resveratrol (Q407329)

Gene Ontology release 2020-05-02

Rhea release 113

resveratrol 3,5-O-dimethyltransferase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

chemical structure

Resveratrol.svg
697 × 402; 3 KB

1 reference

imported from Wikimedia project

German Wikipedia

mass

228.079 dalton

1 reference

501-36-0 (English)

19 October 2016

C₁₄H₁₂O₃

1 reference

501-36-0 (English)

19 November 2016

C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O

1 reference

501-36-0 (English)

19 November 2016

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

1 reference

Stilbenes of the rhytidome of Pinus sibirica and Picea koraiensis

501-36-0 (English)

19 November 2016

3 references

Hydroxystilbenes of the inner bark of Pinus sibirica

Hydroxystilbenes from the bark of Pinus sibirica

Pinus koraiensis

1 reference

Stilbenes of the rhytidome of Pinus sibirica and Picea koraiensis

Humulus lupulus

2 references

Determination of stilbenes in hop pellets from different cultivars

Fate of resveratrol and piceid through different hop processings and storage times

Cyphostemma crotalarioides

3 references

Antifungal activity of resveratrol oligomers fromCyphostemma crotalarioides

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

Cis ε-viniferin: A New Antifungal Resveratrol Dehydrodimer from Cyphostemma crotalarioides Roots

Polygonaceae

1 reference

Inhibition of nitric oxide and inflammatory cytokines in LPS-stimulated murine macrophages by resveratrol, a potent proteasome inhibitor

Artocarpus dadah

1 reference

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

Bauhinia racemosa

1 reference

Pacharin: a new dibenzo(2,3-6,7)oxepin derivative from bauhinia racemosa lamk

Caragana tibetica

1 reference

Antioxidant constituents of Caragana tibetica

Cissus quadrangularis

1 reference

Stilbene Derivatives fromCissusquadrangularis

Eucalyptus crebra

1 reference

Polyphenols of Eucalyptus sideroxylon wood

Eucalyptus decorticans

1 reference

Polyphenols of Eucalyptus sideroxylon wood

Festuca argentina

1 reference

Lignans and a stilbene from Festuca argentina

Gnetum latifolium

1 reference

Stilbenoids from the stem of Gnetum latifolium (Gnetaceae).

Gnetum pendulum

1 reference

Stilbenoids from the lianas of Gnetum pendulum

Gnetum venosum

1 reference

Oligostilbenoids from Gnetum venosum

Nothofagus

1 reference

The polyphenols of Nothofagus species—II.The heartwood of Nothofagus fusca

Parthenocissus tricuspidata

2 references

A resveratrol dimer from Parthenocissus tricuspidata

Two new antioxidant stilbene dimers, parthenostilbenins A and B from Parthenocissus tricuspidata

Phoenix dactylifera

1 reference

Two polyhydroxystilbenes from stems of Phoenix dactylifera

Rumex bucephalophorus

2 references

Resveratrol and Two Monomethylated Stilbenes from Israeli Rumex bucephalophorus and Their Antioxidant Potential

Antioxidant activity and inhibition of alpha-glucosidase by trans-resveratrol, piceid, and a novel trans-stilbene from the roots of Israeli Rumex bucephalophorus L.

Schizocarphus nervosus

1 reference

Homoisoflavanones and stilbenoids from Scilla nervosa

Bolboschoenus fluviatilis

1 reference

The constituents of Scirpus fluviatilis(Torr). A. Gray. I. The structures of two new hydroxystilbene dimers, scirpusin A and B.

Smilax aspera

1 reference

Steroidal saponins from the roots of Smilax aspera subsp. mauritanica

Smilax bracteata

1 reference

Antioxidant phenylpropanoid glycosides from Smilax bracteata

Trifolium campestre

1 reference

Isoflavonoid and stilbene phytoalexins of the genus Trifolium

Vatica rassak

2 references

Oligostilbenoids in stem bark of Vatica rassak

Vaticanol C, a novel resveratrol tetramer, inhibits cell growth through induction of apoptosis in colon cancer cell lines

Vitis coignetiae

1 reference

The production of resveratrol by Vitis vinifera and other members of the Vitaceae as a response to infection or injury

Vitis riparia

1 reference

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

Yucca periculosa

1 reference

Antioxidant and insect growth regulatory activities of stilbenes and extracts from Yucca periculosa

