eriodictyol (Q3459685)

eriodictyol 3'-O-methyltransferase activity

1 February 2021

1 reference

reference URL

http://geneontology.org/external2go/rhea2go

1 February 2021

chemical structure

Eriodictyol.png
671 × 438; 8 KB

0 references

mass

288.063 dalton

1 reference

ERIODICTYOL (English)

19 October 2016

1 reference

C₁₅H₁₂O₆

1 reference

ERIODICTYOL (English)

19 October 2016

canonical SMILES

C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O

1 reference

ERIODICTYOL (English)

19 October 2016

isomeric SMILES

C1[C@H](OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O

1 reference

Huazhongilexone is not 3',5,5',7-Tetrahydroxyflavanone. Preparation of 3',5'-Dimethoxy-5,7-dihydroxyflavanone.

ERIODICTYOL (English)

19 October 2016

1 reference

Onopordum laconicum

1 reference

Flavonoids of Onopordum sibthorpianum and Onopordum laconicum

Eupatorium album

1 reference

External Flavonoids of 12 Species of North American Eupatorieae (Asteraceae)

Eupatorium hyssopifolium

1 reference

External Flavonoids of 12 Species of North American Eupatorieae (Asteraceae)

Eupatorium rotundifolium

1 reference

External Flavonoids of 12 Species of North American Eupatorieae (Asteraceae)

Eupatorium serotinum

1 reference

External Flavonoids of 12 Species of North American Eupatorieae (Asteraceae)

Hazardia squarrosa

1 reference

Flavonoid aglycones in the resin of Hazardia squarrosa var. Grindelioides

Luetkea pectinata

1 reference

Flavonoids of Luetkea pectinata (Rosaceae: Spiraeoideae)

Rubus phoenicolasius

1 reference

Flavonoid-Aglyka als Drüsenprodukte der Moosrose (Rosa centifolica cv. muscosa) und der Japanischen Weinbeere (Rubus phoenicolasius) / Flavonoid Aglycones as Glandular Products in Rosa centifolia cv. muscosa and in Rubus phoenicolasius

Anthemis altissima

2 references

Sesquiterpene lactones from Anthemis altissima and their anti-Helicobacter pylori activity

Sesquiterpene lactones from Anthemis altissima and their anti-Helicobacter pylori activity

peanut

4 references

Constituents of Useful Plants. IX. Constituents of Arachis hypogaea L.

Analysis of enantiomeric flavanones in plant extracts by high-performance liquid chromatography on a cellulose triacetate based chiral stationary phase

Depression of Aflatoxin Production by Flavonoid-Type Compounds from Peanut Shells

Constituents of Useful Plants. IX. Constituents of Arachis hypogaea L.

Chrysothamnus viscidiflorus

2 references

Leaf surface flavonoids of Chrysothamnus

Leaf surface flavonoids of Chrysothamnus

Dipteryx odorata

2 references

Potential cancer chemopreventive constituents of the seeds of Dipteryx odorata (tonka bean).

Potential cancer chemopreventive constituents of the seeds of Dipteryx odorata (tonka bean).

Elsholtzia bodinieri

1 reference

Three new flavonoid glycosides isolated from Elsholtzia bodinieri.

Erycibe expansa

1 reference

Structures of new flavonoids, erycibenins D, E, and F, and NO production inhibitors from Erycibe expansa originating in Thailand

Eysenhardtia subcoriacea

2 references

Antioxidant aryl-prenylcoumarin, flavan-3-ols and flavonoids from Eysenhardtia subcoriacea.

Antioxidant aryl-prenylcoumarin, flavan-3-ols and flavonoids from Eysenhardtia subcoriacea.

