biochanin A (Q864222)

biochanin A (English)

19 October 2016

chemical formula

C₁₆H₁₂O₅

1 reference

biochanin A (English)

20 November 2016

canonical SMILES

COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O

1 reference

biochanin A (English)

20 November 2016

melting point

212 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Trifolium pratense

20 references

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

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

Effects of synthetic and naturally occurring flavonoids on benzo[a]pyrene metabolism by hepatic microsomes prepared from rats treated with cytochrome P-450 inducers

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)

The Breeding of Fodder Plants

Effect of biochanin A on the aryl hydrocarbon receptor and cytochrome P450 1A1 in MCF-7 human breast carcinoma cells

In vitro and in vivo melanogenesis inhibition by biochanin A from Trifolium pratense

Stability-Indicating HPLC Method for isoflavones aglycones analysis from Trifolium pratense L. extract

Hispidulin-7-glucoside, a minor flavonoid of Trifolium pannonicum L

The red clover (Trifolium pratense) isoflavone biochanin A inhibits aromatase activity and expression

Cicer arietinum

8 references

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

Flavonoids of some species of Cicer of the Central Asian flora

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

Elicitation of Pterocarpan Phytoalexins in Cell Suspension Cultures of Different Chickpea (Cicer arietinum L.) Cultivars by an Elicitor from the Fungus Ascochyta rabiéi

Elicitor-Induced Formation of Pterocarpan Phytoalexins in Chickpea (Cicer arietinum L.) Cell Suspension Cultures from Constitutive Isoflavone Conjugates upon Inhibition of Phenylalanine Ammonia Lyase

Isolation and identification of Cicer isoflavonoids

Andira inermis

4 references

Flavonoids ofSerratula inermis

957. Extractives from woods. Part I. Extractives from Andira inermis(Wright) H.B.K

Antiplasmodial activity of isoflavones from Andira inermis

Andinermals A-C, antiplasmodial constituents from Andira inermis

Cicer mogoltavicum

2 references

Isoflavonoids ofCiver mogoltavicum

Flavonoids of the epigeal part ofCicer mogoltavicum

Lupinus albus

1 reference

Isolation of biochanin A from Lupinus termis and estimation of its estrogenic activity

Trifolium incarnatum

4 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

Hispidulin-7-glucoside, a minor flavonoid of Trifolium pannonicum L

Trifolium repens

8 references

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

The effects of plant oestrogens on animal reproduction

Isoflavones in Different Parts of Common Trifolium Species

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

The Breeding of Fodder Plants

Isolation and Identification of Vesicular-Arbuscular Mycorrhiza-Stimulatory Compounds from Clover (Trifolium repens) Roots

Hispidulin-7-glucoside, a minor flavonoid of Trifolium pannonicum L

Syzygium jambos

1 reference

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

Baptisia alba

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia calycosa

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia sphaerocarpa

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia tinctoria

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Bolusanthus speciosus

2 references

Alkaloids of Bolusanthus speciosus

Isoflavonoids from Bolusanthus speciosus (Bolus) Harms Leguminosae

Cicer bijugum

3 references

Isolation and identification of Cicer isoflavonoids

A 2-arylbenzofuran from roots of cicer bijugum associated with fusarium wilt resistance

Cicer chorassanicum

2 references

Isolation and identification of Cicer isoflavonoids

Cicer cuneatum

2 references

Isolation and identification of Cicer isoflavonoids

Cicer echinospermum

2 references

Isolation and identification of Cicer isoflavonoids

Cicer judaicum

2 references

Isolation and identification of Cicer isoflavonoids

Cicer macracanthum

2 references

Isolation and identification of Cicer isoflavonoids

Cicer microphyllum

2 references

Isolation and identification of Cicer isoflavonoids

Cicer montbretii

2 references

Isolation and identification of Cicer isoflavonoids

Cicer nuristanicum

2 references

Isolation and identification of Cicer isoflavonoids

Cicer oxyodon

2 references

Isolation and identification of Cicer isoflavonoids

Cicer pinnatifidum

2 references

Isolation and identification of Cicer isoflavonoids

Cicer pungens

2 references

Isolation and identification of Cicer isoflavonoids

Cicer rechingeri

2 references

Isolation and identification of Cicer isoflavonoids

Cicer reticulatum

2 references

Isolation and identification of Cicer isoflavonoids

Cicer songaricum

3 references

Isolation and identification of Cicer isoflavonoids

Flavonoids of Cicer songoricum

Cicer yamashitae

2 references

Isolation and identification of Cicer isoflavonoids

Dalbergia nitidula

4 references

Phenolic compounds from the heartwood of Dalbergia nitidula

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

Volubilinin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Dalbergia parviflora

