ε-viniferin (Q5383943)

Epsilon-viniferin (English)

(2R,3S)-cis-epsilon-viniferin

5 October 2016

stereoisomer of

2 references

inferred from InChIKey

2 references

inferred from InChIKey

2 references

inferred from InChIKey

(2S,3R)-trans-epsilon-viniferin

1 reference

(2S,3R)-cis-epsilon-viniferin

1 reference

5-[(2R,3S)-6-hydroxy-2-(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol

1 reference

(2R,3S)-trans-epsilon-viniferin

1 reference

(+)-cis-epsilon-viniferin

1 reference

chemical formula

C₂₈H₂₂O₆

1 reference

Epsilon-viniferin (English)

20 November 2016

canonical SMILES

C1=CC(=CC=C1C=CC2=CC(=CC3=C2C(C(O3)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O)O

1 reference

Epsilon-viniferin (English)

20 November 2016

isomeric SMILES

C1=CC(=CC=C1/C=C/C2=CC(=CC3=C2[C@H]([C@@H](O3)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O)O

1 reference

Oligostilbenes from Carex kobomugi

Epsilon-viniferin (English)

20 November 2016

2 references

Kobophenol A, a unique tetrastilbene from Ohwi (Cyperaceae)

Dipterocarpus grandiflorus

1 reference

Two New Resveratrol (=5-[(1E)-2-(4-Hydroxyphenyl)ethenyl]benzene-1,3-diol) Tetramers with a Tetrahydrofuran Ring fromDipterocarpus grandiflorus

Upuna borneensis

1 reference

Resveratrol derivatives from Upuna borneensis

Vitis vinifera

8 references

3-Hydroxy-3-methylglutaryl-CoA (HMG-CoA) reductase inhibitory effect of Vitis vinifera

First symmetrical bicyclo[6.6.0]tetradecane resveratrol tetramer from stalks of vitis vinifera (Vitaceae)

Oligostilbenes from the roots of Vitis amurensis

Determination of stilbenes (delta-viniferin, trans-astringin, trans-piceid, cis- and trans-resveratrol, epsilon-viniferin) in Brazilian wines.

Profiling of resveratrol oligomers, important stress metabolites, accumulating in the leaves of hybrid Vitis vinifera (Merzling × Teroldego) genotypes infected with Plasmopara viticola

Histological study of the responses of two Vitis vinifera cultivars (resistant and susceptible) to Plasmopara viticola infections

Structure elucidation of peonidin 3,7-o-β-diglucoside isolated from Garnacha Tintorera (Vitis vinifera L.) grapes.

Survey of grapevine Vitis vinifera stem polyphenols by liquid chromatography-diode array detection-tandem mass spectrometry.

Gnetum parvifolium

2 references

A dimeric stilbene from Gnetum parvifolium

Stilbenoids in lianas of Gnetum parvifolium.

Rheum coreanum

1 reference

Inhibition of human low density lipoprotein and high density lipoprotein oxidation by oligostilbenes from rhubarb

Sophora leachiana

2 references

A flavonostilbene and two stilbene oligomers in roots of Sophora leachiana

Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae)

Sophora alopecuroides

2 references

Six flavonostilbenes and a flavanone in roots of Sophora alopecuroides

Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae)

Vitis coignetiae

2 references

Vitisin A and cis-vitisin A, strongly hepatotoxic plant oligostilbenes from Vitis coignetiae (Vitaceae)

Powerful hepatoprotective and hepatotoxic plant oligostilbenes, isolated from the Oriental medicinal plant Vitis coignetiae (Vitaceae)

Cyphostemma crotalarioides

2 references

Antifungal activity of resveratrol oligomers fromCyphostemma crotalarioides

Cyphostemmins A-B, two new antifungal oligostilbenes from Cyphostemma crotalarioides (Vitaceae)

Gnetum gnemon

1 reference

Stilbene derivatives from Gnetum gnemon Linn.

Gnetum hainanense

1 reference

Five new stilbene dimers from the lianas of Gnetum hainanense

Gnetum klossii

2 references

Phenolic Constituents of Gnetum klossii

Phenolic constituents of Lyonia ovalifolia

Gnetum latifolium

1 reference

Stilbenoids from the stem of Gnetum latifolium (Gnetaceae).

Hopea parviflora

1 reference

Stilbenoids in the stem bark of Hopea parviflora

Parthenocissus tricuspidata

2 references

A resveratrol dimer from Parthenocissus tricuspidata

A resveratrol dimer from Parthenocissus tricuspidata

Shorea disticha

1 reference

Distichol an antibacterial polyphenol from Shorea disticha

Sophora davidii

1 reference

Stilbene oligomers in roots of Sophora davidii

Vatica rassak

1 reference

Oligostilbenoids in stem bark of Vatica rassak

Vitis riparia

1 reference

Disease resistance of Vitis spp. and the production of the stress metabolites resveratrol, ε-viniferin, α-viniferin and pterostilbene

Carex fedia

2 references

New 3,5,4'-trihydroxystilbene (resveratrol) oligomers from Carex fedia Nees var. miyabei (Franchet) T. Koyama (Cyperaceae).

