(Q5172335)

inferred from SMILES

mass

472.35526 dalton

1 reference

Corosolic acid (English)

(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,11R,12aR,14bR)-10,11-dihydroxy-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

7 October 2016

stereoisomer of

2 references

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

inferred from InChI

2 references

(1S,2R,4aS,6aR,6aS,6bR,8aS,10R,11R,12aR,14bS)-10,11-dihydroxy-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

2 references

(1S,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-10,11-dihydroxy-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

2 references

1 reference

(1R,2S,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-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

1 reference

1 reference

C₃₀H₄₈O₄

1 reference

Corosolic acid (English)

7 October 2016

canonical SMILES

CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O

1 reference

Corosolic acid (English)

7 October 2016

isomeric SMILES

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

1 reference

Pentacyclic triterpenoids from Prunella vulgaris

Corosolic acid (English)

7 October 2016

5 references

Triterpenoids from Prunella vulgaris

Anti-allergic and anti-inflammatory triterpenes from the herb of Prunella vulgaris

Triterpenoid Saponins from the Spikes ofPrunella vulgaris

Anti-allergic and anti-inflammatory triterpenes from the herb of Prunella vulgaris

Isodon henryi

1 reference

Two New C(20)-Oxygenatedent-Kaurene Diterpenoids fromIsodon henryi

Myrtus communis L.

1 reference

New α-Glucosidase Inhibitors and Antibacterial Compounds fromMyrtus communis L.

Chaenomeles sinensis

1 reference

Antitumor-promoting constituents from Chaenomeles sinensis KOEHNE and their activities in JB6 mouse epidermal cells

Dracocephalum kotschyi

1 reference

Two new monoterpene glycosides and trypanocidal terpenoids from Dracocephalum kotschyi

Melaleuca leucadendra

2 references

Ursane triterpenoids from leaves of melaleuca leucadendron

New Triterpenes from the Heartwood ofMelaleuca leucadendronL.

Monochaetum vulcanicum

1 reference

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

Olea europaea

1 reference

Production of triterpene acids by cell suspension cultures of Olea europaea

Psidium guajava

1 reference

Triterpenoids from the leaves of Psidium guajava

Ternstroemia gymnanthera

1 reference

Ursane- and oleanane-type triterpenes from Ternstroemia gymnanthera callus tissues

Actinidia polygama

3 references

Triterpenoids from the fruit galls of Actinidia polygama

Triterpenoids from callus tissue of Actinidia polygama

Triterpenoids from callus tissue of Actinidia polygama

Agrimonia pilosa

1 reference

Phenolic Components from the Aerial Parts of Agrimonia pilosa

Alchemilla alpina

1 reference

Alchemilla faeroensis

1 reference

Alchemilla vulgaris

1 reference

Arnebia euchroma

1 reference

Tormentic Acid and 2alpha-Hydroxyursolic Acid from Arnebia euchroma

Callicarpa pentandra

1 reference

Four new clerodane diterpenoids from Callicarpa pentandra

Cowania mexicana

1 reference

Triterpene Acids from Cowainea mexicana

Purshia mexicana

1 reference

Triterpene Acids from Cowainea mexicana

Crataegus pinnatifida

1 reference

Corosolic acid isolated from the fruit of Crataegus pinnatifida var. psilosa is a protein kinase C inhibitor as well as a cytotoxic agent

Diospyros melanoxylon

2 references

Triterpene acids from Diospyros melanoxylon

Diospyros melanoxylon Leaves: A Rich Source of Pentacyclic Triterpenes

Elsholtzia ciliata

1 reference

Studies on the Chemical Constituents of Elsholtzia herb.

Enkianthus cernuus

1 reference

6β-Hydroxyursolic acid and other triterpenoids of Enkianthus cernuus

Eriobotrya japonica

5 references

Antioxidant flavonoids and chlorogenic acid from the leaves of Eriobotrya japonica

Polyhydroxylated Triterpenes from Eriobotrya japonica

A New Triterpene Ester from Eriobotrya japonica.

Anti-inflammatory and antitumor-promoting effects of the triterpene acids from the leaves of Eriobotrya japonica

Anti-metastatic properties of the leaves of Eriobotrya japonica

Eucalyptus occidentalis

1 reference

Isolation from Eucalyptus occidentalis and identification of a new kaempferol derivative that induces apoptosis in human myeloid leukemia cells

Eucalyptus perriniana

1 reference

Triterpenoids from Eucalyptus perriniana cultured cells

Eucalyptus robusta

1 reference

A New Triterpenic Acid from Schefflera impressa

Ficus pumila

1 reference

Constituents of Ficus pumila Leaves.

