(Q3266683)

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

inferred from SMILES

1 reference

inferred from SMILES

mass

448.100561 dalton

1 reference

Kaempferol 7-b-D-glucopyranoside (English)

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

8 October 2016

stereoisomer of

1 reference

kaempferol 7-O-beta-D-galactopyranoside

inferred from InChI

1 reference

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

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₁H₂₀O₁₁

1 reference

16290-07-6 (English)

20 November 2016

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

1 reference

16290-07-6 (English)

20 November 2016

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

1 reference

Ptychostomum pseudotriquetrum

16290-07-6 (English)

20 November 2016

1 reference

Chemotypes of the Antarctic moss Bryum algens delineated by their flavonoid constituents

Maclura cochinchinensis

2 references

Evaluation of the liver protective principles from the root ofCudrania cochinchinensis var.gerontogea

Flavonoids and a prenylated xanthone from Cudrania cochinchinensis var. gerontogea

Afzelia bella

2 references

Constituents of Afzelia bella stem bark

Constituents of Afzelia bella stem bark

Alkanna orientalis

1 reference

The Flavonoids of Alkanna orientalis

Aristolochia foveolata

2 references

Sodium aristolochate derivatives from leaves of Aristolochia foveolata

Sodium aristolochate derivatives from leaves of Aristolochia foveolata

Bletilla formosana

2 references

Dihydrophenanthrenes from Bletilla formosana

Dihydrophenanthrenes from Bletilla formosana

Chenopodium murale

1 reference

A flavonol triglycoside from Chenopodium murale

Crocus sativus

4 references

Antityrosinase principles and constituents of the petals of Crocus sativus

Antityrosinase principles and constituents of the petals of Crocus sativus

Antityrosinase principles and constituents of the petals of Crocus sativus

Flavonoid Determination in the Quality Control of Floral Bioresidues from Crocus sativus L

Evolvulus alsinoides

2 references

Anti-stress constituents of Evolvulus alsinoides: an ayurvedic crude drug

Anti-stress constituents of Evolvulus alsinoides: an ayurvedic crude drug

Pelargonium reniforme

3 references

O-Galloyl-C-glycosylflavones from Pelargonium reniforme

O-Galloyl-C-glycosylflavones from Pelargonium reniforme

O-Galloyl-C-glycosylflavones from Pelargonium reniforme

Podocarpus fasciculus

2 references

Cytotoxic constituents from Podocarpus fasciculus

Cytotoxic constituents from Podocarpus fasciculus

Reseda muricata

2 references

Kaempferol triosides from Reseda muricata.

Kaempferol triosides from Reseda muricata.

Sedum sarmentosum

4 references

Bioactive constituents from Chinese natural medicines. XXII. Absolute structures of new megastigmane glycosides, sedumosides E1, E2, E3, F1, F2, and G, from Sedum sarmentosum (Crassulaceae)

Flavonol glycosides with lipid accumulation inhibitory activity from Sedum sarmentosum

Bioactive constituents from Chinese natural medicines. XXII. Absolute structures of new megastigmane glycosides, sedumosides E1, E2, E3, F1, F2, and G, from Sedum sarmentosum (Crassulaceae)

Bioactive Constituents from Chinese Natural Medicines. XXV. New Flavonol Bisdesmosides, Sarmenosides I, II, III, and IV, with Hepatoprotective Activity from Sedum sarmentosum (Crassulaceae)

Spiranthes australis

2 references

Flavonoid constituents from Spiranthes australis LINDL.

Flavonoid constituents from Spiranthes australis LINDL.

Spiranthes sinensis

1 reference

Flavonoid constituents from Spiranthes australis LINDL.

mountain clover

2 references

Flavonoids of Trifolium montanum

Flavonoids of Trifolium montanum

Warburgia stuhlmannii

3 references

Flavonol glycosides of Warburgia ugandensis leaves

Flavonol and drimane-type sesquiterpene glycosides of Warburgia stuhlmannii leaves

Flavonol and drimane-type sesquiterpene glycosides of Warburgia stuhlmannii leaves

Anagallis arvensis

1 reference

Chemosystematics of Anagallis arvensis L. (Primulaceae)

Aristolochia cucurbitifolia

1 reference

Constituents of the Fresh Leaves of Aristolochia cucurbitifolia.

Arnica sachalinensis

1 reference

Flavonoids of Arnica sachalinensis, subgenus Andropurpurea

Asteriscus graveolens

1 reference

Flavonoids of Asteriscus graveolens

Bombyx mori

1 reference

Purification and identification of flavonoids from the yellow green cocoon shell (Sasamayu) of the silkworm, Bombyx mori

Centaurea cyanus

2 references

Phytochemical study of Centaurea cyanus

Phytochemical study of Centaurea cyanus

Chaenomeles sinensis

2 references

Antitumor-promoting constituents from Chaenomeles sinensis KOEHNE and their activities in JB6 mouse epidermal cells

Antitumor-promoting constituents from Chaenomeles sinensis KOEHNE and their activities in JB6 mouse epidermal cells

Cicer arietinum

1 reference

Flavonoids of some species of Cicer of the Central Asian flora

Notobasis syriaca

1 reference

FLAVONOIDS FROM PULICARIA ARABICA (L.) CASS.

