(Q15424791)

4',5-Dihydroxy-7-glucosyloxyflavanone

Prunin (English)

5 October 2016

2 references

inferred from InChIKey

(R)-5-Hydroxy-2-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)chroman-4-one

inferred from InChI

1 reference

(2S)-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₁H₂₂O₁₀

1 reference

Prunin (English)

5 October 2016

C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O

1 reference

Prunin (English)

5 October 2016

C1[C@H](OC2=CC(=CC(=C2C1=O)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)C4=CC=C(C=C4)O

1 reference

Flavonoids of Phlomis aurea and P. floccosa

Prunin (English)

5 October 2016

1 reference

Phlomis floccosa

1 reference

Flavonoids of Phlomis aurea and P. floccosa

Vachellia farnesiana var. farnesiana

1 reference

Chemical composition of Acacia farnesiana (L) Willd fruits and its activity against Mycobacterium tuberculosis and dysentery bacteria

Holarrhena pubescens

1 reference

Constituents of the leaves of Holarrhena pubescens

Phyllanthus emblica

1 reference

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

Juniperus communis

1 reference

Neolignan and flavonoid glycosides in Juniperus communis var. depressa

Ipomoea nil

1 reference

Flavonoids in the acyanic flowers of Pharbitis nil

Cynara scolymus

1 reference

The flavonoids of Cynara sibthorpiana

Podocarpus nivalis

1 reference

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

Prunus davidiana

3 references

Antihyperlipidemic effect of flavonoids from Prunus davidiana

Improvement of hyperglycemia and hyperlipemia in streptozotocin-diabetic rats by a methanolic extract of Prunus davidiana stems and its main component, prunin

Phytochemical study onPrunus davidiana

Viscum articulatum

2 references

Flavanone and diphenylpropane glycosides and glycosidic acyl esters from Viscum articulatum

Two new phenolic glycosides from Viscum articulatum

Abies nephrolepis

1 reference

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

Acer pictum

1 reference

Two new hepatoprotective stilbene glycosides from Acer mono leaves

Antirrhinum majus

2 references

The chemistry of flower pigmentation in Antirrhinum majus. II. Glycosides of PPmmYY, PPMMYY, ppmmYY and ppMMYY color genotypes

The Chemistry of Flower Pigmentation in Antirrhinum majus. V.1Pigments of Yellow Antirrhinum majus,2,3Genotype ppmmyy4

Breynia fruticosa

1 reference

Glycosides from Breynia fruticosa and Breynia rostrata

Citrus medica

1 reference

Chemical constituents from the peels of Citrus sudachi

Citrus sudachi

1 reference

Chemical constituents from the peels of Citrus sudachi

Crotalaria assamica

1 reference

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

Dracocephalum tanguticum

1 reference

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

Neocheiropteris fortunei

1 reference

Effects of eleven flavonoids from the osteoprotective fraction of Drynaria fortunei (KUNZE) J. SM. on osteoblastic proliferation using an osteoblast-like cell line

Helichrysum arenarium

2 references

Medicinal flowers. XXX. Eight new glycosides, everlastosides F-M, from the flowers of Helichrysum arenarium

Medicinal flowers. XXVII. New flavanone and chalcone glycosides, arenariumosides I, II, III, and IV, and tumor necrosis factor-alpha inhibitors from everlasting, flowers of Helichrysum arenarium

Pelargonium reniforme

1 reference

O-Galloyl-C-glycosylflavones from Pelargonium reniforme

Pinus massoniana

1 reference

Flavonoid glycosides from needles of Pinus massoniana

Populus tremuloides

1 reference

Cytotoxic phenolic compounds in leaf buds of Populus tremuloides

Prunus spachiana

1 reference

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

Prunus amygdalus

1 reference

Antioxidative phenolic compounds isolated from almond skins (Prunus amygdalus Batsch).

Prunus dulcis

1 reference

Antioxidative phenolic compounds isolated from almond skins (Prunus amygdalus Batsch).

Prunus avium

4 references

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

Flavanone glucosides in callus and phloem of Prunus avium: Identification and stimulation of their synthesis

Specific accumulation of o-diphenols in stressed leaves of Prunus avium

Antioxidative phenolic compounds isolated from almond skins (Prunus amygdalus Batsch).

Prunus mume

1 reference

Notes- Flavonoids of Various Prunus Species. VIII. The Flavonoids in the Wood of Prunus mume

Prunus nipponica

1 reference

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

Viscum coloratum

2 references

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

Antioxidative flavanone glycosides from the branches and leaves of Viscum coloratum

Anisomeles indica

1 reference

Flavonoid Glycosides from Anisomeles ovata

Cuscuta reflexa

1 reference

Constituents of Cuscuto Reflexa are anti-HIV Agents

Cynara cardunculus

1 reference

The flavonoids of Cynara sibthorpiana

Erythroxylum rufum

1 reference

Flavonoids of Erythroxylum rufum and Erythroxylum ulei

Hydrangea macrophylla

1 reference

Absolute Stereostructures of 3S-Phyllodulcin, 3R- and 3S-Phyllodulcin Glycosides, and 3R- and 3S-Thunberginol H Glycosides from the Leaves of Hydrangea macrophylla SERINGE var. thunbergii MAKINO

Momordica foetida

1 reference

Plants traditionally used against malaria: phytochemical and pharmacological investigation of Momordica foetida

Robinsonia masafuerae

1 reference

FLAVONOID EVOLUTION IN ROBINSONIA (COMPOSITAE) OF THE JUAN FERNANDEZ ISLANDS

Salix caprea

1 reference

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

Vaccinium macrocarpon

1 reference

Inhibition of uropathogenic Escherichia coli by cranberry juice: a new antiadherence assay