Ampelopsis japonica

1 reference

The constituents of the roots of Ampelopsis japonica

peanut

8 references

A dienyl stilbene phytoalexin from Arachis hypogaea

Resveratrol and Piceid Levels in Natural and Blended Peanut Butters

Plant foods and herbal sources of resveratrol

trans-resveratrol content in commercial peanuts and peanut products

Occurrence of resveratrol in edible peanuts

Isolation, Purification, and Liquid Chromatographic Determination of Stilbene Phytoalexins in Peanuts

Analysis of trans-resveratrol in peanuts and peanut butters consumed in Korea

Comparison of extraction methods for the quantification of selected phytochemicals in peanuts (Arachis hypogaea).

Artocarpus gomezianus

1 reference

Tyrosinase inhibitors from Artocarpus gomezianus

Botrytis cinerea

1 reference

Metabolism of stilbene phytoalexins by Botrytis cinerea: 1. Characterization of a resveratrol dehydrodimer

Chamaecrista dentata

1 reference

Constituents of Cassia laevigata

Chamaecrista greggii

1 reference

Cassanes and anthraquinones from Chamaecrista greggii

Cyperus longus

2 references

Structures and Radical Scavenging Activities of Novel Norstilbene Dimer, Longusone A, and New Stilbene Dimers, Longusols A, B, and C, from Egyptian Herbal Medicine Cyperus longus

Structures of novel norstilbene dimer, longusone A, and three new stilbene dimers, longusols A, B, and C, with antiallergic and radical scavenging activities from Egyptian natural medicine Cyperus longus.

Elephantorrhiza goetzei

1 reference

A new stilbene glycoside from Elephantorrhiza goetzei

Festuca arundinacea

1 reference

Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the poaceae

Festuca versuta

1 reference

Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the poaceae

Gnetum gnemonoides

1 reference

Four New Glucosides of Stilbene Oligomers from the Stem of Gnetum gnemonoides

Gnetum hainanense

1 reference

Five new stilbene dimers from the lianas of Gnetum hainanense

Gnetum klossii

2 references

Phenolic constituents of Lyonia ovalifolia

Phenolic Constituents of Gnetum klossii

Gnetum montanum

2 references

Constituents of Gnetum montanum

Stilbene Derivatives fromGnetum montanumMarkgr. f.megalocarpumMarkgr.

Gnetum parvifolium

1 reference

Stilbenoids in lianas of Gnetum parvifolium.

Holodiscus discolor

1 reference

A stilbene xyloside from Holodiscus discolor bark

Hopea utilis

1 reference

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

Hordeum brevisubulatum

1 reference

Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the poaceae

Hydrangea macrophylla

1 reference

Development of bioactive functions in hydrangeae dulcis folium. III. On the antiallergic and antimicrobial principles of hydrangeae dulcis folium. (1). Thunberginols A, B, and F

Iris halophila

1 reference

Halophilols A and B, two new stilbenes from Iris halophila

Lolium multiflorum

1 reference

Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the poaceae

Lolium perenne

1 reference

Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the poaceae

Lolium persicum

1 reference

Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the poaceae

Lolium rigidum

1 reference

Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the poaceae

Lolium temulentum

1 reference

Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the poaceae

Lonchocarpus utilis

1 reference

Anticancer action of cubé insecticide: correlation for rotenoid constituents between inhibition of NADH:ubiquinone oxidoreductase and induced ornithine decarboxylase activities

Maackia amurensis

3 references

Isoflavones and stilbenes of the heartwood ofMaackia amurensis

Determination of phenolic components in ethanolic extracts from wood of Maackia amurensis

Isoflavonoid production by callus cultures of Maackia amurensis

Maclura pomifera

1 reference

Phenolics from osage orange wood cleavage of oxyresveratrol

Chinese peony

1 reference

Antioxidative activity of resveratrol and its derivatives isolated from seeds of Paeonia lactiflora

Parthenocissus quinquefolia

1 reference

Stilbene derivatives in the stem of parthenocissus quinquefolia

Picea abies

2 references

Stilbenes from Picea abies bark

Anti-leukaemic compounds derived from stilbenes in Picea abies bark

Poa alsodes

1 reference

Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the poaceae

Pterolobium hexapetalum

1 reference

Phenanthrene and stilbenes from Pterolobium hexapetallum

Rheum maximowiczii

1 reference

Phenylbutanoids and stilbene derivatives of Rheum maximowiczii

Rheum palaestinum

1 reference

Anti-platelet stilbenes from aerial parts of Rheum palaestinum

rhubarb

5 references

Effects of stilbene constituents from rhubarb on nitric oxide production in lipopolysaccharide-activated macrophages