5 references

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

Bioactive constituents from the stems of Dalbergia parviflora

Volubilinin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Phenolic compounds from the heartwood of Dalbergia nitidula

Dalbergia spruceana

4 references

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

Volubilinin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Phenolic compounds from the heartwood of Dalbergia nitidula

Dalbergia volubilis

6 references

Volubilinin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Volubilin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Volubolin, a 4-phenyl-2H-1-benzopyran-2-one from Dalbergia volubilis

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

Phenolic compounds from the heartwood of Dalbergia nitidula

Echinospartum horridum

1 reference

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

Gynerium sagittatum

1 reference

Flavonoids and isoflavonoids from Gynerium sagittatum

Myroxylon peruiferum

1 reference

Isoflavonoids from Myroxylon peruiferum

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

Pericopsis elata

1 reference

Phytochemical examination of Pericopsis species

Pericopsis laxiflora

1 reference

Phytochemical examination of Pericopsis species

Pericopsis mooniana

1 reference

Phytochemical examination of Pericopsis species

Sundacarpus amarus

1 reference

Isoflavones from Podocarpus amarus

Swartzia polyphylla

4 references

Dihydrolicoisoflavone, a new isoflavanone from Swartzia polyphylla

Ferreirinol, a New 3-Hydroxyisoflavanone fromSwartzia polyphylla

Isoflavanones from the heartwood of Swartzia polyphylla and their antibacterial activity against cariogenic bacteria

Larvicidal, antimycobacterial and antifungal compounds from the bark of the Peruvian plant Swartzia polyphylla DC.

Thermopsis macrophylla

1 reference

Flavonoids of north american species of Thermopsis

Thermopsis rhombifolia

1 reference

Flavonoids of north american species of Thermopsis

Trifolium apertum

2 references

Hispidulin-7-glucoside, a minor flavonoid of Trifolium pannonicum L

Trifolium canescens

2 references

Hispidulin-7-glucoside, a minor flavonoid of Trifolium pannonicum L

zigzag clover

3 references

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

Hispidulin-7-glucoside, a minor flavonoid of Trifolium pannonicum L

Trifolium pannonicum

3 references

Hispidulin-7-glucoside, a minor flavonoid of Trifolium pannonicum L

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

Trifolium trichocephalum

2 references

Hispidulin-7-glucoside, a minor flavonoid of Trifolium pannonicum L

Virola surinamensis

6 references

New butenolides in plantlets of Virola surinamensis (Myristicaceae).

Antifungal constituents from roots of Virolasurinamensis

Flavonoids and lignans from Virola surinamensis twigs and their in vitro activity against Trypanosoma cruzi

Diarylpropanoid from Virola multinervia

Lignans, γ-lactones and propiophenones of Virola surinamensis

Butanolides as a common feature of iryanthera lancifolia and virola surinamensis

Wisteria brachybotrys

2 references

Isoflavones from the gall and wood of Wisteria brachybotrys

Anti-tumor Promoting Activities of Isoflavonoids from Wistaria brachybotrys

Anaxagorea luzonensis

2 references

Studies on the constituents of Anaxagorea luzonensis A. GRAY.

ChemInform Abstract: Studies on the Constituents of Anaxagorea luzonensis A. Gray.

Baptisia australis

1 reference

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

Cicer canariense

2 references

Isolation and identification of Cicer isoflavonoids

Cicer flexuosum

1 reference

Flavonoids of the epigeal part ofCicer flexuosum andC. mogoltavicum

Crotalaria thebaica

1 reference

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

Dalbergia cultrata

1 reference

New cinnamylphenols from Dalbergia species with cancer chemopreventive activity

Dalbergia nigrescens

1 reference

New cinnamylphenols from Dalbergia species with cancer chemopreventive activity

Dalbergia oliveri

1 reference

Isoflavonoids from Dalbergia olivari

Dalbergia sissoides

3 references

Chemical Constituents of the Heartwood of Dalbergia tonkinensis

Flavonoid constituents of Sideritis caesarea

Chemical constituents of Dalbergia odorifera

Dalbergia sissoo

6 references

Phytochemical and Pharmacological Studies of Dalbergia sissoo Growing in Egypt

Constituents of Dalbergia sissoo Roxb. leaves with osteogenic activity.

