genistein (Q415957)

Gene Ontology release 2019-11-16

response to genistein

subject has role

reactant

1 reference

Gene Ontology release 2020-05-02

soy isoflavones

0 references

chemical structure

Genistein.svg
512 × 242; 11 KB

1 reference

image of molecular model or crystal lattice model

German Wikipedia

Genistein-3D-balls.png
2,000 × 1,125; 374 KB

depicts

ball-and-stick model

0 references

mass

270.053 dalton

1 reference

genistein (English)

19 October 2016

C₁₅H₁₀O₅

1 reference

genistein (English)

19 November 2016

C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O

1 reference

genistein (English)

19 November 2016

300 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Vigna radiata

1 reference

Antifungal Phytoalexins in Phaseolus aureus Roxb

Trifolium pratense

18 references

Effects of phytoestrogens derived from red clover on atherogenic adhesion molecules in human endothelial cells.

Determination of isoflavones in red clover by capillary electrophoresis with electrochemical detection

Pressurized liquid extraction versus other extraction techniques in micropreparative isolation of pharmacologically active isoflavones from Trifolium L. species.

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

Reversed-phase high-performance liquid chromatographic determination of isoflavones in plant materials after isolation by solid-phase extraction

Quantification of isoflavones in red clover by high-performance liquid chromatography

Isoflavones in Different Parts of Common Trifolium Species

Comparison of the in vitro estrogenic activities of compounds from hops (Humulus lupulus) and red clover (Trifolium pratense)

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

High Performance Liquid Chromatographic Separation of Isoflavones and Structural Elucidation of Isoflavone 7-O-glucoside 6''-malonates from Cicer arietinum

The distribution of oestrogenic isoflavones in the genus Trifolium

The Breeding of Fodder Plants

New genistein monogalactoside from the aerial part of Trifolium pratense

Trifoside — An isoflavone from Trifolium pratense

The occurrence of genistein in subterranean clover (T. subterraneum, L.) and other trifolium species.

Notizen: Isoflavonoid Phytoalexins from Leaves of Trifolium arvense

liquorice

5 references

Blockade of the dioxin pathway by herbal medicine Formula Bupleuri Minor: identification of active entities for suppression of AhR activation.

Flavonoids of the epigeal part of Glycyrrhiza glabra

Flavonoid variation in the leaves of Glycyrrhiza glabra

Glabranin — A new flavonone from Glycyrrhiza glabra

An isoflavan phytoalexin from leaves of Glycyrrhiza glabra

Lupinus albus

9 references

Fungitoxic dihydrofuranoisoflavones and related compounds in white lupin, Lupinus albus

Accumulation of Isoflavones in Lupin Seedings Treated with Copper Chloride

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

Application of gas chromatography-mass spectrometry to the identification of isoflavonoids in lupine root extracts

Biosynthesis of White Lupin Isoflavonoids from [U-C]l-Phenylalanine and Their Release into the Culture Medium

New coumaronochromones from white lupin, Lupinus albus L. (Leguminosae).

Fungitoxic Isoflavones from Lupinus albus and other Lupinus Species

Production and Release of Isoflavonoids by Lupin Cell Cultures

Epigenetic control of a cell wall scopoletin peroxidase by lupisoflavone in Lupinus

Trifolium incarnatum

2 references

High Performance Liquid Chromatographic Separation of Isoflavones and Structural Elucidation of Isoflavone 7-O-glucoside 6''-malonates from Cicer arietinum

Isoflavones in Different Parts of Common Trifolium Species

Syzygium jambos

1 reference

A general method for the dereplication of flavonoid glycosides utilizing high performance liquid chromatography/mass spectrometric analysis

Styphnolobium japonicum

8 references

Inhibitory effects of isoflavones on lipid peroxidation by reactive oxygen species

Sophoricoside analogs as the IL-5 inhibitors from Sophora japonica

A new coumaronochromone from Sophora japonica

Analysis and processing of Chinese herbal drugs. VIII: The study of sophorae floe

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

Five flavonoid compounds from Echinosophora koreensis

Ficus nervosa

1 reference

Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa

Acacia adunca

3 references

A phytochemical survey of the Australian species of Acacia

Acacia baileyana

3 references

A phytochemical survey of the Australian species of Acacia

Acacia binervata

3 references

A phytochemical survey of the Australian species of Acacia

Acacia calamifolia

3 references

A phytochemical survey of the Australian species of Acacia

Acacia cardiophylla

3 references

A phytochemical survey of the Australian species of Acacia

Acacia chrysotricha

3 references

A phytochemical survey of the Australian species of Acacia

Acacia clunies-rossiae

3 references

A phytochemical survey of the Australian species of Acacia

Acacia concurrens

3 references

A phytochemical survey of the Australian species of Acacia

Acacia constablei

3 references

A phytochemical survey of the Australian species of Acacia

Acacia cultriformis

3 references

A phytochemical survey of the Australian species of Acacia

Acacia dealbata

3 references

A phytochemical survey of the Australian species of Acacia

Acacia deanei

3 references

A phytochemical survey of the Australian species of Acacia

Acacia decurrens

3 references

A phytochemical survey of the Australian species of Acacia

Acacia elata

3 references

A phytochemical survey of the Australian species of Acacia

Acacia falciformis

3 references

A phytochemical survey of the Australian species of Acacia

Acacia filicifolia

3 references

A phytochemical survey of the Australian species of Acacia

Acacia fimbriata

3 references

A phytochemical survey of the Australian species of Acacia

Acacia holosericea

3 references

A phytochemical survey of the Australian species of Acacia

Acacia irrorata

3 references

A phytochemical survey of the Australian species of Acacia

Acacia kettlewelliae

3 references

A phytochemical survey of the Australian species of Acacia

Acacia lanigera

3 references

A phytochemical survey of the Australian species of Acacia

Acacia leucoclada

3 references

A phytochemical survey of the Australian species of Acacia

Acacia longifolia

3 references

A phytochemical survey of the Australian species of Acacia

Acacia mabellae

3 references

A phytochemical survey of the Australian species of Acacia

Acacia mearnsii

3 references

A phytochemical survey of the Australian species of Acacia

Acacia melanoxylon

3 references

A phytochemical survey of the Australian species of Acacia

Acacia mollifolia

3 references

A phytochemical survey of the Australian species of Acacia

Acacia neriifolia

3 references

A phytochemical survey of the Australian species of Acacia

Acacia obtusifolia

3 references

A phytochemical survey of the Australian species of Acacia

Acacia oshanesii

3 references

A phytochemical survey of the Australian species of Acacia

Acacia oswaldii

3 references

A phytochemical survey of the Australian species of Acacia

Acacia parramattensis

3 references

A phytochemical survey of the Australian species of Acacia

Acacia pycnantha

3 references

A phytochemical survey of the Australian species of Acacia

Acacia retinodes

3 references

A phytochemical survey of the Australian species of Acacia

Acacia rigens

3 references

A phytochemical survey of the Australian species of Acacia

Acacia silvestris

3 references

A phytochemical survey of the Australian species of Acacia

Acacia terminalis

3 references

A phytochemical survey of the Australian species of Acacia

Acacia trachyphloia

3 references

A phytochemical survey of the Australian species of Acacia

Acacia verniciflua

3 references

A phytochemical survey of the Australian species of Acacia

Acacia vestita

3 references

A phytochemical survey of the Australian species of Acacia

Apios americana

1 reference

Isoflavonoid phytoalexins from fungus-inoculated leaves of Apios tuberosa

Baptisia alba

2 references

Distribution of flavonoids in the genus baptisia (leguminosae)

