19533-92-7 Usage
Description
2α,3β-Dihydroxylup-20(29)-en-28-oic acid is a pentacyclic triterpenoid compound characterized by the presence of an additional alpha-hydroxy group at position 2 on the betulinic acid structure. This unique feature distinguishes it from other triterpenoids and suggests potential biological activities and applications. It has been isolated from the plant Breynia fruticosa, indicating its natural occurrence and potential for extraction and utilization in various industries.
Uses
Used in Pharmaceutical Industry:
2α,3β-Dihydroxylup-20(29)-en-28-oic acid is used as a pharmaceutical compound for its potential therapeutic properties. The presence of the alpha-hydroxy group at position 2 may confer specific biological activities, such as anti-inflammatory, anti-tumor, or anti-viral effects. Further research and development are needed to explore its full potential and optimize its use in drug formulations.
Used in Cosmetic Industry:
In the cosmetic industry, 2α,3β-Dihydroxylup-20(29)-en-28-oic acid may be used as an active ingredient in skincare products due to its triterpenoid nature. Triterpenoids are known for their beneficial effects on the skin, such as moisturizing, anti-aging, and soothing properties. The additional alpha-hydroxy group could enhance these effects, making it a valuable component in cosmetic formulations.
Used in Nutraceutical Industry:
2α,3β-Dihydroxylup-20(29)-en-28-oic acid can also be utilized in the nutraceutical industry as a dietary supplement or functional food ingredient. Its potential health benefits, such as anti-inflammatory and anti-oxidative properties, could be harnessed to promote overall wellness and support specific health conditions when incorporated into nutraceutical products.
Used in Agricultural Industry:
In agriculture, 2α,3β-Dihydroxylup-20(29)-en-28-oic acid may find applications as a natural pesticide or growth promoter. Its potential biological activities could be leveraged to protect crops from pests or to enhance plant growth and yield. Further research is required to determine its efficacy and safety in agricultural settings.
Check Digit Verification of cas no
The CAS Registry Mumber 19533-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,3 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19533-92:
(7*1)+(6*9)+(5*5)+(4*3)+(3*3)+(2*9)+(1*2)=127
127 % 10 = 7
So 19533-92-7 is a valid CAS Registry Number.
19533-92-7Relevant articles and documents
Expedient Synthesis of Alphitolic Acid and Its Naturally Occurring 2- O-Ester Derivatives
Park, Somin,Cho, Jihee,Jeon, Hongjun,Sung, Sang Hyun,Lee, Seunghee,Kim, Sanghee
, p. 895 - 902 (2019/05/14)
The expedient synthesis of alphitolic acid (1) as well as its natural C-3-epimer and 2-O-ester derivatives was accomplished in a few steps from the readily commercially available betulin (9). A Rubottom oxidation delivered an α-hydroxy group in a stereo- and chemoselective manner. The diastereoselective reduction of the α-hydroxy ketone was key to accessing the 1,2-diol moiety of this class of natural products. Our concise and stereoselective synthetic protocol allowed the gram-scale synthesis of these natural products, which will facilitate future biological evaluations.
Efficient access to isomeric 2,3-dihydroxy lupanes: first synthesis of alphitolic acid
Hao, Jia,Zhang, Xueli,Zhang, Pu,Liu, Jun,Zhang, Luyong,Sun, Hongbin
experimental part, p. 7975 - 7984 (2009/12/06)
Alphitolic acid (3) is a naturally occurring lupane type of pentacyclic triterpene, which possesses various pharmacological properties. Efficient synthesis of 3 has been accomplished in 10 steps with an overall yield of 19% starting from the readily avail