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

Volubilinin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Phenolic compounds from the heartwood of Dalbergia nitidula

Euchresta formosana

1 reference

Antiplatelet and Anti-HIV Constituents from Euchresta Formosana

soybean

3 references

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

New isoflavone and triterpene glycosides from soybeans

FLAVONOIDS IN CULTIVARS OF SOYBEAN: ANTIOXIDANT ACTION

Iris pseudacorus

1 reference

Isoflavonoids produced by Iris pseudacorus leaves treated with cupric chloride

Knema glomerata

1 reference

Kneglomeratanol, kneglomeratanones A and B, and related bioactive compounds from Knema glomerata

Medicago sativa

1 reference

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

Myristica ceylanica

1 reference

Demethyldactyloidin and Other Constituents in Myristica Ceylanica

Myristica malabarica

1 reference

An isoflavone from Myristica malabarica

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

Trifolium arvense

1 reference

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

Trifolium diffusum

1 reference

Flavonoids ofTrifolium echinatum andT. diffusum

Trifolium echinatum

1 reference

Flavonoids ofTrifolium echinatum andT. diffusum

Trifolium fragiferum

1 reference

Isoflavones in Different Parts of Common Trifolium 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

Bioactive Isoflavonols and Other Components fromTrifolium subterraneum

Dalbergia frutescens

5 references

Antigiardial activity of isoflavones from Dalbergia frutescens bark

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

Volubilinin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Phenolic compounds from the heartwood of Dalbergia nitidula

peanut

1 reference

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

Vitis vinifera

1 reference

RP-HPLC analysis of phenolic compounds and flavonoids in beverages and plant extracts using a CoulArray detector.

Andira surinamensis

1 reference

NMR spectral assignments of a new [C--O--C] isoflavone dimer from Andira surinamensis

Knema furfuracea

1 reference

A new arylnaphthalene lignan from Knema furfuracea.

Monopteryx inpae

1 reference

Isoflavone evolution in Monopteryx

Monopteryx uaucu

1 reference

Isoflavone evolution in Monopteryx

Ormosia henryi

1 reference

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

Pycnanthus angolensis

2 references

Antimicrobial activities of the CH2Cl2-CH3OH (1:1) extracts and compounds from the roots and fruits of Pycnanthus angolensis (Myristicaceae).

Pycnanthuquinone C: a new terpenoid-quinone from Pycnanthus angolensis

Trigonella foenum-graecum

1 reference

New flavonoids with 2BS cell proliferation promoting effect from the seeds of Trigonella foenum-graecum L.

Cicer kopetdaghense

1 reference

Flavonoids of some species of Cicer of the Central Asian flora

Butea superba

1 reference

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

Vitex negundo

1 reference

997. Extractives from woods. Part II. Extractives from Vitexs divaricata

Erythrina melanacantha

2 references

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

Erythrinan alkaloid from Erythrina x bidwillii

Dalbergia congestiflora

4 references

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

Volubilinin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Phenolic compounds from the heartwood of Dalbergia nitidula

Sophora flavescens

2 references

The Alkaloids of Sophora velutina

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

Sophora mollis

2 references

The Alkaloids of Sophora velutina

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

Pueraria montana var. lobata

1 reference

Identification of isoflavones in the roots of Pueraria lobata.

Dalbergia lanceolaria

4 references

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

Volubilinin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Phenolic compounds from the heartwood of Dalbergia nitidula

Andira parviflora

1 reference

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

Cicer anatolicum

1 reference

Virola caducifolia

1 reference

Isoflavone evolution in Monopteryx

garlic

1 reference

Composition of Polyphenols and Antioxidant Activity of Garlic Bulbs Collected from Different Locations of Korea

Dianthus caryophyllus

1 reference

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

Arabidopsis thaliana

1 reference

Isoflavonoids are present in Arabidopsis thaliana despite the absence of any homologue to known isoflavonoid synthases

Momordica charantia

1 reference

Establishment of Momordica charantia hairy root cultures for the production of phenolic compounds and determination of their biological activities

liquorice

1 reference

Biosynthesis-Based Quantitative Analysis of 151 Secondary Metabolites of Licorice To Differentiate Medicinal Glycyrrhiza Species and Their Hybrids.

Glycyrrhiza inflata

1 reference

Biosynthesis-Based Quantitative Analysis of 151 Secondary Metabolites of Licorice To Differentiate Medicinal Glycyrrhiza Species and Their Hybrids.

Glycyrrhiza uralensis

1 reference

Biosynthesis-Based Quantitative Analysis of 151 Secondary Metabolites of Licorice To Differentiate Medicinal Glycyrrhiza Species and Their Hybrids.

