hydroxyresveratrol (Q7116143)

29700-22-9 (English)

5 October 2016

C₁₄H₁₂O₄

1 reference

29700-22-9 (English)

19 November 2016

C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O

1 reference

29700-22-9 (English)

19 November 2016

C1=CC(=C(C=C1O)O)/C=C/C2=CC(=CC(=C2)O)O

1 reference

In-vitro and in-vivo anti-inflammatory effect of oxyresveratrol from Morus alba L.

29700-22-9 (English)

19 November 2016

4 references

Hepatoprotective and free radical scavenging activities of prenylflavonoids, coumarin, and stilbene from Morus alba

A novel stilbene glucoside, oxyresveratrol 3'-O-beta-glucopyranoside, from the root bark of Morus alba

Pancreatic lipase inhibitory constituents from Morus alba leaves and optimization for extraction conditions

Morus macroura

2 references

A stilbene dimer, andalasin B, from the root trunk of Morus macroura

Andalasin A, a new stilbene dimer from Morus macroura

Sorocea muriculata

1 reference

Sorocenols G and H, anti-MRSA oxygen heterocyclic Diels-Alder-type adducts from Sorocea muriculata roots.

Artocarpus dadah

1 reference

Constituents of the bark and twigs of Artocarpus dadah with cyclooxygenase inhibitory activity

Artocarpus gomezianus

1 reference

Artoindonesianins N and O, new prenylated stilbene and prenylated arylbenzofuran derivatives from Artocarpus gomezianus

Artocarpus reticulatus

1 reference

Prenylated flavonoids and related compounds of the Indonesian Artocarpus (Moraceae)

Schoenocaulon officinale

1 reference

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

Milicia excelsa

2 references

Excelsaoctaphenol, a stilbene dimer from Chlorophora excelsa

Metabolites from Chlorophora excelsa: Possible intermediates in the biogenesis of a pentasubstituted stilbene

Gnetum hainanense

1 reference

Five new stilbene dimers from the lianas of Gnetum hainanense

Maclura pomifera

3 references

Flavanones and xanthones from Maclura pomifera

Phenolics from osage orange wood cleavage of oxyresveratrol

A stilbene from the heartwood of Maclura pomifera: Note

Melaleuca leucadendra

1 reference

Biologically Active constituents of Melaleuca leucadendron: Inhibitors of Induced Histamine Release from Rat Mast Cells

Morus mongolica

1 reference

On the Structure of Sanggenon Q, A New Diels-Alder Type Adduct from Morus mongolica Schneider

Veratrum grandiflorum

2 references

Antifungal stress compounds from Veratrum grandiflorum leaves treated with cupric chloride

The Phenolic Substances of white Hellebore (Veratrum Grandiflorum Loes fil.) II

Prunus dulcis

1 reference

Characterisation of stilbenes in California almonds (Prunus dulcis) by UHPLC-MS

Artocarpus heterophyllus

1 reference

Anti-inflammatory effects of phenolic compounds isolated from the fruits of Artocarpus heterophyllus

Bagassa guianensis

1 reference

Secondary metabolites of Bagassa guianensis Aubl. wood: a study of the chemotaxonomy of the Moraceae family

Fatsia japonica

1 reference

Triterpene saponins and other constituents from Fatsia japonica

Gnetum montanum

1 reference

Stilbene Derivatives fromGnetum montanumMarkgr. f.megalocarpumMarkgr.

Spirotropis longifolia

1 reference

Secondary metabolites from Spirotropis longifolia (DC) Baill and their antifungal activity against human pathogenic fungi

Morus

1 reference

Phytochemical profiles of different mulberry (Morus sp.) species from China

Vitis vinifera

1 reference

Stir bar sorptive extraction with gas chromatography-mass spectrometry for the determination of resveratrol, piceatannol and oxyresveratrol isomers in wines

Artocarpus lacucha

1 reference

Constituents of the bark and twigs of Artocarpus dadah with cyclooxygenase inhibitory activity

Prunus avium

1 reference

Characterisation of stilbenes in California almonds (Prunus dulcis) by UHPLC-MS

breadfruit

1 reference

Chemical constituents of the fruits of Artocarpus altilis

Identifiers

InChI

InChI=1S/C14H12O4/c15-11-4-3-10(14(18)8-11)2-1-9-5-12(16)7-13(17)6-9/h1-8,15-18H/b2-1+

1 reference

PDHAOJSHSJQANO-OWOJBTEDSA-N

29700-22-9 (English)

19 November 2016

2 references

29700-22-9 (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

29700-22-9

2 references

Global Substance Registration System

UNII

6V071CP5CR

hydroxyresveratrol (English)

PDHAOJSHSJQANO-OWOJBTEDSA-N

19 November 2016

InChIKey

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=29700-22-9

1 reference

Oxyresveratrol (English)

19 November 2016

1 reference

29700-22-9 (English)

19 November 2016

mapping relation type

1 reference

OXYRESVERATROL (English)

19 November 2016

1 reference

splash10-0a4j-0910000000-59fb6af87749967847bd

OXYRESVERATROL (English)

19 November 2016

1 reference

inferred from InChIKey

SCHEMBL988358

1 reference

based on heuristic

inferred from InChIKey

1 reference

0 references

EC number

608-401-8

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.108.380

27 December 2018

ECHA Substance Infocard ID

4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]benzene-1,3-diol (English)

quotation

CAS no.: 29700-22-9 (English)

100.108.380

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.108.380

27 December 2018

4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]benzene-1,3-diol (English)

quotation

CAS no.: 29700-22-9 (English)

0 references

2 references

Oxyresveratrol (English)

5 October 2016

based on heuristic

inferred from InChIKey

UNII

6V071CP5CR

1 reference

Global Substance Registration System

UNII

6V071CP5CR

hydroxyresveratrol (English)

19 November 2016

0 references

1 reference