The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae)

Baptisia bracteata

2 references

Distribution of flavonoids in the genus baptisia (leguminosae)

The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae)

Baptisia calycosa

2 references

Distribution of flavonoids in the genus baptisia (leguminosae)

The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae)

Baptisia cinerea

2 references

Distribution of flavonoids in the genus baptisia (leguminosae)

The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae)

Baptisia lanceolata

2 references

Distribution of flavonoids in the genus baptisia (leguminosae)

The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae)

Baptisia lecontei

2 references

The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae)

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia megacarpa

2 references

Distribution of flavonoids in the genus baptisia (leguminosae)

The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae)

Baptisia nuttalliana

2 references

Distribution of flavonoids in the genus baptisia (leguminosae)

The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae)

Baptisia perfoliata

2 references

Distribution of flavonoids in the genus baptisia (leguminosae)

The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae)

Baptisia tinctoria

2 references

Distribution of flavonoids in the genus baptisia (leguminosae)

The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae)

Cajanus cajan

1 reference

A new isoflavone glucoside from Cajanus cajan

Desmodium gangeticum

2 references

The Structure of Desmocarpin, a Pterocarpan Phytoalexin from Desmodium gangeticum

Isoflavanones from the allelopathic aqueous root exudate of Desmodium uncinatum.

Desmodium uncinatum

3 references

Isoflavanones from the allelopathic aqueous root exudate of Desmodium uncinatum.

Isoflavanones from the Allelopathic Aqueous Root Exudate of Desmodium uncinatum.

The Structure of Desmocarpin, a Pterocarpan Phytoalexin from Desmodium gangeticum

Sophora koreensis

5 references

Five flavonoid compounds from Echinosophora koreensis

Three 2′,4′,6′-trioxygenated flavanones in roots of Echinosophora koreensis

Three 2′,4′,6′-Trioxygenated flavanones in roots of Echinosophora koreensis

Echinospartum horridum

1 reference

5-O-methylbiochanin a, a new isoflavone from Echinospartum horridum

Erythrina burttii

4 references

Two prenylated flavonoids from the stem bark of Erythrina burttii.

Isolation of jamaicin and lisetin and their determination in Piscidia erythrina L. by high-performance liquid chromatography

Three new cinnamylphenols in heartwood of Erythrina crista-galli

Erythrina indica

4 references

Two prenylated flavonoids from the stem bark of Erythrina burttii.

Isolation of jamaicin and lisetin and their determination in Piscidia erythrina L. by high-performance liquid chromatography

Three new cinnamylphenols in heartwood of Erythrina crista-galli

Erythrina variegata

4 references

Two prenylated flavonoids from the stem bark of Erythrina burttii.

Isolation of jamaicin and lisetin and their determination in Piscidia erythrina L. by high-performance liquid chromatography

Three new cinnamylphenols in heartwood of Erythrina crista-galli

Euchresta formosana

2 references

Cytotoxic coumaronochromones from the roots of Euchresta formosana.

Antiplatelet and Anti-HIV Constituents from Euchresta Formosana

Ficus cordata

3 references

Antimicrobial activity of the crude extracts and compounds from Ficus chlamydocarpa and Ficus cordata (Moraceae).

Ficusins A and B, Two New Cyclic-Monoterpene-substituted Isoflavones from Ficus septica Barm. F.

Ficus spp. (fig): ethnobotany and potential as anticancer and anti-inflammatory agents

Ficus nymphaeifolia

3 references

Ficus spp. (fig): ethnobotany and potential as anticancer and anti-inflammatory agents

Ficusins A and B, Two New Cyclic-Monoterpene-substituted Isoflavones from Ficus septica Barm. F.

Antimicrobial activity of the crude extracts and compounds from Ficus chlamydocarpa and Ficus cordata (Moraceae).

Ficus septica

3 references

Ficusins A and B, Two New Cyclic-Monoterpene-substituted Isoflavones from Ficus septica Barm. F.

Ficus spp. (fig): ethnobotany and potential as anticancer and anti-inflammatory agents

Antimicrobial activity of the crude extracts and compounds from Ficus chlamydocarpa and Ficus cordata (Moraceae).

Genista ephedroides

1 reference

Hypericum scabrum

1 reference

Prenylated benzophenones and xanthones from Hypericum scabrum.

Lablab purpureus

1 reference

Phytoalexins of Hyacinth Bean (Lablab niger)

Laburnum anagyroides

1 reference

Isoflavones from pods of laburnum anagyroides

Lespedeza cyrtobotrya

2 references

Studies on the constituentes of Lespedeza cyrtobotrya Miq. I. The structures of a new chalcone and two new isoflav-3-ens.

Melanin synthesis inhibitors from Lespedeza cyrtobotrya

Lupinus arboreus

3 references

Fungitoxic Isoflavones from Lupinus albus and other Lupinus Species

Quantitative flavonoid variation in Lupinus sericeus

Lupinus arcticus

3 references

Fungitoxic Isoflavones from Lupinus albus and other Lupinus Species

Quantitative flavonoid variation in Lupinus sericeus

Lupinus elegans

3 references

Fungitoxic Isoflavones from Lupinus albus and other Lupinus Species

Quantitative flavonoid variation in Lupinus sericeus

Lupinus luteus

6 references

Fungitoxic Isoflavones from Lupinus albus and other Lupinus Species

Flavonoid aglycones of Lupinus luteus

New Complex Isoflavones in the Roots of Yellow Lupin (Lupinus luteusL., cv. Barpine)

Isoflavones of the roots of Lupinus luteus

Quantitative flavonoid variation in Lupinus sericeus

Lupinus mutabilis

3 references

Fungitoxic Isoflavones from Lupinus albus and other Lupinus Species

Quantitative flavonoid variation in Lupinus sericeus

Lupinus nanus

3 references

Fungitoxic Isoflavones from Lupinus albus and other Lupinus Species

Quantitative flavonoid variation in Lupinus sericeus

Lupinus sericeus

3 references

Quantitative flavonoid variation in Lupinus sericeus

Fungitoxic Isoflavones from Lupinus albus and other Lupinus Species

Lupinus subcarnosus

3 references

Fungitoxic Isoflavones from Lupinus albus and other Lupinus Species

Quantitative flavonoid variation in Lupinus sericeus

Lupinus texensis

4 references

Flavonoids from Lupinus texensis and their free radical scavenging activity

Fungitoxic Isoflavones from Lupinus albus and other Lupinus Species

Quantitative flavonoid variation in Lupinus sericeus

Maackia amurensis

7 references

Chemical Studies on the Oriental Plant Drugs. XXXV. The Chemical Constituents of the Heartwood of Maackia amurensis var. buergeri.

