20248-08-2 Usage
Description
α-Amyrenone is a triterpenoid compound found in various plant species, such as the bark of the White birch tree (Betula pubescens) and the resin of the gumbo-limbo tree (Bursera simaruba). It is recognized for its bioactive properties, including anti-inflammatory, antioxidant, and anticancer activities, making it a promising candidate for the development of new drugs and natural products for various diseases. Additionally, its antioxidant properties have attracted interest in the cosmetic and skincare industry.
Uses
Used in Pharmaceutical Industry:
α-Amyrenone is used as a potential therapeutic agent for various diseases due to its anti-inflammatory, antioxidant, and anticancer properties. It is being studied for its potential in the development of new drugs and natural products that can target a range of health conditions.
Used in Cosmetic and Skincare Industry:
α-Amyrenone is used as an ingredient in cosmetic and skincare products for its antioxidant properties. Its ability to protect the skin from oxidative stress and promote overall skin health makes it a valuable component in formulations aimed at maintaining youthful and radiant skin.
Check Digit Verification of cas no
The CAS Registry Mumber 20248-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,4 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20248-08:
(7*2)+(6*0)+(5*2)+(4*4)+(3*8)+(2*0)+(1*8)=72
72 % 10 = 2
So 20248-08-2 is a valid CAS Registry Number.
20248-08-2Relevant articles and documents
Hepatoprotective triterpenes from Sedum sarmentosum
He, Aimin,Wang, Mingshi,Hao, Hongyan,Zhang, Decheng,Lee, Kuo-Hsiung
, p. 2607 - 2610 (1998)
The known δ-amyrone, 3-epi-δ-amyrin, δ-amyrin as well as a new hydroperoxy triterpene, 18β-hydroperoxy-olean-12-en-3-one (named sarmentolin) were isolated as hepatoprotective agents from Sedum sarmentosum. Their structures were elucidated by spectral analysis and chemical reactions.