(+)-taxifolin (Q412191)

(+)-taxifolin 5'-hydroxylase activity

inferred from SMILES

part of

1 reference

reference URL

http://geneontology.org/external2go/rhea2go

1 February 2021

chemical structure

(+)-Taxifolin.svg
359 × 196; 17 KB

1 reference

German Wikipedia

Taxifolin structure.svg
512 × 279; 24 KB

0 references

mass

304.058302724 dalton

1 reference

inferred from isomeric SMILES

stereoisomer of

(+)-epitaxifolin

2 references

inferred from InChIKey

1 reference

1 reference

C₁₅H₁₂O₇

2 references

O=C1C=2C(O)=CC(O)=CC2OC(C3=CC=C(O)C(O)=C3)C1O

0 references

isomeric SMILES

OC1=C(C([C@H](O)[C@@H](C2=CC(O)=C(O)C=C2)O3)=O)C3=CC(O)=C1

1 reference

Characterisation of Phenolic Constituents from Juvenile and Mature Needles of Norway Spruce by Means of High Performance Liquid Chromatography-Mass Spectrometry

3 references

Preparative separation of phenolic compounds from Picea abies by high-speed counter-current chromatography

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

Larix gmelinii

2 references

Antioxidant Activity of a Dihydroquercetin Isolated fromLarix gmelinii (Rupr.) Rupr. Wood

Flavonoids ofLarix dahurica. I

Silybum marianum

10 references

A simple device allowing UV-detection of the active substances of Silybum marianum (L.) Gaertner on TLC plates devoid of fluorescent indicator

Complete Isolation and Characterization of Silybins and Isosilybins from Milk Thistle (Silybum marianum).

Silybum marianum

Determination of silymarine in the extract from the dried silybum marianum fruits by high performance liquid chromatography and capillary electrophoresis

Flavonolignans, Kaempferol 3-Sulphate and Other Flavonoids from Silybum marianum subsp. anatolicum

Milk thistle nomenclature: why it matters in cancer research and pharmacokinetic studies

Milk Thistle,Silybum marianum(L.) Gaertn., Flower Head Development and Associated Marker Compound Profile

Milk thistle and prostate cancer: differential effects of pure flavonolignans from Silybum marianum on antiproliferative end points in human prostate carcinoma cells.

Complete isolation and characterization of silybins and isosilybins from milk thistle (Silybum marianum).

Enhanced accumulation of flavonolignans in Silybum marianum cultured roots by methyl jasmonate

Equisetum arvense

2 references

Naringenin, dihydrokaempferol, and dihydroquercetin from Equisetum arvense

Phenolic acids of Equisetum arvense

Acacia carneorum

1 reference

Metabolites from the purple heartwood of Mimosoideae. Part 2. Acacia carnei maiden: isolation, synthesis, and reactions of crombeone

Anthemis altissima

1 reference

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

Arabidopsis thaliana

2 references

The Arabidopsis TDS4 gene encodes leucoanthocyanidin dioxygenase (LDOX) and is essential for proanthocyanidin synthesis and vacuole development.

Evidence for oxidation at C-3 of the flavonoid C-ring during anthocyanin biosynthesis.

Brassica carinata

1 reference

Pigmentation in the developing seed coat and seedling leaves of Brassica carinata is controlled at the dihydroflavonol reductase locus

Cleistopholis glauca

1 reference

Novel oligorhamnosides from the stem bark of Cleistopholis glauca

Colophospermum mopane

1 reference

Stereochemistry and biogenesis of mopanols and peltogynols and associated flavanoids from Colophospermum mopane

Genista corsica

2 references

A new isoflavone from Genista corsica

A new isoflavone from Genista saharae (Fabaceae)

Juglans mandshurica

3 references

Inhibition of human immunodeficiency virus type 1 reverse transcriptase and ribonuclease H activities by constituents of Juglans mandshurica

Anti-human immunodeficiency virus-type 1 activity of constituents from Juglans mandshurica

Anti-complement activity of constituents from the stem-bark of Juglans mandshurica

Kadsura heteroclita

1 reference

Compounds from Kadsura heteroclita and related anti-HIV activity

Lippia origanoides

2 references

Chemical constituents from Lippia sidoides and cytotoxic activity

Chemical constituents from Pteris multifida and cytotoxic activity

Lippia sidoides

2 references

Chemical constituents from Lippia sidoides and cytotoxic activity

Chemical constituents from Pteris multifida and cytotoxic activity

Opuntia ficus-indica

1 reference

Secondary metabolites from Opuntia ficus-indica var. saboten.

