genistin (Q5533221)

inferred from SMILES

mass

432.105647 dalton

1 reference

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

Genistin (English)

5 October 2016

2 references

inferred from InChIKey

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

2 references

inferred from InChIKey

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

2 references

inferred from InChIKey

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

1 reference

chemical formula

C₂₁H₂₀O₁₀

1 reference

Genistin (English)

18 November 2016

C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O

1 reference

Genistin (English)

18 November 2016

C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O

1 reference

Genistin (English)

18 November 2016

Adenocarpus complicatus

1 reference

Potential Value of Plants as Sources of New Antifertility Agents II *

Lupinus albus

3 references

Detection of isoflavonoids and their glycosides by liquid chromatography/electrospray ionization mass spectrometry in root extracts of lupin (Lupinus albus)

New Isoflavone Glucosides from White Lupin (Lupinus albus L.)

Production and Release of Isoflavonoids by Lupin Cell Cultures

Achlys triphylla

1 reference

Four flavonol glycosides from Achlys triphylla

Calycotome villosa

2 references

Flavonoids from Calicotome villosa

Flavonoids from Calicotome villosa

Chaenomeles sinensis

3 references

Tissue factor inhibitory flavonoids from the fruits of Chaenomeles sinensis

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

Chamaecytisus supinus

1 reference

Flavonoids and Alkaloids of Chamaecytisus hirsutus and Chamaecytisus supinus

Cicer arietinum

1 reference

High-performance liquid chromatography of isoflavones and phytoalexins from Cicer arietinum

Eriosema tuberosum

2 references

Isoflavonoid glycosides from eriosema tuberosum

Isoflavonoid glycosides from eriosema tuberosum

Ficus septica

2 references

Phenanthroindolizidine Alkaloids and Their Cytotoxicity from the Leaves of Ficus septica

Phenanthroindolizidine Alkaloids and Their Cytotoxicity from the Leaves of Ficus septica

Flemingia paniculata

2 references

New salicylic acid and isoflavone derivatives from Flemingia paniculata.

New salicylic acid and isoflavone derivatives from Flemingia paniculata.

Genista ephedroides

1 reference

Flavonoids fromGenista ephedroides

Genista morisii

2 references

Estradiol-antagonistic activity of phenolic compounds from leguminous plants.

Flavonoids and isoflavonoids from Genista morisii

Genista lydia

1 reference

Ulceroprotective activity of the flavonoids ofGenista rumelica Vel

Lespedeza davidii

1 reference

Chemical constituents from Sinacalia davidii

Lupinus luteus

2 references

Isoflavones of the roots of Lupinus luteus

Isoflavones of the roots of Lupinus luteus

Lupinus polyphyllus

1 reference

Isoflavone Glycoside Formation in Transformed and Non-Transformed Suspension and Hairy Root Cultures of Lupinus polyphyllus and Lupinus hartwegii

Lupinus pubescens

1 reference

ALKALOIDS AND ISOFLAVONOIDS FROM LUPINUS PUBESCENS BENTH

Maackia amurensis

3 references

Isoflavonoids of the bark and leaves ofMaackia amurensis

Isoflavonoid composition of a callus culture of the relict tree Maackia amurensis Rupr. et Maxim

Isoflavonoids of the bark and leaves ofMaackia amurensis

Flemingia macrophylla

2 references

A flavonol C-glycoside from Moghania macrophylla

A flavonol C-glycoside from Moghania macrophylla

Neorautanenia amboensis

1 reference

Isoflavone Glycosides from Neorautanenia amboensis

Prunus avium

2 references

Prunetin 5-O-β-d-glucopyranoside, an isoflavone from the peduncle of Prunus avium and P. Cerasus

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

Prunus cerasus

2 references

Prunetin 5-O-β-d-glucopyranoside, an isoflavone from the peduncle of Prunus avium and P. Cerasus

Antioxidant polyphenols from tart cherries (Prunus cerasus).

Punica granatum

1 reference

Oestrogen content of pomegranate seeds

Retama sphaerocarpa

4 references

An isoflavone glucoside from Retama sphaerocarpa boissier

Cytotoxic activity of flavonoids and extracts from Retama sphaerocarpa Boissier

An isoflavone glucoside from Retama sphaerocarpa boissier

Phytochemical Study of Retama sphaerocarpa

Selaginella sinensis

1 reference

Chemical constituents of Carlesia sinensis

Thermopsis dolichocarpa

1 reference

Flavonoids of Thermopsis dolichocarpa

Trifolium pratense

5 references

Identification of isoflavone conjugates in red clover (Trifolium pratense) by liquid chromatography–mass spectrometry after two-dimensional solid-phase extraction

Determination of isoflavone glucoside malonates in Trifolium pratense L. (red clover) extracts: quantification and stability studies.

