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Details

Stereochemistry ABSOLUTE
Molecular Formula C32H52O2
Molecular Weight 468.7541
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of .BETA.-AMYRIN ACETATE

SMILES

CC(=O)O[C@H]1CC[C@@]2(C)[C@@H](CC[C@]3(C)[C@@H]2CC=C4[C@@H]5CC(C)(C)CC[C@]5(C)CC[C@@]34C)C1(C)C

InChI

InChIKey=UMRPOGLIBDXFNK-ZYGITSNFSA-N
InChI=1S/C32H52O2/c1-21(33)34-26-13-14-30(7)24(28(26,4)5)12-15-32(9)25(30)11-10-22-23-20-27(2,3)16-17-29(23,6)18-19-31(22,32)8/h10,23-26H,11-20H2,1-9H3/t23-,24-,25+,26-,29+,30-,31+,32+/m0/s1

HIDE SMILES / InChI

Molecular Formula C32H52O2
Molecular Weight 468.7541
Charge 0
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Description

Beta-Amyrin Acetate is β-Amyrin derivative with potent anti-inflammatory, anti-diabetic, anti-hyperlipidemic activities.

Originator

Approval Year

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

PubMed

Patents

Sample Use Guides

In Vivo Use Guide
In 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced inflammation mouse model Beta-Amyrin Acetate shows potent anti-inflammatory activity with ID50=0.75mkM/ear
Route of Administration: Topical
In Vitro Use Guide
The murine microglia cell line, BV2, was used for activity evaluation. BV2 cells were cultured in Dulbecco’s modified Eagle medium (Gibco, USA) supplemented with 5% fetal bovine serum (Hyclone). Cells were treated with Beta-Amyrin Acetate (up to 50 mkM). Production of NO was measured by the accumulation of nitrite in the culture medium 24 h after stimulation with LPS (0.5 mkg/ml) or IFN (20 ng/ml) by the Griess reagent.
Substance Class Chemical
Record UNII
AM1H7102OC
Record Status Validated (UNII)
Record Version