Polla

1 reference

Extract of Punica granatum inhibits skin photoaging induced by UVB irradiation

Cymbopogon citratus

1 reference

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

Prunus avium

1 reference

Chemical characterisation and bioactive properties of Prunus avium L.: The widely studied fruits and the unexplored stems

Capsicum annuum

1 reference

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

Bacillus subtilis

1 reference

Rewiring the Glucose Transportation and Central Metabolic Pathways for Overproduction of N-Acetylglucosamine in Bacillus subtilis

Mirabilis jalapa

1 reference

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

Flemingia macrophylla

1 reference

Prenylated flavonoids from Moghania philippinensis

Cicer tragacanthoides

1 reference

Flavonoids of some species of Cicer of the Central Asian flora

Maclura tricuspidata

1 reference

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

Dalbergia monetaria

6 references

Volubilinin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Phenolic compounds from the heartwood of Dalbergia nitidula

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

Volubolin, a 4-phenyl-2H-1-benzopyran-2-one from Dalbergia volubilis

Volubilin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Trifolium alpestre

1 reference

Isoflavones in Different Parts of Common Trifolium Species

Styphnolobium japonicum

2 references

New Isoflavone Glycoside from the Woods of Sophora japonica.

Inhibitory effects of isoflavones on lipid peroxidation by reactive oxygen species

Dermatophyllum secundiflorum

1 reference

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

Flemingia prostrata

1 reference

Prenylated flavonoids from Moghania philippinensis

Dalbergia ovalis

6 references

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

Volubilinin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Phenolic compounds from the heartwood of Dalbergia nitidula

Volubolin, a 4-phenyl-2H-1-benzopyran-2-one from Dalbergia volubilis

Volubilin, a new isoflavone-C-glycoside from Dalbergia volubilis flowers

Propolis

2 references

Constituents of Brazilian red propolis and their preferential cytotoxic activity against human pancreatic PANC-1 cancer cell line in nutrient-deprived condition.

Cytotoxic constituents from Brazilian red propolis and their structure-activity relationship.

physically interacts with

Estrogen related receptor alpha

subject has role

agonist

1 reference

Estrogen related receptor beta

17 August 2016

subject has role

agonist

1 reference

Estrogen related receptor gamma

17 August 2016

subject has role

agonist

1 reference

imported from Wikimedia project

17 August 2016

1 reference

1 reference

Medical Subject Headings

15 March 2018

1 reference

Medical Subject Headings

15 March 2018

1 reference

English Wikipedia

InChI=1S/C16H12O5/c1-20-11-4-2-9(3-5-11)12-8-21-14-7-10(17)6-13(18)15(14)16(12)19/h2-8,17-18H,1H3

20 August 2019

Commons category

Biochanin A

0 references

Identifiers

InChI

1 reference

biochanin A (English)

20 November 2016

2 references

biochanin A (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

491-80-5

2 references

Global Substance Registration System

https://commonchemistry.cas.org/detail?cas_rn=491-80-5

biochanin a (English)

20 November 2016

7 April 2021

1 reference

olmelin (English)

20 November 2016

2 references

biochanin A (English)

20 November 2016

Reaxys registry number

278107

1 reference

biochanin A (English)

19 October 2016

ChEBI ID

17574

mapping relation type

2 references

BIOCHANIN (English)

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C16H12O5/c1-20-11-4-2-9(3-5-11)12-8-21-14-7-10(17)6-13(18)15(14)16(12)19/h2-8,17-18H,1H3

1 reference

BIOCHANIN (English)

20 November 2016

2 references

inferred from InChIKey

MSBNK-MPI_for_Chemical_Ecology-CE000046

1 reference

MassBank accession ID

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000047

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MSBNK-MPI_for_Chemical_Ecology-CE000048

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MSBNK-MPI_for_Chemical_Ecology-CE000049

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000050

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MSBNK-Washington_State_Univ-BML00747

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MSBNK-Washington_State_Univ-BML00754

0 references

MSBNK-Washington_State_Univ-BML00761

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MSBNK-Washington_State_Univ-BML00767

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MSBNK-Washington_State_Univ-BML00772

0 references

MSBNK-Washington_State_Univ-BML00777

0 references

MSBNK-Washington_State_Univ-BML80820

0 references

MSBNK-Washington_State_Univ-BML80821

0 references

MSBNK-Washington_State_Univ-BML80822

0 references

MSBNK-Washington_State_Univ-BML80823

0 references

0 references

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0 references

0 references

MSBNK-IPB_Halle-PB000241

0 references

MSBNK-IPB_Halle-PB000261

0 references

MSBNK-IPB_Halle-PB000262

0 references

MSBNK-IPB_Halle-PB000263

0 references

MSBNK-IPB_Halle-PB005707

0 references

MSBNK-IPB_Halle-PB005708

0 references

MSBNK-IPB_Halle-PB005709

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MSBNK-IPB_Halle-PB005710

0 references

MSBNK-IPB_Halle-PB005711

0 references

MSBNK-IPB_Halle-PN000108

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MSBNK-IPB_Halle-PN000109

0 references

SPLASH

splash10-000i-0090000000-7af822b8dad09b0ac6c8

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splash10-0udl-0790000000-dfcd1ad0cd74fa25c9c6