Isoflavones and stilbenes of the heartwood ofMaackia amurensis

Determination of phenolic components in ethanolic extracts from wood of Maackia amurensis

Isoflavonoids of the bark and leaves ofMaackia amurensis

Isoflavonoid production by callus cultures of Maackia amurensis

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

Method for the quantitative determination of the isoflavones and polyhydroxystilbenes of Maackia amurensis

Neorautanenia amboensis

1 reference

Isoflavone Glycosides from Neorautanenia amboensis

Ononis spinosa

3 references

High-performance liquid chromatographic analysis of flavonoids from Ononis spinosa L.

Determination of isoflavones from Ononis spinosa L. extracts by high-performance liquid chromatography with ultraviolet diode-array detection

High Performance Liquid Chromatographic Separation of Isoflavones and Structural Elucidation of Isoflavone 7-O-glucoside 6''-malonates from Cicer arietinum

Ormosia monosperma

1 reference

Anti-oral microbial activity of isoflavonoids in root bark of Ormosia monosperma

Pericopsis laxiflora

1 reference

Phytochemical examination of Pericopsis species

Phaseolus vulgaris

5 references

Post-Infectional Compounds From the French Bean Phaseolus vulgaris; Isolation and Identification of Genistein and 2',4',5,7-Tetrahydroxyisoflavone

Phaseollin formation and metabolism in Phaseolus vulgaris

Isoflavonoids from Phaseolus coccineus

Induced and Constitutive Isoflavonoids in Phaseolus mungo L. Leguminosae

Germplasm characterization of Zolfino landraces (Phaseolus vulgaris L.) by flavonoid content

Prunus cerasus

1 reference

Antioxidant polyphenols from tart cherries (Prunus cerasus).

Pterocarpus angolensis

1 reference

A novel α-hydroxydihydrochalcone from the heartwood of Pterocarpus angolensis D.C.: absolute configuration, synthesis, photochemical transformations, and conversion into α-methyldeoxybenzoins

Securidaca inappendiculata

1 reference

Xanthones from the stems of Securidaca inappendiculata

Dermatophyllum secundiflorum

4 references

Isoflavonoids from Sophora secundiflora, S. arizonica and S. gypsophila

Five flavonoid compounds from Echinosophora koreensis

Tephrosia sinapou

1 reference

Potential cancer chemopreventive flavonoids from the stems of Tephrosia toxicaria

Thermopsis alterniflora

2 references

Thermopsis macrophylla

2 references

Thermopsis mollis

2 references

Thermopsis rhombifolia

2 references

Thermopsis villosa

2 references

Wisteria brachybotrys

1 reference

Isoflavones from the gall and wood of Wisteria brachybotrys

maize

2 references

Chemical constituents of the style of Zea mays L. with glycation inhibitory activity

Effect of Pr and pr alleles on anthocyanin biosynthesis in zea mays

Apis mellifera

1 reference

Characterization and antioxidant properties of six Algerian propolis extracts: ethyl acetate extracts inhibit myeloperoxidase activity

Achlys triphylla

1 reference

Chemical Constituents in the Genus Achlys

Andira inermis

2 references

Flavonoids ofSerratula inermis

Antiplasmodial activity of isoflavones from Andira inermis

Ascochyta salicorniae

1 reference

Ascosalipyrrolidinone A, an antimicrobial alkaloid, from the obligate marine fungus Ascochyta salicorniae

Astragalus verrucosus

1 reference

Antimicrobial and antifungal activity of crude extracts and isolated saponins from Astragalus verrucosus

Baptisia australis

3 references

High Performance Liquid Chromatographic Separation of Isoflavones and Structural Elucidation of Isoflavone 7-O-glucoside 6''-malonates from Cicer arietinum

The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae)

Distribution of flavonoids in the genus baptisia (leguminosae)

Bolusanthus speciosus

2 references

Isoflavonoids from Bolusanthus speciosus (Bolus) Harms Leguminosae

Antimicrobial and antioxidant flavonoids from the root wood of Bolusanthus speciosus

Calycotome villosa

1 reference

Flavonoids from Calicotome villosa

Chamaecytisus hirsutus

1 reference

Flavonoids and Alkaloids of Chamaecytisus hirsutus and Chamaecytisus supinus

Chamaecytisus supinus

1 reference

Flavonoids and Alkaloids of Chamaecytisus hirsutus and Chamaecytisus supinus

Cicer arietinum

2 references

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

High Performance Liquid Chromatographic Separation of Isoflavones and Structural Elucidation of Isoflavone 7-O-glucoside 6''-malonates from Cicer arietinum

Cladrastis platycarpa

1 reference

A New Pterocarpan from the Heartwood of Cladrastis platycarpa

Craspedolobium schochii

1 reference

Constituents of Craspedolobium schochii

Crotalaria retusa

1 reference

Identification of the Flavonoids in Papilionaceae Flowers Using Paper Chromatography

Crotalaria thebaica

1 reference

Isoflavones and a saponin from Crotalaria thebaica (Del.) DC growing in Egypt

Dalbergia oliveri

1 reference

Isoflavonoids from Dalbergia olivari

Dalbergia parviflora

1 reference

Flavonoids from the heartwood of the Thai medicinal plant Dalbergia parviflora and their effects on estrogenic-responsive human breast cancer cells

Dalbergia sissoo

2 references

Phytochemical and Pharmacological Studies of Dalbergia sissoo Growing in Egypt

Constituents of Dalbergia sissoo Roxb. leaves with osteogenic activity.

Desmodium velutinum

1 reference

Identification of the Flavonoids in Papilionaceae Flowers Using Paper Chromatography

Eriosema tuberosum

1 reference

Isoflavonoid glycosides from eriosema tuberosum

Ficus pumila

1 reference

Flavonoids from Ficus pumila

Flemingia paniculata

1 reference

New salicylic acid and isoflavone derivatives from Flemingia paniculata.