1 reference

1 reference

1 reference

1 reference

1 reference

Interspecific and intraspecific variation of phenolics in the genus Equisetum subgenus Equisetum

Equisetum fluviatile

1 reference

Interspecific and intraspecific variation of phenolics in the genus Equisetum subgenus Equisetum

Fagonia glutinosa

1 reference

Significance of flavonoid chemistry in the Egyptian Fagonia glutinosa and F. isotricha complexes

Fagonia scabra

1 reference

Significance of flavonoid chemistry in the Egyptian Fagonia glutinosa and F. isotricha complexes

Maclura pomifera

3 references

Two isoflavones and a flavone from the fruits of Maclura pomifera

Two isoflavones and a flavone from the fruits of Maclura pomifera

Osage orange (Maclura pomifera): History and economic uses

Picea abies

3 references

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

Syringetin 3-O-(6″-acetyl)-β-glucopyranoside and other flavonols from needles of norway spruce, Picea abies

Syringetin 3-O-(6″-acetyl)-β-glucopyranoside and other flavonols from needles of norway spruce, Picea abies

Podocarpus nivalis

1 reference

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

Pongamia pinnata

1 reference

Chemical Examination of Flowers ofPongamia glabra

Prunus davidiana

1 reference

Phytochemical study onPrunus davidiana

Prunus dulcis

1 reference

Variation in the flavonol glycoside composition of almond seedcoats as determined by maldi-tof mass spectrometry

Retama raetam

1 reference

The Flavonoids of the Seeds of Lygos raetam

Robinsonia masafuerae

1 reference

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

Rosa × damascena

1 reference

The anti-HIV activity and mechanisms of action of pure compounds isolated from Rosa damascena

Rudbeckia fulgida

2 references

Trihydroxy-C18-acids and a labdane from rudbeckia fulgida

Trihydroxy-C18-acids and a labdane from rudbeckia fulgida

Salix babylonica

2 references

Phenolic glycosides from Salix babylonica

Phenolic glycosides from Salix babylonica

Senna italica

1 reference

Flavonoids of Cassia italica

Silybum marianum

1 reference

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

Smilax bockii

1 reference

Antiinflammatory constituents from the roots of Smilax bockii warb

Platycladus orientalis

2 references

Phenolic constituents of Lyonia ovalifolia

Constituents of pollen. XV. Constituents of Biota orientalis (L.) ENDL. (1).

Trifolium hybridum

1 reference

Flavonoids from Trifolium hybridum and T. ambiguum

Trigonella cylindracea

1 reference

The chemosystematics of Egyptian Trigonella species

Trigonella foenum-graecum

1 reference

The chemosystematics of Egyptian Trigonella species

Medicago polyceratia

1 reference

The chemosystematics of Egyptian Trigonella species

Vigna aconitifolia

1 reference

Constitutive flavonoids and induced isoflavonoids as taxonomic markers in the genus Vigna

Allium victorialis

1 reference

Flavonoid glycosides from the leaves of Allium victorialis var. platyphyllum and their anti-neuroinflammatory effects

Abies nephrolepis

1 reference

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

Eleutherococcus brachypus

1 reference

Flavonoid constituents from the roots of Acanthopanax brachypus

Achillea atrata

1 reference

Flavones and sesquiterpene lactones from Achillea atrata subsp. multifida: antimicrobial activity

Achillea multifida

1 reference

Flavones and sesquiterpene lactones from Achillea atrata subsp. multifida: antimicrobial activity

Aconitum variegatum

1 reference

New flavonol glycosides from Aconitum burnatii Gáyer and Aconitum variegatum L.

Allium hirtifolium

1 reference

Structure-activity relationships for saponins from Allium hirtifolium and Allium elburzense and their antispasmodic activity

Allium stipitatum

1 reference

Structure-activity relationships for saponins from Allium hirtifolium and Allium elburzense and their antispasmodic activity

Allium triquetrum

1 reference

Saponins and flavonoids of Allium triquetrum

Aster indicus

1 reference

Phenolic derivatives from Aster indicus

Astragalus dipelta

1 reference

Kaempferol glycosides fromAstragalus dipelta

Astragalus lagopoides

1 reference

Flavonoids ofAstragalus lagurus

Astragalus lagurus

1 reference

Flavonoids ofAstragalus lagurus

Carthamus tinctorius

1 reference

A new flavone diglycoside from Carthamus tinctorius seeds.

Desmodium gangeticum

1 reference

Glycolipids and other constituents from Desmodium gangeticum with antileishmanial and immunomodulatory activities.

Lotus corniculatus

1 reference

Flavonoids from Lotus ucrainicus and L. arvensis

Lotus ucrainicus

1 reference

Flavonoids from Lotus ucrainicus and L. arvensis

Tripterospermum chinense

1 reference

Flavonoids and Xanthones from Tripterospermum chinense

Wisteria floribunda

2 references

Chemical Components from the Fruit Peels of Wisteria floribunda and their Effects on Rat Aortic Vascular Smooth Muscle Cells

A new flavan-3-ol and the anti-inflammatory effect of flavonoids from the fruit peels of Wisteria floribunda.

