126223-28-7 , Ginsenoside Rg4 ,
20(Z)-Ginsenoside F4
Cas:126223-28-7
C42H70O12 / 767.00
MFCD22200428
Ginsenoside RG4 is a saponin compound that is extracted from the root of Korean red ginseng. This natural compound has gained a lot of attention from the scientific community due to its potential therapeutic applications. In this paper, we will explore the definition, physical and chemical properties, synthesis and characterization, 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 of Ginsenoside RG4.
Definition and Background:
Ginsenoside RG4 is a saponin compound that belongs to the ginsenoside family. The compound is extracted from the root of Korean red ginseng, which has been used for centuries in traditional medicine practices in Korea, China, and Japan. Ginsenoside RG4 was first isolated in 1984, and since then, it has become a subject of intense research due to its potential therapeutic applications.
Synthesis and Characterization:
There are various methods to obtain Ginsenoside RG4, including extraction, isolation, and synthesis. The most common method is the extraction of the compound from the root of Korean red ginseng. The extracted compound is then purified using various chromatographic techniques. Characterization of Ginsenoside RG4 is performed using various spectroscopic and analytical techniques, including nuclear magnetic resonance (NMR), high-performance liquid chromatography (HPLC), and mass spectrometry (MS).
Analytical Methods:
To quantify and analyze Ginsenoside RG4, various methods have been developed, including HPLC, MS, and NMR. These methods are widely used by researchers to ensure the purity, stability, and concentration of the compound.
Biological Properties:
Ginsenoside RG4 has been found to exhibit various therapeutic effects, including anti-cancer, anti-inflammatory, anti-oxidant, and neuroprotective activities. The compound has been shown to induce apoptosis in various cancer cells, including breast, colon, and lung cancer cells. In addition, Ginsenoside RG4 has been found to modulate the immune system, improve cognitive function, and provide cardiovascular protection.
Toxicity and Safety in Scientific Experiments:
In scientific experiments, Ginsenoside RG4 has been found to be safe and non-toxic, with no adverse effects on animals or humans. However, more studies are needed to determine the long-term safety and toxicity of the compound.
Applications in Scientific Experiments:
Ginsenoside RG4 has been widely studied for its potential therapeutic applications in various fields, including cancer, Alzheimer's disease, and cardiovascular disease. The compound has also been found to have potential applications in anti-aging, stress relief, and skin care.
Current State of Research:
Currently, the research on Ginsenoside RG4 is focused on its therapeutic applications in various fields, including cancer, neurodegenerative diseases, and cardiovascular diseases. The compound has also been studied for its anti-inflammatory properties and potential applications in skin care.
Potential Implications in Various Fields of Research and Industry:
Ginsenoside RG4 has numerous potential implications in various fields of research and industry. The compound could potentially be used in the development of new anti-cancer drugs, neuroprotective agents, and anti-aging products. In addition, the compound may have applications in the food industry and as a dietary supplement.
Limitations and Future Directions:
Despite its promising potential, the use of Ginsenoside RG4 has several limitations. One of the main limitations is the low availability of the compound due to the difficulty in extracting and synthesizing it. Additionally, the mechanism of action of the compound is not fully understood, and more research is needed to determine the optimal dosage and administration of the compound. Future research should focus on developing more efficient and cost-effective synthesis methods, exploring the underlying mechanism of action, and conducting clinical trials to determine the safety and efficacy of the compound in humans.
Conclusion:
Ginsenoside RG4 is a promising natural compound that has shown potential therapeutic applications in various fields. The compound has been found to exhibit anti-cancer, anti-inflammatory, anti-oxidant, and neuroprotective activities. However, more research is needed to determine the optimal dosage and administration of the compound, as well as its long-term safety and toxicity. Despite its limitations, Ginsenoside RG4 presents a promising avenue for the development of new drugs and anti-aging products.
Ginsenoside F4 is a saponin that is found in Panax ginseng and other plants. It has been shown to scavenge reactive oxygen species, which are implicated in cancer, inflammation, and aging. Ginsenoside F4 has been shown to have anti-inflammatory properties by inhibiting the production of inflammatory cytokines such as TNF-α, IL-1β, IL-6, and IL-8. This saponin also inhibits the growth of bacteria such as Listeria monocytogenes and Bacillus subtilis. Ginsenoside F4 has been shown to inhibit proliferation of cancer cells in human breast cancer cells (MCF7) through an activation of the JNK pathway.
CAS Number | 126223-28-7 |
Product Name | Ginsenoside RG4 |
IUPAC Name | (2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-2-[[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-dihydroxy-4,4,8,10,14-pentamethyl-17-[(2Z)-6-methylhepta-2,5-dien-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol |
Molecular Formula | C42H70O12 |
Molecular Weight | 767 |
InChI | InChI=1S/C42H70O12/c1-20(2)11-10-12-21(3)23-13-16-41(8)29(23)24(44)17-27-40(7)15-14-28(45)39(5,6)36(40)25(18-42(27,41)9)52-38-35(33(49)31(47)26(19-43)53-38)54-37-34(50)32(48)30(46)22(4)51-37/h11-12,22-38,43-50H,10,13-19H2,1-9H3/b21-12-/t22-,23+,24+,25-,26+,27+,28-,29-,30-,31+,32+,33-,34+,35+,36-,37-,38+,40+,41+,42+/m0/s1 |
SMILES | CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CC4(C(CC(C5C4(CCC5C(=CCC=C(C)C)C)C)O)C6(C3C(C(CC6)O)(C)C)C)C)CO)O)O)O)O)O |
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