2111-46-8 Usage
Chemical Class
Triterpenoids
Triterpenoids are a large group of naturally occurring organic compounds derived from plants and fungi.
Pharmacological Activities
Anti-inflammatory, antioxidant, and anti-cancer properties
These activities suggest potential therapeutic uses in various medical conditions.
Medicinal Applications
Treating diabetes and cardiovascular diseases
The compound's properties may help manage or alleviate symptoms of these conditions.
Drug Candidate
Studied for potential use in pharmaceutical research
Its diverse biological activities make it a promising candidate for further research and development.
Natural Source
Derived from plants and fungi
The compound is sourced from natural organisms, which may contribute to its potential therapeutic benefits.
Significance in Medicinal Chemistry
Represents a significant area of interest
The compound's versatile biological activities make it a valuable subject for research in the field of medicinal chemistry and drug development.
Chemical Structure
11α,12α-Epoxy-13α-methyl-27-noroleana-14-ene-3β-ol acetate
This complex structure is responsible for the compound's various pharmacological properties and potential applications.
Acetate Derivative
The compound is an acetate ester
The acetate group may influence the compound's solubility, stability, or biological activity.
Stereochemistry
Contains multiple stereocenters (α and β)
The stereochemistry of the compound can affect its biological activity and interactions with target molecules.
Functional Groups
Epoxy, methyl, and acetate groups
Biological Target
Potential interactions with various cellular receptors or enzymes
The compound may exert its pharmacological effects by interacting with specific biological targets.
Synthetic Methods
May involve chemical synthesis or extraction from natural sources
The methods used to obtain the compound can impact its purity, yield, and potential for large-scale production.
Check Digit Verification of cas no
The CAS Registry Mumber 2111-46-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2111-46:
(6*2)+(5*1)+(4*1)+(3*1)+(2*4)+(1*6)=38
38 % 10 = 8
So 2111-46-8 is a valid CAS Registry Number.
2111-46-8Relevant articles and documents
STUDIES ON OXIDATI0N OF TRITERPENOIDS: PART VII. TRANSFORMATION OF OLEANANE AND URSANE SKELETONS TO 11α,12α-OXIDOTRITERPENOIDS WITH HYDROGEN PEROXIDE AND SELENIUM DIOXIDE AND THEIR CARBON-13 NMR DATA.
Pradhan, Bhim Prasad,Chakraborty, Satyajit,Weyerstahl, Peter
, p. 4487 - 4496 (2007/10/02)
Hydrogen peroxide-selenium dioxide in t-butanol has been found to be a good reagent for the preparation of 11α,12α-oxidotriterpenoids of oleanane and ursane skeletons; whereas α-amyrin and β-amyrin acetates furnished 11α,12α-epoxyurs-14-en-3β-yl acetate (4c) and 11α,12α-epoxytaraxer-14-en-3β-yl acetate (4a) respectively, uvaol and ursolic acid/methyl ester gave 11α,12α-epoxyurs-28->13-olide-3β-ol (5d); erythrodiol (3c) and oleanolic acid (3b)/methyl ester (3d) afforded 11α,12α-epoxy-oleanan-28->13-olide-3β-ol (5); olean-12-en-2α,3β,28-yl triacetate (3j) on similar reaction furnished 11α,12α-epoxytaraxer-14-en-3β-ol-2α,28-yl diacetate (4d) and 11α,12α-epoxytaraxer-14-en-2α,3β-diol-28-ylacetate (4e).