Pelargonium reniforme

1 reference

O-Galloyl-C-glycosylflavones from Pelargonium reniforme

Polygala caudata

1 reference

Xanthones from Polygala caudata

Pseudotsuga menziesii

2 references

Pseudotsuganol, a biphenyl-linked pinoresinol–dihydroquercetin from douglas-fir bark: isolation of the first true flavonolignan

Douglas-fir polyphenols and heartwood formation

Rhamnus disperma

1 reference

Polyphenolic metabolites of Rhamnus disperma

Spatholobus suberectus

1 reference

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

Thymus vulgaris

1 reference

Isolation and structure elucidation of radical scavengers from Thymus vulgaris leaves.

Xanthoceras sorbifolia

1 reference

Inhibitory effects on HIV-1 protease of constituents from the wood of Xanthoceras sorbifolia.

Anastatica hierochuntica

3 references

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

Anaxagorea luzonensis

2 references

Studies on the constituents of Anaxagorea luzonensis A. GRAY.

ChemInform Abstract: Studies on the Constituents of Anaxagorea luzonensis A. Gray.

Andira inermis

1 reference

Flavonoids ofSerratula inermis

peanut

1 reference

A flavonoid antioxidant in Spanish peanuts(Arachia hypogoea)

Artabotrys hexapetalus

1 reference

Flavonoids from Artabotrys hexapetalus

Baccharis scandens

1 reference

Diterpenoids from chilean Baccharis species

Bauhinia purpurea

1 reference

Chemical Constituents of Heartwood ofBauhinia purpurea

Berchemia formosana

1 reference

Chemical Constituents fromBerchemia formosana

Berchemia racemosa

1 reference

Constituents of Berchemia racemosa Sieb. et Zucc

Calceolaria hypericina

1 reference

Phenylpropanoid glycosides from Calceolaria hypericina

Crataegus flava

1 reference

A new eudesmanolide from Crataegus flava fruits.

Crotalaria nitens

1 reference

Phytochemical studies on Crotalaria laburnifolia

Cryptomeria japonica

1 reference

Flavonoids and lignans from leaves of Cryptomeria japonica

Cuscuta reflexa

1 reference

Constituents of Cuscuto Reflexa are anti-HIV Agents

Drimys winteri

1 reference

Isolation and identification of active compounds from Drimys winteri barks.

Erythroxylum rufum

1 reference

Flavonoids of Erythroxylum rufum and Erythroxylum ulei

Eucalyptus globulus

2 references

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

Phenolic compounds from the branches of Eucalyptus maideni

Ficus pumila

1 reference

Flavonoids from Ficus pumila

Hypericum japonicum

2 references

Chromone glycosides and flavonoids from hypericum japonicum

A new phloroglucinol diglycoside derivative from Hypericum japonicum Thunb

Juniperus chinensis

1 reference

Free radical scavengers from the heartwood of Juniperus chinensis

Matthiola incana

1 reference

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

Mimusops elengi

1 reference

Triterpenoid saponins of Mimusops elengi

Origanum vulgare

1 reference

Oregano flavonoids as lipid antioxidants

Phoebe formosana

1 reference

Polar Chemical Constituents fromPhoebe formosana

Pinus contorta

2 references

Isolation of dihydromyricetin and dihydroquercetin from bark of pinus contorta

Isolation of quercetin, myricetin, and their respective dihydro-compounds by Sephadex LH-20 chromatography

Pinus ponderosa

1 reference

Chemistry of toxic range plants. Water-soluble lignols of Ponderosa pine needles

Pinus sylvestris

3 references

Flavonoid variability within Pinus sylvestris

Phenolics from inner bark of Pinus sylvestris

Flavonoids from Pinus sylvestris needles and their variation in trees of different origin grown for nearly a century at the same area

Platycodon grandiflorum

1 reference

Phytochemical Studies of Seeds of Medicinal Plants. II. A New Dihydroflavonol Glycoside and a New 3-Methyl-1-butanol Glycoside from Seeds of Platycodon grandiflorum A. DE CANDOLLE.

