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  • 10338-51-9, Salidroside, Rhodioloside, 红景天苷, CAS:10338-51-9
  • 10338-51-9, Salidroside, Rhodioloside, 红景天苷, CAS:10338-51-9
10338-51-9, Salidroside, Rhodioloside, 红景天苷, CAS:10338-51-910338-51-9, Salidroside, Rhodioloside, 红景天苷, CAS:10338-51-9

10338-51-9, Salidroside, Rhodioloside, 红景天苷, CAS:10338-51-9

10338-51-9, Salidroside,
Rhodioloside,
红景天苷,
CAS:10338-51-9
C14H20O7 / 300.30

红景天苷, Salidroside

Salidroside is a natural compound that belongs to the group of compounds known as sesquiterpene lactones. It has been shown to have biological properties in vitro, such as apoptosis induction, autophagy inhibition, and control of cell transformation. Salidroside has also been shown to inhibit skin tumor formation in vivo and to reduce the expression of pro-apoptotic proteins. The apoptosis pathway is a major target for salidroside because it may be involved in the regulation of DNA damage responses. Salidroside has been shown to induce apoptosis by inhibiting dinucleotide phosphate (DNP) synthase and activating caspases. This activation is mediated by the protein kinase C (PKC), which leads to activation of caspase-3, poly(ADP-ribose) polymerase, and other pro-apoptotic proteins. Salidroside also induces apoptosis through a pathway involving mitochondria and Bcl.

Salidroside (Sal), also known as rhodioloside, is a glycoside compound and an active ingredient that can be found in Rhodiola rosea (R. rosea) and other species of Rhodiola. R. Rosea, also known as golden root, is a perennial plant that is native to the Arctic regions of Europe, Asia, and America and has been traditionally used for centuries to treat a wide range of ailments, including fatigue, depression, and anxiety. Salidroside was first isolated and identified in R. rosea in the 1960s and has since been the subject of numerous scientific studies due to its potential therapeutic properties.

Physical and Chemical Properties

Salidroside is a glucoside of tyrosol, a phenolic compound, and has the chemical formula C14H20O7. Salidroside is a highly water-soluble compound and has a melting point of 215-218°C. It is a brownish-yellow powder that is stable at room temperature when stored in a dry and cool place, such as in an airtight container.

Synthesis and Characterization

Being a natural compound, Salidroside can be extracted from the roots of R. rosea. However, to obtain a more concentrated form of Salidroside, chemical synthesis has been explored. Chemical synthesis of Salidroside has been achieved via the coupling of tyrosol with glucose. The synthesized Salidroside has been characterized using various techniques, including nuclear magnetic resonance (NMR spectroscopy), infrared spectroscopy (FT-IR), and mass spectrometry (MS).

Analytical Methods

Several analytical methods have been developed to determine the content of Salidroside in plant extracts or synthesized compounds. These methods include high-performance liquid chromatography (HPLC), gas chromatography (GC-MS), and capillary electrophoresis (CE). Of these methods, HPLC is the most commonly used technique due to its sensitivity and accuracy.

Biological Properties

Salidroside has been shown to possess a wide range of biological properties that may have therapeutic applications in various diseases. One of the most well-studied properties of Salidroside is its antioxidative activity. Salidroside has been shown to scavenge free radicals and protect cells from oxidative stress. Additionally, Salidroside has demonstrated anti-inflammatory, anti-cancer, neuroprotective, cardioprotective, and anti-fatigue properties in various cell and animal models.

Toxicity and Safety in Scientific Experiments

Overall, Salidroside has a good safety profile and low toxicity in animal models and human trials. However, some studies have reported potential adverse effects of Salidroside, including gastrointestinal disturbances, headaches, and muscle pains, at higher doses.

Applications in Scientific Experiments

Salidroside has a broad range of potential therapeutic applications in various diseases. Studies have shown that Salidroside has a protective effect against radiation-induced damage, inhibits the proliferation of cancer cells, and enhances immunity in animal models. Moreover, Salidroside may also alleviate symptoms of depression, anxiety, and cognitive impairment in humans.

Current State of Research

Research on Salidroside is ongoing, and many studies have demonstrated its potential therapeutic applications. The number of studies on Salidroside has increased significantly over the past decade, indicating that researchers are increasingly interested in elucidating its mechanism of action and potential therapeutic uses.

Potential Implications in Various Fields of Research and Industry

Salidroside has various potential implications in various fields of research and industry. In the medical field, Salidroside may be used as a natural alternative to conventional drugs in treating various diseases, including cancer, cardiovascular diseases, and neurological disorders. Additionally, Salidroside may also be used in the cosmetics industry due to its antioxidative and anti-inflammatory properties.

Limitations and Future Directions

While Salidroside has many potential therapeutic applications, several limitations should be considered. For instance, the bioavailability of Salidroside is relatively low due to its poor solubility and first-pass metabolism in the liver. To overcome this limitation, several strategies, such as drug delivery systems and prodrugs, have been explored. Additionally, further research is needed to ascertain the long-term safety and efficacy of Salidroside in humans as most studies have been limited to animal models.

Future Directions

Several future directions can be identified for Salidroside research, including:

1. Investigating the role of Salidroside in regulating gut microbiota and its potential implications in gut health and diseases.

2. Exploring the effect of Salidroside on cellular senescence and its potential implications in aging-related diseases.

3. Investigating the potential of Salidroside in enhancing the therapeutic efficacy of conventional chemotherapeutic drugs in cancer treatment.

4. Developing novel formulations of Salidroside to improve its bioavailability and efficacy in human trials.

In conclusion, Salidroside is a natural compound with a variety of potential therapeutic applications in various diseases. Its antioxidative and anti-inflammatory properties make it an attractive candidate for drug development. However, further research is needed to elucidate its mechanism of action and potential implications in various fields of research and industry.

CAS Number10338-51-9
Product NameSalidroside
IUPAC Name(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol
Molecular FormulaC14H20O7
Molecular Weight300.3 g/mol
InChIInChI=1S/C14H20O7/c15-7-10-11(17)12(18)13(19)14(21-10)20-6-5-8-1-3-9(16)4-2-8/h1-4,10-19H,5-7H2/t10-,11-,12+,13-,14-/m1/s1
InChI KeyILRCGYURZSFMEG-RKQHYHRCSA-N
Synonymsbeta-D-glucopyranoside, 2-(4-hydroxyphenyl)ethyl-, rhodioloside, rhodosin, salidroside, salidroside, (-)-, sallidroside
Canonical SMILESC1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O
Isomeric SMILESC1=CC(=CC=C1CCO[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O

CAS No: 10338-51-9 Synonyms: Rhodioloside2-(4-Hydroxyphenyl)ethyl-b-D-glucopyranosideTyrosol glucoside 

 Chemical Formula: C14H20O7 Molecular Weight: 300.30

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