CAS 20248-08-2
:α-Amyrenone
Description:
α-Amyrenone is a triterpenoid compound characterized by its pentacyclic structure, which is derived from the natural product α-amyrin. It is typically found in various plant species and is known for its potential biological activities, including anti-inflammatory and antimicrobial properties. The molecular formula of α-Amyrenone reflects its complex structure, and it exhibits a melting point that indicates its solid state at room temperature. This compound is often studied for its role in traditional medicine and its potential applications in pharmaceuticals. In terms of solubility, α-Amyrenone is generally more soluble in organic solvents than in water, which is common for many terpenoids. Its chemical behavior can be influenced by the presence of functional groups, making it a subject of interest in organic synthesis and natural product chemistry. Overall, α-Amyrenone represents a significant compound in the study of natural products and their applications in health and industry.
Formula:C30H48O
InChI:InChI=1S/C30H48O/c1-25(2)15-16-27(5)17-18-29(7)20(21(27)19-25)9-10-23-28(6)13-12-24(31)26(3,4)22(28)11-14-30(23,29)8/h22-23H,9-19H2,1-8H3/t22-,23+,27+,28-,29+,30+/m0/s1
InChI key:InChIKey=KPUDOJPVQQJLGI-CKARLABJSA-N
SMILES:C[C@]12[C@@]3(C)C(=C4[C@@](C)(CC3)CCC(C)(C)C4)CC[C@@]1([C@]5(C)[C@@](CC2)(C(C)(C)C(=O)CC5)[H])[H]
Synonyms:- Olean-13(18)-en-3-one
- δ-Amyrenone
- δ-Amyrone
- 3-Oxo-Δ13(18)-oleanene
- (6aR,6bS,8aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,13,14,14a-dodecahydro-1H-picen-3-one
- α-Amyrenone
- 5α-Olean-13(18)-en-3-one
- 13(18)-Oleanen-3-one
- δ-Amyrenane
- Delta-Amyrone
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
δ-Amyrenone
CAS:δ-Amyrenone (Delta-Amyrone), isolated from S. lineare, has anti-inflammatory effects.Formula:C30H48OPurity:99.68%Color and Shape:SolidMolecular weight:424.713(18)-Oleanen-3-one
CAS:Controlled Product<p>13(18)-Oleanen-3-one (13EO) is a chemical compound that has been shown to have antiviral activity against HIV. It was developed as a potential treatment for AIDS in the 1990s and has been shown to inhibit the virus at an early stage of its life cycle. The mechanism of action is not yet fully understood, but it appears that 13EO inhibits the reverse transcription process by binding to the RNA polymerase enzyme. Treatment with 13EO also reduces symptoms of hepatitis caused by Rhamnitrin and may be effective for treating herpes simplex infections. 13EO binds to chloride ions in the human body, which may account for its inhibition of viral replication.<br>13EO has been shown to increase production of β-amyrin and stilbene derivatives in cells. These compounds are known to have anti-inflammatory effects and may play a role in the antiviral activity seen with 13EO treatment.</p>Formula:C30H48OPurity:Min. 95%Molecular weight:424.7 g/mol