Phlomis nissolii

3 references

Flavonoids from Phlomis nissolii

Flavonoids from Phlomis nissolii

Flavonoids from Phlomis nissolii

Rhamnus disperma

3 references

Polyphenolic metabolites of Rhamnus disperma

Polyphenolic metabolites of Rhamnus disperma

Polyphenolic metabolites of Rhamnus disperma

Rhodiola sachalinensis

2 references

Bioactive constituents from Chinese natural medicines. XXVI. Chemical structures and hepatoprotective effects of constituents from roots of Rhodiola sachalinensis

Bioactive constituents from Chinese natural medicines. XXVI. Chemical structures and hepatoprotective effects of constituents from roots of Rhodiola sachalinensis

Saracha punctata

2 references

A novel antiprotozoal aminosteroid from Saracha punctata

A novel antiprotozoal aminosteroid from Saracha punctata

Spatholobus suberectus

2 references

Bioactive constituents of Spatholobus suberectus in regulating tyrosinase-related proteins and mRNA in HEMn cells

Bioactive constituents of Spatholobus suberectus in regulating tyrosinase-related proteins and mRNA in HEMn cells

Anastatica hierochuntica

7 references

Anastatins A and B, New Skeletal Flavonoids with Hepatoprotective Activities from the Desert Plant Anastatica hierochuntica

Melanogenesis inhibitors from the desert plant Anastatica hierochuntica in B16 melanoma cells

Anastatins A and B, New Skeletal Flavonoids with Hepatoprotective Activities from the Desert Plant Anastatica hierochuntica

Anastatins A and B, new skeletal flavonoids with hepatoprotective activities from the desert plant Anastatica hierochuntica.

Melanogenesis inhibitors from the desert plant Anastatica hierochuntica in B16 melanoma cells

Melanogenesis inhibitors from the desert plant Anastatica hierochuntica in B16 melanoma cells

Anastatins A and B, new skeletal flavonoids with hepatoprotective activities from the desert plant Anastatica hierochuntica.

Searsia retinorrhoea

1 reference

A weakly antimalarial biflavanone from Rhus retinorrhoea

Thymus numidicus

1 reference

Secondary metabolites from Thymus numidicus Poiret.

Aglaia rubiginosa

3 references

Cytotoxic constituents of the twigs and leaves of Aglaia rubiginosa.

Cytotoxic Constituents of the Twigs and Leaves of Aglaia rubiginosa

Cytotoxic constituents of the twigs and leaves of Aglaia rubiginosa.

Allagopappus dichotomus

1 reference

Sesquiterpene Lactones and Other Constituents of Allagopappus Species

Allagopappus viscosissimus

1 reference

Germacranolides fromAllagopappus viscosissimus

Ambrosia artemisioides

1 reference

Eudesmanolides, 5,10-bis-epi-eudesmanes and oplopanone derivatives from Ambrosia artemisioides

Ambrosia bidentata

2 references

Exudate flavonoids in some solanaceae

Exudate Flavonoids in ThreeAmbrosiaSpecies

Argemone mexicana

2 references

Flavonoids in the seeds of Argemone mexicana: a reappraisal

Flavonoids in the seeds of Argemone mexicana: a reappraisal

tarragon

1 reference

Acetylenes and Other Constituents from Artemisia dracunculus

Artemisia xanthochloa

2 references

Prenylated coumarates from Artemisia xanthochroa

Prenylated coumarates from Artemisia xanthochroa

Baccharis genistelloides

2 references

Studies on the constituents of Baccharis genistelloides.

Studies on the constituents of Baccharis genistelloides.

Baccharis salicifolia

1 reference

Diterpene glycosides and other constituents from argentinian baccharis species

Bauhinia purpurea

1 reference

Chemical Constituents of Heartwood ofBauhinia purpurea

Berchemia racemosa

1 reference

Constituents of Berchemia racemosa Sieb. et Zucc

Bracteantha viscosa

2 references

Exudate flavonoids from two australian asteraceae, Bracteantha viscosa and cassinia quinquefaria

Constituents of helichrysum viscosum var. bracteatum DC.