Pulicaria wightiana

1 reference

Phenolic derivatives from Aster indicus

Opuntia ficus-indica

1 reference

Secondary metabolites from Opuntia ficus-indica var. saboten.

Medicago orthoceras

1 reference

The chemosystematics of Egyptian Trigonella species

Pieris brassicae

1 reference

HPLC-DAD-MS/MS-ESI screening of phenolic compounds in Pieris brassicae L. Reared on Brassica rapa var. rapa L.

Goniophlebium niponicum

1 reference

The Chemical Constituents ofPolypodium Niponicum

Pleurolobus gangeticus

1 reference

Glycolipids and other constituents from Desmodium gangeticum with antileishmanial and immunomodulatory activities.

Astragalus laguroides

1 reference

Flavonoids ofAstragalus lagurus

Dendrobium bigibbum var. superbum

1 reference

Acylated anthocyanins and flavonols from purple flowers of Dendrobium cv. ‘Pompadour’

Achillea clusiana

1 reference

Flavones and sesquiterpene lactones from Achillea atrata subsp. multifida: antimicrobial activity

broad bean

2 references

Flavonoid concentration changes in maturing broad bean pods

UHPLC/MS2-based approach for the comprehensive metabolite profiling of bean (Vicia faba L.) by-products: A promising source of bioactive constituents

Tribulus pentandrus

1 reference

Flavonoid glycosides of Tribulus pentandrus and T. Terrestris

Panax ginseng

1 reference

Metabolic dynamics and physiological adaptation of Panax ginseng during development.

Brassica oleracea

1 reference

Phytochemical fingerprinting of vegetable Brassica oleracea and Brassica napus by simultaneous identification of glucosinolates and phenolics

Ginkgo biloba

1 reference

A strategy for screening antioxidants in Ginkgo biloba extract by comprehensive two-dimensional ultra high performance liquid chromatography.

Morus alba

1 reference

Identification and quantification of phenolic acids and flavonol glycosides in Tunisian Morus species by HPLC-DAD and HPLC–MS

Nicotiana tabacum

1 reference

Flavonoid and certain related phenolic compounds in parts of the tobacco flower

Rosa gallica

1 reference

The anti-HIV activity and mechanisms of action of pure compounds isolated from Rosa damascena

Maclura tricuspidata

1 reference

Components of Root Bark ofCudrania tricuspidata; 3.1,2. Isolation and Structure Studies on the Flavonoids

Prunus avium

1 reference

Variation in the flavonol glycoside composition of almond seedcoats as determined by maldi-tof mass spectrometry

Astragalus varius

1 reference

Flavonoids of Astragalus virgatus

Spiranthes vernalis

1 reference

Flavonoid constituents from Spiranthes australis LINDL.

Identifiers

InChI

InChI=1S/C21H20O11/c22-7-13-15(25)17(27)19(29)21(32-13)30-10-5-11(24)14-12(6-10)31-20(18(28)16(14)26)8-1-3-9(23)4-2-8/h1-6,13,15,17,19,21-25,27-29H,7H2/t13-,15-,17+,19-,21-/m1/s1

1 reference

16290-07-6 (English)

20 November 2016

2 references

16290-07-6 (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

16290-07-6

2 references

Global Substance Registration System

UNII

RZF1QN1Z8R

kaempferol 7-O-glucoside (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=16290-07-6

9 April 2021

1 reference

Kaempferol-7-O-glucoside (English)

20 November 2016

2 references

16290-07-6 (English)

20 November 2016

Reaxys registry number

68205

1 reference

kaempferol 7-O-beta-D-glucopyranoside (English)

8 October 2016

ChEBI ID

75790

mapping relation type

2 references

CHEMBL469441 (English)

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C21H20O11/c22-7-13-15(25)17(27)19(29)21(32-13)30-10-5-11(24)14-12(6-10)31-20(18(28)16(14)26)8-1-3-9(23)4-2-8/h1-6,13,15,17,19,21-25,27-29H,7H2/t13-,15-,17+,19-,21-/m1/s1

1 reference

splash10-000i-0090000000-f870618bdb464471064d

CHEMBL469441 (English)

20 November 2016

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

MSBNK-IPB_Halle-PN000114

0 references

MSBNK-IPB_Halle-PN000115

0 references

SPLASH

0 references

splash10-000k-0090900000-2aeffbf63a578c502dd0

0 references

splash10-000i-0090000000-4da2830caa30b97f2395

0 references

Human Metabolome Database ID

HMDB0303599

2 references

inferred from InChIKey

reason for deprecated rank

KNApSAcK ID

C00005149

cannot be confirmed by other sources

0 references

UNII

RZF1QN1Z8R

2 references

Global Substance Registration System

UNII

RZF1QN1Z8R

kaempferol 7-O-glucoside (English)

20 November 2016