(Q6871627)

(2S,3S,4S,5R)-6-{[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

inferred from SMILES

1 reference

inferred from SMILES

chemical structure

Miquelianin.svg
512 × 444; 40 KB

0 references

mass

478.075 dalton

1 reference

Quercituron (English)

3',4',5,7-Tetrahydroxyflavon-3-yl alpha-D-glucopyranosiduronic acid

7 October 2016

stereoisomer of

2 references

Quercetin 3-O-beta-D-galacturonopyranoside

inferred from InChI

2 references

(2R,3R,4R,5S,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid

inferred from InChI

1 reference

(2S,3S,4R,5S,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid

2 references

inferred from InChI

chemical formula

C₂₁H₁₈O₁₃

1 reference

Quercituron (English)

19 November 2016

canonical SMILES

C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O

1 reference

Quercituron (English)

19 November 2016

isomeric SMILES

C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)C(=O)O)O)O)O)O)O

1 reference

Heterophylliins A,B,C,D and E, ellagitannin monomers and dimers from Corylus heterophylla Fisch.

Quercituron (English)

19 November 2016

1 reference

Callistemon citrinus

1 reference

An acylated flavonol glycoside and hydrolysable tannins from Callistemon lanceolatus flowers and leaves

Callistemon lanceolatus

1 reference

An acylated flavonol glycoside and hydrolysable tannins from Callistemon lanceolatus flowers and leaves

Foeniculum vulgare

4 references

An Acylated Kaempferol Glycoside from Flowers of and

Q28333020

Comparative study of the flavonoids of some local members of the umbelliferae

Identification by HPLC−DAD and HPLC−MS Analyses and Quantification of Constituents of Fennel Teas and Decoctions

Hypericum hirsutum

1 reference

Miquelianin and other polyphenols from Hypericum hirsutum

Phaseolus vulgaris

2 references

Composition and Content of Flavonol Glycosides in Green Beans and Their Fate during Processing

Flavonoids ofPhaseolus vulgaris

Polygonum salicifolium

1 reference

Phenylvaleric acid and flavonoid glycosides from Polygonum salicifolium

Reynoutria sachalinensis

1 reference

Antioxidant activity of anthraquinones and flavonoids from flower of Reynoutria sachalinensis

Schinus molle

1 reference

Antioxidant flavonol glycosides from Schinus molle

Acmella ciliata

1 reference

New phenolic compounds of Acmella ciliata

Alnus sieboldiana

1 reference

Alnusnins A and B from the leaves of Alnus sieboldiana

peanut

1 reference

Spermidine and flavonoid conjugates from peanut (Arachis hypogaea) flowers

Arnica chamissonis

1 reference

Acetylated and other flavonoid glycosides from Arnica chamissonis

Campanula glomerata

1 reference

Phenolic compounds of Campanula glomerata

Centella asiatica

2 references

The anti-thrombotic active constituents from Centella asiatica

A new triterpene glycoside from Centella erecta

Centella erecta

1 reference

A new triterpene glycoside from Centella erecta

Clematis rehderiana

1 reference

A new flavone C-glycoside from Clematis rehderiana.

Clematis stans

1 reference

Studies on the constituents of Clematis species. VI. The constituents of Clematis stans Sieb. et Zucc

Cornus mas

1 reference

Quali-quantitative analysis of flavonoids of Cornus mas L. (Cornaceae) fruits

Cyclocarya paliurus

1 reference

Phenolic compounds from the leaves of Cyclocarya paliurus (Batal.) Ijinskaja and their inhibitory activity against PTP1B

Diospyros cathayensis

1 reference

Flavonol glycosides in leaves of two Diospyros species

Diospyros zombensis

1 reference

Cytotoxic naphthoquinones, molluscicidal saponins and flavonols from Diospyros zombensis

Epilobium hirsutum

1 reference

Polyphenolic metabolites of Epilobium hirsutum

Eucalyptus consideniana

1 reference

Polyphenols from Eucalyptus consideniana and Eucalyptus viminalis

Eucalyptus globulus

1 reference

Marker constituents of the natural antioxidant Eucalyptus leaf extract for the evaluation of food additives.

