22425-82-7 Usage
Description
Methyl maslinate is a flavonoid, a type of organic compound, that is naturally found in various plants and fruits such as apples, strawberries, and grapes. It has been studied for its potential therapeutic properties, including antioxidant, anti-inflammatory, and anti-cancer effects, as well as its potential role in promoting cardiovascular health and preventing age-related diseases. Researchers are interested in this compound due to its diverse biological activities and potential health benefits, but further studies are needed to fully understand its mechanisms of action and potential applications in medicine and nutrition.
Uses
Used in Pharmaceutical Industry:
Methyl maslinate is used as a therapeutic agent for its potential antioxidant, anti-inflammatory, and anti-cancer effects. Its diverse biological activities make it a promising candidate for the development of new medications.
Used in Nutrition Industry:
Methyl maslinate is used as a nutritional supplement for its potential health benefits, including promoting cardiovascular health and preventing age-related diseases. Its presence in various fruits makes it a natural and appealing option for consumers seeking to improve their overall health.
Used in Research:
Methyl maslinate is used as a subject of study in scientific research to further understand its mechanisms of action and explore its potential applications in medicine and nutrition. As more is learned about this compound, it may lead to the development of new treatments and preventative measures for various health conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 22425-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,2 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22425-82:
(7*2)+(6*2)+(5*4)+(4*2)+(3*5)+(2*8)+(1*2)=87
87 % 10 = 7
So 22425-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C31H50O4/c1-26(2)13-15-31(25(34)35-8)16-14-29(6)19(20(31)17-26)9-10-23-28(5)18-21(32)24(33)27(3,4)22(28)11-12-30(23,29)7/h9,20-24,32-33H,10-18H2,1-8H3/t20-,21-,22?,23-,24+,28+,29-,30-,31+/m1/s1
22425-82-7Relevant articles and documents
Different pathways for the deoxygenation of the A-ring of natural triterpene compounds
Parra, Andres,Lopez, Pilar E.,Garcia-Granados, Andres
scheme or table, p. 177 - 196 (2010/05/18)
Some deoxygenation pathways were tested to remove the hydroxyl groups of the natural triterpenes oleanolic acid and maslinic acid to obtain a practical starting material for the semisynthesis of other interesting organic synthons. Different deoxygenation processes were carried out starting from these triterpenic acids or from several derivatives such as methyl esters and epoxy derivatives. The hydroxyl groups were transformed into some intermediate compounds including xanthyl, thiocarbonyl or tosyl derivatives. The opening of the oxirane ring between C-2 and C-3 was also achieved through different methods using deoxygenating reagents such as Me3SiCl/NaI, WCl 4/n-BuLi and Cp2TiCl.
Further triterpenes from Melissa officinalis L
Brieskorn,Krause
, p. 603 - 612 (2007/10/11)
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