(Q27136369)

(3S,4aR,6aR,6bS,8aS,11R,12S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol

Uvaol (English)

7 October 2016

1 reference

(3S,4aS,6aR,6bS,8aS,11R,12S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol

2 references

(3R,4aS,6aR,6bS,8aS,11R,12S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol

1 reference

(3S,4aS,6aR,6bS,8aS,11S,12S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol

1 reference

urs-12-ene-3β,28-diol

1 reference

chemical formula

C₃₀H₅₀O₂

1 reference

Uvaol (English)

7 October 2016

CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO

1 reference

Uvaol (English)

7 October 2016

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)O)C)C)[C@@H]2[C@H]1C)C)CO

1 reference

Role of Nitric Oxide and Hydrogen Sulfide in the Vasodilator Effect of Ursolic Acid and Uvaol from Black Cherry Prunus serotina Fruits

Uvaol (English)

7 October 2016

1 reference

Olea europaea

3 references

Pentacyclic triterpene acids in olives

Production of triterpene acids by cell suspension cultures of Olea europaea

Cardiotonic and antidysrhythmic effects of oleanolic and ursolic acids, methyl maslinate and uvaol

Crataegus monogyna

1 reference

A comparison of the composition of epicuticular wax from red raspberry (Rubus idaeus L.) and hawthorn (Crataegus monogyna Jacq.) flowers

Rubus idaeus

1 reference

A comparison of the composition of epicuticular wax from red raspberry (Rubus idaeus L.) and hawthorn (Crataegus monogyna Jacq.) flowers

Hippophae rhamnoides

2 references

Chemical investigation ofHippophaë rhamnoides. I. The main components of the unsaponifiable part of an extract of the fruit pulp

Chemical investigation ofHippophaë rhamnoides. II. Main components of the neutral reaction of the saponification products of an extract of the leaves of the sea buckthorn

Salvia tomentosa

1 reference

Further Flavones and Triterpenes and the New 6-Hydroxyluteolin 5-β-D-Glucoside From Salvia tomentosa

Diospyros blancoi

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros ismailii

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros lotus

2 references

Naphthoquinones and triterpenes from some asian Diospyros species

Pharmacology and chemotaxonomy of Diospyros

Diospyros maingayi

2 references

Naphthoquinones and triterpenes from some asian Diospyros species

Pharmacology and chemotaxonomy of Diospyros

Diospyros siamang

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros singaporensis

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros sumatrana

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros wallichii

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros argentea

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Psidium guajava

2 references

Chemical Constituents of the Leaves of Psidium guajava

Chemical constituents from the leaves of Psidium guajava

Diospyros kaki

3 references

Effect of five triterpenoid compounds isolated from leaves of Diospyros kaki on stimulus-induced superoxide generation and tyrosyl phosphorylation in human polymorphonuclear leukocytes

Pharmacology and chemotaxonomy of Diospyros

A new 18,19-secoursane triterpene from the leaves of Diospyros kaki

Euphorbia micractina

1 reference

Chemical Constituents of the Roots of Euphorbia micractina

Alibertia edulis

2 references

An oleanane acid from Alibertia edulis

Constituintes químicos de Arrabidaea samydoides (Bignoniaceae)

Eucalyptus robusta

1 reference

Studies on the chemical constituents of Eucalyptus robusta Sm.: Isolation and identification of robustaol B and other constituents

Rhododendron ellipticum

1 reference

Quercetin 5,4′-dimethyl ether from Rhododendron ellipticum

Empetrum nigrum

1 reference

A new skeletal triterpenoid isolated from Empetrum nigrum

Nierembergia hippomanica

1 reference

7,8-dihydroajugasterone C, norhygrine and other constituents of Nierembergia hippomanica