Genista burdurensis

1 reference

Alkaloids of Genista burdurensis

Genista morisii

3 references

Estradiol-antagonistic activity of phenolic compounds from leguminous plants

Flavonoids and isoflavonoids from Genista morisii

Glycine canescens

1 reference

Leaf flavonoids of Glycine subgenus Glycine in relation to systematics

Glycine clandestina

1 reference

Leaf flavonoids of Glycine subgenus Glycine in relation to systematics

Glycine falcata

1 reference

Leaf flavonoids of Glycine subgenus Glycine in relation to systematics

Glycine latifolia

1 reference

Leaf flavonoids of Glycine subgenus Glycine in relation to systematics

Glycine tabacina

1 reference

Leaf flavonoids of Glycine subgenus Glycine in relation to systematics

Glycine tomentella

1 reference

Leaf flavonoids of Glycine subgenus Glycine in relation to systematics

Sophora pachycarpa

1 reference

Flavonoids ofGoebelia pachycarpa

Iris pseudacorus

1 reference

Isoflavonoids produced by Iris pseudacorus leaves treated with cupric chloride

Lespedeza floribunda

2 references

Melanin synthesis inhibitors from Lespedeza floribunda

Studies on the constituentes of Lespedeza cyrtobotrya Miq. I. The structures of a new chalcone and two new isoflav-3-ens.

Lonchocarpus utilis

1 reference

Anticancer action of cubé insecticide: correlation for rotenoid constituents between inhibition of NADH:ubiquinone oxidoreductase and induced ornithine decarboxylase activities

Lupinus angustifolius

1 reference

Isoflavonoids as insect feeding deterrents and antifungal components from root ofLupinus angustifolius.

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

Medicago sativa

2 references

Forage Estrogens, Detection of Daizein, Formononetin, Genistein, and Biochanin A in Forages

Estrogenic activity of some isoflavone derivatives

Mucuna membranacea

1 reference

Chemical Constituents from Mucuna membranacea

Ougeinia dalbergioides

1 reference

High-performance liquid chromatographic analysis of genistein and other isoflavonoids from heartwood of Ougeinia dalbergioides

Portulaca oleracea

1 reference

Two Antioxidant Alkaloids from Portulaca oleracea L.

Prunus cerasoides

1 reference

Puddumin-A, a New Flavanone Glucoside from Prunus cerasoides

Pseudomonas

1 reference

A specific inhibitor for tyrosine protein kinase from Pseudomonas

Pseudosophora alopecuroides

1 reference

Flavonoids ofPseudosophora alopecuroides

Cullen corylifolia

1 reference

The presence of three isoflavonoid compounds in Psoralea corylifolia

Cullen corylifolium

1 reference

The presence of three isoflavonoid compounds in Psoralea corylifolia

Punica granatum

2 references

Oestrogen content of pomegranate seeds

Diverse Phytochemicals and Bioactivities in the Ancient Fruit and Modern Functional Food Pomegranate (Punica granatum).

Saussurea japonica

1 reference

A New Triterpene and a New Lignan fromSaussurea japonica

Spartium junceum

1 reference

Quantitative determination of flavonoids inSpartium junceum

Spatholobus suberectus

1 reference

A New Flavanone from Spatholobus Suberectus Dunn

Streptomyces griseus

1 reference

Isoflavonoids from Streptomycetes: Origins of Genistein, 8-Chlorogenistein, and 6,8-Dichlorogenistein

Streptosporangium vulgare

1 reference

K-254-I (genistein), a new inhibitor of Ca2+ and calmodulin-dependent cyclic nucleotide phosphodiesterase from Streptosporangium vulgare.

Thermopsis montana

1 reference

Alkaloids of Heimia montana

Trifolium arvense

1 reference

Pressurized liquid extraction versus other extraction techniques in micropreparative isolation of pharmacologically active isoflavones from Trifolium L. species.

Trifolium fragiferum

1 reference

Isoflavones in Different Parts of Common Trifolium Species

zigzag clover

1 reference

Pressurized liquid extraction versus other extraction techniques in micropreparative isolation of pharmacologically active isoflavones from Trifolium L. species.

mountain clover

1 reference

Isoflavones in Different Parts of Common Trifolium Species

Trifolium rubens

1 reference

Pressurized liquid extraction versus other extraction techniques in micropreparative isolation of pharmacologically active isoflavones from Trifolium L. species.

Trifolium aureum

1 reference

Flavonoids ofTrifolium strepens

Trifolium subterraneum

4 references

The effects of plant oestrogens on animal reproduction

Isoflavonoids do not inhibit in vivo lipid peroxidation in subjects with high-normal blood pressure

Isoflavones in Different Parts of Common Trifolium Species

The distribution of oestrogenic isoflavones in the genus Trifolium

Ulex europaeus

1 reference

Isoflavones from root bark of gorse

Vigna mungo

1 reference

Induced and Constitutive Isoflavonoids in Phaseolus mungo L. Leguminosae

Ophiocordyceps sinensis

1 reference

Anti-inflammatory principles from Cordyceps sinensis

Dalbergia frutescens

1 reference

Antigiardial activity of isoflavones from Dalbergia frutescens bark

peanut

1 reference

Comparison of extraction methods for the quantification of selected phytochemicals in peanuts (Arachis hypogaea).

Glycine

3 references

Compositional changes induced by UV-B radiation treatment of common bean and soybean seedlings monitored by capillary electrophoresis with diode array detection

Isoflavonoid content of Hong Kong soy foods.

Phytoestrogen content of foods consumed in Canada, including isoflavones, lignans, and coumestan

Ammopiptanthus mongolicus

1 reference

Three New Isoflavonoids from the Aerial Parts ofAmmopiptanthus mongolicus

Butea frondosa

1 reference

Osteogenic activity of constituents from Butea monosperma

Butea monosperma

1 reference

Osteogenic activity of constituents from Butea monosperma

Desmodium styracifolium

4 references

Flavonoid compounds from Desmodium styracifolium of Vietnamese origin

Isoflavanones and their O-glycosides from Desmodium styracifolium

The Structure of Desmocarpin, a Pterocarpan Phytoalexin from Desmodium gangeticum

Isoflavanones from the allelopathic aqueous root exudate of Desmodium uncinatum.

Ficus glumosa

1 reference

Ceramides and cytotoxic constituents from Ficus glumosa Del. (Moraceae)

Genista cadasonensis

1 reference

Endemic Sardinian plants: the case of Genista cadasonensis Valsecchi

Genista pichisermolliana

1 reference

A new alpinumisoflavone derivative from Genista pichisermolliana

Genista sessilifolia

2 references

Flavonoids and isoflavonoids from Genista sessilifolia DC. Growing in Turkey

Genista tinctoria

2 references

LXXIX.—The colouring matters contained in dyer's broom (Genista tinctoria) and heather (Calluna vulgaris)

Genista tricuspidata

1 reference

Flavonoids and isoflavonoids from Genista tricuspidata

Ormosia henryi

1 reference

Polyprenylated isoflavanone and isoflavonoids from Ormosia henryi and their cytotoxicity and anti-oxidation activity

