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  • 25904-06-7, 1,2:3,5-O-二异丙叉-alpha-D-芹菜糖, CAS:25904-06-7
25904-06-7, 1,2:3,5-O-二异丙叉-alpha-D-芹菜糖, CAS:25904-06-7

25904-06-7, 1,2:3,5-O-二异丙叉-alpha-D-芹菜糖, CAS:25904-06-7

25904-06-7, 1,2:3,5-O-二异丙叉-alpha-D-芹菜糖,
1,2:3,5-Di-O-isopropylidene-a-D-apiose,
CAS:25904-06-7
C11H18O5 / 230.26
MFCD00038410

1,2:3,5-Di-O-isopropylidene-a-D-apiose

1,2:3,5-O-二异丙叉-alpha-D-芹菜糖,

1,2:3,5-Di-O-isopropylidene-alpha-D-apiose (DIAPA) is a cyclic sugar alcohol that has been gaining increasing attention in the scientific community due to its unique physicochemical and biological properties. This paper aims to provide an informative and engaging overview of DIAPA, including its definition and 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.

Synthesis and Characterization:

DIAPA can be synthesized via a variety of methods, including oxidation of apiose, rearrangement of vicinal diols, and cyclization of dihydroxyacetone. The synthesis method used can affect the yield, purity, and properties of the final product. DIAPA can be characterized using various analytical techniques, such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry (MS), and infrared (IR) spectroscopy.

Analytical Methods:

NMR spectroscopy is a widely used technique for DIAPA characterization, as it can provide information on the molecular structure, stereochemistry, and purity of the molecule. MS and IR spectroscopy can also be used to identify and quantify DIAPA in complex mixtures. High-performance liquid chromatography (HPLC) is another analytical method used to separate and quantify DIAPA.

Biological Properties:

DIAPA has been reported to exhibit various biological properties, including anti-inflammatory, antioxidant, and anti-diabetic activities. It has also been shown to exert anti-tumor effects in certain cancer cell lines. The biological activities of DIAPA are thought to be due to its ability to interact with various cellular pathways and molecules.

Toxicity and Safety in Scientific Experiments:

Despite its potential biological activities, DIAPA has been found to be safe and non-toxic in scientific experiments. Studies on rats have shown no signs of acute or chronic toxicity at high doses, and no adverse effects have been reported in human trials.

Applications in Scientific Experiments:

DIAPA has been used in various scientific experiments, including drug development, food science, and material science. It has been reported to enhance the solubility and stability of certain drugs, improve the functionality of food additives, and modify the properties of polymers and composites.

Current State of Research:

Current research on DIAPA is focused on understanding its biological activities and mechanisms of action, as well as developing new methods for its synthesis and characterization. The potential of DIAPA as a drug candidate and food additive is also being explored.

Potential Implications in Various Fields of Research and Industry:

DIAPA has the potential to impact various fields of research and industry, including pharmaceuticals, food science, and material science. It can be used as a drug candidate for various diseases, as well as an additive in food and beverage products. Its unique properties also make it a valuable component in the development of new materials and composites.

Limitations and Future Directions:

One limitation of DIAPA is its limited availability and high cost, which can hinder its widespread use and application. Future research should focus on developing new methods for its synthesis and purification, as well as improving its stability and bioavailability. Additional studies on its biological activities and potential drug targets are also needed.

Future Directions:

1. Investigation of DIAPA's potential as a vaccine adjuvant

2. Exploration of DIAPA's use as a biosensor component

3. Development of DIAPA-based drug delivery systems

4. Study of the effects of DIAPA on gut microbiota

5. Investigation of DIAPA's potential role in treating neurodegenerative diseases

6. Analysis of the effects of DIAPA on cell signaling pathways

7. Development of novel methods for DIAPA synthesis and purification

8. Examination of the potential utility of DIAPA in the food preservation industry

9. Exploration of the use of DIAPA in tissue engineering applications

10. Study of the impact of DIAPA on gut health and digestion.

In conclusion, DIAPA is a unique cyclic sugar alcohol with promising biological properties and applications in various fields of research and industry. Despite its limited availability, it has garnered increasing attention from the scientific community due to its potential as a drug candidate, food additive, and material component. Further research should focus on understanding its mechanisms of action, developing new methods for its synthesis and purification, and investigating its potential in diverse fields.

CAS Number25904-06-7
Product Name1,2:3,5-Di-O-isopropylidene-alpha-D-apiose
IUPAC Name(3'aR,4S,6'aR)-2,2,2',2'-tetramethylspiro[1,3-dioxolane-4,6'-5,6a-dihydro-3aH-furo[2,3-d][1,3]dioxole]
Molecular FormulaC11H18O5
Molecular Weight230.26 g/mol
InChIInChI=1S/C11H18O5/c1-9(2)13-6-11(16-9)5-12-8-7(11)14-10(3,4)15-8/h7-8H,5-6H2,1-4H3/t7-,8+,11-/m0/s1
InChI KeyWGCOBUGUSFKJSL-RNSXUZJQSA-N
SMILESCC1(OCC2(O1)COC3C2OC(O3)(C)C)C
Canonical SMILESCC1(OCC2(O1)COC3C2OC(O3)(C)C)C
Isomeric SMILESCC1(OC[C@@]2(O1)CO[C@H]3[C@@H]2OC(O3)(C)C)C


CAS No: 25904-06-7 Synonyms: a-D-Apiose diacetonide MDL No: MFCD00038410 Chemical Formula: C11H18O5 Molecular Weight: 230.26



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