115009-57-9

Basic information

• Product Name: Icariside F2
• Synonyms: Icariside F2
• CAS NO: 115009-57-9
• Molecular Formula: C₁₈H₂₆O₁₀
• Molecular Weight: 402.39304
• Mol File: 115009-57-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: ?20°C
• CAS DataBase Reference: Icariside F2(CAS DataBase Reference)
• NIST Chemistry Reference: Icariside F2(115009-57-9)
• EPA Substance Registry System: Icariside F2(115009-57-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 115009-57-9(Hazardous Substances Data)

Usage

General Description

Icariside F2 is a chemical compound that belongs to the family of flavonoids, which are a class of plant pigments. It is derived from Epimedium koreanum, a herb that has been traditionally used in Chinese medicine for its potential health benefits. Icariside F2 has been studied for its anti-inflammatory, antioxidant, and neuroprotective properties, which may contribute to its potential therapeutic effects in conditions such as neurodegenerative diseases, cancer, and osteoporosis. Its ability to modulate various cellular signaling pathways and to inhibit the activity of enzymes involved in inflammatory and oxidative processes makes it a promising candidate for further research and development of potential therapeutic applications.

Upstream product

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Downstream Products

• 639-97-4 D-apiose 

Relevant articles and documents

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The synthetic apiosyl-glucosides having (S)-3,7-dimethyl-1,6-octadien-3- yl (linalyl); (R)-1-methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl (terpineyl); (E) and (Z)-3,7-dimethyl-2,6-octadien-1-yl (geranyl and neryl); (S)-3,7- dimethyl-6-octen-1-yl (citronellyl); benzyl and 2-phenylethyl as aglycon moiety were prepared using the stereospecific trichloroacetimidate Schmidt method. The key intermediate diholoside 1,2,3,4-tetra-O-acetyl-6-O-[(3-C- acetoxymethyl)-2,3-di-O-acetyl-β-D-erythrofuranosyl)-β-D-glucopyranose was obtained by Kochetkov glycosylation of a branched-chain tetrofuranose cyanoethylidene derivative. The NMR data (1H and 13C) of the synthetic compounds and the glycosylation shifts of the apiose moiety are reported. The synthetic apiosyl-glucosides having (S)-3,7-dimethyl-1,6-octadien-3-yl (linalyl); (R)-1-methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl (terpineyl); (E) and (Z)-3,7-dimethyl-2,6-octadien-1-yl (geranyl and neryl); (S)-3,7-dimethyl-6-octen-1-yl (citronellyl); benzyl and 2-phenylethyl as aglycon moiety were prepared using the stereospecific trichloroacetimidate Schmidt method. The key intermediate diholoside 1,2,3,4-tetra -O-acetyl-6-O-[ (3-C-acetoxymethyl) -2,3-di-O-acetyl-β-D-erythrofuranosyl)-β-D-glucopyranose was obtained by Kochetkov glycosylation of a branched-chain tetrofuranose cyanoethylidene derivative. The NMR data (1H and 13C) of the synthetic compounds and the glycosylation shifts of the apiose moiety are reported.