155301-58-9 Usage
General Description
Alisol E 23-acetate, also known as 23-acetylalisol E, is a natural triterpenoid compound found in the roots of the medicinal plant Alisma orientale. It has been traditionally used in Chinese medicine for its anti-inflammatory, anti-tumor, and anti-osteoporotic properties. Studies have shown that Alisol E 23-acetate has potential therapeutic effects in treating liver diseases, cardiovascular diseases, and inflammatory disorders. It has also demonstrated hepatoprotective and neuroprotective activities, making it a promising candidate for the development of new pharmaceutical drugs. Additionally, it has been investigated for its potential role in the treatment of metabolic diseases such as obesity and diabetes. Overall, Alisol E 23-acetate shows promise as a versatile and potent natural compound with numerous potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 155301-58-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,3,0 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155301-58:
(8*1)+(7*5)+(6*5)+(5*3)+(4*0)+(3*1)+(2*5)+(1*8)=109
109 % 10 = 9
So 155301-58-9 is a valid CAS Registry Number.
155301-58-9Relevant articles and documents
Stability and structure studies on alisol A 24-acetate
Makabel, Bolat,Zhao, Yuying,Wang, Bin,Bai, Yanjing,Zhang, Qingying,Wu, Li,Lv, Yang
, p. 41 - 45 (2008)
Alisol A 24-acetate is one of the main active triterpenoid compounds isolated from Rhizoma Alismatis, which is a famous Traditional Chinese Medicine, and has been determined for the quality control of this crude drug. In this study, alisol A 24-acetate was found to be unstable in solvents and its stability in different solvents was investigated in detail. The results showed that alisol A 24-acetate and 23-acetate inter-transformed in solvents and the transformation rate was more rapid in protic solvents than in aprotic solvents. Moreover, both alisol A 24-acetate and 23-acetate were deacetylated to yield alisol A when kept in methanol for a long time. This is the first report on the structural transformation between alisol A 24-acetate, alisol A 23-acetate and alisol A. In addition, the single crystal X-ray structure of alisol A 24-acetate and the NMR data of alisol A 23-acetate were also reported for the first time.
