Ursolic acid acetate (Q72515925)

(1S,2R,4aS,6aR,6aS,6bR,8aR,12aR,14bS)-10-acetyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid

inferred from SMILES

1 reference

inferred from SMILES

mass

498.37091008 dalton

1 reference

(1S,2R,4aS,6aR,6aS,6bR,8aS,10S,12aR,14bR)-10-acetyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid

inferred from SMILES

stereoisomer of

2 references

inferred from InChIKey

(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-acetyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid

inferred from InChI

1 reference

(1S,2S,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-acetyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₃₂H₅₀O₄

0 references

canonical SMILES

O=C(OC1CCC2(C)C3CC=C4C5C(C)C(C)CCC5(C(=O)O)CCC4(C)C3(C)CCC2C1(C)C)C

0 references

isomeric SMILES

C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OC(=O)C)C)C)[C@@H]2[C@H]1C)C)C(=O)O

0 references

found in taxon

Ternstroemia japonica

1 reference

Jacaranone and related compounds from the fresh fruits of Ternstroemia japonica and their antioxidative activity

Ternstroemia gymnanthera

1 reference

Jacaranone and related compounds from the fresh fruits of Ternstroemia japonica and their antioxidative activity

Actinidia polygama

2 references

Triterpenoids from callus tissue of Actinidia polygama

Triterpenoids from the fruit galls of Actinidia polygama

Sanguisorba alpina

1 reference

Triterpenoids from Sanguisorba alpina

Cynomorium songaricum

2 references

Inhibitory effects of ursolic acid derivatives from Cynomorium songaricum, and related triterpenes on human immunodeficiency viral protease

Triterpenes from Cynomorium songaricium--analysis of HCV protease inhibitory activity, quantification, and content change under the influence of heating

Achyrocline bogotensis

1 reference

Cyclobutane dimers from the Colombian medicinal plant Achyrocline bogotensis.

Acridocarpus vivy

1 reference

Cytotoxic triterpenoids from Acridocarpus vivy from the Madagascar rain forest.

Cornus kousa

1 reference

Lipid peroxidation, cyclooxygenase enzyme and tumor cell proliferation inhibitory compounds in Cornus kousa fruits

Coussarea paniculata

1 reference

New cytotoxic lupane triterpenoids from the twigs of Coussarea paniculata.

Cussonia bancoensis

1 reference

Saponins from Cussonia bancoensis and their inhibitory effects on nitric oxide production.

Diospyros castanea

1 reference

Diospyros cauliflora

1 reference

Diospyros curranii

1 reference

Diospyros ebenum

1 reference

Diospyros evena

1 reference

Diospyros ferrea

1 reference

Diospyros hirsuta

1 reference

Diospyros kaki

1 reference

Triterpenoids from the leaves of Diospyros kaki (persimmon) and their inhibitory effects on protein tyrosine phosphatase 1B.

Diospyros leucomelas

1 reference

Diospyros lotus

2 references

Triterpenoids ofDiospyros lotus

Diospyros montana

1 reference

Diospyros morrisiana

1 reference

Diospyros quaesita

1 reference

Enkianthus cernuus

1 reference

6β-Hydroxyursolic acid and other triterpenoids of Enkianthus cernuus

Euphorbia paralias

1 reference

Phytochemical study of Euphorbia paralias

Ficus microcarpa

2 references

Ficus spp. (fig): ethnobotany and potential as anticancer and anti-inflammatory agents

Cytotoxic triterpenes from the aerial roots of Ficus microcarpa.

Gonocaryum calleryanum

1 reference

A secoiridoid and other constituents of Gonocaryum calleryanum

Leptopetalum biflorum

1 reference

New Anthraquinones from the Roots ofHedyotisdichotoma

Hyptis brevipes

1 reference

Bioactive 5,6-dihydro-alpha-pyrone derivatives from Hyptis brevipes

Isatis tinctoria

1 reference

A comprehensive metabolite profiling of Isatis tinctoria leaf extracts

Lasianthus gardneri

1 reference

A new 3,4-seco-lupane derivative from Lasianthus gardneri

Lavandula canariensis

1 reference

Triterpenes from Lavandula canariensis

Lavandula gibsonii

1 reference

Aromatic monoterpenes from Lavandula gibsonii☆

Leucothoe grayana

1 reference

A NEW DITERPENOID FROMLEUCOTHOE GRAYANAMAX.

