical processes. This paper provides an overview of 1-thio-beta-D-glucose pentaacetate, including its definition, background, 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

1-Thio-beta-D-glucose pentaacetate is a thio-sugar derivative of glucose, which is a monosaccharide and the most abundant sugar in nature. The thio-group in this compound replaces the oxygen atom in the hydroxyl group at the C-1 position of glucose. This substitution results in the formation of a thioether linkage that alters the properties of the sugar, making it more hydrophobic and less reactive than the corresponding hydroxyl sugar. Thio-sugars are found in certain bacteria and play crucial roles in pathogenesis and other biological processes.

Synthesis and Characterization

1-Thio-beta-D-glucose pentaacetate can be synthesized by reacting glucose with thioacetic acid in the presence of a catalyst such as hydrochloric acid. The product is obtained in moderate yield and requires careful purification to remove impurities. Characterization of the compound is performed by various spectroscopic techniques, including IR, 1H-NMR, and 13C-NMR spectroscopy.

Analytical Methods

Several analytical methods have been developed to determine the purity and identity of 1-thio-beta-D-glucose pentaacetate, including thin-layer chromatography, HPLC, and mass spectrometry. These methods are used to monitor the synthesis and purification of the compound and to analyze its properties and behavior in various chemical and biological systems.

Biological Properties

Thio-sugars have been found to play important roles in several biological processes, including bacterial pathogenesis, host-pathogen interactions, and regulation of gene expression. 1-Thio-beta-D-glucose pentaacetate has been reported to inhibit the growth of certain bacteria and to interfere with bacterial biofilm formation. It also shows potential as an inhibitor of enzymes involved in carbohydrate metabolism, such as alpha-glucosidase.

Toxicity and Safety in Scientific Experiments

Studies on the toxicity and safety of 1-thio-beta-D-glucose pentaacetate have shown that the compound is relatively non-toxic and safe for use in scientific experiments. However, as with any chemical substance, care should be taken when handling and using this compound to avoid accidental exposure or ingestion.

Applications in Scientific Experiments

1-Thio-beta-D-glucose pentaacetate has several potential applications in various fields of research and industry, including:

1. Chemical synthesis: Thio-sugars are promising molecules for the development of new drugs and materials. 1-Thio-beta-D-glucose pentaacetate can be used as a building block for the synthesis of more complex thio-sugars and other related compounds.

2. Biological studies: Thio-sugars are used as probes to investigate the role of sugar modifications in biological processes. 1-Thio-beta-D-glucose pentaacetate can be used to study the interactions of thio-sugars with enzymes, receptors, and other biomolecules.

3. Microbial control: Thio-sugars have antimicrobial properties, and 1-Thio-beta-D-glucose pentaacetate can be used as a potential agent to control the growth of certain bacteria and to prevent bacterial biofilm formation.

4. Carbohydrate metabolism: Thio-sugars have been shown to be inhibitors of enzymes involved in carbohydrate metabolism, and 1-Thio-beta-D-glucose pentaacetate can be used as a tool to study the kinetics and mechanisms of carbohydrate metabolism.

Current State of Research

Research on thio-sugars, including 1-Thio-beta-D-glucose pentaacetate, is ongoing and has led to the discovery of several new compounds with unique properties and potential applications. Recent studies have focused on the synthesis, characterization, and biological properties of these compounds, as well as their potential use in drug discovery and other related fields.

Potential Implications in Various Fields of Research and Industry

The unique properties of 1-Thio-beta-D-glucose pentaacetate and other thio-sugars hold promise for their potential use in various fields of research and industry, including:

1. Drug discovery: Thio-sugars are being investigated as potential leads for the development of new drugs, particularly antibiotics, anticancer drugs, and antiviral agents.

2. Materials science: Thio-sugars are being explored for their potential use in materials science, particularly in the development of new materials that exhibit unique properties, such as electrical conductivity, and mechanical strength.

3. Food science: Thio-sugars are being investigated for their potential use as food additives to enhance flavor and as food preservatives to inhibit the growth of certain bacteria.

Limitations

Despite the potential applications of 1-Thio-beta-D-glucose pentaacetate and other thio-sugars, there are several limitations that need to be addressed, including:

1. Limited supply: Thio-sugars are not widely available, and their synthesis can be challenging and expensive.

2. Limited stability: Thio-sugars are less stable than their corresponding oxygen sugars and can undergo hydrolysis or oxidation under certain conditions.

3. Limited understanding: The biological properties of thio-sugars are not fully understood, and further research is needed to elucidate their mechanisms of action and potential therapeutic applications.

Future Directions

Several future directions can be identified for 1-thio-beta-D-glucose pentaacetate and other thio-sugars, including:

1. Development of new synthetic methods: New synthetic methods are needed to improve the yields and purity of thio-sugars and to enable the synthesis of more complex structures.

2. Investigation of the biological properties: Further studies are needed to investigate the biological properties of thio-sugars and their potential use as therapeutic agents.

3. Investigation of the mechanisms of action: Further studies are needed to elucidate the mechanisms of action of thio-sugars in biological systems and to identify potential targets for drug development.

4. Applications in industry: Thio-sugars have potential applications in various industries, including pharmaceuticals, materials science, and food science. Further research is needed to develop and optimize these applications.

Conclusion

1-Thio-beta-D-glucose pentaacetate is a member of the thio-sugar family with unique properties that make it a promising molecule for various fields of research and industry. The synthesis, characterization, and biological properties of this compound have been investigated, and further research is needed to elucidate its potential applications and mechanisms of action. Thio-sugars have shown promise as leads for drug development and as materials with unique properties, and further research is needed to explore these and other potential applications.

CAS Number13639-50-4
Product Name1-Thio-beta-D-glucose pentaacetate
IUPAC Name[(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-acetylsulfanyloxan-2-yl]methyl acetate
Molecular FormulaC16H22O10S
Molecular Weight406.405 g/mol
InChIInChI=1S/C16H22O10S/c1-7(17)22-6-12-13(23-8(2)18)14(24-9(3)19)15(25-10(4)20)16(26-12)27-11(5)21/h12-16H,6H2,1-5H3/t12-,13-,14+,15-,16+/m1/s1
InChI KeyCFAJEDWNNGFOQV-LJIZCISZSA-N
SMILESCC(=O)OCC1C(C(C(C(O1)SC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C
Canonical SMILESCC(=O)OCC1C(C(C(C(O1)SC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C
Isomeric SMILESCC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)SC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C


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