Brickellia vernicosa

2 references

Flavonoids of Brickellia vernicosa

Flavonoids of Brickellia vernicosa

Calycotome villosa

2 references

Flavonoids from Calicotome villosa

Flavonoids from Calicotome villosa

Carthamus tinctorius

1 reference

6-hydroxykaempferol and its glycosides from Carthamus tinctorius petals

Chromolaena tyleri

1 reference

4-Hydroxyfla Vanones FromChromolena Tyleri.Evidence of A Characteristic Ei-Ms

Chrysanthemum indicum

2 references

Studies on the monoamine oxidase inhibitors of medicinal plants I. Isolation of MAO-B inhibitors fromChrysanthemum indicum

Medicinal flowers. VI. Absolute stereostructures of two new flavanone glycosides and a phenylbutanoid glycoside from the flowers of Chrysanthemum indicum L.: their inhibitory activities for rat lens aldose reductase

Conyza pallidiflora

1 reference

Diterpenes and sesquiterpene xylosides from east africanConyza species

Crataegus microphylla

1 reference

Flavonoids of Crataegus microphylla

Croton steenkampianus

3 references

Bioactive diterpenes and other constituents of Croton steenkampianus

Bioactive diterpenes and other constituents of Croton steenkampianus

Bioactive diterpenes and other constituents of Croton steenkampianus

Cyclopia sessiliflora

1 reference

In vitro Superoxide Anion Radical Scavenging Ability of Honeybush Tea ( Cyclopia )

Encelia actonii

1 reference

Encelia asperifolia

1 reference

Encelia frutescens

1 reference

Encelia laciniata

1 reference

Encelia stenophylla

1 reference

Encelia ventorum

1 reference

Encelia virginensis

1 reference

Eriodictyon californicum

2 references

Isolation of potential cancer chemopreventive agents from Eriodictyon californicum

Isolation of potential cancer chemopreventive agents from Eriodictyon californicum

Eucalyptus globulus

1 reference

Lipid peroxidation inhibitory activity of some constituents isolated from the stem bark of Eucalyptus globulus

Gaillardia tontalensis

1 reference

Chemotaxonomy of the argentinian species of Gaillardia

Genista morisii

1 reference

Flavonoids and isoflavonoids from Genista morisii

Haplopappus remyanus

2 references

Friedolabdanes and other constituents from chileanHaplopappus species

Friedolabdanes and other constituents from chileanHaplopappus species

Centromadia fitchii

1 reference

Foliar flavonoid exudates and sectional taxonomy of Hemizonia

Deinandra greeneana

1 reference

Foliar flavonoid exudates and sectional taxonomy of Hemizonia

Deinandra kelloggii

1 reference

Foliar flavonoid exudates and sectional taxonomy of Hemizonia

Deinandra lobbii

2 references

Foliar flavonoid exudates and sectional taxonomy of Hemizonia

Flavonoids from the external leaf resins of four hemizonia species (asteraceae)

Deinandra minthornii

1 reference

Foliar flavonoid exudates and sectional taxonomy of Hemizonia

Deinandra pentactis

2 references

Foliar flavonoid exudates and sectional taxonomy of Hemizonia

Flavonoids from the external leaf resins of four hemizonia species (asteraceae)

Deinandra streetsii

1 reference

Foliar flavonoid exudates and sectional taxonomy of Hemizonia

Hypericum hircinum

2 references

Quercetin as the Active Principle of Hypericum hircinum Exerts a Selective Inhibitory Activity against MAO-A: Extraction, Biological Analysis, and Computational Study

Quercetin as the Active Principle ofHypericumhircinumExerts a Selective Inhibitory Activity against MAO-A: Extraction, Biological Analysis, and Computational Study

Kalmia latifolia

1 reference

Flavonoids from the leaves of Kalmia latifolia

Lyonia ovalifolia

1 reference

Studies on the Constituents of the Leaves of Lyonia ovalifolia DRUDE in Nepal

Cyperus pluribracteatus

2 references

Five flavans from Mariscus psilostachys

Five flavans from Mariscus psilostachys

Matthiola incana

1 reference

Relationship between Flower Development, Anthocyanin Accumulation and Activity o f Enzymes Involved in Flavonoid Biosynthesis in Matthiola incana R. Br

basil

2 references

Basil (Ocimum basilicum L.)