Analysis of flavonoids from red clover by liquid chromatography—electrospray mass spectrometry

LC-ESI-MS study of the flavonoid glycoside malonates of red clover (Trifolium pratense)

New genistein monogalactoside from the aerial part of Trifolium pratense

Dalbergia sissoo

1 reference

Constituents of Dalbergia sissoo Roxb. leaves with osteogenic activity.

Glycine

1 reference

Isoflavonoid content of Hong Kong soy foods.

Streptomyces

3 references

Termisoflavones A-C, Isoflavonoid Glycosides from Termite-Associated Streptomyces sp. RB1.

Chemical Identification of Isoflavonoids from a Termite-Associated sp. RB1 and Their Neuroprotective Effects in Murine Hippocampal HT22 Cell Line

Termisoflavones AC, Isoflavonoid Glycosides from Termite-Associated Streptomyces sp. RB1

Sorbus cuspidata

1 reference

Neurocytoprotective effects of the bioactive constituents of Pueraria thomsonii in 6-hydroxydopamine (6-OHDA)-treated nerve growth factor (NGF)-differentiated PC12 cells

Desmodium styracifolium

1 reference

Flavonoid compounds from Desmodium styracifolium of Vietnamese origin

Genista pichisermolliana

1 reference

A new alpinumisoflavone derivative from Genista pichisermolliana

Genista sessilifolia

1 reference

Flavonoids and isoflavonoids from Genista sessilifolia DC. Growing in Turkey

Mucuna birdwoodiana

1 reference

Two new isoflavone glycosides from Mucuna birdwoodiana

Prunus spachiana

1 reference

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

Thermopsis alterniflora

1 reference

Flavonoids of Thermopsis alterniflora

Thermopsis lupinoides

1 reference

Isoflavonoids in the roots of Thermopsis fabacea D.C. (Leguminosae).

reversed clover

1 reference

Flavonoids from Trifolium resupinatum var. microcephalum

Trifolium subterraneum

1 reference

Bioactive Isoflavonols and Other Components fromTrifolium subterraneum

Chamaecytisus eriocarpus

1 reference

Flavonoids and Alkaloids from Chamaecytisus eriocarpus

Thermopsis californica

1 reference

Isoflavonoids in the roots of Thermopsis fabacea D.C. (Leguminosae).

Griffitharia vestita

1 reference

Neurocytoprotective effects of the bioactive constituents of Pueraria thomsonii in 6-hydroxydopamine (6-OHDA)-treated nerve growth factor (NGF)-differentiated PC12 cells

Genista tridentata

2 references

The opposing effects of the flavonoids isoquercitrin and sissotrin, isolated from Pterospartum tridentatum, on oral glucose tolerance in rats

Flavonoids of an extract of Pterospartum tridentatum showing endothelial protection against oxidative injury

Chamaecytisus pygmaeus

1 reference

Flavonoids and Alkaloids from Chamaecytisus eriocarpus

Grona styracifolia

1 reference

Flavonoid compounds from Desmodium styracifolium of Vietnamese origin

Neorautanenia mitis

1 reference

Isoflavone Glycosides from Neorautanenia amboensis

Thermopsis lanceolata

1 reference

Isoflavonoids in the roots of Thermopsis fabacea D.C. (Leguminosae).

Pueraria montana var. lobata

4 references

Isoflavone glucosides exist as their 6''-O-malonyl esters in Pueraria lobata and its cell suspension cultures.

Studies on the constituents of Pueraria lobata. III. Isoflavonoids and related compounds in the roots and the voluble stems.

Constituents of the roots of Pueraria lobata inhibit formation of advanced glycation end products (AGEs)

Dual High-Resolution α-Glucosidase and Radical Scavenging Profiling Combined with HPLC-HRMS-SPE-NMR for Identification of Minor and Major Constituents Directly from the Crude Extract of Pueraria lobata

Glycine soja

1 reference

Secondary metabolites from Glycine soja and their growth inhibitory effect against Spodoptera litura

chia

1 reference

Phytochemical profile and nutraceutical potential of chia seeds (Salvia hispanica L.) by ultra high performance liquid chromatography.

Glycine max

23 references

Histochemistry. VI. Tocopherols and isoflavones in soybeans (Glycine max MERRILL, seeds).

A new isoflavone glycoside in soybean seeds(Glycine max Merrill), glycitein 7-O-.BETA.-D-(6''-O-acetyl)-glucopyranoside.