Leptospermum scoparium

2 references

Three Lupane Derivatives fromLeptospermum scoparium

Flavonoids from Leptospermum scoparium

Eucalyptus globulus

1 reference

Terpenoids and other constituents of Eucalyptus globulus

Shorea robusta

1 reference

Triterpenoids from Shorea robusta resin

Maclura pomifera

1 reference

New Lupane Triterpene Fatty Acid Ester from Leaves ofMaclura pomifera

Syzygium formosanum

1 reference

Terpenoids of Syzygium formosanum

Vochysia ferruginea

1 reference

6beta-hydroxymaslinic acid, a triterpene from Vochysia ferruginea

Eucalyptus saligna

1 reference

Constituents of the leaves of Eucalyptus saligna

Debregeasia salicifolia

1 reference

Antimicrobial triterpenes from Debregeasia salicifolia

Callistemon citrinus

1 reference

An alkenol and C-methylated flavones from Callistemon lanceolatus leaves

Callistemon lanceolatus

1 reference

An alkenol and C-methylated flavones from Callistemon lanceolatus leaves

Englerophytum magalismontanum

1 reference

Notes on Activity Tests and Constituents of two Supposed Medicinal Plants from South Africa, Englerophytum magalismontanum and Diospyros lycioides desf. subsp. sericea†

Euphorbia retusa

2 references

Triterpenes from Euphorbia broteri

Triterpenes from Euphorbia rigida.

Isodon coetsa

1 reference

Diterpenoid constituents from Rabdosia coetsa

Crataegus pinnatifida

2 references

Chitin synthase II inhibitory activity of ursolic acid, isolated from Crataegus pinnatifida

Inhibitory effect of triterpenes from Crataegus pinatifida on HIV-I protease

Arctostaphylos columbiana

1 reference

Phytochemical Investigation of Arctostaphylos columbiana Piper and Arctostaphylos patula Greene (Ericaceae)

Arctostaphylos patula

1 reference

Phytochemical Investigation of Arctostaphylos columbiana Piper and Arctostaphylos patula Greene (Ericaceae)

Woodwardia radicans

1 reference

Triterpenoids from Woodwardia radicans

Ilex latifolia

1 reference

Triterpenoids from the Stem Bark of Adina cordifolia

Diospyros melanoxylon

1 reference

Diospyros melanoxylon Leaves: A Rich Source of Pentacyclic Triterpenes

Origanum dictamnus

1 reference

Triterpenes from amaracus dictamnus

Origanum pampaninii

1 reference

Diterpenes from the Genus Amaracus

Salvia lanata

1 reference

Salvia lanata Roxb.

Baccharis coridifolia

1 reference

Plant Anticancer Agents XXXVI. Schottenol Glucoside from Baccharis coridifolia and Ipomopsis aggregata1

Calluna vulgaris

1 reference

Triterpenoids and steroids of some species of the order Ericales

Microtropis fokienensis

2 references

Cytotoxic triterpenoids from the leaves of Microtropis fokienensis

Cytotoxic dihydroagarofuranoid sesquiterpenes from the stem of Microtropis fokienensis

Eriobotrya japonica

1 reference

11beta-Hydroxysteroid dehydrogenase 1 inhibiting constituents from Eriobotrya japonica revealed by bioactivity-guided isolation and computational approaches

alpenrose

1 reference

Ferruginenes A-C from Rhododendron ferrugineum and their cytotoxic evaluation

Euphorbia paralias

1 reference

Phytochemical study of Euphorbia paralias

Nuxia sphaerocephala

1 reference

Clerodane and labdane diterpenoids from Nuxia sphaerocephala

Baccharis dracunculifolia

1 reference

In vitro antileishmanial, antiplasmodial and cytotoxic activities of phenolics and triterpenoids from Baccharis dracunculifolia D. C. (Asteraceae).

Cydonia oblonga

1 reference

Antioxidant and antiproliferative activities of phytochemicals from Quince (Cydonia vulgaris) peels

Cydonia vulgaris

1 reference

Antioxidant and antiproliferative activities of phytochemicals from Quince (Cydonia vulgaris) peels

Cylicodiscus gabunensis

1 reference

Triterpenoid derivatives from Cylicodiscus gabunensis

Euonymus alatus

1 reference

Triterpenes of Euonymus alatus and their cytotoxic activity

Leucothoe keiskei

1 reference

Ein Bestandteil der Blätter von <I>Leucothoe Keiskei</I> Miq

Morus alba

1 reference

Inhibitory effects of constituents from Morus alba var. multicaulis on differentiation of 3T3-L1 cells and nitric oxide production in RAW264.7 cells.

Morus alba var. multicaulis

1 reference

Inhibitory effects of constituents from Morus alba var. multicaulis on differentiation of 3T3-L1 cells and nitric oxide production in RAW264.7 cells.

