(Q105033280)

English

(2S,3R,4S,5R,6R)-2-[3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

chemical compound

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Statements

instance of

type of chemical entity

0 references

subclass of

(3R,4S,5S,6R)-2-{3-hydroxy-5-[(1E)-2-(4-hydroxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

based on heuristic

inferred from SMILES

2-[3-Hydroxy-5-[2-(4-hydroxyphenyl)vinyl]phenoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

1 reference

based on heuristic

inferred from SMILES

(2S,4S,5S)-2-[3-hydroxy-5-[(Z)-2-(4-hydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

based on heuristic

inferred from SMILES

mass

390.131467664 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

(2R,3S,4R,5R,6S)-2-[3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

based on heuristic

inferred from InChIKey

Resveratrol 3-Glucoside

2 references

based on heuristic

inferred from InChIKey

1 reference

(2S,3R,4S,5S,6R)-2-[3-hydroxy-5-[2-(4-hydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

based on heuristic

inferred from InChI

Glycosylated resveratrol

1 reference

1 reference

C₂₀H₂₂O₈

0 references

canonical SMILES

OC1=CC=C(C=C1)C=CC=2C=C(O)C=C(OC3OC(CO)C(O)C(O)C3O)C2

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isomeric SMILES

OC[C@H]1O[C@@H](Oc2cc(O)cc(/C=C/c3ccc(O)cc3)c2)[C@H](O)[C@@H](O)[C@H]1O

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found in taxon

Ampelopsis heterophylla var. hancei

1 reference

stated in

Ampelopsins E, E, H and cis-ampelopsin E, oligostilbenes from Ampelopsis brevipedunculata var. Hancei roots

Fagopyrum megacarpum

1 reference

stated in

Studies on nepalese crude drugs. XXVIII. Chemical constituents of Bhote Khair, the underground parts of Eskemukerjea megacarpum HARA.

Eucalyptus decorticans

1 reference

stated in

Polyphenols of Eucalyptus sideroxylon wood

Eucalyptus pruinosa

1 reference

stated in

Polyphenols of Eucalyptus sideroxylon wood

Lysidice brevicalyx

1 reference

stated in

Targeted isolation and structure elucidation of stilbene glycosides from the bark of Lysidice brevicalyx Wei guided by biological and chemical screening

Schoenocaulon officinale

1 reference

stated in

Stilbene and 2-arylbenzofuran glucosides from the rhizomes of Schoenocaulon officinale

Sorghum bicolor

1 reference

stated in

Accumulation of trans-piceid in sorghum seedlings infected with Colletotrichum sublineolum

Upuna borneensis

1 reference

stated in

Acetophenone C-glucosides and stilbene O-glucosides in Upuna borneensis

Vatica rassak

1 reference

stated in

Oligostilbenoids in stem bark of Vatica rassak

Veratrum grandiflorum

1 reference

stated in

Antifungal stress compounds from Veratrum grandiflorum leaves treated with cupric chloride

Picea jezoensis

1 reference

stated in

Stilbene biosynthesis in the needles of spruce Picea jezoensis.

Ampelopsis glandulosa var. hancei

1 reference

stated in

Ampelopsins E, E, H and cis-ampelopsin E, oligostilbenes from Ampelopsis brevipedunculata var. Hancei roots

Picea abies

2 references

stated in

Bio-Guided Isolation of Methanol-Soluble Metabolites of Common Spruce (Picea abies) Bark by-Products and Investigation of Their Dermo-Cosmetic Properties

stated in

Phenolic extractives from root bark of Picea abies

Foeniculum vulgare

1 reference

stated in

Phenolic glycosides from Foeniculum vulgare fruit and evaluation of antioxidative activity

broad bean

1 reference

stated in

UHPLC-ESI-QTOF-MS-based metabolic profiling of Vicia faba L. (Fabaceae) seeds as a key strategy for characterization in foodomics

Kalmia procumbens

1 reference

stated in

A stilbene and dihydrochalcones with radical scavenging activities from Loiseleuria procumbens

Identifiers

InChI

InChI=1S/C20H22O8/c21-10-16-17(24)18(25)19(26)20(28-16)27-15-8-12(7-14(23)9-15)2-1-11-3-5-13(22)6-4-11/h1-9,16-26H,10H2/b2-1+/t16-,17+,18+,19-,20-/m1/s1

0 references

InChIKey

HSTZMXCBWJGKHG-JTHNCSCQSA-N

0 references

1 reference

26 December 2021

1 reference

(Q105033280)

(2S,3R,4S,5R,6R)-2-[3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Statements

Identifiers

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