Euphorbia sanctae-catharinae

1 reference

Flavonol glycosides of Euphorbia retusa and E. sanctae-catharinae

Gaultheria miqueliana

1 reference

Components of the Leaves of Gaultheria Miqueliana TAKEDA

Gaultheria pyroloides

1 reference

Components of the Leaves of Gaultheria Miqueliana TAKEDA

Hamamelis virginiana

1 reference

Phenolic compounds from leaves ofHamamelis virginiana

Hedysarum coronarium

1 reference

Condensed tannins and flavonoids from the forage legume sulla (Hedysarum coronarium).

Hypericum aucheri

1 reference

Biflavone, flavonol, and xanthone glycosides from Hypericum aucheri

Hypericum henryi

1 reference

Polycyclic polyprenylated acylphloroglucinols and chromone O-glucosides from Hypericum henryi subsp. uraloides

Hypericum laricifolium

1 reference

Constituents of Hypericum laricifolium and their cyclooxygenase (COX) enzyme activities

Hypericum perforatum

3 references

Flavonoids from Hypericum perforatum show antidepressant activity in the forced swimming test

Phenolic compounds from Hypericum perforatum

Variation in the composition of the essential oils, phenolic compounds and mineral elements of Hypericum perforatum L. growing in Estonia

Morella rubra

1 reference

A Triterpenoid and phenolic compounds from Myrica rubra seeds

Myrica rubra

1 reference

A Triterpenoid and phenolic compounds from Myrica rubra seeds

Nelumbo nucifera

3 references

Anti-HIV benzylisoquinoline alkaloids and flavonoids from the leaves of Nelumbo nucifera, and structure-activity correlations with related alkaloids

Antioxidative effect and active components from leaves of Lotus ( Nelumbo nucifera ).

Simultaneous qualitative assessment and quantitative analysis of flavonoids in various tissues of lotus (Nelumbo nucifera) using high performance liquid chromatography coupled with triple quad mass spectrometry

Populus grandidentata

1 reference

Studies on the Leaves of the Family Salicaceae. II.1Quercetin-3-glucosiduronic Acid from Populus grandidentata Leaves2

Rosa lucieae

1 reference

Purgative activity and principals of the fruits of Rosa multiflora and R. wichuraiana

Rosa wichuraiana

1 reference

Purgative activity and principals of the fruits of Rosa multiflora and R. wichuraiana

Rubus adenotrichus

1 reference

Analysis of phenolic compounds in two blackberry species (Rubus glaucus and Rubus adenotrichus) by high-performance liquid chromatography with diode array detection and electrospray ion trap mass spectrometry

Rubus glaucus

1 reference

Analysis of phenolic compounds in two blackberry species (Rubus glaucus and Rubus adenotrichus) by high-performance liquid chromatography with diode array detection and electrospray ion trap mass spectrometry

Salvia blepharophylla

1 reference

Clerodane diterpenoids from Salvia blepharophylla

Tamarix nilotica

2 references

A new ferulic acid ester and other constituents from Tamarix nilotica leaves.

Flavonoids of the flowers of tamarix nilotica

Theobroma grandiflorum

1 reference

New bioactive polyphenols from Theobroma grandiflorum ("cupuaçu").

Gaultheria pyrolifolia

1 reference

Components of the Leaves of Gaultheria Miqueliana TAKEDA

Rosa luciae

1 reference

Purgative activity and principals of the fruits of Rosa multiflora and R. wichuraiana

Dracocephalum ruyschiana

1 reference

Flavone tetraglycosides and benzyl alcohol glycosides from the Mongolian medicinal plant Dracocephalum ruyschiana.