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Onopordum myriacanthum

1 reference

Sesquiterpene lactones and elemane derivatives from Onopordon myriacanthum

Origanum vulgare

2 references

Oregano flavonoids as lipid antioxidants

Polar Constituents from the Aerial Parts ofOriganum vulgareL. Ssp.hirtumGrowing Wild in Greece

Peucephyllum schottii

2 references

Sesquiterpene lactones from Peucephyllum schottii

Sesquiterpene lactones from Peucephyllum schottii

Phyllanthus emblica

2 references

Two new acylated flavanone glycosides from the leaves and branches of Phyllanthus emblica

Two new acylated flavanone glycosides from the leaves and branches of Phyllanthus emblica

Populus tremula

2 references

Cinnamrutinoses A and B, glycosides of Populus tremula

Cinnamrutinoses A and B, glycosides of Populus tremula

Premna resinosa

1 reference

Flavonoids from Three Ethiopian Species of Premna

Prunus persica

1 reference

FLAVONOIDS AND CYANOGENIC GLYCOSIDES FROM THE LEAVES AND STEM BARK OF PRUNUS PERSICA (L.) BATSCH (MEET GHAMR) PEACH LOCAL CULTIVAR IN ASSIUT REGION

Rhamnus lycioides

1 reference

Flavonoids of Rhamnus lycioides; Part 2

Rhamnus pallasii

2 references

Flavonoids from Rhamnus pallasii

Flavonoids from Rhamnus pallasii

Sarcophyte sanguinea

2 references

Exocarpic acid and other compounds from tubers and inflorescences of Sarcophyte sanguinea

Exocarpic acid and other compounds from tubers and inflorescences of Sarcophyte sanguinea

Solanum hindsianum

2 references

Isolation of Eriodictyol Identical with Huazhongilexone from Solanum hindsianum.

Isolation of Eriodictyol Identical with Huazhongilexone from Solanum hindsianum.

Sorghum bicolor

1 reference

Glucosylated flavonoids and other phenolic compounds from sorghum

Stifftia chrysantha

1 reference

Flavonóides das flores de Stiffitia chrysantha Mikan

Tessaria dodoneifolia

1 reference

Sesquiterpenes and flavonoids from Tessaria species

Thymus herba-barona

1 reference

Free flavonoid aglycones from Thymus herba barona and its monoterpenoid chemotypes

Thymus moroderi

1 reference

Flavonoid Aglycones of Thymus moroderi

Thymus piperella

1 reference

Highly Methylated 6-Hydroxyflavones and Other Flavonoids from Thymus piperella

Vellozia glabra

2 references

Variations in the lipophilic and vacuolar flavonoids of the genus Vellozia

Differences in flavonoid patterns between genera within the velloziaceae

Vernonia syringifolia

2 references

Glaucolides and hirsutinolides from african Vernonia species

Glaucolides and hirsutinolides from african Vernonia species

Viburnum cotinifolium

2 references

Flavonoid from Viburnum cotinifolium

Flavonoid from Viburnum cotinifolium

Wyethia angustifolia

2 references

Flavonoids of Wyethia angustifolia and W. helenioides

Flavonoids of Wyethia angustifolia and W. helenioides

Wyethia glabra

2 references

Flavonoids from Wyethia glabra

Flavonoids from Wyethia glabra

Agnorhiza invenusta

2 references

Flavonoids of Wyethia section Agnorhiza

Flavonoids of Wyethia section Agnorhiza

Xanthoceras sorbifolia

1 reference

A new coumarin glycoside from the husks of Xanthoceras sorbifolia

Bauhinia glauca

1 reference

Potential therapeutic agents for circulatory diseases from Bauhinia glauca Benth.subsp. pernervosa. (Da Ye Guan Men).

Paulownia tomentosa

1 reference

Cholinestrase inhibitory effects of geranylated flavonoids from Paulownia tomentosa fruits.

