132185-84-3 Usage
Description
5beta-Hydroxycostic acid, also known as (2R,4aR,8aS)-Decahydro-8a-hydroxy-4a-methyl-α,8-bis(methylene)-2-naphthaleneacetic acid, is a naturally occurring organic compound extracted from the roots of Saussurea lappa and Laggera pterodonta. It is characterized by its unique chemical structure and may possess anti-viral properties.
Uses
Used in Traditional Chinese Medicine:
5beta-Hydroxycostic acid is used as a traditional Chinese medicine ingredient for its potential therapeutic effects. It is believed to have various health benefits, including anti-viral properties, which may help in treating certain viral infections.
Used in Pharmaceutical Industry:
5beta-Hydroxycostic acid is used as a pharmaceutical compound for its potential anti-viral properties. It may be utilized in the development of new drugs or therapies to combat viral infections, offering an alternative to conventional treatments.
Used in Cosmetics Industry:
5beta-Hydroxycostic acid may be used as an active ingredient in cosmetics for its potential skin health benefits. Its anti-viral properties could be harnessed to create products that promote skin health and protect against harmful viral infections.
Used in Research and Development:
5beta-Hydroxycostic acid is used as a research compound for further investigation into its properties and potential applications. Scientists and researchers may study its chemical structure, anti-viral effects, and other possible uses to expand our understanding of this compound and its potential benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 132185-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,1,8 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132185-84:
(8*1)+(7*3)+(6*2)+(5*1)+(4*8)+(3*5)+(2*8)+(1*4)=113
113 % 10 = 3
So 132185-84-3 is a valid CAS Registry Number.
132185-84-3Relevant articles and documents
Eudesmane and megastigmane glucosides from Laggera alata
Zheng, Qunxiong,Xu, Zhaojun,Sun, Xianfeng,Yao, Wei,Sun, Handong,Cheng, Christopher H. K.,Zhao, Yu
, p. 835 - 839 (2007/10/03)
Four eudesmane glucosides, alatosides A-D (1-4), and one megastigmane glucoside, alatoside E (5), were isolated from the BuOH fraction of Laggera alata along with six known compounds. Structures of the new compounds were elucidated by a combination of chemical and spectroscopic methods. Alatosides A-E were characterized as: 1α-O-(β-D-glucopyranosyloxyl)-7-epi-eudesma-11-en-2β, 4α-diol (1), 2β-O-(β-D-glucopyranosyloxyl)-eudesma-4α-hydroxyl-11(13)- en-12-oic-acid (2), 5β-O-β-D-glucopyranosyloxyl)-eudesma-4(15), 11(13)-dien-12-oic-acid (3), 5α-O-(β-D-glucopyranosyloxyl)-eudesma-3,11 (13)-dien-12-oic acid (4) and 3β-O-(β-D-glucopyranosyloxyl)-megastigma-9-one (5), respectively. Based on the chemical characteristics of eudesmane derivatives isolated from the Laggera genus, it was suggested that there are probably two different biogenetic pathways for these secondary metabolites in this genus.