Antioxidant constituents from rhubarb: structural requirements of stilbenes for the activity and structures of two new anthraquinone glucosides

Inhibitors from rhubarb on lipopolysaccharide-induced nitric oxide production in macrophages: structural requirements of stilbenes for the activity

Study on anti-Oketsu activity of rhubarb II. Anti-allergic effects of stilbene components from Rhei undulati Rhizoma (dried rhizome of Rheum undulatum cultivated in Korea).

Anti-allergic activity of stilbenes from Korean rhubarb (Rheum undulatum L.): structure requirements for inhibition of antigen-induced degranulation and their effects on the release of TNF-alpha and IL-4 in RBL-2H3 cells

Rheum undulatum

5 references

Effects of stilbene constituents from rhubarb on nitric oxide production in lipopolysaccharide-activated macrophages

Antioxidant constituents from rhubarb: structural requirements of stilbenes for the activity and structures of two new anthraquinone glucosides

Inhibitors from rhubarb on lipopolysaccharide-induced nitric oxide production in macrophages: structural requirements of stilbenes for the activity

Study on anti-Oketsu activity of rhubarb II. Anti-allergic effects of stilbene components from Rhei undulati Rhizoma (dried rhizome of Rheum undulatum cultivated in Korea).

Anti-allergic activity of stilbenes from Korean rhubarb (Rheum undulatum L.): structure requirements for inhibition of antigen-induced degranulation and their effects on the release of TNF-alpha and IL-4 in RBL-2H3 cells

Salacia lehmbachii

1 reference

Four stilbenes from Salacia lehmbachii

Smilax glabra

1 reference

A new flavanone isolated from rhizoma smilacis glabrae and the structural requirements of its derivatives for preventing immunological hepatocyte damage

Smilax perfoliata

1 reference

Studies on chemical constituents of rhizomes of Smilax trinervula

Upuna borneensis

2 references

Resveratrol derivatives from Upuna borneensis

A New Resveratrol Hexamer from Upuna borneensis

Vaccinium angustifolium

1 reference

Resveratrol in raw and baked blueberries and bilberries

Vaccinium macrocarpon

1 reference

An LC-MS method for analyzing total resveratrol in grape juice, cranberry juice, and in wine

Vaccinium myrtillus

2 references

Resveratrol in raw and baked blueberries and bilberries

Resveratrol, pterostilbene, and piceatannol in vaccinium berries

Veratrum grandiflorum

2 references

Antifungal stress compounds from Veratrum grandiflorum leaves treated with cupric chloride

The Phenolic Substances of White Hellebore (Veratrum Grandiflorum Hoes. Fil.) I

Veratrum taliense

2 references

Inhibition of xanthine and monoamine oxidases by stilbenoids from Veratrum taliense.

Steroidal Alkaloids and Stilbenoids from Veratrum taliense

Vitis davidii

1 reference

Oligostilbenes from vitis betulifolia

Vitis rupestris

1 reference

HPLC Analysis of Grapevine Phytoalexins Coupling Photodiode Array Detection and Fluorometry

Yucca schidigera

4 references

Inhibition of inducible nitric oxide synthase expression by yuccaol C from Yucca schidigera roezl

Antimutagenic effect of resveratrol against Trp-P-1.

Resveratrol and other phenolics from the bark of Yucca schidigera roezl.

Yucca schidigera bark: phenolic constituents and antioxidant activity

Broussonetia papyrifera

1 reference

Aromatase inhibitors from Broussonetia papyrifera

Dracaena cochinchinensis

1 reference

Anti-Helicobacter pylori and thrombin inhibitory components from Chinese dragon's blood, Dracaena cochinchinensis

Lens culinaris

1 reference

Changes in the content of bioactive polyphenolic compounds of lentils by the action of exogenous enzymes. Effect on their antioxidant activity

Vitis labrusca

2 references

Contents of resveratrol, piceid, and their isomers in commercially available wines made from grapes cultivated in Japan

Hydroxylated Stilbenes in Selected American Wines

Vitis rotundifolia

1 reference

Hydroxylated Stilbenes in Selected American Wines

Streptomyces avermitilis

3 references

Regioselective hydroxylation of trans-resveratrol via inhibition of tyrosinase from Streptomyces avermitilis MA4680

Microbial transformation of resveratrol by endophyte Streptomyces sp. A12 isolated from Polygonum cuspidatum

Unique secondary metabolites of a Streptomyces strain isolated from extreme salty wetland show antioxidant and antibacterial activities

Ammopiptanthus mongolicus

1 reference

ChemInform Abstract: (+)-3α-Hydroxylupanine, a New Alkaloid from Ammopiptanthus mongolicus (Maxim.) Cheng F.

