38242-02-3

Usage

Uses

Used in Pharmaceutical Applications:
β-Amyrenonol is used as a therapeutic agent for its anti-inflammatory, antioxidant, and anti-cancer properties. It has been investigated for the treatment of arthritis, prostate cancer, and other inflammatory conditions, demonstrating potential in alleviating symptoms and improving patient outcomes.
Used in Cosmetic and Skincare Industry:
β-Amyrenonol is used as an active ingredient in cosmetic and skincare products for its anti-aging and skin-protective effects. It contributes to maintaining skin health, reducing the appearance of wrinkles, and providing protection against environmental stressors.
Further research is needed to better understand the mechanisms of action of β-Amyrenonol and to explore its potential clinical uses in various applications.

Upstream product

• 107657-18-1 3β-hydroxyolean-12-en-11-one acetate 
• 2118-84-5 3β-benzoyloxy-oleanen-(12)-one-(11) 
• 71-43-2 benzene 
• 559-70-6 beta-amyrin 

Downstream Products

• 94530-87-7 3β-hydroxy-olean-9(11),12-diene 
• 41694-47-7 3β-benzoyloxy-oleana-9(11),12-diene 
• 107657-18-1 3β-hydroxyolean-12-en-11-one acetate 

Relevant academic research and scientific papers

Rearrangement and oxidation of β-amyrin promoted by growing cells of Lecanicillium muscarinium

Microbial transformation of β-amyrin by growing cells of the fungus Lecanicillium muscarinium (former Cephalosporium aphidicola) was successfully accomplished after 15 days of incubation with orbital shaking at 120 rpm. Two products purified by column chr

Triterpene esters: Natural products from dorstenia arifolia (moraceae)

The phytochemical study of Dorstenia arifolia Lam. (Moraceae) has led to the identification of 18 triterpenes esterified by fatty acids, five triterpenes without esterification, 12 triterpenes esterified by acetic acid, together with a known furanocoumarin: α-amyrin (1), β-amyrin (2) α-amyrin acetate (3) β-amyrin acetate (4), α-amyrin octanoate (5), β-amyrin octanoate (6), α-amyrin decanoate (7), β-amyrin decanoate (8), α-amyrin dodecanoate (9), β-amyrin dodecanoate (10), α-amyrin tetradecanoate (11), β-amyrin tetradecanoate (12), α-amyrin hexadecanoate (13), β-amyrin hexadecanoate (14), glutinol (15), glutinyl acetate (16), 11-oxo-α-amyrin (17), 11-oxo-β-amyrin (18), 11-oxo-α-amyrin acetate (19), 11-oxo- β-amyrin acetate (20) 11-oxo-α-amyrin octanoate (21) 11-oxo-β-amyrin octanoate (22), 11-oxo-α-amyrin decanoate (23), 11-oxo-β-amyrin decanoate (24) 11-oxo-α-amyrin dodecanoate (25) 11-oxo-β-amyrin dodecanoate (26), ursa-9(11),12-dien-3-yl acetate (27), oleana-9(11),12-dien-3-yl acetate (28), ursa-9(11),12-dien-3-yl decanoate (29), oleana- 9(11),12-dien-3-yl decanoate (30), 12,13-epoxyolean-3-yl acetate (31), 12,13-epoxyolean- 9(11)en-3-yl acetate (32), taraxeryl acetate (33), lupenyl acetate (34), lanosta-8,24-dien-3- yl acetate (35) and psoralen (36). The identification of the triterpene compounds isolated as isomeric mixtures obtained from the hexane extract was based mainly in mass spectra and 13C-NMR data. The long-chain alkanoic acid esters of the triterpenes α- and β-amyrin; 11-oxo-α- and 11-oxo-β-amyrin; ursa- and olean-9(11),12-dien-3-yl; have not been reported before in the literature as constituents of the Dorstenia genus.

Functionalisation of Saturated Hydrocarbons. Part 6. Selective Oxidation of Steroids and Related Compounds

The oxidation of a series of steroids by the Gif system gives, almost without exception, the 20-ketone as major isolated product.The side-chain cleavage is made more selective by modification of rings A or B.The oxidation of oleana-1,12-diene-3,11-dione has also been studied and the two principal products have been identified.