470-55-3 , D-水苏糖,
Stachyose,
Cas:470-55-3
MFCD00006631
C24H42O21 / 666.59
Non-reducing storage and transport sugar in woody plants; used as a sweetener.
Stachyose is a tetrasaccharide composed of two glucose molecules, one fructose, and one galactose, linked by alpha-1,6 glycosidic bonds. It is a common oligosaccharide found in many plants, particularly legumes, serving as a reserve carbohydrate. Stachyose has attracted attention due to its potential applications in various fields of research and industry, including food, medicine, and agriculture.
Physical and Chemical Properties
Stachyose is a white crystalline solid with a sweet taste and a water-soluble property. Its molecular weight is 666.6 g/mol, and its density is 1.43 g/cm3. Stachyose is a reducing sugar, and its hydrolysis yields glucose, fructose, and galactose.
Synthesis and Characterization
Stachyose can be synthesized through a variety of methods, including enzymatic synthesis, chemical synthesis, and microbial fermentation. The most common approach involves enzymatic synthesis, which utilizes glycosyltransferases and their corresponding donor and acceptor compounds. The product is then purified and characterized using various analytical techniques, including high-performance liquid chromatography (HPLC), nuclear magnetic resonance (NMR) spectroscopy, and mass spectrometry (MS).
Analytical Methods
Stachyose can be measured using various analytical methods, including HPLC, capillary electrophoresis (CE), and thin-layer chromatography (TLC). These methods rely on different principles, such as separation of compounds based on their physical and chemical properties, and detection of specific compounds using specific reagents or detectors.
Biological Properties
Stachyose has been shown to exert various biological activities, such as immune modulating, anticancer, and prebiotic effects. Studies have demonstrated that stachyose can enhance the growth and activity of beneficial gut bacteria, such as bifidobacteria and lactobacilli, while inhibiting the growth of harmful bacteria such as E. coli. Stachyose has also been shown to enhance the immune response by increasing the expression of certain cytokines, such as interleukin-2 (IL-2) and interferon-gamma (IFN-gamma). Additionally, stachyose has been found to exhibit anticancer effects by inhibiting the growth and migration of cancer cells in vitro.
Toxicity and Safety in Scientific Experiments
Stachyose has been found to be generally safe and non-toxic in scientific experiments, with no observed adverse effects on animals or humans. However, some studies have reported mild gastrointestinal disturbances, such as diarrhea and flatulence, in individuals consuming high amounts of stachyose.
Applications in Scientific Experiments
Stachyose has numerous applications in various fields of research and industry. In food science, stachyose can be used as a prebiotic ingredient, adding nutritional value and improving the texture and quality of food. In medicine, stachyose has potential as an anticancer agent, immune booster, and anti-inflammatory agent. In agriculture, stachyose can be used as a fertilizer or supplement for crops, improving their growth and resistance to pests and diseases. Additionally, stachyose has been used as a cryoprotectant to prevent damage to cells during freezing and thawing.
Current State of Research
Stachyose has been extensively researched in recent years, with numerous studies exploring its biological properties and potential applications. However, there are still gaps in our understanding of stachyose, particularly regarding its mechanism of action and long-term effects on human health.
Potential Implications in Various Fields of Research and Industry
Stachyose has the potential to revolutionize various industries, including food, medicine, and agriculture. As a prebiotic ingredient, stachyose can improve the nutritional value and health benefits of food products without sacrificing taste or texture. In medicine, stachyose has potential as a natural anticancer agent, immune booster, and anti-inflammatory agent, with the potential to reduce the need for synthetic drugs with adverse side effects. In agriculture, stachyose can improve crop yields and quality, reducing the need for chemical fertilizers and pesticides.
Limitations and Future Directions
Despite the promising potential of stachyose, there are certain limitations and challenges that must be addressed. First of all, the synthesis of stachyose is still relatively costly and time-consuming, limiting its commercial viability. Additionally, more research is needed to fully understand the mechanisms of action and long-term effects of stachyose on human health. Lastly, the applications of stachyose in various fields of research and industry require further exploration and optimization.
Future Directions
There are numerous future directions for research and development of stachyose. Some potential areas of exploration include:
1. Development of more cost-effective and efficient synthesis methods for stachyose.
2. Optimization of the use of stachyose as a prebiotic ingredient in food products, including exploration of its potential applications in functional foods.
3. Exploration of the potential therapeutic applications of stachyose as an anticancer agent, immune booster, and anti-inflammatory agent.
4. Evaluation of the potential use of stachyose as a natural fertilizer or supplement for crops, including exploration of its effects on soil health and environmental sustainability.
5. Development of new methods for the delivery of stachyose in various applications, such as encapsulation or modification of stachyose to improve its bioavailability and efficacy.
6. Investigation of the long-term effects and safety of stachyose consumption on human health, particularly in vulnerable populations such as children and pregnant women.
In conclusion, stachyose is a versatile and promising compound with numerous potential applications in various fields of research and industry. More research and development are needed to fully unlock its potential and overcome the current limitations and challenges.
CAS Number | 470-55-3 |
Product Name | Stachyose |
IUPAC Name | (2S,3R,4S,5R,6R)-2-[[(2R,3R,4S,5R,6S)-6-[[(2R,3S,4S,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol;hydrate |
Molecular Formula | C24H42O21 |
Molecular Weight | 684.6 g/mol |
InChI | InChI=1S/C24H42O21.H2O/c25-1-6-10(28)14(32)17(35)21(41-6)39-3-8-11(29)15(33)18(36)22(42-8)40-4-9-12(30)16(34)19(37)23(43-9)45-24(5-27)20(38)13(31)7(2-26)44-24;/h6-23,25-38H,1-5H2;1H2/t6-,7-,8-,9-,10+,11+,12-,13-,14+,15+,16+,17-,18-,19-,20+,21+,22+,23-,24+;/m1./s1 |
InChI Key | UQZIYBXSHAGNOE-XNSRJBNMSA-N |
SMILES | C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O.O |
Synonyms | stachyose, stachyose hydrate, stachyose tetrahydrate |
Canonical SMILES | C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O.O.O.O.O |
Isomeric SMILES | C([C@@H]1[C@@H]([C@@H]([C@H]([C@H](O1)OC[C@@H]2[C@@H]([C@@H]([C@H]([C@H](O2)OC[C@@H]3[C@H]([C@@H]([C@H]([C@H](O3)O[C@]4([C@H]([C@@H]([C@H](O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O.O.O.O.O |
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