892869-59-9 Usage
Description
(2Z)-2-(Hydroxymethylene)-3-oxoolean-12-en-28-oic acid phenylmethyl ester, also known as ursolic acid phenylmethyl ester, is a chemical compound derived from ursolic acid, a naturally occurring triterpenoid found in various plant sources. It is characterized by a hydroxymethylene group and a ketone group, and is typically esterified with a phenylmethyl ester. Ursolic acid phenylmethyl ester has been studied for its potential pharmacological properties, including anti-inflammatory, anti-cancer, and anti-diabetic effects. It has also shown promise as a potential therapeutic agent for various diseases and conditions, making it a subject of ongoing research in the field of medicinal chemistry and drug development.
Uses
Used in Pharmaceutical Industry:
Ursolic acid phenylmethyl ester is used as a potential therapeutic agent for various diseases and conditions due to its pharmacological properties, such as anti-inflammatory, anti-cancer, and anti-diabetic effects.
Used in Drug Development:
Ursolic acid phenylmethyl ester is used as a subject of ongoing research in the field of medicinal chemistry and drug development, as it has shown promise as a potential therapeutic agent for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 892869-59-9 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, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 892869-59:
(8*8)+(7*9)+(6*2)+(5*8)+(4*6)+(3*9)+(2*5)+(1*9)=249
249 % 10 = 9
So 892869-59-9 is a valid CAS Registry Number.
InChI:InChI=1/C38H52O4/c1-33(2)17-19-38(32(41)42-24-25-11-9-8-10-12-25)20-18-36(6)27(28(38)22-33)13-14-30-35(5)21-26(23-39)31(40)34(3,4)29(35)15-16-37(30,36)7/h8-13,23,28-30,39H,14-22,24H2,1-7H3/b26-23-/t28-,29-,30+,35-,36+,37+,38-/m0/s1
892869-59-9Relevant 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.