61854-36-2 Usage
Description
DeMethoxycapillarisin is a flavonoid derivative found in the Artemisia capillaris Thunberg, a plant widely used in traditional Chinese medicine. It exhibits various biological activities, such as anti-inflammatory, anti-oxidative, and hepatoprotective effects, making it a promising compound for therapeutic applications.
Used in Pharmaceutical Industry:
DeMethoxycapillarisin is used as a therapeutic agent for the treatment of liver diseases, as it effectively reduces hepatic inflammation and oxidative stress, thereby protecting the liver from damage.
Used in Anticancer Applications:
DeMethoxycapillarisin is used as an anticancer agent, showing potential in inhibiting the growth of cancer cells. Its pharmacological activities make it a promising candidate for further research and development in cancer treatment.
Used in Traditional Chinese Medicine:
DeMethoxycapillarisin is used as a key component in traditional Chinese medicine formulations, leveraging its anti-inflammatory, anti-oxidative, and hepatoprotective properties to treat various health conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 61854-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,5 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61854-36:
(7*6)+(6*1)+(5*8)+(4*5)+(3*4)+(2*3)+(1*6)=132
132 % 10 = 2
So 61854-36-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H10O6/c16-8-1-3-10(4-2-8)20-14-7-12(19)15-11(18)5-9(17)6-13(15)21-14/h1-7,16-18H
61854-36-2Relevant articles and documents
Synthesis of Demethoxycapillarisin, a Naturally Occurring 2-Phenoxychromone, and Related Compounds
Takeno, Hidekazu,Hashimoto, Masashi,Koma, Yoshiyasu,Horiai, Haruo,Kikuchi, Hiroyuki
, p. 474 - 475 (2007/10/02)
Demethoxycapillarisin (1), a naturally occurring 2-phenoxychromone, and the related compounds (2) - (4) have been synthesized via a route involving, as a key step, an intramolecular Wittig reaction between a phosphorus ylide and a carbonate.