Bagassa guianensis

1 reference

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

Cayratia japonica

1 reference

Two new resveratrol tetramers isolated from Cayratia japonica (Thunb.) Gagn. with strong inhibitory activity on fatty acid synthase and antioxidant activity

Fagopyrum megacarpum

1 reference

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

Eucalyptus wandoo

1 reference

Hydroxystilbenes of Eucalyptus wandoo

Gnetum macrostachyum

2 references

A new antioxidant flavonoid from the lianas of Gnetum macrostachyum

Macrostachyols A-D, new oligostilbenoids from the roots of Gnetum macrostachyum

Juniperus excelsa

1 reference

Isoflavones and stilbenes from Juniperus macropoda

Juniperus polycarpos var. seravschanica

1 reference

Isoflavones and stilbenes from Juniperus macropoda

Larix gmelinii

1 reference

Polyphenolic compounds from Larix gmelinii phloem

Paeonia × suffruticosa

1 reference

Three new oligostilbenes from the seeds of Paeonia suffruticosa

Pholidota chinensis

1 reference

Stilbene derivatives from Pholidota chinensis and their anti-inflammatory activity

Plasmopara viticola

1 reference

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

Rumex hastatus

1 reference

Hastatusides A and B: Two New Phenolic Glucosides fromRumex hastatus

Rumex nepalensis

1 reference

Bioactive compounds from Rumex plants

Smilax corbularia

1 reference

Estrogenic and anti-estrogenic compounds from the Thai medicinal plant, Smilax corbularia (Smilacaceae).

Smilax excelsa

1 reference

Bioactive chemical constituents from Smilax excelsa

Spirotropis longifolia

1 reference

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

Syagrus romanzoffiana

1 reference

alpha-Glucosidase inhibitors from the seeds of Syagrus romanzoffiana.

Vateria indica

1 reference

Chemical constituents in the leaves of Vateria indica

Vitis amurensis

1 reference

Polyphenols from Vitis amurensis stems

Vitis chunganensis

1 reference

Chunganenol: an unusual antioxidative resveratrol hexamer from Vitis chunganensis

Hultholia mimosoides

1 reference

Potential anti-inflammatory diterpenoids from the roots of Caesalpinia mimosoides Lamk

Chesneya mongolica

1 reference

ChemInform Abstract: (+)-3α-Hydroxylupanine, a New Alkaloid from Ammopiptanthus mongolicus (Maxim.) Cheng F.

Calligonum leucocladum

1 reference

New stilbene derivatives from Calligonum leucocladum.

Stuhlmannia moavi

1 reference

Bioactive compounds from Stuhlmannia moavi from the Madagascar dry forest

Morus

1 reference

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

Vaccinium arboreum

1 reference

Resveratrol, pterostilbene, and piceatannol in vaccinium berries

Vaccinium vitis-idaea

1 reference

Resveratrol, pterostilbene, and piceatannol in vaccinium berries

Causonis japonica

1 reference

Two new resveratrol tetramers isolated from Cayratia japonica (Thunb.) Gagn. with strong inhibitory activity on fatty acid synthase and antioxidant activity

Lycopersicon

1 reference

Detection and quantitation of resveratrol in tomato fruit (Lycopersicon esculentum Mill.).

Juniperus scopulorum

1 reference

Isoflavones and stilbenes from Juniperus macropoda

Gnetum gnemon

1 reference

Stilbene derivatives from Gnetum gnemon Linn.

Humulus scandens

1 reference

Two new phenolic constituents of Humulus japonicus and their cytotoxicity test in vitro

Humulus japonicus

1 reference

Two new phenolic constituents of Humulus japonicus and their cytotoxicity test in vitro

Picea jezoensis

1 reference

Stilbene biosynthesis in the needles of spruce Picea jezoensis.

