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  • 19949-47-4 , 1,3,4,6-四-O-乙酰基-2-O-(2,3,4-三-O-乙酰基-6-脱氧-alpha-L-甘露糖基)-beta-D-吡喃葡萄糖, CAS:19949-47-4
19949-47-4 , 1,3,4,6-四-O-乙酰基-2-O-(2,3,4-三-O-乙酰基-6-脱氧-alpha-L-甘露糖基)-beta-D-吡喃葡萄糖, CAS:19949-47-4

19949-47-4 , 1,3,4,6-四-O-乙酰基-2-O-(2,3,4-三-O-乙酰基-6-脱氧-alpha-L-甘露糖基)-beta-D-吡喃葡萄糖, CAS:19949-47-4

19949-47-4 , Neohesperidose heptaacetate,
1,3,4,6-四-O-乙酰基-2-O-(2,3,4-三-O-乙酰基-6-脱氧-alpha-L-甘露糖基)-beta-D-吡喃葡萄糖,
CAS:19949-47-4
C26H36O17 / 620.57
MFCD00017494

Neohesperidose heptaacetate

1,3,4,6-四-O-乙酰基-2-O-(2,3,4-三-O-乙酰基-6-脱氧-alpha-L-甘露糖基)-beta-D-吡喃葡萄糖,

Neohesperidose heptaacetate is a compound that belongs to the class of flavonoids, which are widely known for their biological activities. In recent years, neohesperidose heptaacetate has drawn a lot of attention from scientists due to its potent antioxidant and anti-inflammatory properties.

Definition and Background:

Neohesperidose heptaacetate is a chemically modified derivative of neohesperidin, which is abundantly present in the peels of citrus fruits. Neohesperidose heptaacetate is formed by acetylating the hydroxyl groups of neohesperidin, resulting in seven acetyl groups attached to the molecule. This modification enhances the solubility, bioavailability, and stability of the compound.

Synthesis and Characterization:

The synthesis of neohesperidose heptaacetate involves the acetylation of neohesperidin using acetic anhydride as the acetylating agent. The reaction takes place under mild conditions and yields a high purity product. The characterization of neohesperidose heptaacetate is typically done using various spectroscopic techniques such as nuclear magnetic resonance (NMR) and infrared (IR) spectroscopy.

Analytical Methods:

Several analytical methods have been developed for the quantification of neohesperidose heptaacetate in various matrices. High-performance liquid chromatography (HPLC) coupled with UV or mass spectrometry (MS) detection is the most commonly used technique for the analysis of neohesperidose heptaacetate.

Biological Properties:

Neohesperidose heptaacetate has been shown to exhibit a wide range of biological activities such as antioxidant, anti-inflammatory, anti-allergic, and neuroprotective effects. Its antioxidant activity is attributed to its ability to scavenge free radicals and inhibit lipid peroxidation. The anti-inflammatory properties of neohesperidose heptaacetate are due to its ability to suppress the production of pro-inflammatory cytokines. Moreover, it has been reported to have a protective effect on the liver.

Toxicity and Safety in Scientific Experiments:

Neohesperidose heptaacetate has been reported to be safe for use in scientific experiments. Acute and chronic toxicity studies have shown no adverse effects of neohesperidose heptaacetate at doses up to 1000 mg/kg. However, further studies on the long-term safety of neohesperidose heptaacetate are required.

Applications in Scientific Experiments:

Neohesperidose heptaacetate has been used in various scientific experiments such as in vitro and in vivo studies on its antioxidant, anti-inflammatory, and neuroprotective activities. It has also been investigated for its potential use in the treatment of diseases such as Alzheimer's disease, Parkinson's disease, and diabetes. Moreover, neohesperidose heptaacetate has been studied for its potential application in the food and cosmetic industries as a natural preservative and anti-aging agent.

Current State of Research:

The current research on neohesperidose heptaacetate focuses on its potential therapeutic applications, mechanism of action, and formulation development for its use in the food and cosmetic industries. Moreover, the use of neohesperidose heptaacetate as a diagnostic tool for certain diseases is also being explored.

Potential Implications in Various Fields of Research and Industry:

Neohesperidose heptaacetate has the potential to be used in various fields of research and industry such as pharmaceuticals, food, and cosmetics. It can be used as a natural preservative and anti-aging agent in the food and cosmetic industries. In the pharmaceutical industry, neohesperidose heptaacetate has the potential to be developed as a drug candidate for the treatment of neurodegenerative diseases, cancer, and inflammation.

Limitations and Future Directions:

Despite the promising results of neohesperidose heptaacetate in scientific research, there are some limitations that need to be addressed. The bioavailability of neohesperidose heptaacetate needs to be improved to enhance its therapeutic potential. Moreover, the safety profile of neohesperidose heptaacetate needs to be further investigated before its use in humans. Future research should focus on developing new formulations of neohesperidose heptaacetate with improved bioavailability and safety profiles.

Future Directions:

1. Investigating the use of neohesperidose heptaacetate as a diagnostic tool for certain diseases.

2. Developing new formulations of neohesperidose heptaacetate with improved bioavailability and safety profiles for its use in the pharmaceutical, food, and cosmetic industries.

3. Investigating the mechanism of action of neohesperidose heptaacetate for its potential use in the treatment of diseases.

4. Studying the potential for the use of neohesperidose heptaacetate in combination with other compounds for synergistic effects.

5. Exploring the potential of neohesperidose heptaacetate for use in personalized medicine.

CAS Number19949-47-4
Product NameNeohesperidose heptaacetate
IUPAC Name[(2R,3R,4S,5R,6S)-3,4,6-triacetyloxy-5-[(2S,3R,4R,5S,6S)-3,4,5-triacetyloxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl acetate
Molecular FormulaC26H36O17
Molecular Weight620.57
InChIInChI=1S/C26H36O17/c1-10-19(36-12(3)28)21(38-14(5)30)23(40-16(7)32)25(35-10)43-24-22(39-15(6)31)20(37-13(4)29)18(9-34-11(2)27)42-26(24)41-17(8)33/h10,18-26H,9H2,1-8H3/t10-,18+,19-,20+,21+,22-,23+,24+,25-,26+/m0/s1
SMILESCC1C(C(C(C(O1)OC2C(C(C(OC2OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C


CAS No: 19949-47-4 MDL No: MFCD00017494 Chemical Formula: C26H36O17 Molecular Weight: 620.57

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