beta-amyrin acetate (Q27273993)

inferred from SMILES

mass

468.397±0 dalton

1 reference

beta-Amyrin acetate (English)

[(3S,4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate

14 October 2016

stereoisomer of

2 references

inferred from InChIKey

[(3S,4aR,6aS,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate

2 references

inferred from InChIKey

[(3R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate

1 reference

[(3R,4aR,6aR,6bS,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate

1 reference

[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate

1 reference

[(3S,4aR,6aR,6bR,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate

1 reference

[(3S,4aS,6aR,6bS,8aS,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate

1 reference

[(3S,4aR,6aR,6bS,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate

1 reference

[(3S,4aS,6aR,6bS,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate

1 reference

[(3S,4aR,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate

1 reference

chemical formula

C₃₂H₅₂O₂

1 reference

beta-Amyrin acetate (English)

14 October 2016

canonical SMILES

CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C

1 reference

beta-Amyrin acetate (English)

14 October 2016

isomeric SMILES

CC(=O)O[C@H]1CC[C@]2([C@H](C1(C)C)CC[C@@]3([C@@H]2CC=C4[C@]3(CC[C@@]5([C@H]4CC(CC5)(C)C)C)C)C)C

1 reference

Triterpenoids Isolated fromParahancornia amapa

beta-Amyrin acetate (English)

14 October 2016

1 reference

Gardenia imperialis

1 reference

Triterpenoid constituents fromGardenia imperialis

Euphorbia larica

1 reference

Chemistry and biological activity of secondary metabolites in Euphorbia from Iran

Excoecaria agallocha

2 references

Pentacyclic triterpenoids from leaves of Excoecaria agallocha

Pentacyclic triterpenoids from leaves of Excoecaria agallocha

Gonocaryum calleryanum

1 reference

A secoiridoid and other constituents of Gonocaryum calleryanum

Quercus glauca

1 reference

Studies on the constituents of Quercus spp. V. Paraffins and triterpenes of Quercus spp. in Japan (author's transl)

Quercus myrsinaefolia

1 reference

Studies on the constituents of Quercus spp. V. Paraffins and triterpenes of Quercus spp. in Japan (author's transl)

Quercus salicina

1 reference

Studies on the constituents of Quercus spp. V. Paraffins and triterpenes of Quercus spp. in Japan (author's transl)

Taraxacum formosanum

2 references

Chemical constituents of Taraxacum formosanum

Chemical constituents of Taraxacum formosanum

Viscum articulatum

1 reference

The inhibition of superoxide anion generation by neutrophils from Viscum articulactum

Viscum coloratum

1 reference

The inhibition of superoxide anion generation in human neutrophils by Viscum coloratum

Periploca laevigata

1 reference

Medicinal Plants of Tunisia. The Structure of Periplocadiol, A New Elemane-Type Sesquiterpene Isolated from the Roots of Periploca laevigata

Sonchus macrocarpus

1 reference

Two eudesmanolides from Sonchus macrocarpus

Acer mandshuricum

1 reference

Triterpene compounds isolated from Acer mandshuricum and their anti-inflammatory activity

Brachylaena ramiflora

2 references

Two new triterpene esters from the twigs of Brachylaena ramiflora from the Madagascar rainforest

Two new triterpene esters from the twigs of Brachylaena ramiflora from the Madagascar rainforest

Haloxylon salicornicum

2 references

In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum

In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum

Toxicodendron sylvestre

1 reference

The regulation of inflammatory cytokine secretion in macrophage cell line by the chemical constituents of Rhus sylvestris

Allium victorialis

1 reference

Alliumonoate: a new cyclopentane derivative from Allium victorialis

Artemisia lehmanniana

1 reference

9β-hydroxy-11β(H),13-dihyhdrosantamarine, a new eudesmanolide fromArtemisia leucotricha

Artocarpus nobilis

1 reference

Glutathione S-transferase inhibitory, free radical scavenging, and anti-leishmanial activities of chemical constituents of Artocarpus nobilis and Matricaria chamomilla

Aspilia mossambicensis

1 reference

A highly oxygenated germacrane fromAspilia eenii and constituents from otherAspilia species

Austroeupatorium inulifolium

1 reference

Nine New Norlabdane Diterpenoids from the Leaves of Austroeupatorium inulifolium

Betula ermanii

1 reference

Cancer chemopreventive activity of oleanane-type triterpenoids from the stem bark of Betula ermanii.