Geum japonicum

1 reference

Triterpenoids and glycosides from Geum japonicum

Hedyotis lawsoniae

1 reference

Studies on the constituents of medicinal and related plants in sri lanka. I. New triterpenes from Hedyotis lawsoniae.

Hyptis capitata

2 references

The cytotoxic principles of Hyptis capitata and the structures of the new triterpenes hyptatic acid-A and -B

Anti-AIDS agents. 30. Anti-HIV activity of oleanolic acid, pomolic acid, and structurally related triterpenoids

Condea verticillata

1 reference

Cytotoxic constituents from Hyptis verticillata

Isodon adenanthus

1 reference

Triterpenoids of Isodon loxothyrsus

Isodon eriocalyx

1 reference

Four new diterpenoids from Isodon eriocalyx var. laxiflora

Isodon loxothyrsus

1 reference

Triterpenoids of Isodon loxothyrsus

Isodon phyllostachys

1 reference

A new ent-kaurane diterpenoid from Isodon phyllostachys

Isodon sculponeatus

1 reference

Cytotoxic ent-Kaurane Diterpenoids from Isodon racemosa (Hemsl) Hara

Lagerstroemia speciosa

4 references

A New Triterpenoid Isolated from Lagerstronemia speciosa (L.) Pers.

Effect of corosolic acid on postchallenge plasma glucose levels.

Screening of plant constituents for effect on glucose transport activity in Ehrlich ascites tumour cells

Active compounds from Lagerstroemia speciosa, insulin-like glucose uptake-stimulatory/inhibitory and adipocyte differentiation-inhibitory activities in 3T3-L1 cells.

Lepechinia caulescens

2 references

Abietanoid acid from Lepechinia caulescens

Di- and triterpenoid acids from Lepechinia caulescens

Leptospermum scoparium

1 reference

Three Lupane Derivatives fromLeptospermum scoparium

Salvia dianthera

1 reference

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

Musanga cecropioides

1 reference

Chemical Studies on the Cecropiaceae: A Novel A-ring Seco Triterpene from Musanga cecropioides

Nepeta eriostachya

1 reference

Ursane triterpenoids from Nepeta eriostachia

Cryptolepis nigrescens

1 reference

Study on chemical constituents of Inula cappa

Perovskia atriplicifolia

1 reference

A new acylated steroid glucoside from Perovskia atriplicifolia

Polylepis incana

1 reference

Chemical investigation of Polylepis incana (Rosaceae)

Potentilla fruticosa

1 reference

Chemical composition of Potentilla fruticosa. II. Triterpenoids

Potentilla tormentilla

1 reference

New Triterpenoid Saponins from the Roots of Potentilla tormentilla

Prunus africana

2 references

Triterpenes from Prunus africana bark

New constituents of Prunus africana bark extract

Prunus zippeliana

1 reference

Constituents of Prunus zippeliana Leaves and Branches.

Scarlet firethorn

1 reference

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

Isodon rubescens

1 reference

Structure and Bonding

Isodon serra

1 reference

Studies on chemical constituents of Rabdosia serra

Rosa davidii

1 reference

Chemical constituents from Sinacalia davidii

Rosa davurica

1 reference

Chemical constituents of pericarps of Rosa davurica Pall., a traditional Chinese medicine

Rosa laevigata

1 reference

Steroids and triterpenoids from Rosa laevigata

Rosa taiwanensis

1 reference

Chemical Constituents from the Root and Aerial Parts ofRosa taiwanensis

Rosa transmorrisonensis

1 reference

Chemical Constituents from the Aerial Part of Rosa Transmorrisonensis

Rubus parvifolius

1 reference

Triterpenoids from the roots ofRubus parvifolius

Rubus ulmifolius

1 reference

In vitro antimicrobial activity of extracts and isolated constituents of Rubus ulmifolius

Salvia canariensis

3 references

A revised structure for the diterpene rosmanol

Terpenoids of Cultivated Salvia canariensis

Diterpenes from the roots of Salvia canariensis

Salvia carduacea

1 reference

A new 24-nor-oleanane triterpenoid from Salvia carduacea

Salvia hierosolymitana

1 reference

Dammarane triterpenes of Salvia hierosolymitana

Salvia paramiltiorrhiza

1 reference

ChemInform Abstract: Diterpenoids From Salvia Paramiltiorrhiza.