Crotalaria sericea

1 reference

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

Crotalaria spectabilis

1 reference

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

Lepisorus fortunei

1 reference

Effects of eleven flavonoids from the osteoprotective fraction of Drynaria fortunei (KUNZE) J. SM. on osteoblastic proliferation using an osteoblast-like cell line

Citrus × paradisi

2 references

Hesperetin 7-O-glucoside and prunin in Citrus species (C. aurantium and C. paradisi). A study of their quantitative distribution in immature fruits and as immediate precursors of neohesperidin and naringin in Citrus aurantium

Glucosylation of exogenous flavanones by grapefruit (Citrus paradisi) cell cultures

Citrus medica var. sarcodactylis

1 reference

Chemical constituents from the peels of Citrus sudachi

Cacao

1 reference

Liquid chromatographic/electrospray ionization tandem mass spectrometric study of the phenolic composition of cocoa (Theobroma cacao).

Paeonia rockii

1 reference

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

Kumquat

1 reference

Chemical constituents from the peels of Citrus sudachi

Prunus itosakura

1 reference

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

Crotalaria juncea

1 reference

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

Citrus japonica

1 reference

Chemical constituents from the peels of Citrus sudachi

1 reference

Prunin

0 references

Identifiers

InChI

InChI=1S/C21H22O10/c22-8-16-18(26)19(27)20(28)21(31-16)29-11-5-12(24)17-13(25)7-14(30-15(17)6-11)9-1-3-10(23)4-2-9/h1-6,14,16,18-24,26-28H,7-8H2/t14-,16+,18+,19-,20+,21+/m0/s1

1 reference

DLIKSSGEMUFQOK-SFTVRKLSSA-N

Prunin (English)

5 October 2016

2 references

DLIKSSGEMUFQOK-SFTVRKLSSA-N

Prunin (English)

5 October 2016

ChEBI release 2020-09-01

CAS Registry Number

529-55-5

1 reference

InChIKey

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=529-55-5

1 reference

Prunin (English)

5 October 2016

1 reference

Prunin (English)

5 October 2016

Reaxys registry number

66743

1 reference

naringenin 7-O-beta-D-glucoside (English)

5 October 2016

ChEBI ID

28327

mapping relation type

1 reference

naringenin 7-O-beta-D-glucoside (English)

5 October 2016

1 reference

MSBNK-Univ_Toyama-TY000160

PRUNIN (English)

5 October 2016

1 reference

MassBank accession ID

0 references

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MSBNK-Univ_Toyama-TY000161

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MSBNK-Univ_Toyama-TY000162

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splash10-00di-0590000000-e40732b0d1dd68f9ac90

0 references

splash10-0fk9-1970000000-eea5a19d9932daa1e0fe

0 references

splash10-0uk9-0930000000-677664c80a37b366e8b1

0 references

splash10-014i-1900000000-781434481d9fc930fc87

0 references

splash10-00di-0790000000-f9c7b124fc21f92b31bb

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splash10-0fk9-1960000000-461c79c9b385107f16f1

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splash10-0uka-0930000000-1e71961ea26405bf0b66

0 references

splash10-0udi-2900000000-fa8ef3184f57c30ae6db

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splash10-0fk9-0980000000-0e86b70556e4d382bc7e

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splash10-00di-0090000000-ee664566643908de2e04

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splash10-00e9-0090800000-bb6d896e019e279809f4

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splash10-00e9-0090800000-a5f475ddf38bcfba17cb

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splash10-00e9-0090500000-a4111e5ea52f785b7965

0 references

splash10-00e9-0090700000-fa1a65cdd6623ad83f45

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splash10-006t-0002344690-0ecda647f03e95cd3092

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splash10-0002-0002345690-424b13449c8123b6e4e7

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splash10-0079-0050900000-e25ed0dbe6236f9f445a

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splash10-00di-0090000000-86d77892c771c706d4e3

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splash10-00di-0090000000-0a38aeae2d155ee2fc36

0 references

splash10-00di-0290000000-04b3670860529362676d

0 references

splash10-0uka-0940000000-1f7c564ea336a00ed3b1

0 references

splash10-0udj-0910000000-c9d458fbf522506e7266

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splash10-001i-0020900000-48ebf5ad7e87093e7fb6

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splash10-00e9-0090500000-59b064eb174fef34b4a1

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splash10-00di-0090000000-0d30d6753f72cea19577

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splash10-00di-0090000000-45715d698cbd3a93005a

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splash10-00di-0590000000-fb0abd825d4bee42ba84

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splash10-00di-0090000000-7a348aba51cc35445f0d

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splash10-001i-0000900030-213d48a9fc89249d0aeb

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splash10-00e9-0090600000-3fa1e0de7ee375e6fb13

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splash10-0g4i-0960000000-4cdbf1aa9926e7c6f413

0 references

splash10-0i2a-0932000000-15724b8eed2ddd8b1f14

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splash10-0gdj-0931000000-330679cf4783d446715c

0 references

splash10-00e9-0090600000-5594c386d7230c06bd74

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DSSTox substance ID

DTXSID40967365

0 references

DSSTOX compound identifier

0 references

0 references

208-464-8

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.007.696

27 December 2018

ECHA Substance Infocard ID

(S)-7-(β-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one (English)

quotation

CAS no.: 529-55-5 (English)

100.007.696

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.007.696

27 December 2018

(S)-7-(β-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one (English)

quotation

CAS no.: 529-55-5 (English)

1 reference

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

naringenin 7-O-beta-D-glucoside (English)

5 October 2016

0 references

0 references

1 reference