Scarlet firethorn

1 reference

Two glucosides from Pyracantha coccinea roots: a new lignan and a new chalcone

Salacia chinensis

1 reference

The absolute stereostructures of three rare D:B-friedobaccharane skeleton triterpenes from the leaves of Salacia chinensis

Sorbus decora

1 reference

Bioassay-guided isolation of the antidiabetic principle from Sorbus decora (Rosaceae) used traditionally by the Eeyou Istchee Cree First Nations

Strychnos spinosa

1 reference

Antitrypanosomal activity of triterpenoids and sterols from the leaves of Strychnos spinosa and related compounds

Vitex cauliflora

1 reference

A new labdane diterpene from Vitex cauliflora Moldenke from the Madagascar rainforest.

Ilex

1 reference

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

Nerium oleander

2 references

Kaneric Acid, a New Triterpene from the Leaves of Nerium oleander

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

Rhaphiolepis loquata

1 reference

11beta-Hydroxysteroid dehydrogenase 1 inhibiting constituents from Eriobotrya japonica revealed by bioactivity-guided isolation and computational approaches

Rhododendron latoucheae

1 reference

Quercetin 5,4′-dimethyl ether from Rhododendron ellipticum

Saussurea muliensis

1 reference

Antimicrobial triterpenoids from Vladimiria muliensis

Gentiana davidii var. formosana

1 reference

A New Acylated Secoiridoid from Gentiana formosana

Rhododendron kotschyi

1 reference

The triterpenoids of some species of rhododendron

Rhododendron groenlandicum

1 reference

Chemical composition of Ledum palustre

Rhododendron tomentosum

1 reference

Chemical composition of Ledum palustre

1 reference

2 references

Triterpenes from Euphorbia broteri

Triterpenes from Euphorbia rigida.

Salvia officinalis

1 reference

Further Flavones and Triterpenes and the New 6-Hydroxyluteolin 5-β-D-Glucoside From Salvia tomentosa

Debregeasia saeneb

1 reference

Antimicrobial triterpenes from Debregeasia salicifolia

Nierembergia linariifolia

1 reference

7,8-dihydroajugasterone C, norhygrine and other constituents of Nierembergia hippomanica

Rhododendron myrtifolium

1 reference

The triterpenoids of some species of rhododendron

Diospyros blancoi

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Moquilea pyrifolia

1 reference

New Lupane Derivatives from the Leaves ofLicania pyrifolia

1 reference

1 reference

Identifiers

InChI

InChI=1S/C30H50O2/c1-19-10-15-30(18-31)17-16-28(6)21(25(30)20(19)2)8-9-23-27(5)13-12-24(32)26(3,4)22(27)11-14-29(23,28)7/h8,19-20,22-25,31-32H,9-18H2,1-7H3/t19-,20+,22+,23-,24+,25+,27+,28-,29-,30-/m1/s1

1 reference

Uvaol (English)

7 October 2016

2 references

Uvaol (English)

7 October 2016

ChEBI release 2020-09-01

2 references

uvaol (English)

7 October 2016

https://commonchemistry.cas.org/detail?cas_rn=545-46-0

9 April 2021

1 reference

Uvaol (English)

7 October 2016

2 references

Uvaol (English)

7 October 2016

ChEBI ID

67894

mapping relation type

2 references

uvaol (English)

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C30H50O2/c1-19-10-15-30(18-31)17-16-28(6)21(25(30)20(19)2)8-9-23-27(5)13-12-24(32)26(3,4)22(27)11-14-29(23,28)7/h8,19-20,22-25,31-32H,9-18H2,1-7H3/t19-,20+,22+,23-,24+,25+,27+,28-,29-,30-/m1/s1

1 reference

UVAOL (English)

7 October 2016

2 references

splash10-059b-5900000000-fd6e8a3360a0b0a72052

1 reference

0 references

splash10-0006-0100900000-4a0d73fcef1863afc64a

0 references

DSSTox substance ID

DTXSID901350099

1 reference

NSC number

159627

0 references

EC number

208-888-3

1 reference

Global Substance Registration System

UNII

W599R31ROT

UVAOL (English)

ECHA Substance Infocard ID

7 October 2016

100.008.081

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.008.081

27 December 2018

Human Metabolome Database ID

Urs-12-ene-3β,28-diol (English)

quotation

CAS no.: 545-46-0 (English)

HMDB0002391

2 references

UNII

W599R31ROT

2 references

Global Substance Registration System

UNII

W599R31ROT

UVAOL (English)

7 October 2016