Platycodon grandiflorus

1 reference

Phytochemical Studies of Seeds of Medicinal Plants. II. A New Dihydroflavonol Glycoside and a New 3-Methyl-1-butanol Glycoside from Seeds of Platycodon grandiflorum A. DE CANDOLLE.

Podocarpus nivalis

1 reference

7-O-methyl-(2R:3R)-dihydroquercetin 5-O-β-D-glucoside and other flavonoids from Podocarpus nivalis

Prunus avium

2 references

Flavonol glycosides of different species and hybrids from the Prunus section eucerasus and the growth-promoting activity of quercetin derivatives

Comparative transcriptome analysis of genes involved in anthocyanin biosynthesis in the red and yellow fruits of sweet cherry (Prunus avium L.).

Prunus cerasus

1 reference

Flavonol glycosides of different species and hybrids from the Prunus section eucerasus and the growth-promoting activity of quercetin derivatives

Prunus fruticosa

1 reference

Flavonol glycosides of different species and hybrids from the Prunus section eucerasus and the growth-promoting activity of quercetin derivatives

Prunus grayana

1 reference

Phenolic glucosides from the heartwood of Prunus grayana

Prunus prostrata

1 reference

Coumarins and Other Constituents of Prunus prostrata

Pterodon emarginatus

1 reference

Further diterpenoids isolated from Pterodon polygalaeflorus

Pulicaria undulata

1 reference

Flavonols of Pulicaria arabica

Scarlet firethorn

1 reference

Flavonoids from Pyracantha coccinea roots

Rhamnus lycioides

1 reference

Flavonoid Constituents of Rhamnus lycioides L.

Rhamnus pallasii

1 reference

Flavonoids from Rhamnus pallasii

Rhododendron abietifolium

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron acuminatum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron aurigeranum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron bagobonum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron beyerinckianum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron brookeanum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron buxifolium

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron crassifolium

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron culminicolum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron dianthosmum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron durionifolium

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron gracilentum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron hooglandii

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron inconspicuum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron intranervatum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron jasminiflorum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron javanicum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron kawakamii

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron konori

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron laetum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron lanceolatum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron leptanthum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron leucogigas

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron macgregoriae

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron meijeri

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron micromalayanum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron nervulosum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron nieuwenhuisii

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron orbiculatum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron phaeochitum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron planecostatum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron pneumonanthum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron polyanthemum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron praetervisum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron rarum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron retusum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron robinsonii

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron rugosum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron searleanum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron stapfianum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron stenophyllum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron suaveolens

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron superbum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron vandeursenii

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron womersleyi

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron wrightianum

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron yelliottii

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Rhododendron zoelleri

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Ribes nigrum

1 reference

Nigrumin-5-p-coumarate and nigrumin-5-ferulate, two unusual nitrile-containing metabolites from black currant (Ribes nigrum) seed

Salix caprea

1 reference

Flavonoids from the Wood of Salix caprea as Inhibitors of Wood-Destroying Fungi

Salix sachalinensis

2 references

Further study on two chemical races of Salix sachalinensis Fr. Schmidt.

Phenolic Compounds from Salix sachalinensis

Sedum reflexum

1 reference

Dihydroflavonols from Cedrus deodara

Sedum rupestre

1 reference

Dihydroflavonols from Cedrus deodara

Sicana odorifera

1 reference

Cucurbita-5,23-diene-3β,25-diol from Sicana odorifera

Smilax glabra

1 reference

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

Sorghum bicolor

1 reference

Glucosylated flavonoids and other phenolic compounds from sorghum

Trachelospermum jasminoides

1 reference

Taxifolin 3-arabinoside from Trachelospermum jasminoides var. Pubescens

Ziziphus jujuba

1 reference

Chemical constituents from the roots of Zizyphus jujuba Mill. var. spinosa

Ziziphus mauritiana

1 reference

Chemical constituents from the roots of Zizyphus jujuba Mill. var. spinosa

Acacia mearnsii

1 reference

α-Amylase and lipase inhibitory activity and structural characterization of acacia bark proanthocyanidins

Betula platyphylla var. japonica

1 reference

Hepatoprotective, superoxide scavenging, and antioxidative activities of aromatic constituents from the bark of Betula platyphylla var. japonica

Streptomyces albidoflavus

1 reference

Isolation, characterization and identification of antibiofouling metabolite from mangrove derived Streptomyces sampsonii PM33

Streptomyces sampsonii

1 reference

Isolation, characterization and identification of antibiofouling metabolite from mangrove derived Streptomyces sampsonii PM33

Abies nephrolepis

1 reference

Phenolic compounds of Abies nephrolepis and their NO production inhibitory activities.

