(Q27136388)

inferred from SMILES

mass

488.350175 dalton

1 reference

Euscaphic acid (English)

2beta-hydroxypomolic acid

7 October 2016

stereoisomer of

2 references

2 references

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

2 references

(1R,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

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

1 reference

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

1 reference

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

1 reference

chemical formula

C₃₀H₄₈O₅

1 reference

Euscaphic acid (English)

7 October 2016

canonical SMILES

CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O

1 reference

Euscaphic 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@]1(C)O)C)C(=O)O

1 reference

Myrianthiphyllin, The First Lignan Cinnamate from Myrianthus arboreus

Euscaphic acid (English)

7 October 2016

2 references

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

Rosa roxburghii

1 reference

Chemical Constituents of Saurauia roxburghii

Rosa laevigata

3 references

Steroids and triterpenoids from Rosa laevigata

Anti-inflammatory secondary metabolites from the leaves of Rosa laevigata

Anti-inflammatory triterpenes from the leaves of Rosa laevigata

Rubus irenaeus

2 references

Chemical Constituents from the Peels of Citrus sudachi

Chemical constituents from the peels of Citrus sudachi

Rubus parkeri

1 reference

Triterpenes from Rubus cochinchinensis

Callicarpa americana

1 reference

Cytotoxic constituents from the fruiting branches of Callicarpa americana collected in southern Florida

Sanguisorba officinalis

3 references

Pomolic acid derivatives from the root of Sanguisorba officinalis

Triterpene glycosides from the roots of Sanguisorba officinalis

Branched-chain sugars of natural occurrence

Lepechinia caulescens

1 reference

Abietanoid acid from Lepechinia caulescens

Musanga cecropioides

4 references

Musangicic acid, a triterpenoid constituent of Musanga cecropioides

Cecropioic acid, a pentacyclic triterpene from Musanga cecropioides

The Chemical Constituents of Musanga cecropioides

Further Triterpenoids of Musanga cecropioides: The Structure of Cecropic Acid

Hoslundia opposita

1 reference

Hosloppin, a New Pyrone-Substituted Flavonoid from Hoslundia opposita

Rosa taiwanensis

1 reference

Chemical Constituents from the Root and Aerial Parts of Rosa taiwanensis

Geum japonicum

2 references

The anticoagulant effects of Geum japonicum extract and its constituents

Anti-HIV triterpene acids from Geum japonicum

Chaenomeles sinensis

1 reference

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

Cotoneaster simonsii

1 reference

Flavonols and isoflavones from Cotoneaster simonsii

Euscaphis japonica

2 references

Studies on constituents of medicinal plants. XIII. Constituents of the pericarps of the capsules of Euscaphis japonica Pax

Cytotoxic Hexacyclic Triterpene Acids from Euscaphis japonica

Jacaranda caucana

1 reference

Jacoumaric acid, a new triterpene ester from Jacaranda caucana

Rubus ellipticus var. obcordatus

1 reference

Triterpenoid saponins from Rubus ellipticus var. obcordatus

Ternstroemia gymnanthera

1 reference

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

Acaena pinnatifida

1 reference

Triterpenoids from Acaena pinnatifida R. et P.

Acanthochlamys bracteata

1 reference

Chemical Constituents of Acanthochlamys bracteata.

Alchemilla alpina

1 reference

Alchemilla faeroensis

1 reference

Alchemilla vulgaris

1 reference

Anchusa strigosa

2 references

New Pyrrolizidine Alkaloids and Glycosides from Anchusa strigosa.

Pyrrolizidine alkaloids from Anchusa strigosa and their antifeedant activity

Eriobotrya deflexa

1 reference

Monoterpene glycosides and triterpene acids from Eriobotrya deflexa

Hedyotis lawsoniae

1 reference

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

Myrianthus libericus

1 reference

Pentacyclic triterpenes from Myrianthus liberecus

Myrianthus serratus

1 reference

An E-ring γ-lactone pentacyclic triterpene from Myrianthus serratus

Paliurus hemsleyanus

1 reference

Triterpenes from Paliurus hemsleyanus

Potentilla tormentilla

1 reference

New Triterpenoid Saponins from the Roots of Potentilla tormentilla

Isodon effusus

1 reference

Terpenoids from Rabdosia effusa HARA.

Rosa bella

1 reference

Chemical Constituents from Fruit of

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 transmorrisonensis

1 reference

Chemical Constituents from the Aerial Part of Rosa Transmorrisonensis

Rosa woodsii

1 reference

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

Rubus sieboldii

1 reference

Novel anti-inflammatory compounds from Rubus sieboldii, triterpenoids, are inhibitors of mammalian DNA polymerases

Rubus ulmifolius

1 reference

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

Complex-toothed flying squirrel

1 reference

Cytotoxic triterpenes from a Chinese medicine, Goreishi

Rubus ellipticus

1 reference

Triterpenoid saponins from Rubus ellipticus var. obcordatus

Vitex negundo var. cannabifolia

1 reference

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

Cecropia pachystachya

1 reference

Natural triterpenoids from Cecropia lyratiloba are cytotoxic to both sensitive and multidrug resistant leukemia cell lines

Centella asiatica

1 reference

A novel triterpene from Centella asiatica.