Moullava spicata

1 reference

Potential anti-inflammatory diterpenoids from the roots of Caesalpinia mimosoides Lamk

Punica granatum

1 reference

Two UGT84 Family Glycosyltransferases Catalyze a Critical Reaction of Hydrolyzable Tannin Biosynthesis in Pomegranate (Punica granatum)

garlic

1 reference

Composition of Polyphenols and Antioxidant Activity of Garlic Bulbs Collected from Different Locations of Korea

Arachis

1 reference

Effect of ultraviolet doses in combined ultraviolet-ultrasound treatments on trans-resveratrol and trans-piceid contents in sliced peanut kernels

Coffea

1 reference

Development of liquid chromatography-tandem mass spectrometry method for analysis of polyphenolic compounds in liquid samples of grape juice, green tea and coffee

Tilia

1 reference

Solid-phase microextraction on-fiber derivatization for the analysis of some polyphenols in wine and grapes using gas chromatography-mass spectrometry.

Streptomyces venezuelae

1 reference

Engineering of plant-specific phenylpropanoids biosynthesis in Streptomyces venezuelae.

Paeonia rockii

1 reference

Bioactive components, antioxidant and antimicrobial activities of Paeonia rockii fruit during development

Iris domestica

3 references

A new stilbene dimer--shegansu B from Belamcanda chinensis

Phenolic constituents of the rhizomes of the Thai medicinal plant Belamcanda chinensis with proliferative activity for two breast cancer cell lines

Shegansu C, a Novel Phenylpropanoid Ester of Sucrose fromBelamcanda chinensis

Vitis vulpina

1 reference

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

Artocarpus lacucha

1 reference

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

Morus alba

2 references

Antioxidant and antityrosinase activity of mulberry (Morus alba L.) twigs and root bark

Isolation and Identification of Antioxidant Polyphenolic Compounds in Mulberry (Morus alba L.) Seeds

Biancaea decapetala

1 reference

Caesaldecan, a Cassane Diterpenoid from the Leaves of Caesalpinia decapetala.

Bistorta elliptica

1 reference

Neuraminidase inhibitors from Reynoutria elliptica

Malus

1 reference

Directly suspended droplet microextraction with in injection-port derivatization coupled to gas chromatography-mass spectrometry for the analysis of polyphenols in herbal infusions, fruits and functional foods

Rheum rhaponticum

5 references

Inhibitors from rhubarb on lipopolysaccharide-induced nitric oxide production in macrophages: structural requirements of stilbenes for the activity

Study on anti-Oketsu activity of rhubarb II. Anti-allergic effects of stilbene components from Rhei undulati Rhizoma (dried rhizome of Rheum undulatum cultivated in Korea).

Antioxidant constituents from rhubarb: structural requirements of stilbenes for the activity and structures of two new anthraquinone glucosides

Effects of stilbene constituents from rhubarb on nitric oxide production in lipopolysaccharide-activated macrophages

Anti-allergic activity of stilbenes from Korean rhubarb (Rheum undulatum L.): structure requirements for inhibition of antigen-induced degranulation and their effects on the release of TNF-alpha and IL-4 in RBL-2H3 cells

Vitis vinifera

49 references

Leaf removal and wine composition of Vitis vinifera L. cv. Nero d'Avola: the volatile aroma constituents.

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

Stilbene content of mature Vitis vinifera berries in response to UV-C elicitation

The production of resveratrol by Vitis vinifera and other members of the Vitaceae as a response to infection or injury

Antioxidant Activity of the Stilbene Astringin, Newly Extracted from Vitis vinifera Cell Cultures

Comparative study of radical scavenger and antioxidant properties of phenolic compounds from Vitis vinifera cell cultures using in vitro tests

Potential cancer-chemopreventive activities of wine stilbenoids and flavans extracted from grape (Vitis vinifera) cell cultures

Direct Analysis of Resveratrol in Wine by Micellar Electrokinetic Capillary Electrophoresis

Delta-viniferin, a resveratrol dehydrodimer: one of the major stilbenes synthesized by stressed grapevine leaves

HPLC Analysis of Grapevine Phytoalexins Coupling Photodiode Array Detection and Fluorometry

Contents of resveratrol, piceid, and their isomers in commercially available wines made from grapes cultivated in Japan

Method to determine resveratrol and pterostilbene in grape berries and wines using high-performance liquid chromatography and highly sensitive fluorimetric detection