Albizia julibrissin

1 reference

Flavonol acylglycosides from flower of Albizia julibrissin and their inhibitory effects on lipid accumulation in 3T3-L1 cells

Allium cepa

1 reference

Antispasmodic saponins from bulbs of red onion, Allium cepa L. var. Tropea

Austrocedrus chilensis

1 reference

The Chemistry of the Natural Order Cupressales. XV. Heartwood Constituents of Austrocedrus chilensis (D.Don), Florin et Boutelje (=Libocedrus chilensis (D.Don)Endl.).

Camellia reticulata

1 reference

Five New Flavonol Glycosides from the Fresh Flowers ofCamellia reticulata

Cercidiphyllum japonicum

1 reference

Polyphenols from the heartwood of Cercidiphyllum japonicum and their effects on proliferation of mouse hair epithelial cells

Crotalaria pallida

1 reference

Anti-inflammatory flavonoids and pterocarpanoid from Crotalaria pallida and C. assamica

Entada phaseoloides

1 reference

Antioxidant phenolic compounds from the stems of Entada phaseoloides

Ficus cordata

1 reference

Pentacyclic Triterpenes and Other Constituents from Ficus cordata (Moraceae)

Chrysophyllum africanum

1 reference

Fatty acid esters of triterpenoids and steroid glycosides from Gambeya africana.

Hylocereus undatus

1 reference

Three new glycosides from Hylocereus undatus

Ichthyothere terminalis

1 reference

Flavonol derivatives of Ichthyothere terminalis

Larix decidua

1 reference

Flavanones from the Heart Wood of Larix decidua Mill. (L. europea D C.).

Larix laricina

1 reference

THE CHEMICAL COMPOSITION OF THE HEARTWOOD EXTRACTIVES OF TAMARACK (LARIX LARICINA (DU ROI) K. KOCH)

Larix sibirica

1 reference

Flavonoids of the bark of Larix sibirica

Origanum dictamnus

1 reference

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

Picea jezoensis

2 references

Structures and radical-scavenging activities of phenolic constituents from the bark of Picea jezoensis var. jezoensis

Anti-tumor-initiating effects of phenolic compounds isolated from the bark of Picea jezoensis var. jezoensis.

Pinus massoniana

1 reference

Flavonoid glycosides from needles of Pinus massoniana

Pittocaulon praecox

1 reference

Eremophilane Derivatives from Pittocaulon praecox

Pittocaulon velatum

1 reference

Seco-eremophiladiolides and eremophilane glucosides from Pittocaulon velatum

Prunus cerasoides

1 reference

Padmatin, a new component of the heartwood of Prunus puddum

Rhododendron decorum

1 reference

Flavonoids from Rhododendron decorum

Rhododendron spinuliferum

1 reference

Chemical constituents from Rhododendron spinuliferum

Brucea javanica

2 references

Flavonoids with DNA strand-scission activity from Rhus javanica var. roxburghiana.

New Phenol Glycosides from the Roots ofRhus Javanicavar.Roxburghiana

Rosa canina

1 reference

Inhibitory effect of quercetin isolated from rose hip (Rosa canina L.) against melanogenesis by mouse melanoma cells

Smilax corbularia

1 reference

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

Rhododendron christianae

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Nelumbo nucifera

1 reference

Chemical constituents from Nelumbo nucifera leaves and their anti-obesity effects

Morus alba

3 references

HPLC-DAD-ESI-MS/MS analysis and antioxidant activities of nonanthocyanin phenolics in mulberry (Morus alba L.).

The novel contributors of anti-diabetic potential in mulberry polyphenols revealed by UHPLC-HR-ESI-TOF-MS/MS.

