euscaphic acid (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

3 references

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

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

Rosa roxburghii

1 reference

Chemical Constituents of Saurauia roxburghii

Rosa laevigata

4 references

Steroids and triterpenoids from Rosa laevigata

Anti-inflammatory triterpenes from the leaves of 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

4 references

Pomolic acid derivatives from the root of Sanguisorba officinalis

Triterpene glycosides from the roots of Sanguisorba officinalis

Triterpene glycosides from the roots of Sanguisorba officinalis

Triterpene glycosides from the roots of Sanguisorba officinalis

Lepechinia caulescens

1 reference

Abietanoid acid from Lepechinia caulescens

Musanga cecropioides

5 references

Musangicic acid, a triterpenoid constituent of Musanga cecropioides

The Chemical Constituents 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 ofRosa taiwanensis

Geum japonicum

3 references

The anticoagulant effects ofGeum japonicum extract and its constituents

Anti-HIV triterpene acids from Geum japonicum

Anti-HIV triterpene acids from Geum japonicum

Chaenomeles sinensis

2 references

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

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

Cotoneaster simonsii

2 references

Flavonols and isoflavones from Cotoneaster simonsii

Flavonols and isoflavones from Cotoneaster simonsii

Euscaphis japonica

3 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

Cytotoxic Hexacyclic Triterpene Acids from Euscaphis japonica

Jacaranda caucana

1 reference

Jacoumaric acid, a new triterpene ester from Jacaranda caucana

Rubus ellipticus var. obcordatus

2 references

Triterpenoid saponins from Rubus ellipticus var. obcordatus

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

3 references

Monoterpene glycosides and triterpene acids from Eriobotrya deflexa

Monoterpene glycosides and triterpene acids from Eriobotrya deflexa

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

2 references

Triterpenes from Paliurus hemsleyanus

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

2 references

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

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

Rosa sericea

1 reference

Chemical constituents from fruits of Ligustrum lucidum

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

Synurus excelsus

1 reference

Phytochemical Constituents of Palm Oil

Complex-toothed flying squirrel

1 reference

Cytotoxic triterpenes from a Chinese medicine, Goreishi

Vitex altissima

2 references

Flavonoids, triterpenoids and a lignan from Vitex altissima

Flavonoids, triterpenoids and a lignan from Vitex altissima

Rubus ellipticus

2 references

Triterpenoid saponins from Rubus ellipticus var. obcordatus

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 ofPhotinia serrulata

Photinia serrulata

1 reference

Triterpenoids from the Edible Leaves ofPhotinia 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 ofGeum 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 ofPhotinia serrulata

Staphylea japonica

1 reference

Cytotoxic Hexacyclic Triterpene Acids from Euscaphis japonica

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

Human Metabolome Database ID

1 reference

0 references

HMDB0036651

2 references

1 reference

euscaphic acid (English)

7 October 2016

UNII

LG23EX5V2J

1 reference

0 references

1 reference

euscaphic acid (English)