Kalanchoe pinnata

1 reference

Triterpenoids and phenanthrenes from leaves of Bryophyllum pinnatum

Camellia oleifera

1 reference

Camelliols A-C, three novel incompletely cyclized triterpene alcohols from sasanqua oil (Camellia sasanqua)

Camellia sasanqua

1 reference

Camelliols A-C, three novel incompletely cyclized triterpene alcohols from sasanqua oil (Camellia sasanqua)

Cirsium palustre

1 reference

Chemical constituents of chloroform and petroleum extracts from Cirsium palustre flower heads

Cynara cardunculus

1 reference

Inhibitory effect of the flowers of artichoke (Cynara cardunculus) on TPA-induced inflammation and tumor promotion in two-stage carcinogenesis in mouse skin

Delia coronariae

1 reference

Trypanosomicidal kaurane diterpenes from Wedelia paludosa

Dorstenia excentrica

1 reference

Furocoumarins of three species of the genus Dorstenia

Elephantopus mollis

1 reference

Antitumor agents XXXVIII: Isolation and structural elucidation of novel germacranolides and triterpenes from Elephantopus mollis

Erythrophleum fordii

1 reference

New diterpenoids and the bioactivity of Erythrophleum fordii

Eucalyptus camaldulensis

1 reference

Ovarian antiproliferative activity directed isolation of triterpenoids from fruits of Eucalyptus camaldulensis Dehnh

Euphorbia bivonae

1 reference

Chemical constituents and antiproliferative activity of Euphorbia bivonae

Euphorbia decipiens

1 reference

New Bioactive Diterpenoid from Euphorbia decipiens

Euphorbia polycaulis

1 reference

New Bioactive Diterpenoid from Euphorbia decipiens

Euphorbia ferganensis

1 reference

β-Amyrin and β-amyrin acetate fromEuphorbia ferganensis

Euphorbia sororia

1 reference

Isoprenoids of Euphorbia sororia. I. Triterpenoids

Ficus pumila

1 reference

New Sterols and Triterpenoids of Ficus pumila Fruit.

Ficus sarmentosa var. thunbergii

1 reference

Triterpenoid Constituents of Ficus thunbergii.

Ganoderma applanatum

1 reference

Chemical constituents of Ganoderma applanatum of British Columbia forests

Gamochaeta serpyllifolia

1 reference

Neue obliquin-derivate aus Helichrysum serpyllifolium

Plecostachys serpyllifolia

1 reference

Neue obliquin-derivate aus Helichrysum serpyllifolium

Syncarpha canescens

1 reference

Neue obliquin-derivate aus Helichrysum serpyllifolium

Heliotropium ellipticum

1 reference

Antimicrobial activity of triterpenoids from Heliotropium ellipticum

Hoya australis

1 reference

Investigations on Hoya Species. I

Ixeris chinensis

1 reference

Composite Constituents: Thirty-Nine Triterpenoids Including Two Novel Compounds from Ixeris chinensis.

Lactuca indica

1 reference

Composite constituent: lactucenyl acetate, a novel migrated lupane triterpenoid from Lactuca indica revision of structure of tarolupenyl acetate

Litsea sericea

1 reference

24-Methylene-25-methylcycloartanol and 24α-ethyl-5α-cholestan-3α-ol from Neolitsea sericea

Machaerium incorruptibile

1 reference

Triterpenoids isolated from Machaerium incorruptibile

Magnolia kachirachirai

1 reference

Secondary Metabolites from Magnolia kachirachirai

Maquira coriacea

1 reference

Constituents of the trunk bark of Maquira coriacea.