Psorothamnus polydenius

2 references

Antiprotozoal compounds from Psorothamnus polydenius

Antiprotozoal compounds from Psorothamnus polydenius

Anethum graveolens

1 reference

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Coriandrum sativum

1 reference

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Hyssopus officinalis

1 reference

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Lippia graveolens

1 reference

Identification and quantification of flavonoids of Mexican oregano (Lippia graveolens) by LC-DAD-ESI/MS analysis

Matricaria chamomilla

1 reference

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Melissa officinalis

1 reference

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Mentha spicata

1 reference

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

parsley

2 references

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Determination of Flavonoids in Plant Material by HPLC with Diode-Array and Electro-Array Detections

Pimpinella anisum

1 reference

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Salvia officinalis

2 references

Seasonal variations of phenolic compounds and biological properties in sage (Salvia officinalis L.).

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Thymus

1 reference

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Tilia tomentosa

1 reference

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Vachellia pennatula

1 reference

Terpenes, Coumarins, and Flavones from Acacia pennatula

Acer pictum

1 reference

Two new hepatoprotective stilbene glycosides from Acer mono leaves

Annona ambotay

1 reference

Geovanine, a new azaanthracene alkaloid from Annona ambotay aubl.

Anthemis auriculata

1 reference

Linear Sesquiterpene Lactones fromAnthemisauriculataand Their Antibacterial Activity

Cota palaestina

1 reference

Sesquiterpene Lactones fromAnthemis melanolepisand Their Antibacterial and Cytotoxic Activities. Prediction of Their Pharmacokinetic Profile

Artemisia vulgaris

1 reference

Estrogenic Flavonoids fromArtemisia vulgarisL.

Baccharis reticularia

1 reference

Five diterpenes and other constituents from nine Baccharis species

Baccharis linearifolia

1 reference

Five diterpenes and other constituents from nine Baccharis species

Baccharis varians

1 reference

Five diterpenes and other constituents from nine Baccharis species

Balanophora harlandii

1 reference

A New Hydrolyzable Tannin fromBalanophora harlandiiwith Radical-Scavenging Activity

Centaurea spruneri

1 reference

Antimicrobial activity of secondary metabolites isolated from Centaurea spruneri Boiss.& Heldr

Chrysanthemum morifolium

1 reference

Xanthine oxidase inhibitors from the flowers of Chrysanthemum sinense

Dalbergia parviflora

1 reference

Cytotoxicity of chemical constituents from the stems of Dalbergia parviflora

Chrysanthemum naktongense

1 reference

Sesquiterpenes and other constituents from Dendranthema zawadskii var. latilobum

Dracocephalum tanguticum

1 reference

Flavonoids from Dracocephalum tanguticum and their cardioprotective effects against doxorubicin-induced toxicity in H9c2 cells

Pogostemon stellatus

1 reference

Anti-inflammatory, cyclooxygenase (COX)-2, COX-1 inhibitory and antioxidant effects of Dysophylla stellata Benth.

Flourensia campestris

1 reference

Constituents of two Flourensia species

Garcinia conrauana

2 references

Lactones, flavonoids and benzophenones from Garcinia conrauana and Garcinia mannii

Pyrones from the bark of Garcinia conrauana: Conrauanalactone, a novel C20 derived α-pyrone

Genista corsica

1 reference

A new isoflavone from Genista corsica

Genista pichisermolliana

1 reference

A new alpinumisoflavone derivative from Genista pichisermolliana

Larix gmelinii

1 reference

Polyphenolic compounds from Larix gmelinii phloem

Limonium aureum

1 reference

Flavonoids of Limonium aureum

Limonium sinense

1 reference

Flavonoids and phenolics from Limonium sinense

Millettia duchesnei

1 reference

Rotenoid derivatives and other constituents of the twigs of Millettia duchesnei

Origanum dictamnus

1 reference

Depsides and other polar constituents from Origanum dictamnus L. and their in vitro antimicrobial activity in clinical strains.

