105330-59-4 Usage
Description
(2R,3S)-3,4-Dihydro-2-(3-hydroxy-4-methoxyphenyl)-5,7-dimethoxy-2H-1-benzopyran-3-ol, commonly known as dihydromorin, is a naturally occurring phenolic compound belonging to the flavonoid class. It is found in plants such as Morus alba and is recognized for its antioxidant properties. Dihydromorin has garnered attention for its potential health benefits, which include anti-inflammatory, anti-cancer, and cardioprotective effects. Additionally, it has been studied for its possible role in managing diabetes and obesity, making it a compound of interest for researchers exploring natural bioactive substances for medicinal applications.
Uses
Used in Pharmaceutical Development:
Dihydromorin is utilized as a key component in the development of new pharmaceuticals or supplements due to its diverse range of health benefits. Its antioxidant properties, along with its anti-inflammatory, anti-cancer, and cardioprotective effects, make it a promising candidate for the treatment and prevention of various diseases.
Used in Anti-Inflammatory Applications:
In the field of anti-inflammatory research, dihydromorin is employed for its potential to reduce inflammation, which is a common factor in many chronic diseases. Its natural anti-inflammatory properties could offer a safer alternative to synthetic drugs.
Used in Anti-Cancer Applications:
Dihydromorin is used as an anti-cancer agent, where it may contribute to the inhibition of tumor growth and the prevention of cancer progression. Its natural bioactivity could be harnessed to develop novel cancer therapies or to complement existing treatments.
Used in Cardiovascular Health:
In the cardiovascular health industry, dihydromorin is used for its cardioprotective effects, potentially reducing the risk of heart diseases by improving vascular health and reducing inflammation associated with cardiovascular conditions.
Used in Diabetes and Obesity Management:
Dihydromorin is used in the management of diabetes and obesity, where its potential to regulate blood sugar levels and influence metabolic processes could offer natural support for individuals with these conditions, contributing to better health outcomes.
Each of these applications highlights the versatility and potential of dihydromorin as a natural compound with significant implications for human health and the development of future therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 105330-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,3 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105330-59:
(8*1)+(7*0)+(6*5)+(5*3)+(4*3)+(3*0)+(2*5)+(1*9)=84
84 % 10 = 4
So 105330-59-4 is a valid CAS Registry Number.
105330-59-4Relevant articles and documents
An efficient synthesis of the four mono methylated isomers of (+)-catechin including the major metabolites and of some dimethylated and trimethylated analogues through selective protection of the catechol ring
Cren-Olive, Cecile,Lebrun, Stephane,Rolando, Christian
, p. 821 - 830 (2007/10/03)
The four monomethylated isomers of (+)-catechin in positions 3′, 4′, 5 and 7, two dimethylated derivatives, the 5,7-dimethylcatechin and the 3′, 4′-dimethylcatechin and two trimethylated isomers of (+)-catechin in positions 3′, 5, 7 and 4′, 5, 7 were synthesized by a new method based on successive and selective protections of the various phenol functions present on (+)-catechin. The key step was the selective protection of the catechol ring with dichlorodiphenylmethane and di-tert-butyldichlorosilane.