Liriope muscari

1 reference

cis-Eudesmane sesquiterpene glycosides from Liriope muscari and Ophiopogon japonicus

Ludwigia octovalvis

1 reference

Three new oleanane-type triterpenes from Ludwigia octovalvis with cytotoxic activity against two human cancer cell lines

Melaleuca ericifolia

1 reference

Antiproliferative triterpenes from Melaleuca ericifolia.

Melaleuca leucadendra

1 reference

Ursane triterpenoids from leaves of melaleuca leucadendron

Salvia dianthera

1 reference

Sesquiterpenoid constituents of Meriandra benghalensis (Labiatae). X-ray structure analysis

Microtropis japonica

1 reference

Cytotoxic triterpenoids from the stems of Microtropis japonica.

Monochaetum vulcanicum

1 reference

A new ursane triterpene from Monochaetum vulcanicum that inhibits DNA polymerase beta lyase

Morus australis

1 reference

Bioactive constituents of Morus australis and Broussonetia papyrifera

Myrianthus arboreus

1 reference

Studies on Nigerian Medicinal Plants: Components of the Stems of Myrianthus arboreus

Nerium oleander

1 reference

Three new triterpenes from Nerium oleander and biological activity of the isolated compounds

Plantago major

1 reference

Ursolic acid from Plantago major, a selective inhibitor of cyclooxygenase-2 catalyzed prostaglandin biosynthesis

Plumeria obtusa

1 reference

Two triterpenoids from the leaves of Plumeria obtusa

Prostanthera melissifolia

1 reference

Phenylethanoid glycosides from Prostanthera melissifolia

Salvia breviflora

1 reference

Diterpenes from Salvia breviflora☆

Salvia chionopeplica

1 reference

Abietane diterpenoids from Salvia chinopeplica

Clinopodium acinos

1 reference

Secondary Metabolites from Satureja Species. New Triterpenoid from Satureja acinos

Sideritis soluta

1 reference

A chemotaxonomic study of nine Canarian Sideritis species

Sideritis discolor

1 reference

A chemotaxonomic study of nine Canarian Sideritis species

Strychnos vanprukii

1 reference

New 3-O-acyl betulinic acids from Strychnos vanprukii Craib

Syzygium formosanum

1 reference

Terpenoids of Syzygium formosanum

Vatica cinerea

1 reference

Natural anti-HIV agents. Part IV. Anti-HIV constituents from Vatica cinerea.

Verbena officinalis

1 reference

3α,24-dihydroxy-urs-12-en-28-oic acid from verbena officinalisfn1fn1RRL communication No. 2251.

Leucoblepharis subsessilis

1 reference

Antifertility chromene from Blepharispermum subsessile

Chaenomeles speciosa

2 references

Inhibition of PGHS-1 and PGHS-2 by Triterpenoid Acids from Chaenomelis Fructus

Antioxidant, anti-inflammatory and anti-influenza properties of components from Chaenomeles speciosa

Desfontainia fulgens

1 reference

Triterpenoids from Desfontainia spinosa

Desfontainia spinosa

1 reference

Triterpenoids from Desfontainia spinosa

Ligustrum obtusifolium

1 reference

Studies on the Constituents of Ligustrum Species. IX. On the Components of the Fruits of Ligustrum obtusifolium SIEB. et ZUCC. (3)

Pieris japonica

2 references

Triterpenoids of the bark of Pieris japonica D. Don.

Triterpenoids of the bark of Pieris japonica D. Don.

Prunella vulgaris

1 reference

Pentacyclic triterpenoids from Prunella vulgaris

Scaevola floribunda

2 references

Chemistry of Fijian Plants. 13.1Floribundal, a Nonglycosidic Bisiridoid, and Six Novel Fatty Esters of δ-Amyrin fromScaevola floribunda

Chemistry of Fijian Plants. 13.1Floribundal, a Nonglycosidic Bisiridoid, and Six Novel Fatty Esters of δ-Amyrin fromScaevola floribunda

yerba mate

1 reference

Evaluation of ursolic acid isolated from Ilex paraguariensis and derivatives on aromatase inhibition

Alchornea laxiflora

1 reference

Two New Fatty Acid Derivatives from the Stem Bark of Alchornea laxiflora (Euphorbiaceae)

Anaphalis margaritacea

1 reference

Flavonoids and triterpenoids from Anaphalis margaritacea

Diospyros maritima

1 reference

Chemical constituents from the stems of Diospyros maritima

Garcinia lateriflora

1 reference

Proteasome-inhibitory and cytotoxic constituents of Garcinia lateriflora: absolute configuration of caged xanthones