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

Maclura cochinchinensis

1 reference

Flavonoids, including an unusual flavonoid-Mg2+ salt, from roots of Cudrania cochinchinensis

Larix gmelinii var. gmelinii

1 reference

Flavonoids ofLarix dahurica. I

Plectocephalus chilensis

1 reference

Chemical Constituents of Centaurea brugueriana

Selenicereus undatus

1 reference

Three new glycosides from Hylocereus undatus

Persicaria salicifolia

1 reference

Inhibitory compound of tyrosinase activity from the sprout of Polygonum hydropiper L. (Benitade).

Persicaria orientalis

1 reference

Simultaneous determination of eight components in Polygonum orientale by ultra performance liquid chromatography(UPLC) method

Maclura pomifera

1 reference

Osage orange (Maclura pomifera): History and economic uses

Punica granatum

1 reference

A "White" Anthocyanin-less Pomegranate (Punica granatum L.) Caused by an Insertion in the Coding Region of the Leucoanthocyanidin Dioxygenase (LDOX; ANS) Gene

asparagus

1 reference

Transcriptome analysis of Asparagus officinalis reveals genes involved in the biosynthesis of rutin and protodioscin

Momordica charantia

1 reference

Identification and Characterization of Phenylpropanoid Biosynthetic Genes and Their Accumulation in Bitter Melon (Momordica charantia).

Magnolia denudata

1 reference

Analysis of Metabolites in White Flowers of Magnolia Denudata Desr. and Violet Flowers of Magnolia Liliiflora Desr.

Magnolia liliiflora

1 reference

Analysis of Metabolites in White Flowers of Magnolia Denudata Desr. and Violet Flowers of Magnolia Liliiflora Desr.

Rhododendron culminicola

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Persicaria decipiens

1 reference

Inhibitory compound of tyrosinase activity from the sprout of Polygonum hydropiper L. (Benitade).

Myrsine lancifolia

1 reference

Trypanocidal activity of flavonoids and limonoids isolated from Myrsinaceae and Meliaceae active plant extracts

Rhododendron christi

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Ziziphus spina-christi

1 reference

PHYTOCHEMICAL STUDY OF THE LEAVES OF ZIZIPHUS SPINA-CHRISTI L. WILLD

Annona ambotay

1 reference

Geovanine, a new azaanthracene alkaloid from Annona ambotay aubl.

Fragaria

1 reference

Overall dietary polyphenol intake in a bowl of strawberries: The influence of Fragaria spp. in nutritional studies

Gambeya africana

1 reference

Fatty acid esters of triterpenoids and steroid glycosides from Gambeya africana.

Lotus pedunculatus

1 reference

Localized Changes in Flavonoid Biosynthesis in Roots of Lotus pedunculatus after Infection by Rhizobium loti

Great yellow gentian

1 reference

Differential accumulation of pelargonidin glycosides in petals at three different developmental stages of the orange-flowered gentian (Gentiana lutea L. var. aurantiaca)

Annona muricata

1 reference

Antioxidant, DNA protective efficacy and HPLC analysis of Annona muricata (soursop) extracts

Phaseolus vulgaris

1 reference

Alpha-amylase, α-glucosidase and lipase inhibiting activities of polyphenol-rich extracts from six common bean cultivars of Southern Italy, before and after cooking.

Eucomis autumnalis

1 reference

Physiological role of phenolic biostimulants isolated from brown seaweed Ecklonia maxima on plant growth and development.

Paeonia rockii

1 reference

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

Persicaria lapathifolia

1 reference

Inhibitory compound of tyrosinase activity from the sprout of Polygonum hydropiper L. (Benitade).

Berchemia floribunda

1 reference

Constituents of Berchemia racemosa Sieb. et Zucc

Rhododendron latoucheae

1 reference

Flavonoid patterns and phytogeography: the genus Rhododendron section Vireya

Xanthoceras sorbifolium

1 reference

Inhibitory effects on HIV-1 protease of constituents from the wood of Xanthoceras sorbifolia.