Patrinia rupestris

1 reference

Chemical Constituents from the Roots ofPatrinia Rupestris

Pinus sibirica

1 reference

Phenolic Compounds from Pinus sibirica Shells

Prunus spachiana

1 reference

Flavonoids of Various Prunus Species. V. The Flavonoids in the Wood of Prunus verecunda

Prunus avium

2 references

Flavonoids of Various Prunus Species. V. The Flavonoids in the Wood of Prunus verecunda

Expression and Anthocyanin Biosynthesis-Modulating Potential of Sweet Cherry (Prunus avium L.) MYB10 and bHLH Genes

Prunus campanulata

1 reference

Flavonoids of Various Prunus Species. II. The Flavonoids in the Wood of Prunus speciosa

Prunus maximowiczii

1 reference

Flavonoids of Various Prunus Species. V. The Flavonoids in the Wood of Prunus verecunda

Prunus nipponica

1 reference

Flavonoids of Various Prunus Species. V. The Flavonoids in the Wood of Prunus verecunda

Prunus leveilleana

1 reference

Flavonoids of Various Prunus Species. V. The Flavonoids in the Wood of Prunus verecunda

Prunus verecunda

1 reference

Flavonoids of Various Prunus Species. V. The Flavonoids in the Wood of Prunus verecunda

Brucea javanica

1 reference

New Phenol Glycosides from the Roots ofRhus Javanicavar.Roxburghiana

Scutellaria baicalensis

1 reference

Four flavonoids from Scutellaria baicalensis

Selaginella labordei

1 reference

Bioactive compounds of inhibiting xanthine oxidase from Selaginella labordei

Smilax corbularia

1 reference

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

Viscum coloratum

1 reference

The inhibition of superoxide anion generation in human neutrophils by Viscum coloratum

Oncosiphon grandiflorum

1 reference

Glaucolides, fulvenoguaianolides and other sesquiterpene lactones from Pentzia species

Ziziphus jujuba

1 reference

Flavonoids from Leaves of Ziziphus jujuba

Vitis vinifera

1 reference

Determination of Flavonoids in Plant Material by HPLC with Diode-Array and Electro-Array Detections

Vaccinium vitis-idaea

1 reference

Determination of Flavonoids in Plant Material by HPLC with Diode-Array and Electro-Array Detections

Malus domestica

1 reference

Determination of Flavonoids in Plant Material by HPLC with Diode-Array and Electro-Array Detections

Camellia sinensis

2 references

Determination of Flavonoids in Plant Material by HPLC with Diode-Array and Electro-Array Detections

Flavonoid biosynthesis in the tea plant Camellia sinensis: properties of enzymes of the prominent epicatechin and catechin pathways.

Punica granatum

1 reference

Diverse Phytochemicals and Bioactivities in the Ancient Fruit and Modern Functional Food Pomegranate (Punica granatum).

Schnella guianensis

1 reference

Flavonoid and other constituents of Bauhinia manca

Garcinia kola

2 references

Lactones, flavonoids and benzophenones from Garcinia conrauana and Garcinia mannii

Pyrones from the bark of Garcinia conrauana: Conrauanalactone, a novel C20 derived α-pyrone

broccoli

1 reference

Determination of Flavonoids in Plant Material by HPLC with Diode-Array and Electro-Array Detections

Tilia mandshurica

1 reference

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Rhaponticum carthamoides

1 reference

Chemistry and pharmacology of Rhaponticum carthamoides: a review.

Ambrosia salsola

1 reference

Flavonoids from the Leaf Resin of Hymenoclea salsola T. & G. (Asteraeeae)

Gleditsia japonica

1 reference

Antibacterial phenolic compounds from the spines of Gleditsia sinensis Lam

Prunus serrulata var. pubescens

1 reference

Flavonoids of Various Prunus Species. V. The Flavonoids in the Wood of Prunus verecunda

Chamomilla recutita

1 reference

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Cyperus trigonellus

1 reference

Five flavans from Mariscus psilostachys

Toxicodendron vernicifluum

1 reference

Neuroprotective and anti-inflammatory effects of flavonoids isolated from Rhus verniciflua in neuronal HT22 and microglial BV2 cell lines

Rosmarinus officinalis

3 references

ULTRASONICALLY ASSISTED EXTRACTION OF PHENOLIC COMPOUNDS FROM AROMATIC PLANTS: COMPARISON WITH CONVENTIONAL EXTRACTION TECHNICS

RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity.