Manilkara kauki

1 reference

Triterpenoids of mimusops manilkara trunk bark

Neolitsea sericea

1 reference

24-Methylene-25-methylcycloartanol and 24α-ethyl-5α-cholestan-3α-ol from Neolitsea sericea

Periploca sepium

1 reference

Chemical constituents of stem bark from Periploca sepium

Phyllanthus flexuosus

1 reference

Triterpene dienols and other constituents from the bark of Phyllanthus flexuosus

Picris hieracioides

1 reference

Composite Constituents: Forty-Two Triterpenoids Including Eight Novel Compounds Isolated from Picris hieracioides subsp. japonica.

Plumeria rubra

1 reference

Minor secondary metabolic products from the stem bark of Plumeria rubra Linn. displaying antimicrobial activities.

Trifoliate orange

1 reference

Anti-human immunodeficiency virus-1 constituents of the bark of Poncirus trifoliata

Rhododendron formosanum

1 reference

Two isomeric epoxysitosterols from Rhododendron formosanum: 1H and 13C NMR chemical shift assignments

Saussurea elegans

1 reference

Components ofSaussurea elegans

Taraxacum japonicum

1 reference

Anti-carcinogenic activity of Taraxacum plant. II.

Taraxacum platycarpum

1 reference

Constituents from the roots of Taraxacum platycarpum and their effect on proliferation of human skin fibroblasts

Tetradium glabrifolium

1 reference

Constituents of Leaves of Tetradium Glabrifolium

Trachelospermum asiaticum

1 reference

The triterpenoids of Trachelospermum asiaticum var. intermedium

Baccharoides anthelmintica

1 reference

4α-methylvernosterol and other sterols from Vernonia anthelmintica seeds

Hilliardiella aristata

1 reference

Glaucolides and other constituents from south african Vernonia species

Viburnum furcatum

1 reference

Three iridoid glycosides from Viburnum furcatum

Viburnum mathewsii

1 reference

Three iridoid glycosides from Viburnum furcatum

Aspilia paludosa

1 reference

Trypanosomicidal kaurane diterpenes from Wedelia paludosa

Sphagneticola trilobata

1 reference

Trypanosomicidal kaurane diterpenes from Wedelia paludosa

Zanthoxylum ailanthoides

1 reference

Chemical Constituents from the Root Bark of FormosanZanthoxylum Ailanthoides

maize

1 reference

Investigations on the Δ23-, Δ24(28)- and Δ25-Sterols of zea mays

Forsythia viridissima

1 reference

Chemical constituents from the fruits of Forsythia suspensa and their antimicrobial activity.

Goniophlebium niponicum

1 reference

Fern constituents: pentacyclic triterpenoids isolated from Polypodium niponicum and P. formosanum

Taraxacum mongolicum

1 reference

Chemical constituents of Taraxacum formosanum

Identifiers

InChI

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

1 reference

beta-Amyrin acetate (English)

14 October 2016

1 reference

Global Substance Registration System

beta-Amyrin acetate (English)

14 October 2016

2 references

UNII

AM1H7102OC

beta-amyrin acetate (English)

14 October 2016

https://commonchemistry.cas.org/detail?cas_rn=1616-93-9

9 April 2021

1 reference

.beta.-Amyrin acetate (English)

14 October 2016

2 references

beta-Amyrin acetate (English)

matched by identifier from

14 October 2016

ChEBI ID

190930

mapping relation type

exact match

2 references

matched by identifier from

ChEBI release 2022-06-13

International Chemical Identifier

InChI

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

1 reference

DSSTOX compound identifier

beta-AMYRIN ACETATE (English)

14 October 2016

1 reference

0 references

0 references

0 references

2 references

Global Substance Registration System

UNII

AM1H7102OC

beta-amyrin acetate (English)

matched by identifier from

14 October 2016