Agarista salicifolia

1 reference

Comparison of flavonoid profiles of Agauria salicifolia (Ericaceae) by liquid chromatography-UV diode array detection-electrospray ionisation mass spectrometry

Erigeron breviscapus

1 reference

Characterization of phenolic compounds in Erigeron breviscapus by liquid chromatography coupled to electrospray ionization mass spectrometry

Apocynum venetum

1 reference

Comprehensive separation and identification of chemical constituents from Apocynum venetum leaves by high-performance counter-current chromatography and high performance liquid chromatography coupled with mass spectrometry

Poacynum venetum

1 reference

Comprehensive separation and identification of chemical constituents from Apocynum venetum leaves by high-performance counter-current chromatography and high performance liquid chromatography coupled with mass spectrometry

Philadelphus lewisii

1 reference

A search for flavonoid variation in Philadelphus lewisii

Diplusodon ciliiflorus

1 reference

Flavonoids of Diplusodon (Lythraceae)

Diplusodon uninervius

1 reference

Flavonoids of Diplusodon (Lythraceae)

Diplusodon orbicularis

1 reference

Flavonoids of Diplusodon (Lythraceae)

Cichorium intybus

2 references

Flavonoids and other phenolics of Cichorium and related members of the Lactuceae (Compositae)

The role of sesquiterpene lactones and phenolics in the chemical defence of the chicory plant

Coriandrum sativum

1 reference

Comparative study of the flavonoids of some local members of the umbelliferae

Ridolfia segetum

1 reference

Comparative study of the flavonoids of some local members of the umbelliferae

Cyclospermum leptophyllum

1 reference

Comparative study of the flavonoids of some local members of the umbelliferae

Ammoides pusilla

1 reference

Comparative study of the flavonoids of some local members of the umbelliferae

Anethum graveolens

3 references

Comparative study of the flavonoids of some local members of the umbelliferae

9-Hydroxypiperitone beta-D-glucopyranoside and other polar constituents from dill (Anethum graveolens L.) herb

UV-Induced biosynthesis of quercetin 3-O-β-D-glucuronide in dill cell cultures

Oenothera odorata

1 reference

Organ- and Tissue-specific Biosynthesis of Flavonoids in Seedlings ofOenothera odorata(Onagraceae)

Betula pubescens

2 references

High-performance liquid chromatographic separation and identification of phenolic compounds from leaves of Betula pubescens and Betula pendula

Flavonoid Glycosides from Betula pubescens and Betula pendula

Betula pendula

3 references

High-performance liquid chromatographic separation and identification of phenolic compounds from leaves of Betula pubescens and Betula pendula

Effect of Sample Preparation Method on Birch (Betula pendula Roth) Leaf Phenolics

Flavonoid Glycosides from Betula pubescens and Betula pendula

Fuchsia fulgens

1 reference

Leaf flavonoid and other phenolic glycosides as indicators of parentage in six ornamental Fuchsia species and their hybrids

Saururus chinensis

2 references

Flavonol glycosides with free radical-scavenging activity of Saururus chinensis

Hepatoprotective flavonol glycosides ofSaururus chinensis herbs

Alchemilla speciosa

1 reference

Flavonoid glycosides from Alchemilla speciosa

Eucalyptus cypellocarpa

1 reference

Cypellocarpins A−C, Phenol Glycosides Esterified with Oleuropeic Acid, fromEucalyptus cypellocarpa.

Arnica mollis

1 reference

Flavonoid glycosides from Arnica amplexicaulis and Arnica mollis

Arnica amplexicaulis

1 reference

Flavonoid glycosides from Arnica amplexicaulis and Arnica mollis

Ligularia amplexicaulis

1 reference

Flavonoid glycosides from Arnica amplexicaulis and Arnica mollis

Arnica longifolia

1 reference

Thirty-seven flavonoids from flowers ofArnica longifolia

Oenothera rosea

1 reference

FLAVONOID SURVEY OF OENOTHERA (ONAGRACEAE): SECTS. GAUROPSIS, HARTMANNIA, KNEIFFIA, PARADOXUS, AND XYLOPLEURUM

Oenothera speciosa

1 reference

FLAVONOID SURVEY OF OENOTHERA (ONAGRACEAE): SECTS. GAUROPSIS, HARTMANNIA, KNEIFFIA, PARADOXUS, AND XYLOPLEURUM

Rubus ulmifolius

1 reference

In vitro antimicrobial activity of extracts and isolated constituents of Rubus ulmifolius