Phytochemical Profiling of Flavonoids, Phenolic Acids, Terpenoids, and Volatile Fraction of a Rosemary (Rosmarinus officinalis L.) Extract.

Daucus carota

1 reference

Inhibition of flavonoid biosynthesis by gibberellic acid in cell suspension cultures of Daucus carota L

Artemisia annua

1 reference

Phytochemical analysis of a herbal tea from Artemisia annua L.

Dianthus caryophyllus

1 reference

Purification and properties of a new S-adenosyl-L-methionine:flavonoid 4'-O-methyltransferase from carnation (Dianthus caryophyllus L.)

Glycyrrhiza uralensis

1 reference

Identification and Enrichment of α-Glucosidase-Inhibiting Dihydrostilbene and Flavonoids from Glycyrrhiza uralensis Leaves

mandarin orange

1 reference

Discrimination of Citrus reticulata Blanco and Citrus reticulata 'Chachi' as well as the Citrus reticulata 'Chachi' within different storage years using ultra high performance liquid chromatography quadrupole/time-of-flight mass spectrometry based m

Capsicum annuum

1 reference

Integrative analysis of metabolome and transcriptome reveals the mechanism of color formation in pepper fruit (Capsicum annuum L.).

Escherichia coli

1 reference

Luminmycins A-C, cryptic natural products from Photorhabdus luminescens identified by heterologous expression in Escherichia coli.

Berchemia floribunda

1 reference

Constituents of Berchemia racemosa Sieb. et Zucc

Rhodiola rosea

1 reference

Bioactive constituents from Chinese natural medicines. XXVI. Chemical structures and hepatoprotective effects of constituents from roots of Rhodiola sachalinensis

Malus pumila

1 reference

Determination of Flavonoids in Plant Material by HPLC with Diode-Array and Electro-Array Detections

Cheniella glauca

1 reference

Potential therapeutic agents for circulatory diseases from Bauhinia glauca Benth.subsp. pernervosa. (Da Ye Guan Men).

Thymus longiflorus

1 reference

Flavonoid Aglycones of Thymus moroderi

Xanthoceras sorbifolium

1 reference

A new coumarin glycoside from the husks of Xanthoceras sorbifolia

Baccharis venosa

1 reference

Studies on the constituents of Baccharis genistelloides.

Baccharis sagittalis

1 reference

Studies on the constituents of Baccharis genistelloides.

Lippia origanoides

1 reference

Identification and quantification of flavonoids of Mexican oregano (Lippia graveolens) by LC-DAD-ESI/MS analysis

Citrus × deliciosa

1 reference

Discrimination of Citrus reticulata Blanco and Citrus reticulata 'Chachi' as well as the Citrus reticulata 'Chachi' within different storage years using ultra high performance liquid chromatography quadrupole/time-of-flight mass spectrometry based m

Onopordum boissierianum

1 reference

Flavonoids of Onopordum sibthorpianum and Onopordum laconicum

Thymus vulgaris

3 references

Analysis of enantiomeric flavanones in plant extracts by high-performance liquid chromatography on a cellulose triacetate based chiral stationary phase

Protein glycation inhibitors from thyme (Thymus vulgaris)

Antiperoxidative components in Thymus vulgaris

Xerochrysum bracteatum

3 references

Exudate Flavonoids in Several Asteroideae and Cichorioideae (Asteraceae)

5,7,3′,4′5′-pentahydroxyflavanone in the bracts of helichrysum bracteatum

Obliquin derivatives and other constituents from Australian Helichrysum species

Prunus itosakura

1 reference

Flavonoids of Various Prunus Species. V. The Flavonoids in the Wood of Prunus verecunda

Eutrochium fistulosum

1 reference

External Flavonoids of 12 Species of North American Eupatorieae (Asteraceae)

Xerochrysum subundulatum

1 reference

Obliquin derivatives and other constituents from Australian Helichrysum species

Satureja cuneifolia

1 reference

Isolation of Vasodilatory Active Flavonoids from the Traditional RemedySatureja obovata