Incarvillea arguta

1 reference

A New Cyclooxygenase Inhibitor from Incarvillea arguta

Incarvillea diffusa

1 reference

A New Cyclooxygenase Inhibitor from Incarvillea arguta

Ixora coccinea

1 reference

Ixorapeptide I and ixorapeptide II, bioactive peptides isolated from Ixora coccinea

Morella rubra

2 references

Bioactive constituents of Chinese natural medicines. VII. Inhibitors of degranulation in RBL-2H3 cells and absolute stereostructures of three new diarylheptanoid glycosides from the bark of Myrica rubra

Inhibitors of nitric oxide production from the bark of Myrica rubra: structures of new biphenyl type diarylheptanoid glycosides and taraxerane type triterpene

Myrica rubra

2 references

Bioactive constituents of Chinese natural medicines. VII. Inhibitors of degranulation in RBL-2H3 cells and absolute stereostructures of three new diarylheptanoid glycosides from the bark of Myrica rubra

Inhibitors of nitric oxide production from the bark of Myrica rubra: structures of new biphenyl type diarylheptanoid glycosides and taraxerane type triterpene

Nuxia sphaerocephala

1 reference

Clerodane and labdane diterpenoids from Nuxia sphaerocephala

Medinilla fengii

1 reference

A new ferulic acid ester, a new ellagic acid derivative, and other constituents from pachycentria formosana: effects on neutrophil pro-inflammatory responses

Syncarpia glomulifera

1 reference

Biologically active triterpenoids of Syncarpia glomulifera bark extract from Paluma, north Queensland, Australia

Tripterygium hypoglaucum

2 references

Triterpenoids from Tripterygium wilfordii

Terpenoids from Tripterigyum hypoglaucum

Vatica affinis

1 reference

Three hydroxy ellagic acid methyl ethers, chrysophanol and scopoletin from Shorea worthingtonii and Vatica obscura

Ilex

1 reference

Triterpenoids from Brazilian Ilex species and their in vitro antitrypanosomal activity.

Salvia

2 references

Flavonoids from Salvia nicolsoniana

New Triterpenoids from Salvia nicolsoniana

Rosmarinus officinalis

2 references

Rofficerone: A New Triterpenoid from Rosmarinus officinalis

Rosmarinus officinalis leaves as a natural source of bioactive compounds.

Diospyros multiflora

1 reference

Triterpenoids ofDiospyros lotus

Diospyros melanoxylon

1 reference

Triterpene acids from Diospyros melanoxylon

Perilla frutescens

1 reference

Cytotoxic activity of Perilla frutescens var. japonica leaf extract is due to high concentrations of oleanolic and ursolic acids

Oldenlandia diffusa

1 reference

A comparable, chemical and pharmacological analysis of the traditional Chinese medicinal herbs Oldenlandia diffusa and O. corymbosa and a new valuation of their biological potential

Mangifera indica

1 reference

Differences in the chemical constituents of Mangifera indica, infected with Aspergillus niger and Fusarium moniliformae

Psidium guajava

1 reference

Four new triterpenoids from the leaves of Psidium guajava

Prunus avium

1 reference

Composition of the cuticle of developing sweet cherry fruit

Phellodendron amurense

1 reference

Rapid identification and comparative analysis of the chemical constituents and metabolites of Phellodendri amurensis cortex and Zhibai dihuang pill by ultra-performance liquid chromatography with quadrupole TOF-MS.

Morus indica

1 reference

Bioactive constituents of Morus australis and Broussonetia papyrifera

Tripterygium wilfordii

2 references

Terpenoids from Tripterigyum hypoglaucum

Triterpenoids from Tripterygium wilfordii

Salvia officinalis

1 reference

Flavonoids from Salvia nicolsoniana

Identifiers

InChI

InChI=1S/C32H50O4/c1-19-11-16-32(27(34)35)18-17-30(7)22(26(32)20(19)2)9-10-24-29(6)14-13-25(36-21(3)33)28(4,5)23(29)12-15-31(24,30)8/h9,19-20,23-26H,10-18H2,1-8H3,(H,34,35)/t19-,20+,23+,24-,25+,26+,29+,30-,31-,32+/m1/s1

0 references

InChIKey

PHFUCJXOLZAQNH-OTMOLZNZSA-N

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CAS Registry Number

7372-30-7

1 reference

InChIKey

PHFUCJXOLZAQNH-OTMOLZNZSA-N

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=7372-30-7

0 references

mapping relation type

exact match

1 reference