New 3,5,4′-Trihydroxystilbene (Resveratrol) Oligomers from Carex fedia Nees var. miyabei (Franchet) T. Koyama (Cyperaceae)

Carex pumila

2 references

(-)-.EPSILON.-Viniferin and related oligostilbenes from Carex pumila Thunb. (Cyperaceae).

(−)-ε-Viniferin and Related Oligostilbenes fromCarex pumitaThunb. (Gyperaceae)

Gnetum montanum

1 reference

Constituents of Gnetum montanum

Hopea utilis

1 reference

Hopeafuran and a C-glucosyl resveratrol isolated from stem wood of Hopea utilis

Iris halophila

1 reference

Halophilols A and B, two new stilbenes from Iris halophila

Sophora moorcroftiana

2 references

Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae)

Stilbene oligomers in roots of Sophora davidii

Sophora stenophylla

1 reference

Phenolic Compounds Isolated from the Roots of Sophora stenophylla.

Vateria indica

2 references

Two new oligostilbenes with dihydrobenzofuran from the stem bark of Vateria indica

Chemical constituents in the leaves of Vateria indica

Vatica albiramis

1 reference

Resveratrol oligomers from Vatica albiramis

Dipterocarpus hasseltii

1 reference

Cytotoxic resveratrol oligomers from the tree bark of Dipterocarpus hasseltii.

Plasmopara viticola

2 references

Profiling of resveratrol oligomers, important stress metabolites, accumulating in the leaves of hybrid Vitis vinifera (Merzling × Teroldego) genotypes infected with Plasmopara viticola

Histological study of the responses of two Vitis vinifera cultivars (resistant and susceptible) to Plasmopara viticola infections

Shorea roxburghii

1 reference

A new dimeric resveratrol from the roots of Shorea roxburghii

Vatica pauciflora

1 reference

New resveratrol oligomers in the stem bark of Vatica pauciflora

Vitis ficifolia

1 reference

Resveratrol derivatives from the roots of Vitis thunbergii

Vitis heyneana

2 references

Resveratrol derivatives from the roots of Vitis thunbergii

Two Lignan Glycosides from Vitis thunbergii

Vitis vulpina

1 reference

Disease resistance of Vitis spp. and the production of the stress metabolites resveratrol, ε-viniferin, α-viniferin and pterostilbene

Rheum

1 reference

New resveratrol oligomer derivatives from the roots of Rheum lhasaense

Commons category

Epsilon-Viniferin

0 references

Identifiers

InChI

InChI=1S/C28H22O6/c29-20-7-2-16(3-8-20)1-4-18-11-24(33)15-25-26(18)27(19-12-22(31)14-23(32)13-19)28(34-25)17-5-9-21(30)10-6-17/h1-15,27-33H/b4-1+/t27-,28+/m1/s1

1 reference

Epsilon-viniferin (English)

20 November 2016

2 references

Epsilon-viniferin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

62218-08-0

2 references

Global Substance Registration System

UNII

0K8Z2K6Y7O

ε-viniferin (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=62218-08-0

10 April 2021

1 reference

Epsilon-viniferin (English)

20 November 2016

2 references

Epsilon-viniferin (English)

matched by identifier from

20 November 2016

Reaxys registry number

4278292

1 reference

(-)-trans-epsilon-viniferin (English)

5 October 2016

ChEBI ID

10556

mapping relation type

2 references

EPSILON-VINIFERIN (English)

matched by identifier from

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C28H22O6/c29-20-7-2-16(3-8-20)1-4-18-11-24(33)15-25-26(18)27(19-12-22(31)14-23(32)13-19)28(34-25)17-5-9-21(30)10-6-17/h1-15,27-33H/b4-1+/t27-,28+/m1/s1

1 reference

EPSILON-VINIFERIN (English)

20 November 2016

1 reference

MassBank accession ID

MSBNK-RIKEN-PR304252

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

splash10-0a4j-0009100000-efe998b03cfeb059aa10

0 references

KNApSAcK ID

C00002905

reason for deprecated rank

cannot be confirmed by other sources

1 reference

Global Substance Registration System

(-)-trans-epsilon-viniferin (English)

5 October 2016

2 references

UNII

0K8Z2K6Y7O

ε-viniferin (English)

matched by identifier from

20 November 2016

0 references

1 reference

(-)-trans-epsilon-viniferin (English)