Shorea robusta

2 references

Triterpenoids from the resin of Shorea robusta

Triterpenoids from the resin of Shorea robusta

Sorbus aucuparia

1 reference

TRITERPENOIDS AND FLAVONOIDAL GLYCOSIDE FROM FRUITS OF SORBUS AUCUPARIA (DC) CULTIVATED IN EGYPT

Symphoricarpos albus

1 reference

The occurrence of lanosterol and 24-methylenelanost-8-en-3β-ol in leaves of symphoricarpus albus

Terminalia chebula

1 reference

2α-Hydroxymicromeric acid, a pentacyclic triterpene from Terminalia chebula

Terminalia glabrescens

1 reference

Chemical constituents from Terminalia glabrescens

Tiarella polyphylla

1 reference

Structure determination of a new lupane-type triterpene, tiarellic acid, isolated from Tiarella polyphylla

Trema micrantha

1 reference

Vitexin, paprazine and terpenoids from Trema micrantha.

Trema orientale

1 reference

Xanthones and Other Constituents of Trema orientalis

Tripterygium wilfordii

1 reference

Immunosuppressive terpenoids from extracts of Tripterygium wilfordii

Complex-toothed flying squirrel

1 reference

Cytotoxic triterpenes from a Chinese medicine, Goreishi

Vismia guianensis

1 reference

New prenylated anthraquinones and xanthones from Vismia guineensis

Vitex altissima

1 reference

Flavonoids, triterpenoids and a lignan from Vitex altissima

Vitex peduncularis

1 reference

Triterpenoids and Flavonoids of Vitex peduncularis

Vochysia ferruginea

1 reference

6beta-hydroxymaslinic acid, a triterpene from Vochysia ferruginea

Crepidiastrum chelidoniifolium

1 reference

The inhibition of diacylglycerol acyltransferase by terpenoids from Youngia koidzumiana.

Ziziphus jujuba

1 reference

Chemical Constituents from the Seeds of Ziziphus jujuba var. spinosa (Bunge) Hu

Euscaphis japonica

1 reference

Cytotoxic Hexacyclic Triterpene Acids from Euscaphis japonica

Rhododendron brachycarpum

1 reference

Rhododendric acid A, a new ursane-type PTP1B inhibitor from the endangered plant Rhododendron brachycarpum G. Don

alpenrose

1 reference

Ferruginenes A-C from Rhododendron ferrugineum and their cytotoxic evaluation

Symplocos lancifolia

1 reference

Triterpenoid saponins from Symplocos lancifolia

Actinidia chinensis

1 reference

Two new triterpenoids from the roots of Actinidia chinensis

Baccharis dracunculifolia

1 reference

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

Dolichandra unguis-cati

1 reference

Triterpenoids from Bignonia unguiscati Roots.

Careya arborea

1 reference

Triterpenoid sapogenols from the leaves of Careya arborea: Structure of careyagenolide

Centella asiatica

1 reference

Antiproliferative constituents from Umbelliferae plants VII. Active triterpenes and rosmarinic acid from Centella asiatica

Cunila lythrifolia

1 reference

Triterpenoid acids from Cunila lythrifolia

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

Dipterocarpus hispidus

1 reference

Terpenes of Dipterocarpus and Doona species

Eucalyptus exserta

1 reference

Two new triterpenoids from the bark of Eucalyptus exserta and their molluscicidal and cytotoxic activities.

Gentiana dahurica

1 reference

Triterpenoids and Iridoid Glycosides from Gentiana dahurica

Juglans regia

1 reference

Antiproliferative triterpenes from the leaves and twigs of Juglans sinensis on HSC-T6 cells

Photinia serratifolia

1 reference

Triterpenoids from the Edible Leaves ofPhotinia serrulata

Photinia serrulata

1 reference

Triterpenoids from the Edible Leaves ofPhotinia serrulata

Planchonella duclitan

1 reference

Triterpene Acids from the Leaves ofPlanchonella Duclitan(Blanco) Bakhuizan

Premna tomentosa

1 reference

Cytotoxic clerodane diterpenoids from the leaves of Premna tomentosa.

Prunus dulcis

1 reference

Antiproliferative terpenoids from almond hulls (Prunus dulcis): identification and structure-activity relationships

Prunus serrulata var. spontanea

1 reference

A new pentacyclic triterpenoid glucoside from Prunus serrulata var. spontanea

Justicia procumbens

1 reference

Antibacterial lignans and triterpenoids from Rostellularia procumbens

Salvia cana

1 reference

Diterpenes from the roots of Salvia canariensis

Salvia miltiorrhiza

1 reference

Triterpenoids from the Flowers of Salvia miltiorrhiza

Salvia virgata

1 reference

Terpenoids from Salvia willeana and S. Virgata

Symplocos paniculata

1 reference

Inhibition of protein tyrosine phosphatase 1B by ursane-type triterpenes isolated from Symplocos paniculata

Ugni molinae

1 reference

Topical anti-inflammatory activity of 2alpha-hydroxy pentacyclic triterpene acids from the leaves of Ugni molinae

Viburnum erubescens

1 reference

Hederagenic acid and other constituents of Viburnum erubescens

Vitex agnus-castus

1 reference

A new diterpenoid glucoside and two new diterpenoids from the fruit of Vitex agnus-castus

Perilla frutescens var. frutescens

1 reference

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

Actinidia valvata

1 reference

Corosolic acid induces apoptosis through mitochondrial pathway and caspase activation in human cervix adenocarcinoma HeLa cells.