Phaseolus lunatus

4 references

Inducible isoflavonoids from the lima bean, Phaseolus lunatus

Isoflavonoids from Phaseolus coccineus

Post-Infectional Compounds From the French Bean Phaseolus vulgaris; Isolation and Identification of Genistein and 2',4',5,7-Tetrahydroxyisoflavone

Induced and Constitutive Isoflavonoids in Phaseolus mungo L. Leguminosae

Piscidia piscipula

1 reference

Diverse oxygenated isoflavonoids from Piscidia erythrina

Sundacarpus amarus

1 reference

Isoflavones from Podocarpus amarus

Prunus leveilleana

1 reference

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

Prunus verecunda

1 reference

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

Sophora alopecuroides

1 reference

Flavonoids ofPseudosophora alopecuroides

Spirotropis longifolia

1 reference

Secondary metabolites from Spirotropis longifolia (DC) Baill and their antifungal activity against human pathogenic fungi

Stellaria media

1 reference

Stellaria media (L.) Vill.- A plant with immense therapeutic potentials: phytochemistry and pharmacology

Wisteriopsis reticulata

1 reference

Anticancer effects of flavonoid derivatives isolated from Millettia reticulata Benth in SK-Hep-1 human hepatocellular carcinoma cells

Genista tridentata

2 references

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

Craspedolobium unijugum

1 reference

Constituents of Craspedolobium schochii

Chamaecytisus pygmaeus

1 reference

Flavonoids and Alkaloids from Chamaecytisus eriocarpus

Butea superba

1 reference

Isolation of New Isoflavonolignans, Butesuperins A and B, from a Thai Miracle Herb, Butea superba

Ardisia colorata

1 reference

Death receptor 5 targeting activity-guided isolation of isoflavones from Millettia brandisiana and Ardisia colorata and evaluation of ability to induce TRAIL-mediated apoptosis

Genista hispanica

1 reference

Genista radiata

1 reference

Bowdichia nitida

1 reference

Natürlich vorkommende Chinone, XXIV1) Über die Inhaltsstoffe vonBowdichia nitida Benth.: Erstmalige Isolierung eines Isoflavonchinons

Genista tridens

1 reference

Genista sericea

1 reference

Genista salzmannii

1 reference

Genista subcapitata

1 reference

Lespedeza juncea

1 reference

Studies on the constituentes of Lespedeza cyrtobotrya Miq. I. The structures of a new chalcone and two new isoflav-3-ens.

Genista linifolia

1 reference

Genista albida

1 reference

Garcinia oblongifolia

1 reference

Two xanthones with a 1,1-dimethylallyl group in root bark of Garcinia subelliptica

Genista stenopetala

1 reference

Genista triacanthos

1 reference

Genista hystrix

1 reference

Lupinus pilosus

3 references

Fungitoxic Isoflavones from Lupinus albus and other Lupinus Species

Quantitative flavonoid variation in Lupinus sericeus

Homo sapiens

2 references

Preparation of Homologous Pyrazolonedicarboxylates

Three new homoisoflavanone glycosides from the bulbs of Ornithogalum caudatum

Genista pulchella

1 reference

Genista microphylla

1 reference

Pterocarpus marsupium

1 reference

A novel α-hydroxydihydrochalcone from the heartwood of Pterocarpus angolensis D.C.: absolute configuration, synthesis, photochemical transformations, and conversion into α-methyldeoxybenzoins

Sophora flavescens

3 references

Five flavonoid compounds from Echinosophora koreensis

Genista lobelii

1 reference

Erythrina latissima

4 references

Two prenylated flavonoids from the stem bark of Erythrina burttii.

Isolation of jamaicin and lisetin and their determination in Piscidia erythrina L. by high-performance liquid chromatography

Three new cinnamylphenols in heartwood of Erythrina crista-galli

Genista acanthoclada

1 reference

Cajanus scarabaeoides

1 reference

A new isoflavone glucoside from Cajanus cajan

Genista depressa

1 reference

Pueraria tuberosa

3 references

Puerariafuran, a new inhibitor of advanced glycation end products (AGEs) isolated from the roots of Pueraria lobata

Isoflavonoids from Pueraria mirifica and their estrogenic activity.

Isoflavonoids and the other constituents in callus tissues of Pueraria lobata.

Genista obtusiramea

1 reference

Genista scorpius

1 reference

Pterocarpus indicus

1 reference

A novel α-hydroxydihydrochalcone from the heartwood of Pterocarpus angolensis D.C.: absolute configuration, synthesis, photochemical transformations, and conversion into α-methyldeoxybenzoins

Genista canariensis

1 reference

Genista spartioides

1 reference

Genista ulicina

1 reference

Genista monspessulana

1 reference

Pinus koraiensis

3 references

Fungitoxic Isoflavones from Lupinus albus and other Lupinus Species

Quantitative flavonoid variation in Lupinus sericeus

Genista sagittalis

1 reference

Genista cupanii

1 reference

Genista anglica

1 reference

Neonotonia wightii

1 reference

A new isoflavone phytoalexin from fungus-inoculated stems of Glycine wightii

Neorautanenia mitis

1 reference

Isoflavone Glycosides from Neorautanenia amboensis

Glycyrrhiza

1 reference

Phenolic constituents of licorice. III. Structures of glicoricone and licofuranone, and inhibitory effects of licorice constituents on monoamine oxidase

Streptomyces

4 references

Flavones and New Isoflavone Derivatives from Microorganisms: Isolation and Structure Elucidation

Amorphane sesquiterpenes from a marine Streptomyces sp.

Flavonoids with mosquito larval toxicity

Amorphane Sesquiterpenes from a Marine Streptomyces sp.1

Pueraria

1 reference

Puerariae radix isoflavones and their metabolites inhibit growth and induce apoptosis in breast cancer cells.

Flemingia macrophylla

4 references

A flavonol C-glycoside from Moghania macrophylla

Neuroprotective flavonoids from Flemingia macrophylla

Isoflavones of Moghania macrophylla

Prenylated flavonoids from Moghania philippinensis

Crotalaria pallida

1 reference

Anti-inflammatory constituents and new pterocarpanoid of Crotalaria pallida

Sophora tonkinensis

3 references

Five flavonoid compounds from Echinosophora koreensis

Thermopsis fabacea

1 reference

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

Pueraria montana var. thomsonii

2 references

Inhibitors for expression of IgE receptor on human mast cell from Puerariae Flos

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

Sophora tonkinensis var. tonkinensis

1 reference

Studies on the Constituents of Sophora Species. IV. : Constituents of the Root of Sophora angustifolia SIEB. et ZUCC. (1)

Ulex gallii

1 reference

Isoflavones from root bark of gorse

Trifolium repens

5 references

Forage Estrogens, Detection of Daizein, Formononetin, Genistein, and Biochanin A in Forages

High Performance Liquid Chromatographic Separation of Isoflavones and Structural Elucidation of Isoflavone 7-O-glucoside 6''-malonates from Cicer arietinum

Isoflavones in Different Parts of Common Trifolium Species

The effects of plant oestrogens on animal reproduction

The Breeding of Fodder Plants

Trifolium pannonicum

1 reference

Pressurized liquid extraction versus other extraction techniques in micropreparative isolation of pharmacologically active isoflavones from Trifolium L. species.