Direct HPLC Analysis of cis- and trans-Resveratrol and Piceid Isomers in Spanish Red Vitis vinifera Wines

Induction of Phytoalexin (Resveratrol) Synthesis in Grapevine Leaves Treated with Aluminum Chloride (AlCl3)

Piceid, the major resveratrol derivative in grape juices

Study of polyphenols in grape berries by reversed-phase high-performance liquid chromatography

LIQUID CHROMATOGRAPHY WITH MULTI-CHANNEL ELECTROCHEMICAL DETECTION FOR THE DETERMINATION OF RESVERATROL IN WINE, GRAPE JUICE, AND GRAPE SEED CAPSULES WITH AUTOMATED SOLID PHASE EXTRACTION

Method for the quantitative extraction of resveratrol and piceid isomers in grape berry skins. Effect of powdery mildew on the stilbene content.

Effect of Postharvest Ultraviolet Irradiation on Resveratrol and Other Phenolics of Cv. Napoleon Table Grapes

Resveratrol and a novel tyrosinase in Carignan grape juice

Occurrence of resveratrol and pterostilbene in age-old darakchasava, an ayurvedic medicine from India

An LC-MS method for analyzing total resveratrol in grape juice, cranberry juice, and in wine

Resveratrol content of Palomino fino grapes: influence of vintage and fungal infection.

Comparative Analysis of Concentrations of trans- and cis-Resveratrol in Must and Wine from Eleven Different Grapevines Grown in Hokkaido, Northern Japan.

Plant foods and herbal sources of resveratrol

Determination of trans-resveratrol and other polyphenols in wines by a continuous flow sample clean-up system followed by capillary electrophoresis separation

Stilbene compounds and stilbene synthase expression during ripening, wilting, and UV treatment in grape cv. Corvina

Directly suspended droplet microextraction with in injection-port derivatization coupled to gas chromatography-mass spectrometry for the analysis of polyphenols in herbal infusions, fruits and functional foods

Solid-phase microextraction on-fiber derivatization for the analysis of some polyphenols in wine and grapes using gas chromatography-mass spectrometry.

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

Determination of piceid and resveratrol in Spanish wines deriving from Monastrell (Vitis vinifera L.) grape variety

Polyphenols content in some Italian red wines of different geographical origins

Separation of phenolic compounds by high-performance liquid chromatography with absorbance and fluorimetric detection.

Distinguishing organic wines from normal wines on the basis of concentrations of phenolic compounds and spectral data

RP-HPLC analysis of phenolic compounds and flavonoids in beverages and plant extracts using a CoulArray detector.

Relationship among antioxidant activity, vasodilation capacity, and phenolic content of red wines

Resveratrol Glucosides are Important Components of Commercial Wines

Comparison of polyphenols and aroma in red wines from Portuguese mainland versus Azores Islands

Preliminary study of resveratrol content in Aragón red and rosé wines

Direct determination of phenolic compounds in Sicilian wines by liquid chromatography with PDA and MS detection

Determination of flavonoids and stilbenes in red wine and related biological products by HPLC and HPLC-ESI-MS-MS.

Assay of resveratrol glucosides and isomers in wine by direct-injection high-performance liquid chromatography

Rapid method for resveratrol determination by HPLC with electrochemical and UV detections in wines

Resveratrol Content of Tunisian Wines

Direct liquid chromatographic analysis of resveratrol derivatives and flavanonols in wines with absorbance and fluorescence detection

Analysis of phenolic constituents of biological interest in red wines by high-performance liquid chromatography

Hydroxylated Stilbenes in Selected American Wines

Phenolic compounds and total antioxidant potential of commercial wines

Capillary electrophoretic determination of resveratrol in wines

Festuca rubra

1 reference

Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the poaceae

broad bean

4 references

The identification of gibberellins in immature seeds of Vicia faba, and some chemotaxonomic considerations

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

Fast responses of metabolites in Vicia faba L. to moderate NaCl stress

Kaempferol 3-O-Galactoside, 7-O-Rhamnoside is the Major Green Fluorescing Compound in the Epidermis of Vicia faba

physically interacts with

Prostaglandin-endoperoxide synthase 2

subject has role

enzyme inhibitor

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Peroxisome proliferator activated receptor gamma

17 August 2016

subject has role

enzyme inhibitor

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

17 August 2016

taste receptor type 2

subject has role

agonist

2 references

Comprehensive Analysis of Mouse Bitter Taste Receptors Reveals Different Molecular Receptive Ranges for Orthologous Receptors in Mice and Humans

Bitter taste receptor activation by flavonoids and isoflavonoids: modeled structural requirements for activation of hTAS2R14 and hTAS2R39.

