892869-60-2 Usage
Description
Oleana-2,12-dieno[2,3-d]isoxazol-28-oic acid phenylmethyl ester is a complex chemical compound belonging to the triterpenoids class, featuring an oleanolic acid core and an isoxazole ring. Oleana-2,12-dieno[2,3-d]isoxazol-28-oic acid phenylmethyl ester is known for its potential pharmaceutical properties, with the phenylmethyl ester functional group enhancing its solubility and stability.
Uses
Used in Pharmaceutical Industry:
Oleana-2,12-dieno[2,3-d]isoxazol-28-oic acid phenylmethyl ester is used as a potential drug candidate due to its anti-inflammatory and antioxidant activities. Its development is aimed at creating new therapeutic agents that can address various health conditions, leveraging its beneficial properties to improve patient outcomes.
Further research is necessary to fully explore the pharmacological properties and potential therapeutic applications of Oleana-2,12-dieno[2,3-d]isoxazol-28-oic acid phenylmethyl ester, ensuring its safety and efficacy in treating specific medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 892869-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,2,8,6 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 892869-60:
(8*8)+(7*9)+(6*2)+(5*8)+(4*6)+(3*9)+(2*6)+(1*0)=242
242 % 10 = 2
So 892869-60-2 is a valid CAS Registry Number.
892869-60-2Relevant articles and documents
Pentacyclic triterpenes. Part 3: Synthesis and biological evaluation of oleanolic acid derivatives as novel inhibitors of glycogen phosphorylase
Chen, Jun,Liu, Jun,Zhang, Luyong,Wu, Guanzhong,Hua, Weiyi,Wu, Xiaoming,Sun, Hongbin
, p. 2915 - 2919 (2007/10/03)
Oleanolic acid and its synthetic derivatives have been identified as novel inhibitors of glycogen phosphorylase. Within this series of compounds, 4 (IC50 = 3.3 μM) is the most potent GPa inhibitor. Preliminary structure-activity relationships of the oleanolic acid derivatives are discussed.