Determination of isoflavones in soybean flours, protein concentrates, and isolates

New 6-O-acyl isoflavone glycosides from soybeans fermented with Bacillus subtilis (natto). I. 6-O-succinylated isoflavone glycosides and their preventive effects on bone loss in ovariectomized rats fed a calcium-deficient diet

Soy isoflavone analysis: quality control and a new internal standard

Chemical modification of isoflavones in soyfoods during cooking and processing

Genistein, daidzein, and their .beta.-glycoside conjugates: antitumor isoflavones in soybean foods from American and Asian diets

Isoflavone Content in Commercial Soybean Foods

Isoflavone Composition of American and Japanese Soybeans in Iowa: Effects of Variety, Crop Year, and Location

An investigation on the extraction and concentration of isoflavones in soy-based products

Semi-preparative high-performance liquid chromatographic isolation of soybean isoflavones

"Isolation of 6\"-O-acetylgenistin and 6\"-O-acetyldaidzin from toasted defatted soyflakes"

Improved high-performance liquid chromatographic analysis of phenolic acids and isoflavonoids from soybean protein products

Novel isoflavone, cinnamic acid, and triterpenoid glycosides in soybean molasses

New isoflavone and triterpene glycosides from soybeans

Isoflavones of the oilcake of the seeds of Glycyne hispida

Components Responsible for the Undesirable Taste of Soybean Seeds

Size Exclusion Chromatography of Soybean Proteins and Isoflavones

Coumestrin a coumestan derivative from soybean roots

Flavonoids ofGlycine hispida

Isoflavone glucoside stress metabolites of soybean leaves

Quantification of isoflavones by capillary zone electrophoresis in soybean seeds: effects of variety and environment

FLAVONOIDS IN CULTIVARS OF SOYBEAN: ANTIOXIDANT ACTION

Styphnolobium japonicum

5 references

Flavonol tetraglycosides from fruits of Styphnolobium japonicum (Leguminosae) and the authentication of Fructus Sophorae and Flos Sophorae.

Four new isoflavone triglycosides from Sophora japonica

Sophoricoside analogs as the IL-5 inhibitors from Sophora japonica

New isoflavone glycosides from the woods of Sophora japonica

Isoflavone tetraglycosides from Sophora japonica Leaves.

Ziziphus spina-christi

1 reference

Chemical Constituents from the Seeds of Ziziphus jujuba var. spinosa (Bunge) Hu

Prunus itosakura

1 reference

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

1 reference

Identifiers

InChI

InChI=1S/C21H20O10/c22-7-15-18(26)19(27)20(28)21(31-15)30-11-5-13(24)16-14(6-11)29-8-12(17(16)25)9-1-3-10(23)4-2-9/h1-6,8,15,18-24,26-28H,7H2/t15-,18-,19+,20-,21-/m1/s1

1 reference

ZCOLJUOHXJRHDI-CMWLGVBASA-N

Genistin (English)

18 November 2016

2 references

Genistin (English)

18 November 2016

ChEBI release 2020-09-01

CAS Registry Number

529-59-9

2 references

Global Substance Registration System

UNII

1POG3SCN5T

ZCOLJUOHXJRHDI-CMWLGVBASA-N

genistin (English)

18 November 2016

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=529-59-9

1 reference

Genistin (English)

18 November 2016

1 reference

Genistin (English)

18 November 2016

mapping relation type

1 reference

GENISTIN (English)

18 November 2016

1 reference

splash10-00di-0090000000-d404dfbc41d3867f6729

GENISTIN (English)

18 November 2016

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

0 references

splash10-014i-0090000000-49c48229b35691b20dbc

0 references

splash10-014i-0090000000-8af657f8354899864b05

0 references

splash10-00lr-0060900000-521eca780e4dd8d5bbe8

0 references

splash10-014i-0090000000-9c26b3ed8e9238de44dc

0 references

splash10-00lr-0060900000-cdf08327e0814ca51a1d

0 references

splash10-0159-0090600000-484eafff83f61f3034a6

0 references

splash10-014i-0090300000-67127f6bda660a7058dd

0 references

splash10-00di-0190000000-1e2a13923c2abc3bf607

0 references

DSSTox substance ID

DTXSID3022324

1 reference

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

DSSTOX compound identifier

0 references

0 references

610-921-5

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.120.406

retrieved

27 December 2018

title

4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-5-hydroxy-3-(4-hydroxyphenyl)- (English)

quotation

CAS no.: 529-59-9 (English)

ECHA Substance Infocard ID

100.120.406

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.120.406

retrieved

27 December 2018

title

4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-5-hydroxy-3-(4-hydroxyphenyl)- (English)

quotation

CAS no.: 529-59-9 (English)

0 references

1 reference

Global Substance Registration System

English

title

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

5 October 2016

1 reference

UNII

1POG3SCN5T