Dysoxylum densiflorum

1 reference

Terpenoids from Dysoxylum densiflorum.

Incarvillea arguta

1 reference

A New Cyclooxygenase Inhibitor from Incarvillea arguta

Incarvillea diffusa

1 reference

A New Cyclooxygenase Inhibitor from Incarvillea arguta

Photinia serratifolia

1 reference

Triterpenoids from the Edible Leaves of Photinia serrulata

Photinia serrulata

1 reference

Triterpenoids from the Edible Leaves of Photinia serrulata

Rosa rugosa

2 references

19Alpha-hydroxyursane-type triterpenoids: antinociceptive anti-inflammatory principles of the roots of Rosa rugosa

Euscaphic acid isolated from roots of Rosa rugosa inhibits LPS-induced inflammatory responses via TLR4-mediated NF-κB inactivation in RAW 264.7 macrophages

Justicia procumbens

1 reference

Antibacterial lignans and triterpenoids from Rostellularia procumbens

Eriobotrya japonica

3 references

Anti-inflammatory constituents of topically applied crude drugs. I. Constituents and anti-inflammatory effect of Eriobotrya japonica LINDL

Constituents of Eriobotrya japonica. A Study of Their Antiviral Properties

A New Triterpene Ester from Eriobotrya japonica.

Rosa multiflora

2 references

A-ring contracted triterpenoid from Rosa multiflora

Triterpenoids from roots of Rosa laevigata

Epicharis densiflora

1 reference

Terpenoids from Dysoxylum densiflorum.

Rosa

1 reference

Pentacyclic Triterpenes from the Fruits of Rosa sterilis

Alchemilla monticola

1 reference

Alchemilla xanthochlora

1 reference

Geum macrophyllum

2 references

Anti-HIV triterpene acids from Geum japonicum

The anticoagulant effects of Geum japonicum extract and its constituents

Potentilla erecta

1 reference

New Triterpenoid Saponins from the Roots of Potentilla tormentilla

Rhaphiolepis deflexa

1 reference

Monoterpene glycosides and triterpene acids from Eriobotrya deflexa

Photinia glabra

1 reference

Triterpenoids from the Edible Leaves of Photinia serrulata

Staphylea japonica

1 reference

Cytotoxic Hexacyclic Triterpene Acids from Euscaphis japonica

Vitex altissima

1 reference

Flavonoids, triterpenoids and a lignan from Vitex altissima

Identifiers

InChI

InChI=1S/C30H48O5/c1-17-10-13-30(24(33)34)15-14-27(5)18(22(30)29(17,7)35)8-9-21-26(4)16-19(31)23(32)25(2,3)20(26)11-12-28(21,27)6/h8,17,19-23,31-32,35H,9-16H2,1-7H3,(H,33,34)/t17-,19-,20 ,21-,22-,23-,26 ,27-,28-,29-,30 /m1/s1

1 reference

Euscaphic acid (English)

7 October 2016

2 references

Euscaphic acid (English)

7 October 2016

ChEBI release 2020-09-01

2 references

euscaphic acid (English)

7 October 2016

https://commonchemistry.cas.org/detail?cas_rn=53155-25-2

8 April 2021

1 reference

(2alpha,3alpha)-2,3,19-Trihydroxyurs-12-en-28-oic acid (English)

7 October 2016

2 references

Euscaphic acid (English)

7 October 2016

Reaxys registry number

4912896

1 reference

euscaphic acid (English)

7 October 2016

ChEBI ID

67914

mapping relation type

2 references

euscaphic acid (English)

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C30H48O5/c1-17-10-13-30(24(33)34)15-14-27(5)18(22(30)29(17,7)35)8-9-21-26(4)16-19(31)23(32)25(2,3)20(26)11-12-28(21,27)6/h8,17,19-23,31-32,35H,9-16H2,1-7H3,(H,33,34)/t17-,19-,20 ,21-,22-,23-,26 ,27-,28-,29-,30 /m1/s1

1 reference

EUSCAPHIC ACID (English)

7 October 2016

2 references

1 reference

1 reference

Human Metabolome Database ID

NSC number

733507

0 references

HMDB0036651

2 references

1 reference

euscaphic acid (English)

7 October 2016

UNII

LG23EX5V2J

1 reference

0 references

1 reference

euscaphic acid (English)