87355-32-6 Usage
General Description
Lupeolic acid is a naturally occurring pentacyclic triterpenoid compound that is found in a variety of plants, including fruits, vegetables, and medicinal herbs. It has been studied for its potential biological activities, including anti-inflammatory, antioxidant, anti-tumor, and antimicrobial properties. Lupeolic acid has shown promising results in inhibiting the growth of cancer cells and reducing inflammation in several preclinical studies. Additionally, it has been suggested to have potential therapeutic effects in treating conditions such as diabetes, obesity, and cardiovascular diseases. Overall, lupeolic acid is a compound with diverse pharmacological properties that may have potential applications in the development of new drugs and treatments for various diseases.
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
