87355-32-6 Usage
Description
Lupeolic acid is a naturally occurring pentacyclic triterpenoid compound found in a variety of plants, including fruits, vegetables, and medicinal herbs. It possesses diverse pharmacological properties, such as anti-inflammatory, antioxidant, anti-tumor, and antimicrobial activities, making it a promising candidate for the development of new drugs and treatments for various diseases.
Uses
Used in Pharmaceutical Industry:
Lupeolic acid is used as an anti-inflammatory agent for its ability to reduce inflammation in several preclinical studies. It is also used as an antioxidant, protecting cells from oxidative damage and potentially contributing to the prevention of various diseases.
Used in Oncology:
Lupeolic acid is used as an anti-tumor agent for its potential to inhibit the growth of cancer cells. It has shown promising results in preclinical studies, suggesting its potential use in the development of new cancer treatments.
Used in Metabolic Diseases Treatment:
Lupeolic acid is used as a therapeutic agent for treating conditions such as diabetes, obesity, and cardiovascular diseases due to its potential therapeutic effects in managing these conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 87355-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,5 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87355-32:
(7*8)+(6*7)+(5*3)+(4*5)+(3*5)+(2*3)+(1*2)=156
156 % 10 = 6
So 87355-32-6 is a valid CAS Registry Number.
87355-32-6Relevant articles and documents
Structural analysis of 3-α-acetyl-20(29)-lupene-24-oic acid, a novel pentacyclic triterpene isolated from the gum resin of Boswellia serrata, by NMR spectroscopy
Belsner, Klaus,Buechele, Berthold,Werz, Udo,Simmet, Thomas
, p. 629 - 632 (2003)
3α-Acetyl-20(29)-lupene-24-oic acid (1) was isolated from the gum resin of Boswellia serrata. Its presence evidently suggests, that the oxidosqualene triterpene pathway of Boswellia serrata closely resembles the biosynthetic route already found in other plants. Complete 1H and 13C spectral assignments were derived from 1D and 2D NMR spectra. This is the first compound with the lupene backbone combining a 3α-hydroxy or 3α-acetyl group with the 24-carboxyl group, a configuration which is typical of the classical boswellic acids. Copyright