Pteris vittata

1 reference

Flavonoid glycosides of Pteridaceae from Brazil

Gutierrezia wrightii

1 reference

Flavonoids from Gutierrezia wrightii

Stephanodoria tomentella

1 reference

Flavonoids from Stephanodoria tomentella

Symphyotrichum eatonii

1 reference

Flavonoids of Aster bracteolatus

Vigna radiata

1 reference

Flavonoids of Phaseolus aureus

Mutisia acuminata

1 reference

New chromone, coumarin, and coumestan derivatives from Mutisia acuminata var. hirsuta

Persicaria perfoliata

1 reference

A Chemotaxonomic Study of Flavonoids from Japanese Polygonum Species

Persicaria senticosa

1 reference

A Chemotaxonomic Study of Flavonoids from Japanese Polygonum Species

Polygonum senticosum

1 reference

A Chemotaxonomic Study of Flavonoids from Japanese Polygonum Species

Inula saxatilis

1 reference

Flavonol glycosides from Scolymus hispanicus and Jasonia glutinosa

Tamarix senegalensis

2 references

Flavonoids of the flowers of tamarix nilotica

A new ferulic acid ester and other constituents from Tamarix nilotica leaves.

Symphyotrichum bracteolatum

1 reference

Flavonoids of Aster bracteolatus

Rubus adenotrichos

1 reference

Analysis of phenolic compounds in two blackberry species (Rubus glaucus and Rubus adenotrichus) by high-performance liquid chromatography with diode array detection and electrospray ion trap mass spectrometry

Apocynum cannabinum

1 reference

Comprehensive separation and identification of chemical constituents from Apocynum venetum leaves by high-performance counter-current chromatography and high performance liquid chromatography coupled with mass spectrometry

Chiliadenus glutinosus

1 reference

Flavonol glycosides from Scolymus hispanicus and Jasonia glutinosa

Chamaenerion dodonaei

2 references

Compounds fromEpilobium angustifoliumInhibit the Specific Metallopeptidases ACE, NEP and APN

Induction of neutral endopeptidase activity in PC-3 cells by an aqueous extract of Epilobium angustifolium L. and oenothein B.

Potentilla anserina

1 reference

Flavan-3-ols and flavonoids from Potentilla anserina

Epilobium dodonaei

2 references

Compounds fromEpilobium angustifoliumInhibit the Specific Metallopeptidases ACE, NEP and APN

Induction of neutral endopeptidase activity in PC-3 cells by an aqueous extract of Epilobium angustifolium L. and oenothein B.

Fallopia japonica var. japonica

1 reference

Comparative analysis of bioactivities of four Polygonum species

Sulla coronaria

1 reference

Condensed tannins and flavonoids from the forage legume sulla (Hedysarum coronarium).

Epilobium prantlii

2 references

Compounds fromEpilobium angustifoliumInhibit the Specific Metallopeptidases ACE, NEP and APN

Induction of neutral endopeptidase activity in PC-3 cells by an aqueous extract of Epilobium angustifolium L. and oenothein B.

Pistacia weinmannifolia

1 reference

Gallotannins and related polyphenols from Pistacia weinmannifolia

Vigna radiata var. radiata

1 reference

Flavonoids of Phaseolus aureus

Psidium guajava

1 reference

Cytotoxic phenylethanol glycosides from Psidium guaijava seeds.

Geranium dissectum

1 reference

A chemosystematic study of some geraniaceae

Myrothamnus flabellifolia

1 reference

Qualitative and quantitative phytochemical characterization of Myrothamnus flabellifolia Welw

Myrothamnus flabellifolius

1 reference

Qualitative and quantitative phytochemical characterization of Myrothamnus flabellifolia Welw