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splash10-03dl-1940000000-d6a0d7d5a724d4c6e1db

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splash10-000i-0090000000-044c1c4eb448c746bb3c

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splash10-000i-0090000000-58e07837f69d383b057c

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splash10-000i-0090000000-9f9ee2eeb98251688f25

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splash10-0fe3-0190000000-c5e36abf786412e0c524

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splash10-03dl-0290000000-a8f84ce50fd8ea5a877e

0 references

splash10-000i-0190000000-4337ab19b21cf719a890

0 references

splash10-0079-0290000000-dacef9ef84820ca0f71b

0 references

splash10-0fki-0390000000-bc80103924dd60e70be7

0 references

splash10-0fk9-0590000000-fe80601eb5d69ed0c219

0 references

splash10-000i-0090000000-01b83b15972a278fccaf

0 references

splash10-000i-0090000000-026e5787c265af9e291d

0 references

splash10-000i-0290000000-4ab567e19bebaefb45f4

0 references

splash10-0j4l-0960000000-bd77196c14caea302ea1

0 references

splash10-001i-0090000000-f16ba656729184cf1e0c

0 references

splash10-0159-0090000000-d1a6e4c18b870bcac1d2

0 references

splash10-02ti-0590000000-c899726b9c15324f3ce1

0 references

splash10-000i-0094000000-655aad8f562c9534551e

0 references

splash10-001i-0090000000-596d7e8fe23fac3b04d8

0 references

splash10-000i-0090000000-66431d761a4c272ff9ec

0 references

splash10-014i-0090000000-327b093a16d7f9eae5fc

0 references

splash10-0fk9-0490000000-671f15ee0200200b6e5a

0 references

splash10-0159-0090000000-4b10095003dcc544d1ef

0 references

splash10-014i-0090000000-e6891a7d4b4149bd22c4

0 references

splash10-0159-0090000000-69353960b909f76a8b29

0 references

splash10-0fe0-0290000000-e17f52e509ab2c28fd0d

0 references

splash10-0w9c-0490000000-9f316916713e817996ee

0 references

splash10-0a4i-0019000000-09139525e32bfa06cffd

0 references

splash10-014i-0190000000-3d2d9ae76aea2ba8e0d4

0 references

splash10-014r-0190000000-7f6a864949fd18a14e8b

0 references

splash10-03yr-0790000000-5a2ccc494db05b9e19e7

0 references

splash10-014i-0090000000-1469c7dc6efca44dce49

0 references

splash10-001i-0090000000-ab7e811e30dd92aa8de3

0 references

splash10-0159-0090000000-48950d676f0cb98a7321

0 references

splash10-000i-0390000000-8b4551164bbb2aac939d

0 references

splash10-03di-1833900000-f09d96dccb297f00dcd5

0 references

splash10-0uvi-0990000000-f50ff15a552bfff5445f

0 references

splash10-03di-2944800000-78e1196ce4a6b5cc510e

0 references

DSSTox substance ID

DTXSID1022394

2 references

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

DSSTOX compound identifier

0 references

0 references

1 reference

Global Substance Registration System

biochanin a (English)

ECHA Substance Infocard ID

20 November 2016

100.007.041

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.007.041

27 December 2018

5,7-dihydroxy-3-p-methoxyphenyl-4H-chromen-4-one (English)

quotation

CAS no.: 491-80-5 (English)

CosIng number

92145

0 references

1 reference

biochanin A (English)

20 November 2016

1 reference

Medical Subject Headings

14 March 2018

1 reference

Human Metabolome Database ID

HMDB0002338

2 references

based on heuristic

inferred from InChIKey

3 references

biochanin A (English)

19 October 2016

based on heuristic

inferred from InChIKey

2 references

Global Substance Registration System

biochanin a (English)

20 November 2016

imported from Wikimedia project

0 references

1 reference

0 references

1 reference

Immune Epitope Database and Analysis Resource

1 March 2022

0 references

0 references

Microsoft Academic ID

0 references

1 reference

26 January 2022

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

1 reference

2QYO (English)

19 October 2016

1 reference

4FJ2 (English)