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83207-58-3, Astragaloside, CAS:83207-58-3

83207-58-3, Astragaloside,
Cyclosiversioside F
CAS:83207-58-3
C41H68O14 / 784.97
MFCD16036240

Astragaloside, 黄芪甲苷

Astragaloside IV is a natural product found in the root of Astragalus membranaceus. It has been shown to have significant up-regulation in response to brain injury and to protect neurons from injury. Astragaloside IV also has anti-inflammatory effects and may be a potential therapeutic agent for the treatment of neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. This compound binds to the NF-κB pathway, which prevents activation of pro-inflammatory genes, including Bcl-2 protein, resulting in reduced nitrate reductase activity and decreased kidney injury.

Cyclosiversioside F is an important natural product isolated from the leaves of Acanthopanax senticosus, also known as Siberian ginseng. This compound has received increasing attention in recent years due to its potential applications in various fields of research and industry. In this paper, we aim to provide a comprehensive overview of the physical and chemical properties, synthesis and characterization, biological properties, toxicity and safety in scientific experiments, applications, current state of research, potential implications, limitations, and future directions of Cyclosiversioside F.

of research, potential implications, limitations, and future directions of Cyclosiversioside F.

Physical and Chemical Properties

Cyclosiversioside F is a white powder with a bitter taste and has a melting point of 327-329 °C. The compound is soluble in methanol and water, but insoluble in chloroform and petroleum ether. The chemical structure of Cyclosiversioside F consists of a hydrophilic sugar moiety attached to a hydrophobic aglycone, which makes it amphiphilic in nature.

Synthesis and Characterization

Cyclosiversioside F is mainly obtained from the leaves of Acanthopanax senticosus. However, it can also be synthesized in the laboratory through chemical reactions. The total synthesis of Cyclosiversioside F has not been reported yet, but partial synthesis has been achieved through various methods. Characterization of Cyclosiversioside F can be done using various techniques, including ultraviolet (UV) spectroscopy, high-performance liquid chromatography (HPLC), mass spectrometry (MS), and nuclear magnetic resonance (NMR) spectroscopy.

Analytical Methods

Several analytical methods have been developed for the quantitative and qualitative determination of Cyclosiversioside F in biological and environmental samples. HPLC and MS are the most commonly used techniques for the separation, identification, and quantification of Cyclosiversioside F in plant extracts and food products.

Biological Properties

Cyclosiversioside F has shown potent and diverse biological activities. It exhibits anti-tumor activity by inducing apoptosis and inhibiting the proliferation of various cancer cells, including breast, liver, colon, and lung cancer cells. Additionally, Cyclosiversioside F has anti-inflammatory and immune-modulatory effects by regulating cytokines and interleukins levels. Studies have also shown that Cyclosiversioside F has antiviral, antibacterial, antioxidant, and antifungal properties.

Toxicity and Safety in Scientific Experiments

To date, no significant toxicity or adverse effects of Cyclosiversioside F have been reported in scientific experiments. However, further studies are needed to determine the safety and toxicity profile of Cyclosiversioside F in long-term usage.

Applications in Scientific Experiments

Cyclosiversioside F has broad applications in scientific experiments, including drug discovery, cancer treatment, immunomodulation, and targeted therapies. It has been recommended for exploring its potential in the development of nutraceuticals and functional foods for health promotion.

Current State of Research

Although Cyclosiversioside F has shown potential in various fields of research, much remains to be explored. The current state of research on Cyclosiversioside F includes studies on its pharmacological effects, structural modifications, and mechanism of action.

Potential Implications in Various Fields of Research and Industry

Cyclosiversioside F has potential applications in various fields of research and industry, including medicine, agriculture, cosmetics, and food. Its use in these areas can lead to significant breakthroughs and advancements.

Limitations

Despite its potential, Cyclosiversioside F has some limitations that need to be addressed. It is relatively expensive to obtain and requires complex purification methods. In addition, the low bioavailability of Cyclosiversioside F poses a challenge in its therapeutic applications.

Future Directions

Several future directions can be pursued to better understand the potential of Cyclosiversioside F. These include:

1. Investigation of its structural modifications to enhance its bioavailability and therapeutic efficacy.

2. Examination of its effect on different cell lines and animal models under various conditions

3. Determination of its toxicity and safety profiles in long-term usage.

4. Study of its mechanisms of action in different biological systems.

5. Development of new analytical methods for its detection, purification, and quantification.

Conclusion

Cyclosiversioside F is a promising natural product with various pharmacological benefits that has been attracting increasing attention in recent years. Its potential applications in various fields of research and industry make it an essential compound to be studied further. This comprehensive overview aims to provide a complete understanding of this compound's physical and chemical properties, biological activities, toxicity, safety, applications, limitations, and future directions.

CAS Number83207-58-3
Product NameCyclosiversioside F
IUPAC Name(2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-hydroxy-15-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
Molecular FormulaC41H68O14
Molecular Weight784.97
InChIInChI=1S/C41H68O14/c1-35(2)24(54-33-29(48)26(45)20(44)17-51-33)9-11-41-18-40(41)13-12-37(5)31(39(7)10-8-25(55-39)36(3,4)50)19(43)15-38(37,6)23(40)14-21(32(35)41)52-34-30(49)28(47)27(46)22(16-42)53-34/h19-34,42-50H,8-18H2,1-7H3/t19-,20+,21-,22+,23-,24-,25+,26-,27+,28-,29+,30+,31-,32-,33-,34+,37+,38-,39-,40-,41+/m0/s1
InChI KeyQMNWISYXSJWHRY-AUJDEUPOSA-N
SMILESCC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(CO8)O)O)O)C
SynonymsCyclosiversioside F; (3b,6a,16b,24R)-20,24-Epoxy-16,26-dihydroxy-3-(b-D-xylopyranosyloxy)-9,19-cyclolanostan-6-yl b-D-glucopyranoside


CAS No: 83207-58-3,84687-43-4 Synonyms: Cyclosiversioside F(3b,6a,16b,24R)-20,24-Epoxy-16,26-dihydroxy-3-(b-D-xylopyranosyloxy)-9,19-cyclolanostan-6-yl b-D-glucopyranoside  MDL No: MFCD16036240 Chemical Formula: C41H68O14 Molecular Weight: 784.97


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