Paeonia rockii

1 reference

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

Persicaria amphibia

1 reference

Phenylvaleric acid and flavonoid glycosides from Polygonum salicifolium

Persicaria decipiens

1 reference

Phenylvaleric acid and flavonoid glycosides from Polygonum salicifolium

Pulicaria arabica

1 reference

Flavonols of Pulicaria arabica

Salvia

1 reference

Polyphenolics of Salvia--a review

Eucalyptus camaldulensis

1 reference

Flavonoid glycosides and the chemosystematics of Eucalyptus camaldulensisis

Eucalyptus occidentalis

1 reference

Flavonoid glycosides and the chemosystematics of Eucalyptus camaldulensisis

Eucalyptus viminalis

1 reference

Polyphenols from Eucalyptus consideniana and Eucalyptus viminalis

Salvia officinalis

1 reference

Polyphenolics of Salvia--a review

Identifiers

InChI

InChI=1S/C21H18O13/c22-7-4-10(25)12-11(5-7)32-17(6-1-2-8(23)9(24)3-6)18(13(12)26)33-21-16(29)14(27)15(28)19(34-21)20(30)31/h1-5,14-16,19,21-25,27-29H,(H,30,31)/t14-,15-,16+,19-,21+/m0/s1

1 reference

Quercituron (English)

DUBCCGAQYVUYEU-ZUGPOPFOSA-N

19 November 2016

InChIKey

2 references

Quercituron (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

22688-79-5

2 references

Global Substance Registration System

UNII

RY36PD0CQ2

querciturone (English)

DUBCCGAQYVUYEU-ZUGPOPFOSA-N

19 November 2016

InChIKey

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=22688-79-5

1 reference

Miquelianin (English)

19 November 2016

1 reference

Quercituron (English)

19 November 2016

Reaxys registry number

72004

1 reference

miquelianin (English)

7 October 2016

ChEBI ID

66395

mapping relation type

1 reference

QUERCETIN GLUCURONIDE (English)

19 November 2016

1 reference

splash10-0udi-0509000000-d027162b4a94a785cec7

QUERCETIN GLUCURONIDE (English)

19 November 2016

1 reference

MassBank accession ID

0 references

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splash10-0udi-0902000000-1cea43fa477a39ac419a

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splash10-0udi-0609400000-9fd50528da25d66adfc7

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splash10-0udi-0009000000-e583e72c5e51ea792643

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splash10-0udi-0009000000-494ea400ed0fb8b0c67e

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splash10-0udi-0009000000-30eccaeb6ce3cdd58664

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splash10-00di-0009100000-0153fe2b73d48255e245

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splash10-00di-0009100000-5aab931f53f3616f2719

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splash10-052r-0001900000-b000449b20cec900718d

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splash10-052r-0001900000-b5fab19d441f26e7d9d2

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splash10-004i-0000900000-0f5977f28761ae719b25

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splash10-0udi-0009200000-38a20b83316c1fb308c8

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splash10-0udi-0109000000-5704d1d1f17fd74cc002

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splash10-0udi-0009000000-2bd01afb77f877725a80

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splash10-0udi-1009000000-e4e8edfcb2b14bae3932

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splash10-0udi-2109000000-b95f9e6d2e5cedd5dde0

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splash10-004i-0000900000-affea1f9440606f3970d

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splash10-004i-0002900000-56ca9b01d99e5abed67a

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splash10-0udi-0009200000-cebd27a1282c5a1f5148

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splash10-0udi-0009000000-bbbba690808d942051b1

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splash10-0udi-0009000000-3a722861ad1502d33d48

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splash10-0udi-0319000000-a9dc358cce62bed3c1b3

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splash10-0ufr-0209700000-061af61d2807cac90267

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splash10-0udr-0904000000-a59e3425ec1876236374

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splash10-0udi-0009000000-93be6391e545f9647cb6

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splash10-0xvi-0909900000-ee767fce1a96611b4c85

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splash10-0ui0-0904400000-b132ac68c19e8bd29f0c

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splash10-0udi-0009000000-54756840d043a5bb4a4f

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splash10-0udi-0009000000-948d7a2a6b700876f6ef

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DSSTox substance ID

DTXSID70945358

0 references

DSSTOX compound identifier

DTXCID101373677

0 references

Human Metabolome Database ID

0 references

1 reference

Global Substance Registration System

UNII

RY36PD0CQ2