Licania cariae

2 references

Phytochemical investigations of Licania genus. Flavonoids and triterpenoids from Licania carii

Phytochemical investigations within the genus Duboisia

Moquilea cariae

2 references

Phytochemical investigations of Licania genus. Flavonoids and triterpenoids from Licania carii

Phytochemical investigations within the genus Duboisia

Prunus serrulata f. spontanea

1 reference

A new pentacyclic triterpenoid glucoside from Prunus serrulata var. spontanea

Vitex negundo

1 reference

Anti-inflammatory ursane- and oleanane-type triterpenoids from Vitex negundo var. cannabifolia

Gentiana davidii var. formosana

1 reference

A New Acylated Secoiridoid from Gentiana formosana

Salvia officinalis

1 reference

Bestandteile von Salvia officinalis

Polylepis besseri

1 reference

Chemical investigation of Polylepis incana (Rosaceae)

Geum macrophyllum

1 reference

Triterpenoids and glycosides from Geum japonicum

Alchemilla monticola

1 reference

Alchemilla xanthochlora

1 reference

Potentilla erecta

1 reference

New Triterpenoid Saponins from the Roots of Potentilla tormentilla

Dasiphora fruticosa

1 reference

Chemical composition of Potentilla fruticosa. II. Triterpenoids

Moquilea pyrifolia

1 reference

New Lupane Derivatives from the Leaves ofLicania pyrifolia

Photinia glabra

1 reference

Triterpenoids from the Edible Leaves ofPhotinia serrulata

Prunus avium

1 reference

Antiproliferative terpenoids from almond hulls (Prunus dulcis): identification and structure-activity relationships

Lamiaceae

1 reference

A novel antimicrobial abietane-type diterpene from Salvia albocaerulea.

Identifiers

InChI

InChI=1S/C30H48O4/c1-17-10-13-30(25(33)34)15-14-28(6)19(23(30)18(17)2)8-9-22-27(5)16-20(31)24(32)26(3,4)21(27)11-12-29(22,28)7/h8,17-18,20-24,31-32H,9-16H2,1-7H3,(H,33,34)/t17-,18+,20-,21+,22-,23+,24+,27+,28-,29-,30+/m1/s1

1 reference

Corosolic acid (English)

7 October 2016

2 references

Corosolic acid (English)

7 October 2016

ChEBI release 2020-09-01

2 references

corosolic acid (English)

7 October 2016

https://commonchemistry.cas.org/detail?cas_rn=4547-24-4

8 April 2021

1 reference

Corosolic acid (English)

7 October 2016

2 references

Corosolic acid (English)

7 October 2016

ChEBI ID

67895

mapping relation type

2 references

corosolic acid (English)

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C30H48O4/c1-17-10-13-30(25(33)34)15-14-28(6)19(23(30)18(17)2)8-9-22-27(5)16-20(31)24(32)26(3,4)21(27)11-12-29(22,28)7/h8,17-18,20-24,31-32H,9-16H2,1-7H3,(H,33,34)/t17-,18+,20-,21+,22-,23+,24+,27+,28-,29-,30+/m1/s1

1 reference

COROSOLIC ACID (English)

7 October 2016

2 references

splash10-00di-0000900000-e570b14aa4aa43281f38

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

0 references

splash10-00di-0000900000-151c3f0e61b7d1b62e83

0 references

splash10-00di-0000900001-1a07defbf0bf868504d8

0 references

splash10-00di-0000900000-1c605655d304a7330562

0 references

splash10-00di-0000900000-996c8326bfd2bc120b37

0 references

DSSTox substance ID

DTXSID70904142

1 reference

DSSTOX compound identifier

DTXCID501332027

0 references

EC number

610-253-4

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.125.730

27 December 2018

ECHA Substance Infocard ID

Urs-12-en-28-oic acid, 2,3-dihydroxy-, (2α,3β)- (English)

quotation

CAS no.: 4547-24-4 (English)

100.125.730

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.125.730

27 December 2018

Human Metabolome Database ID

Urs-12-en-28-oic acid, 2,3-dihydroxy-, (2α,3β)- (English)

quotation

CAS no.: 4547-24-4 (English)

HMDB0304746

2 references

UNII

AMX2I57A98

2 references

Global Substance Registration System

UNII

AMX2I57A98

COROSOLIC ACID (English)

7 October 2016