23094-71-5 Usage
General Description
Chebulagic acid is a chemical compound found in the fruits of the Terminalia chebula tree, commonly known as black myrobalan. It belongs to a class of compounds called hydrolyzable tannins, which are known for their antioxidant and anti-inflammatory properties. Chebulagic acid has been shown to possess a wide range of biological activities, including anti-cancer, anti-diabetic, anti-bacterial, and anti-viral effects. It has also demonstrated potential for protecting against liver damage and promoting wound healing. Chebulagic acid is being studied for its potential therapeutic applications in various diseases and conditions, and its natural source in Terminalia chebula has made it an attractive target for further research into its health benefits.
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 articles and documents
Glutathione-mediated conversion of the ellagitannin geraniin into chebulagic acid
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.