Bracteantha acuminata

2 references

Obliquin derivatives and other constituents from Australian Helichrysum species

Obliquin derivatives and other constituents from Australian Helichrysum species

Cota altissima

1 reference

Sesquiterpene lactones from Anthemis altissima and their anti-Helicobacter pylori activity

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

subject has role

metabolite

0 references

Commons category

Eriodictyol

0 references

Identifiers

InChI

InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2/t13-/m0/s1

1 reference

ERIODICTYOL (English)

19 October 2016

2 references

ERIODICTYOL (English)

19 October 2016

ChEBI release 2020-09-01

2 references

eriodictyol (English)

19 October 2016

https://commonchemistry.cas.org/detail?cas_rn=552-58-9

8 April 2021

1 reference

Eriodictyol (English)

19 October 2016

1 reference

ERIODICTYOL (English)

19 October 2016

Reaxys registry number

92358

1 reference

eriodictyol (English)

19 October 2016

ChEBI ID

28412

mapping relation type

2 references

eriodictyol (English)

19 October 2016

International Chemical Identifier

InChI

InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2/t13-/m0/s1

1 reference

ERIODICTYOL (English)

19 October 2016

2 references

inferred from InChIKey

splash10-0f79-0910000000-c48ad5f3958e9c41f5de

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

splash10-000i-0970000000-cb17dd84eda67cc9d6a4

0 references

splash10-000i-0900000000-5c65882b59856d787f67

0 references

splash10-0udi-0910000000-85200d3bfe0ef9f8c6cf

0 references

splash10-0udi-1900000000-c83d3fbbf98b1c8e768d

0 references

splash10-0f79-0950000000-70ad9d5c48c3fd3ab1fe

0 references

splash10-0f79-1930000000-1bd4ad63c015087fbdb2

0 references

splash10-0f79-0900000000-8aa62dd381d8e70390e1

0 references

splash10-000i-0090000000-136edb232ec0a4f9d1f2

0 references

splash10-000i-0190000000-d8e1fd5ccec5438eaa15

0 references

splash10-0w2i-0920000000-c7914e4ae4e49dca7894

0 references

splash10-0udi-0900000000-85b9b7f49e3d96f4d7bc

0 references

splash10-0udi-2900000000-9c0722bb69845cf5bda1

0 references

splash10-000i-0090000000-2b794ccb1be3fc997ee1

0 references

splash10-0f79-0940000000-a705459ecf7518f84511

0 references

splash10-0udr-0900000000-524835586575ac56f221

0 references

splash10-000i-0900000000-b8015bd66a00e2d86143

0 references

splash10-0019-0900000000-5bf07fecf8b640f58a65

0 references

splash10-000i-0900000000-b2b02735735b0219532c

0 references

splash10-0udi-0900000000-6a4b40315f7612bc2fbe

0 references

splash10-0udi-0900000000-100db8442b14b1d1ccdd

0 references

splash10-000i-0090000000-778b9cb4a7b875c6bbec

0 references

splash10-052r-0090000000-9178a74a6239d2ef3882

0 references

splash10-052r-0290000000-287f5fa660d816283c29

0 references

splash10-0019-0090000000-cb3df3f82944d76bf224

0 references

DSSTox substance ID

DTXSID70877706

1 reference

DSSTOX compound identifier

0 references

1 reference

Global Substance Registration System

UNII

Q520486B8Y

eriodictyol (English)

ECHA Substance Infocard ID

19 October 2016

100.008.198

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.008.198

27 December 2018

Human Metabolome Database ID

(S)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4-benzopyrone (English)

quotation

CAS no.: 552-58-9 (English)

0 references

1 reference

HMDB0005810

2 references

based on heuristic

inferred from InChIKey

reason for deprecated rank

KNApSAcK ID

C00000960

cannot be confirmed by other sources

1 reference

Global Substance Registration System

eriodictyol (English)

19 October 2016

2 references

UNII

Q520486B8Y

eriodictyol (English)

19 October 2016

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

0 references

0 references

1 reference

15 January 2022

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

0 references

1 reference

28 October 2013

Microsoft Academic ID

0 references

1 reference

26 January 2022

1 reference

2NNL (English)