16955-55-8

Basic information

• Product Name: salireposide
• Synonyms: salireposide
• CAS NO: 16955-55-8
• Molecular Formula: C₂₀H₂₂O₉
• Molecular Weight: 406.38328
• Mol File: 16955-55-8.mol
• Article Data: 1

Chemical Properties

• Melting Point: 206 °C
• Boiling Point: 676.3°Cat760mmHg
• Flash Point: 240.5°C
• Appearance: /
• Density: 1.485g/cm³
• Vapor Pressure: 3.25E-19mmHg at 25°C
• Refractive Index: 1.652
• PKA: 9.79±0.20(Predicted)
• CAS DataBase Reference: salireposide(CAS DataBase Reference)
• NIST Chemistry Reference: salireposide(16955-55-8)
• EPA Substance Registry System: salireposide(16955-55-8)

Safety Data

• Hazardous Substances Data: 16955-55-8(Hazardous Substances Data)

Usage

Description

Salireposide, a natural chemical compound found in various plant species such as willow trees and common agrimony, is a phenolic glycoside characterized by its phenolic compound attached to a sugar molecule. It is recognized for its anti-inflammatory, antioxidant, and analgesic properties, which make it a potentially valuable compound for medicinal applications. Salireposide has been studied for its potential in treating conditions like arthritis, cancer, and cardiovascular diseases, and it has also demonstrated promise in liver protection and wound healing. Overall, salireposide is a biologically active compound with a range of potential health benefits.

Uses

Used in Pharmaceutical Industry:
Salireposide is used as an anti-inflammatory agent for its ability to reduce inflammation, which can be beneficial in treating conditions such as arthritis.
Used in Antioxidant Applications:
Salireposide is used as an antioxidant to combat oxidative stress and protect cells from damage, which can be useful in preventing and treating various diseases associated with oxidative stress.
Used in Pain Management:
Salireposide is used as an analgesic to alleviate pain, making it a potential candidate for pain management therapies.
Used in Cancer Treatment:
Salireposide is used as a potential cancer treatment agent due to its ability to target and inhibit the growth of cancer cells.
Used in Cardiovascular Disease Management:
Salireposide is used as a therapeutic agent for cardiovascular diseases, potentially helping to improve heart health and reduce the risk of related conditions.
Used in Liver Protection:
Salireposide is used as a hepatoprotective agent to shield the liver from damage caused by toxins, supporting liver health and function.
Used in Wound Healing:
Salireposide is used as a wound healing promoter to facilitate the healing process of various types of wounds, enhancing tissue repair and regeneration.

InChI:InChI=1/C20H22O9/c21-9-15-16(23)17(24)18(25)20(29-15)28-14-7-6-13(22)8-12(14)10-27-19(26)11-4-2-1-3-5-11/h1-8,15-18,20-25H,9-10H2/t15-,16-,17+,18-,20-/m1/s1

Upstream product

• 3233-32-7 hydroquinone monoacetate 
• 18265-35-5 2-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyloxy)-5-acetoxybenzyl(3-methoxy-4-acetoxy)benzoate 
• 1415680-12-4 2-(2,3,4,6-tetra-О-acetyl-β-D-glucopyranozyloxy)-5-acetyloxybenzyl alcohol 
• 1415680-10-2 2-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-5-acetyloxybenzaldehyde 
• 64418-88-8 2-hydroxy-5-acetyloxybenzaldehyde 
• 123-31-9 hydroquinone 

Relevant articles and documents

First total chemical synthesis of natural acyl derivatives of some phenolglycosides of the family Salicaceae

The total synthesis of certain natural phenolglycosides of the family Salicaceae, namely: salireposide, populosides A, B, and C and not occurring in plants desoxysalireposide (2-(β-d-glucopyranosyloxy)-benzylbenzoate) and per-acetate of iso-salireposide (2-(β-d-glucopyranosyloxy)-5-benzoyloxy benzyl alcohol), starting from readily available phenols and glucose was accomplished. A simple method for the synthesis of phenolglycosides derivatives of 2-acyloxy salicyl and gentisyl alcohol was developed. The key step of these natural products' synthesis is a selective removal of acetyl groups in the presence of other acyl groups.