471-67-0 Usage
Triterpene compound
18BETA(H)-OLEANANE is a compound derived from plants, specifically from the triterpenoid group.
Ursane type
It belongs to the ursane type of triterpenoids, which is a subgroup of triterpenes.
Molecular structure
The compound has a unique molecular structure that includes a pentacyclic ring system.
Biological activities
18BETA(H)-OLEANANE has been found to possess various biological activities, such as anti-inflammatory, anti-tumor, and antiviral properties.
Wound healing
The compound has shown potential in promoting wound healing.
Oxidative stress protection
18BETA(H)-OLEANANE has been found to protect against oxidative stress.
Therapeutic potential
Studies have suggested that 18BETA(H)-OLEANANE may have a therapeutic potential in treating a range of diseases, making it an interesting target for further research and potential pharmaceutical development.
Check Digit Verification of cas no
The CAS Registry Mumber 471-67-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 471-67:
(5*4)+(4*7)+(3*1)+(2*6)+(1*7)=70
70 % 10 = 0
So 471-67-0 is a valid CAS Registry Number.
471-67-0Relevant articles and documents
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Ruzicka et al.
, (1938)
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Reduction of Steroid and Triterpenoid α,β-Unsaturated Ketones with Lithium/Ethylenediamine
Pradhan, Bhim Prasad,Chakraborty, Satyajit
, p. 263 - 265 (2007/10/02)
Reduction of less sterically hindered ketone, glochidone (1) with lithium/ethylenediamine (Li/EDA) leads to the reduction of the double bond followed by that of the carbonyl group to afford thermodynamically stable alcohol, lupanol (1b).The sterically hindered α,β-unsaturated ketones such as 11-keto-triterpenoids also furnish saturated alcohols but in small proportions; the other compounds formed are obtained with reduction of the carbonyl group accompanied by dehydration or even deoxygenation.