LiverTox likelihood score

LiverTox toxicity likelihood category E

1 reference

8 April 2021

https://www.ncbi.nlm.nih.gov/books/n/livertox/Resveratrol

21 May 2018

1 reference

non-steroidal anti-inflammatory drug

1 reference

15 March 2018

1 reference

MeSH descriptor ID

C059514

phytogenic antineoplastic agents

15 March 2018

1 reference

15 March 2018

1 reference

MeSH descriptor ID

C059514

platelet aggregation inhibitors

15 March 2018

1 reference

15 March 2018

1 reference

15 March 2018

1 reference

InChI=1S/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1+

15 March 2018

0 references

0 references

0 references

Resveratrol

0 references

topic's main category

Category:Resveratrol

0 references

Identifiers

InChI

1 reference

501-36-0 (English)

19 November 2016

2 references

501-36-0 (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

501-36-0

2 references

resveratrol (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=501-36-0

10 April 2021

1 reference

trans-resveratrol (English)

19 November 2016

2 references

501-36-0 (English)

19 November 2016

Reaxys registry number

1912434

1 reference

trans-resveratrol (English)

19 October 2016

ChEBI ID

45713

mapping relation type

3 references

RESVERATROL (English)

19 November 2016

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1+

1 reference

RESVERATROL (English)

