38242-02-3 Usage
General Description
β-Amyrenonol, also known as 9β-Hydroxy β-amyrin, is a triterpenoid compound found in a variety of plant species. It is a derivative of β-amyrin, a common plant-derived compound with various pharmacological activities. β-Amyrenonol has been found to exhibit anti-inflammatory, antioxidant, and anti-cancer properties in various in vitro and in vivo studies. It has also been investigated for its potential role in the treatment of arthritis, prostate cancer, and other inflammatory conditions. Additionally, β-Amyrenonol has shown potential for use in cosmetic and skincare products due to its anti-aging and skin-protective effects. Overall, β-Amyrenonol is a promising compound with potential therapeutic and cosmetic applications, and further research is needed to better understand its mechanisms of action and potential clinical uses.
Check Digit Verification of cas no
The CAS Registry Mumber 38242-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,4 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38242-02:
(7*3)+(6*8)+(5*2)+(4*4)+(3*2)+(2*0)+(1*2)=103
103 % 10 = 3
So 38242-02-3 is a valid CAS Registry Number.
38242-02-3Relevant articles and documents
Rearrangement and oxidation of β-amyrin promoted by growing cells of Lecanicillium muscarinium
Martins, Leonardo Ribeiro,Takahashi, Jacqueline Aparecida
, p. 767 - 774 (2010)
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
Functionalisation of Saturated Hydrocarbons. Part 6. Selective Oxidation of Steroids and Related Compounds
Barton, Derek H. R.,Boivin, Jean,Hill, Christopher H.
, p. 1797 - 1804 (2007/10/02)
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.
