23094-71-5 Usage
Uses
Used in Pharmaceutical Applications:
Chebulagic acid is used as a therapeutic agent for its anti-cancer properties, targeting a variety of cancer types through its multifaceted biological activities. It also serves as an anti-diabetic, anti-bacterial, and anti-viral agent, leveraging its broad-spectrum biological effects for the treatment and management of different health conditions.
Used in Nutraceutical Applications:
Given its antioxidant and anti-inflammatory properties, chebulagic acid is used as a dietary supplement to promote overall health and well-being, potentially reducing the risk of various diseases associated with oxidative stress and inflammation.
Used in Cosmetic Applications:
The anti-inflammatory and wound healing properties of chebulagic acid make it a valuable ingredient in cosmetic products, particularly those aimed at skin health and regeneration.
Used in Food and Beverage Industry:
Chebulagic acid's antioxidant properties can be utilized in the food and beverage industry to enhance the shelf life of products and contribute to their nutritional value.
Used in Agricultural Applications:
As an anti-bacterial and anti-viral agent, chebulagic acid can be employed in agriculture to improve crop health and resistance against various pathogens, thereby increasing yield and quality.
Each of these applications takes advantage of the unique properties of chebulagic acid, highlighting its potential as a versatile compound for use across multiple industries.
Check Digit Verification of cas no
The CAS Registry Mumber 23094-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,9 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23094-71:
(7*2)+(6*3)+(5*0)+(4*9)+(3*4)+(2*7)+(1*1)=95
95 % 10 = 5
So 23094-71-5 is a valid CAS Registry Number.
23094-71-5Relevant academic research and scientific papers
Tanaka, Takashi,Kouno, Isao,Nonaka, Gen-Ichiro
, p. 34 - 40 (1996)
Geraniin (1), a widely distributed ellagitannin having a dehydrohexahydroxydiphenoyl (DHHDP) ester moiety, was converted into chebulagic acid (2), an ellagitannin having a chebuloyl ester moiety, which was reported to be a potent inhibitor of DNA topoisomerases. This was achieved by addition of the thiol group of glutathione to the six-membered acetal ring form of the DHHDP moiety (1a) with concomitant hydrolytic ring cleavage and subsequent reductive desulfurization with Raney nickel. The concurrent addition of the thiol to the five-membered acetal ring form of the DHHDP group (1b) generated the product 14 and its precursor 13, which are structurally related to naturally occurring ellagitannins isolated from Euphorbiaceous plants. Thus, the rearrangements observed in these reactions may be relevant to the metabolism of DHHDP esters in plants.