Glycyrrhiza uralensis

1 reference

Phenolic constituents of licorice. VIII. Structures of glicophenone and glicoisoflavanone, and effects of licorice phenolics on methicillin-resistant Staphylococcus aureus

snap bean

1 reference

Isoflavonoids from Phaseolus coccineus

Streptomyces xanthophaeus

1 reference

α-Glucosidase inhibitors and phytotoxins from Streptomyces xanthophaeus

Streptomyces filamentosus

1 reference

Roseosporol A, the first isolation of a novel sesquiterpenoid from Streptomyces roseosporus

Erythrina fusca

1 reference

Fuscacarpans A-C, new pterocarpans from the stems of Erythrina fusca

Pueraria montana var. lobata

6 references

In vitro isoflavonoid production in callus from different organs of Pueraria lobata (Wild.) Ohwi.

Puerariafuran, a new inhibitor of advanced glycation end products (AGEs) isolated from the roots of Pueraria lobata

Isoflavonoids and the other constituents in callus tissues of Pueraria lobata.

Tectorigenin, an isoflavone of Pueraria thunbergiana Benth., induces differentiation and apoptosis in human promyelocytic leukemia HL-60 cells

Identification of isoflavones in the roots of Pueraria lobata.

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

Annona muricata

1 reference

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

Dianthus caryophyllus

1 reference

Purification and properties of a new S-adenosyl-L-methionine:flavonoid 4'-O-methyltransferase from carnation (Dianthus caryophyllus L.)

Tripterygium wilfordii

1 reference

Isolation and characterization of a glycosyltransferase with specific catalytic activity towards flavonoids from Tripterygium wilfordii

Ginkgo biloba

1 reference

Quality control evaluation of nutraceutical products from Ginkgo biloba using liquid chromatography coupled to high resolution mass spectrometry

Cymbopogon citratus

1 reference

Pterospartum tridentatum, Gomphrena globosa and Cymbopogon citratus: A phytochemical study focused on antioxidant compounds

Capsicum annuum

1 reference

Integrative analysis of metabolome and transcriptome reveals the mechanism of color formation in pepper fruit (Capsicum annuum L.).

Glycine soja

1 reference

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

Mirabilis jalapa

1 reference

Three new phenolic compounds from a manipulated plant cell culture, Mirabilis jalapa

Glycyrrhiza inflata

1 reference

Screening for bioactive natural products from a 67-compound library of Glycyrrhiza inflata

chia

1 reference

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

Maclura tricuspidata

3 references

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

Flavonoids and a prenylated xanthone from Cudrania cochinchinensis var. gerontogea

Benzylated and prenylated flavonoids from the root barks of Cudrania tricuspidata with pancreatic lipase inhibitory activity

Iris domestica

2 references

Phenolic constituents of Belamcanda chinensis

A New Isoflavonoid from Belamcanda chinensis (L.) DC.

Thermopsis lanceolata

1 reference

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

Desmodium sandwicense

3 references

Isoflavanones from the allelopathic aqueous root exudate of Desmodium uncinatum.

The Structure of Desmocarpin, a Pterocarpan Phytoalexin from Desmodium gangeticum

Isoflavanones from the Allelopathic Aqueous Root Exudate of Desmodium uncinatum.

soybean

34 references

Antileukemic activity of genistein, a major isoflavone present in soy products

Clinical characteristics and pharmacokinetics of purified soy isoflavones: multiple-dose administration to men with prostate neoplasia

Effects of the phytoestrogen genistein on some predictors of cardiovascular risk in osteopenic, postmenopausal women: a two-year randomized, double-blind, placebo-controlled study.

Effects of the phytoestrogen genistein on bone metabolism in osteopenic postmenopausal women: a randomized trial

Tofu and soy drinks contain phytoestrogens

Electrospray characterization of selected medicinal plant extracts

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

Malonyl Isoflavone Glycosides in Soybean Seeds(Glycine max MERRILL).

Analysis of estrogenic activity of foodstuffs and cigarette smoke condensates using a yeast estrogen screening method

Development and validation of an isocratic high-performance liquid chromatographic method for quantitative determination of phytoestrogens in soya bean

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

Isoflavones and Coumestrol in Soybeans and Soybean Products from Australia and Indonesia

"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

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

HPLC isolation and GC-MS identification of genistein, daidzein, and coumestrol from unhydrolyzed soybean root extracts

Phenolic compounds ofGlycine hispida

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

New isoflavone and triterpene glycosides from soybeans

Contents of isoflavones and effect of isoflavones on root hair curling in non-nodulating-Rj1Rj1) soybean plant

Components Responsible for the Undesirable Taste of Soybean Seeds

Genistein accumulation in soybean (Glycine max[L.] Merr.) root systems under suboptimal root zone temperatures

Coumestrin a coumestan derivative from soybean roots

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

Phenolic acids and flavonoids in soybean root and leaf extracts

FLAVONOIDS IN CULTIVARS OF SOYBEAN: ANTIOXIDANT ACTION

Novel process of fermenting black soybean [Glycine max (L.) Merrill] yogurt with dramatically reduced flatulence-causing oligosaccharides but enriched soy phytoalexins.

LDL-antioxidant pterocarpans from roots of Glycine max (L.) Merr

2 references

Isoflavones in Different Parts of Common Trifolium Species

The distribution of oestrogenic isoflavones in the genus Trifolium

Maclura cochinchinensis

2 references

Flavonoids and a prenylated xanthone from Cudrania cochinchinensis var. gerontogea

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

Crotalaria goreensis

1 reference

Identification of the Flavonoids in Papilionaceae Flowers Using Paper Chromatography

Prunus itosakura

1 reference

Flavonoids of Various Prunus Species. VI. The Flavonoids in the Wood of Prunus aequinoctialis, P. nipponica, P. Maximowiczii and P. avium

Flemingia prostrata

1 reference

Prenylated flavonoids from Moghania philippinensis

Deguelia scandens

3 references

Anti-inflammatory isoflavonoids from the stems of Derris scandens

A benzil and isoflavone derivatives from Derris scandens Benth

A new benzil derivative from Derris scandens: Structure-insecticidal activity study

broad bean

4 references

The identification of gibberellins in immature seeds of Vicia faba, and some chemotaxonomic considerations

UHPLC-ESI-QTOF-MS-based metabolic profiling of Vicia faba L. (Fabaceae) seeds as a key strategy for characterization in foodomics

Fast responses of metabolites in Vicia faba L. to moderate NaCl stress

Kaempferol 3-O-Galactoside, 7-O-Rhamnoside is the Major Green Fluorescing Compound in the Epidermis of Vicia faba

physically interacts with

cystic fibrosis transmembrane conductance regulator

1 reference

17 August 2016

1 reference

Estrogen related receptor alpha

17 August 2016

1 reference

Estrogen related receptor beta

17 August 2016

1 reference

Estrogen related receptor gamma

17 August 2016

1 reference

Transient receptor potential cation channel subfamily C member 5

17 August 2016

1 reference

17 August 2016

taste receptor type 2

subject has role

agonist

2 references

Bitter taste receptor activation by flavonoids and isoflavonoids: modeled structural requirements for activation of hTAS2R14 and hTAS2R39.