19 November 2016

2 references

SCHEMBL19425

2 references

MSBNK-MPI_for_Chemical_Ecology-CE000093

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000094

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000095

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000096

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000097

0 references

0 references

0 references

0 references

0 references

0 references

MSBNK-IPB_Halle-PB000641

0 references

MSBNK-IPB_Halle-PB000642

0 references

MSBNK-IPB_Halle-PB000643

0 references

MSBNK-IPB_Halle-PB000661

0 references

MSBNK-IPB_Halle-PB002421

0 references

MSBNK-IPB_Halle-PB002422

0 references

MSBNK-IPB_Halle-PB002423

0 references

MSBNK-IPB_Halle-PB002424

0 references

MSBNK-IPB_Halle-PB003661

0 references

MSBNK-IPB_Halle-PB003662

0 references

MSBNK-IPB_Halle-PB006261

0 references

MSBNK-IPB_Halle-PB006262

0 references

MSBNK-IPB_Halle-PB006263

0 references

SPLASH

splash10-0a4r-1900000000-12ac653b70e86d051e9a

0 references

splash10-0a4l-3900000000-cddc9dc871ae0131587d

0 references

splash10-0aov-4900000000-085c30542d4dbecc9a30

0 references

splash10-004i-0390000000-f8caace8d6c937282e65

0 references

splash10-052r-1900000000-d06e6e1c144b2d48b364

0 references

splash10-0aou-3900000000-bb14be278509155e8ce6

0 references

splash10-016r-8900000000-7a10869ce89fa2c7828f

0 references

splash10-004i-0090000000-d9def7cee71fb7a40786

0 references

splash10-004r-0970000000-f8c7ca07f27bfc1b8bda

0 references

splash10-0006-0900000000-b1333b06db343c38f529

0 references

splash10-014l-0900000000-c856c7fa9653868e5785

0 references

splash10-004r-0950000000-8e44b9aa58ac75282058

0 references

splash10-000f-0900000000-2b750fcfd933ce8809f2

0 references

splash10-004i-0290000000-9742e3e8991c1c0c270d

0 references

splash10-002r-0940000000-07826509d63ca5c6ed72

0 references

splash10-014i-0910000000-2cac03dc9e9b045fdf23

0 references

splash10-002r-0940000000-fb2be32a94602011c1b2

0 references

splash10-000i-0920000000-4b294faea28304389dcf

0 references

splash10-000i-0910000000-7cfbcea1e1b612e05a02

0 references

splash10-000i-0910000000-93888a6f43e37bc70298

0 references

splash10-004i-0090000000-1d87f420c8ebd2cc1629

0 references

splash10-002r-0940000000-9770f309ccec96a06ebd

0 references

splash10-004i-0090000000-c7a1f8bfe9b46981bc5e

0 references

splash10-004r-0890000000-ebaa23d1e834efa6bd82

0 references

splash10-00kf-0900000000-e6ae1092dce4d19b2bfe

0 references

splash10-004i-0090000000-a44a9432674fd77e6bfc

0 references

splash10-004i-0090000000-4dd2b80e73b9e49f1cbe

0 references

splash10-004i-0090000000-295a6f498044f2e40db9

0 references

splash10-004i-0390000000-781b53b7b6e088dbe519

0 references

splash10-0a4i-2910000000-13c9a4f5b540ead6ed51

0 references

splash10-004i-0090000000-ef67f685ae522ab3ee58

0 references

splash10-004i-0090000000-a546ae8e93357865ebb8

0 references

splash10-004i-0390000000-ed050f32b7af9170820a

0 references

splash10-004i-0090000000-f9ff90d98488d6d05587

0 references

splash10-014i-0900000000-79bf3bfcbb7bcdd0ffd2

0 references

splash10-014i-0900000000-9340e3fe04d435cf8475

0 references

splash10-004i-0590000000-4a9b53d6aad6ed8189d2

0 references

splash10-00kf-0900000000-b0f6bf3388d96335d77e

0 references

splash10-0ar9-0910000000-b498b69c984c5f85498e

0 references

splash10-0007-0932700000-e18cd1a1d304b5b4bac2

0 references

splash10-0007-0931800000-1262ced85c7bce9922a1

0 references

splash10-0006-1853900000-4919511a11ec24935434

0 references

NMRShiftDB structure ID

21968

1 reference

imported from Wikimedia project

RTECS number

CZ8987000

1 reference

1 reference

Hazardous Substances Data Bank

28 October 2019

RESVERATROL (English)

10 May 2021

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

0 references

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.121.386

27 December 2018

ECHA Substance Infocard ID

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

quotation

CAS no.: 501-36-0 (English)

100.121.386

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.121.386

27 December 2018

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

quotation

CAS no.: 501-36-0 (English)

1 reference

28 December 2019

RESVERATROL (English)

quotation

CAS no.: 501-36-0 (English)

0 references

1 reference

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

D02.455.426.559.389.150.700.375

resveratrol (English)

19 November 2016

Resveratrol

0 references

MeSH tree code

0 references

D02.455.426.559.389.657.715.500

0 references

D03.633.100.150.266.450.260.777.500

0 references

RxNorm ID

1000492

1 reference

resveratrol (English)

19 November 2016

DrugBank ID

DB02709

1 reference

Human Metabolome Database ID

HMDB0003747

2 references

3 references

trans-resveratrol (English)

19 October 2016

C00044435

2 references

2 references

resveratrol (English)

19 November 2016

PatientsLikeMe treatment ID

0 references

1 reference

resveratrol (English)

Australian Register of Therapeutic Goods ID

19 November 2016

0 references

0 references

1 reference

Gran Enciclopèdia Catalana ID

trans-resveratrol (English)

19 October 2016

0 references

0 references

0 references

0 references

resveratrol

0 references

Gran Enciclopèdia Catalana ID (former scheme)

0 references

1 reference

9 July 2020

Microsoft Academic ID

0 references

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

4JAZ (English)

19 October 2016

1 reference

1DVS (English)

19 October 2016

1 reference

4QOH (English)

19 October 2016

1 reference

4QOJ (English)

19 October 2016

1 reference

3CKL (English)

19 October 2016

1 reference

1U0W (English)

19 October 2016

1 reference

3FTS (English)

19 October 2016

1 reference

2JIZ (English)

19 October 2016

1 reference

4DPN (English)

19 October 2016

1 reference

5BTR (English)

19 October 2016

1 reference

3MNQ (English)

19 October 2016

1 reference

2YDX (English)

19 October 2016

1 reference

2L98 (English)

19 October 2016

1 reference

5CR1 (English)

19 October 2016

1 reference

4QER (English)

19 October 2016

1 reference

1CGZ (English)

19 October 2016

1 reference

4HDA (English)

19 October 2016

1 reference

1Z1F (English)

19 October 2016

1 reference

1SG0 (English)

19 October 2016

1 reference

4Q93 (English)

19 October 2016

1 reference

4PP6 (English)

19 October 2016

1 reference

1 reference

resveratrol (English)