Lotus uliginosus

1 reference

Localized Changes in Flavonoid Biosynthesis in Roots of Lotus pedunculatus after Infection by Rhizobium loti

pomelo

1 reference

Chemistry of toxic range plants. Water-soluble lignols of Ponderosa pine needles

Citrus grandis

1 reference

Chemistry of toxic range plants. Water-soluble lignols of Ponderosa pine needles

Citrus medica

1 reference

Chemistry of toxic range plants. Water-soluble lignols of Ponderosa pine needles

Sedum anglicum

1 reference

Dihydroflavonols from Cedrus deodara

Eucalyptus maidenii

1 reference

Phenolic compounds from the branches of Eucalyptus maideni

Opuntia humifusa

1 reference

Megastigmane Derivatives from the Cladodes of Opuntia humifusa and Their Nitric Oxide Inhibitory Activities in Macrophages

Opuntia vulgaris

1 reference

Megastigmane Derivatives from the Cladodes of Opuntia humifusa and Their Nitric Oxide Inhibitory Activities in Macrophages

Cota altissima

1 reference

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

Opuntia humifusa humifusa

1 reference

Megastigmane Derivatives from the Cladodes of Opuntia humifusa and Their Nitric Oxide Inhibitory Activities in Macrophages

Asteraceae

1 reference

Diterpenes and other constituents fromRelhania species

Dioscorea alata

1 reference

Transciptome analysis reveals flavonoid biosynthesis regulation and simple sequence repeats in yam (Dioscorea alata L.) tubers

1 reference

non-steroidal anti-inflammatory drug

1 reference

InChI=1S/C15H12O7/c16-7-4-10(19)12-11(5-7)22-15(14(21)13(12)20)6-1-2-8(17)9(18)3-6/h1-5,14-19,21H/t14-,15+/m0/s1

Medical Subject Headings

15 March 2018

0 references

Taxifolin

0 references

Identifiers

InChI

1 reference

PubChem

2 references

PubChem

ChEBI release 2020-09-01

CAS Registry Number

480-18-2

1 reference

https://commonchemistry.cas.org/detail?cas_rn=480-18-2

8 April 2021

ChemSpider ID

458

1 reference

Serbo-Croatian Wikipedia

PubChem CID

439533

1 reference

German Wikipedia

Reaxys registry number

93548

0 references

ChEBI ID

17948

mapping relation type

exact match

2 references

English Wikipedia

International Chemical Identifier

InChI

InChI=1S/C15H12O7/c16-7-4-10(19)12-11(5-7)22-15(14(21)13(12)20)6-1-2-8(17)9(18)3-6/h1-5,14-19,21H/t14-,15+/m0/s1

ChEMBL ID

CHEMBL66

1 reference

2 references

inferred from InChIKey

splash10-000i-0190000000-6de8dee651f748512d2e

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

splash10-004i-0090000000-cf06c618e97b36a85565

0 references

splash10-0pc1-0980000000-2d1ecd15f61d12518b21

0 references

splash10-004r-0960000000-22428e71371e23f8c0f1

0 references

splash10-0a4i-0009000000-17d7dd51ffa3375c944c

0 references

splash10-0udi-0009000000-1df32727d81ac0fee4d1

0 references

splash10-0udr-0289000000-4c575af554f3aa37d246

0 references

splash10-0fb9-0911000000-41df9988f9e8f3a17404

0 references

splash10-00fr-0591000000-8c2bb267dbaff0ec8425

0 references

splash10-0fk9-0393000000-2ad9cdbeaebe4832addf

0 references

splash10-0udi-0019000000-f4c2db21ffbf7fdec0ec

0 references

splash10-0ul1-0930000000-805f5b6770fe1b1ed799

0 references

DSSTox substance ID

DTXSID8022450

2 references

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

DSSTOX compound identifier

0 references

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.006.859

ECHA Substance Infocard ID

27 December 2018

title

(2R-trans)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-4-benzopyrone (English)

quotation

CAS no.: 480-18-2 (English)

100.006.859

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.006.859

27 December 2018

title

(2R-trans)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-4-benzopyrone (English)

quotation

CAS no.: 480-18-2 (English)

1 reference

28 December 2019

DIHYDROQUERCETIN (English)

quotation

CAS no.: 480-18-2 (English)

1 reference

1 reference

Medical Subject Headings

14 March 2018

1 reference

Human Metabolome Database ID

HMDB0303943

2 references

inferred from InChIKey

http://kanaya.naist.jp/knapsack_jsp/information.jsp?sname=C_ID&word=C00000677

KNApSAcK ID

C00000677

1 reference

reference URL

UNII

9SOB9E3987

1 reference

EAS93SC1VS

1 reference

0 references

1 reference

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

Serbo-Croatian Wikipedia

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

UMLS CUI

C0075861

1 reference

inferred by common MeSH mappings on source and on Wikidata

UMLS 2023