Comprehensive Analysis of Mouse Bitter Taste Receptors Reveals Different Molecular Receptive Ranges for Orthologous Receptors in Mice and Humans

1 reference

protein kinase inhibitors

1 reference

15 March 2018

1 reference

15 March 2018

1 reference

15 March 2018

0 references

0 references

1 reference

https://en.wikipedia.org/w/index.php?title=Genistein&oldid=949235007

English Wikipedia

Wikimedia import URL

Commons category

Genistein

0 references

Identifiers

InChI

InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)11-7-20-13-6-10(17)5-12(18)14(13)15(11)19/h1-7,16-18H

1 reference

genistein (English)

19 November 2016

2 references

genistein (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

446-72-0

2 references

genistein (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=446-72-0

9 April 2021

1 reference

Genistein (English)

19 November 2016

2 references

genistein (English)

19 November 2016

Reaxys registry number

263823

1 reference

genistein (English)

19 October 2016

mapping relation type

3 references

GENISTEIN (English)

19 November 2016

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)11-7-20-13-6-10(17)5-12(18)14(13)15(11)19/h1-7,16-18H

1 reference

GENISTEIN (English)

19 November 2016

2 references

MSBNK-BGC_Munich-RP017601

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

MSBNK-BGC_Munich-RP017602

0 references

MSBNK-BGC_Munich-RP017603

0 references

MSBNK-BGC_Munich-RP017611

0 references

MSBNK-BGC_Munich-RP017612

0 references

MSBNK-BGC_Munich-RP017613

0 references

MSBNK-Athens_Univ-AU241957

0 references

MSBNK-Athens_Univ-AU241958

0 references

MSBNK-Athens_Univ-AU241959

0 references

MSBNK-Athens_Univ-AU241960

0 references

MSBNK-Athens_Univ-AU241962

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000011

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000012

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000013

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000014

0 references

MSBNK-NaToxAq-NA000026

0 references

MSBNK-NaToxAq-NA000027

0 references

MSBNK-NaToxAq-NA000028

0 references

MSBNK-NaToxAq-NA000029

0 references

MSBNK-NaToxAq-NA000030

0 references

MSBNK-Osaka_Univ-OUF00238

0 references

MSBNK-PFOS_research_group-FFF00193

0 references

MSBNK-PFOS_research_group-FFF00194

0 references

MSBNK-PFOS_research_group-FFF00195

0 references

MSBNK-PFOS_research_group-FFF00196

0 references

MSBNK-PFOS_research_group-FFF00197

0 references

MSBNK-PFOS_research_group-FFF00198

0 references

MSBNK-PFOS_research_group-FFF00199

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

MSBNK-Univ_Toyama-TY000136

0 references

MSBNK-Univ_Toyama-TY000137

0 references

0 references

0 references

0 references

0 references

MSBNK-IPB_Halle-PB000881

0 references

MSBNK-IPB_Halle-PB000882

0 references

MSBNK-IPB_Halle-PB000884

0 references

MSBNK-IPB_Halle-PB000885

0 references

MSBNK-IPB_Halle-PB005712

0 references

MSBNK-IPB_Halle-PB005713

0 references

MSBNK-IPB_Halle-PB005714

0 references

MSBNK-IPB_Halle-PB005715

0 references

MSBNK-IPB_Halle-PB005721

0 references

MSBNK-IPB_Halle-PN000050

0 references

MSBNK-IPB_Halle-PN000051

0 references

SPLASH

splash10-00di-0090000000-02a1637fcc9a07392ba3

0 references

splash10-00di-0290000000-a60723328e71945659e4

0 references

splash10-0v4m-1960000000-5ac1d77b7f1d478f9382

0 references

splash10-0fr6-4910000000-f32b159fe5a08e29fdf8

0 references

splash10-00kf-8900000000-197e5590fe8134de533b

0 references

splash10-014i-9400000000-26d4739286bef040b4f9

0 references

splash10-014i-9300000000-6d84c4f68b9adbb0190f

0 references

splash10-014i-9200000000-c3580569c07b6affd7e1

0 references

splash10-014i-0090000000-9542aa77ed8c84bed45f

0 references

splash10-014i-0090000000-c6b607727a820f778924

0 references

splash10-014i-0190000000-420b0e9cca5700d25589

0 references

splash10-0159-1950000000-e2dfe33be49873b2975d

0 references

splash10-053r-3910000000-667af9dc5d8d490e2c6f

0 references

splash10-001i-5900000000-fc48254c3b9ccf779d62

0 references

splash10-00lr-9800000000-cba29ca84271d6f980a5

0 references

splash10-014i-9300000000-4150dab542ca3ac540a2

0 references

splash10-014i-9100000000-8d38036ee57ded4ff3fb

0 references

splash10-00di-0090000000-76a9cf3dd47ae8f37162

0 references

splash10-00di-0190000000-af442f78e868fd43ac61

0 references

splash10-0uxu-0940000000-c018563cc751d4f71058

0 references

splash10-014l-4900000000-5490c0b819842ba4a872

0 references

splash10-00di-0090000000-2c1c9cb6dfc7a092d3a8

0 references

splash10-00di-0090000000-125841d51722dcc61cba

0 references

splash10-00di-0090000000-124c837f947147cccd5c

0 references

splash10-0g4i-0390000000-32e5ad3ba5c1dab47e34

0 references

splash10-0uxu-0970000000-2cc2b429ddf3d4dc77f4

0 references

splash10-00di-0190000000-8d8291787b0ec5d9dc5e

0 references

splash10-00di-0390000000-f5674c252eb8da406041

0 references

splash10-0fk9-0490000000-3ed2edca3db41c24bf64

0 references

splash10-00di-0090000000-56b7c6f0bc76ae17e1c9

0 references

splash10-00di-0321900000-1dd6fcaf99898bd949df

0 references

splash10-014l-9600000000-b15477d1806070aa2e1c

0 references

splash10-00kf-5910000000-48f270af88a5a591e780

0 references

splash10-0v4m-1960000000-fbd7f2eb8c701be4e7a1

0 references

splash10-00di-0290000000-6a2f647c28daa9287eab

0 references

splash10-00di-0090000000-4045f471e10774927fb0

0 references

splash10-00di-0090000000-b593f863241cb83cbaa8

0 references

splash10-00di-0190000000-cf817be7ff212fa47a0a

0 references

splash10-00di-0090000000-9ce354d07dc39313259b

0 references

splash10-001i-0910000000-e781065a7305ca109957

0 references

splash10-0fr6-2920000000-a32f6ae97952bb96de05

0 references

splash10-00di-0290000000-4592d557e739a114cbfa

0 references

splash10-00di-0390000000-4954518a873e098a93ee

0 references

splash10-0fr6-2920000000-e988d098144d69e2ab01

0 references

splash10-00di-0390000000-09228775cac3366ba894

0 references

splash10-0uxr-0790000000-752271144b920ef9dcdf

0 references

splash10-014i-0090000000-ace47d8eb119a5d9801a

0 references

splash10-00lr-0890000000-a5611c3a49da154342cd

0 references

splash10-003r-0970000000-5c1ad72d644a6f7d8fb2

0 references

splash10-00di-0090000000-14ae481944ad1a1f7ca0

0 references

splash10-014i-0090030000-a3400b0a77da6983528f

0 references

splash10-01b9-0290000000-14651926a70dc054d2f8

0 references

splash10-00xr-0290000000-a66544a19f0800e2da4d

0 references

splash10-014i-0090000000-6cce4c7fc500a4d0e031

0 references

splash10-014i-0090000000-9a9b5a56fe8e96b29727

0 references

splash10-05fs-0024940000-93caab48cbfebe0adfe1

0 references

splash10-00mk-0034930000-4fd902a5138b08f96ec8

0 references

splash10-0uxr-0980000000-d7597f9c07cf1f3dd705

0 references

splash10-0uxr-0980000000-54cb13a53cda72100fea

0 references

splash10-0fwa-0690000000-51644d5d7c7b02b8d60a

0 references

splash10-0006-0970000000-1a4982eb4d7eb25f31ed

0 references

splash10-00xr-0190000000-bfdc73b7c98095774174

0 references

splash10-00xr-0290000000-1b4e4c826cb722d2d4f4

0 references

splash10-00xr-0190000000-7aef74124459eefc260d

0 references

splash10-0uxr-0980000000-5cd85b268b8c09ce869c

0 references

splash10-0a4i-0059000000-9157f7d4e1ab427874b4

0 references

splash10-017i-0590000000-ac80dd1871f3889b2227

0 references

splash10-016r-0590000000-bf36f475b096e2438121

0 references

splash10-0avi-0023930000-1dfc646710db8bcea7f4

0 references

splash10-0600-0024930000-e167c8f3b2cc83df3938

0 references

splash10-0w2c-0890000000-e39869e4de6743dab7a0

0 references

splash10-0uxu-0890000000-08a921b5fef4280f09bc

0 references

splash10-0uxu-0890000000-9cd17bd71a9f622cdb09

0 references

splash10-0a4i-0059000000-2488bce117227c3a4e73

0 references

splash10-0006-0090000000-1bb16c49282b8cebd0f9

0 references

splash10-0006-0090000000-9a0a356da9ba07a275d6

0 references

splash10-0a4i-0059000000-8b2723ae8be3606593e0

0 references

splash10-0a4i-0009000000-d00f7486b124d27b247d

0 references

splash10-0a4i-0009000000-5fc199cfc4cc949e1300

0 references

splash10-01ox-0070090000-474d6eaba4a456f2d780

0 references

splash10-01ox-0060090000-305968de8df4fa9284f2

0 references

splash10-00di-1490000000-7e273097c726d64fddd7

0 references

splash10-0uxs-0940000000-6d7bda0e62f0e046a7db

0 references

splash10-0006-0090000000-a46ae833d36c8b9bb9f4

0 references

splash10-001i-0910000000-7ca449cfd3c648cf0f79

0 references

splash10-00di-0090000000-b38100149f8900d87aea

0 references

splash10-00di-0090000000-fd0cff73611745fc4b3a

0 references

splash10-00di-0090000000-f1126bd6d175c968787e

0 references

splash10-00di-1590000000-337676391a09c9739379

0 references

splash10-014i-0090000000-720c4e1f43db9f50b589

0 references

splash10-014i-0090000000-0e3ca66534f635efb4d8

0 references

splash10-001i-0900000000-ad50062f85b9c32e1426

0 references

splash10-001i-0910000000-6a694e60823635f66757

0 references

splash10-00di-0490000000-8a8038ed373877790e4b

0 references

splash10-00di-0190000000-49c573bd6b3218e32ec0

0 references

splash10-014i-0190000000-3a2edef598996d8ee33a

0 references

splash10-00di-0090000000-17b09902cbc2dacc4f53

0 references

splash10-014j-0930000000-789526dd365eeb43ad9a

0 references

splash10-014i-0190000000-cadb0bf0ffc4c0574ec9

0 references

splash10-014i-0090000000-6db4d2441911d696b121

0 references

RTECS number

NR2392000

1 reference

Hazardous Substances Data Bank

1 reference

28 October 2019

GENISTEIN (English)

10 May 2021

2 references

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

DSSTOX compound identifier

0 references

0 references

1 reference

genistein (English)

ECHA Substance Infocard ID

19 November 2016

100.006.524

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.006.524

27 December 2018

5,7-dihydroxy-3-(4-hydroxyphenyl)-4-benzopyrone (English)

quotation

CAS no.: 446-72-0 (English)

1 reference

28 December 2019

GENISTEIN (English)

CAS no.: 446-72-0 (English)

AGROVOC ID

c_37219

0 references

1 reference

genistein (English)

19 November 2016

Genistein

1 reference

D03.383.663.283.266.450.400.375

14 March 2018

0 references

D03.633.100.150.266.450.400.375

0 references

RxNorm ID

25696

1 reference

genistein (English)

19 November 2016

1 reference

Human Metabolome Database ID

HMDB0003217

2 references

based on heuristic

3 references

genistein (English)

19 October 2016

2 references

genistein (English)

19 November 2016

Natural Product Atlas ID

NPA021027

2 references

based on heuristic

PatientsLikeMe treatment ID

0 references

0 references

1 reference

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

1 reference

30 June 2018

1 reference

Immune Epitope Database and Analysis Resource

1 March 2022

0 references

1 reference

6 April 2020

1 reference

28 October 2013

Microsoft Academic ID

0 references

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

3KGU (English)

19 October 2016

1 reference

3KGT (English)

19 October 2016

1 reference

1QKM (English)

19 October 2016

1 reference

1X7J (English)

19 October 2016

1 reference

1X7R (English)

19 October 2016

1 reference

2QA8 (English)

19 October 2016

1 reference

5AUZ (English)

19 October 2016

1 reference

4FJ1 (English)

19 October 2016

1 reference

inferred by common MeSH mappings on source and on Wikidata

5AV4 (English)

19 October 2016

0 references

1 reference

UMLS 2023