Daidzin (Q3814656)

O=C1C(=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C12)C=4C=CC(O)=CC4

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isomeric SMILES

c1cc(ccc1c2coc3cc(ccc3c2=O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O

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found in taxon

Baptisia arachnifera

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia bracteata

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia calycosa

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia cinerea

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia lanceolata

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia lecontei

1 reference

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

Baptisia megacarpa

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia nuttalliana

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia perfoliata

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia simplicifolia

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Begonia nantoensis

1 reference

Cytotoxic and anti-HIV principles from the rhizomes of Begonia nantoensis

Froelichia floridana

1 reference

Ecdysteroids and a sucrose phenylpropanoid ester from Froelichia floridana

Pueraria

1 reference

On the Constituents of Pueraria Root. (1)

Retama sphaerocarpa

4 references

An isoflavone glucoside from Retama sphaerocarpa boissier

An isoflavone glucoside from Retama sphaerocarpa boissier

Cytotoxic activity of flavonoids and extracts from Retama sphaerocarpa Boissier

An isoflavone glucoside from Retama sphaerocarpa boissier

Thermopsis macrophylla

1 reference

Thermopsis mollis

1 reference

Thermopsis rhombifolia

1 reference

Thermopsis villosa

1 reference

Adenocarpus artemisiifolius

1 reference

Flavonoids as chemosystematic markers for the genus Adenocarpus

Adenocarpus decorticans

1 reference

Flavonoids as chemosystematic markers for the genus Adenocarpus

Cicer arietinum

1 reference

Accumulation of Phenolic Compounds and Phytoalexins in Sliced and Elicitor-Treated Cotyledons of Cicer arietinum L.

Cicer baldshuanicum

1 reference

Flavonoids of some species of Cicer of the Central Asian flora

Cicer flexuosum

1 reference

Flavonoids of some species of Cicer of the Central Asian flora

Erythrina latissima

1 reference

Isoflavone Glycosides from the Root Wood of Erythrina latissima

Flemingia macrophylla

2 references

A flavonol C-glycoside from Moghania macrophylla

A flavonol C-glycoside from Moghania macrophylla

Bituminaria acaulis

2 references

Daidzin from Psoralea acaulis

Daidzin from Psoralea acaulis

Cullen drupaceum

2 references

Flavonoids ofPsoralea drupaceae andReseda luteola

Flavonoids ofPsoralea drupaceae andReseda luteola

Cullen plicatum

2 references

A phenolic cinnamate dimer from Psoralea plicata

A phenolic cinnamate dimer from Psoralea plicata

Pueraria tuberosa

1 reference

Analysis of isoflavones in Puerariae radix by high-performance liquid chromatography with amperometric detection

Punica granatum

1 reference

Oestrogen content of pomegranate seeds

Trifolium pratense

4 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)

Vigna angularis

2 references

Induction of stress metabolite formation in suspension cultures of Vigna angularis

Induction of Phenylalanine Ammonia-Lyase Activation and Isoflavone Glucoside Accumulation in Suspension-Cultured Cells of Red Bean, Vigna angularis, by Phytoalexin Elicitors, Vanadate, and Elevation of Medium pH

Vigna radiata

1 reference

Flavonoids of Phaseolus aureus

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

Phyllolobium chinense

1 reference

Studies on the constituents of leguminous plants. Part XXX. Structures of Three New Acylated Flavonol Glycosides from Astragalus complanatus R. Br.

Genista sessilifolia

1 reference

Flavonoids and isoflavonoids from Genista sessilifolia DC. Growing in Turkey

Maackia amurensis

1 reference

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

Ormosia henryi

1 reference

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

Thermopsis lupinoides

1 reference

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

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

Kartalinia acaulis

1 reference

Daidzin from Psoralea acaulis

Thermopsis lanceolata

1 reference

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

Pueraria montana var. lobata

12 references

Identification of isoflavones in the roots of Pueraria lobata.

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.

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

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

Flavonoids of the rhizomes ofPueraria hirsuta

Separation and purification of isoflavones from Pueraria lobata by high-speed counter-current chromatography

Chemical constituents from roots of Pueraria lobata

Isolation and high performance liquid chromatography (HPLC) of isoflavonoids from the Pueraria root

Effects of isoflavones extracted from kudzu, Pueraria lobata (Willd.) Ohwi, on glyoxalase I activity and the growth of cultured cells.

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

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

Phaseolus vulgaris

1 reference

Biotransformation of common bean (Phaseolus vulgaris L.) flavonoid glycosides by bifidobacterium species from human intestinal origin

Capsicum annuum

1 reference

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

chia

1 reference

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

Ziziphus spina-christi

1 reference

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

soybean

25 references

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

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

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

Electrospray characterization of selected medicinal plant extracts

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

Fabaceae

1 reference

Isolation and high performance liquid chromatography (HPLC) of isoflavonoids from the Pueraria root

subject has role

alcohol deterrents

1 reference

InChI=1S/C21H20O9/c22-8-16-18(25)19(26)20(27)21(30-16)29-12-5-6-13-15(7-12)28-9-14(17(13)24)10-1-3-11(23)4-2-10/h1-7,9,16,18-23,25-27H,8H2/t16-,18-,19+,20-,21-/m1/s1

Medical Subject Headings

15 March 2018

1 reference

Medical Subject Headings

MeSH descriptor ID

C013908

retrieved

15 March 2018

Identifiers

InChI

1 reference

PubChem

2 references

PubChem

https://commonchemistry.cas.org/detail?cas_rn=552-66-9

ChEBI release 2020-09-01

1 reference

6 April 2021

ChemSpider ID

10164919

1 reference

English Wikipedia

PubChem CID

107971

2 references

English Wikipedia

Reaxys registry number

59741

0 references

ChEBI ID

42202

mapping relation type

exact match

3 references

Serbo-Croatian Wikipedia

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C21H20O9/c22-8-16-18(25)19(26)20(27)21(30-16)29-12-5-6-13-15(7-12)28-9-14(17(13)24)10-1-3-11(23)4-2-10/h1-7,9,16,18-23,25-27H,8H2/t16-,18-,19+,20-,21-/m1/s1

ChEMBL ID

CHEMBL486422

1 reference

splash10-0uxr-0190300000-7c009a9b8fd016988c20

1 reference

MassBank accession ID

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splash10-0udi-0090300000-87d938e172f23b8f9266

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splash10-0udi-0090101010-00cce9f1d03944bfc839

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splash10-0udi-0090000000-f372e3204e88dfa0fac6

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splash10-0089-2970000000-19bb9d5854402bda7386

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splash10-0a4i-0190000000-eda4bb0289e93579fe55

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splash10-000i-0030900000-7d29657b93ed6a4bbec3

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splash10-0a4i-0090000000-73a8d0f2baf05f40f6e9

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splash10-0a4i-0290000000-0795fc21c6cff9c0c467

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splash10-0udi-0190200000-21f48ac2697d0d52ecd2

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splash10-0udi-0090000000-a2bf7f7ca15d756d6c5f

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splash10-0udi-0090000000-981712685cf4f281fd3a

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splash10-0udi-0090005000-9e868b1cf42d82a91b13

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splash10-0udi-0090005100-6b4e53251bdae012c62c

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splash10-0a4i-0090000000-e747acf3658b3277b4e4

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splash10-0a4i-0090000000-2688cee77d9a5929a7c4

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splash10-004i-0090000000-dcd9745d3194e3b63cb0

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splash10-004i-0090000000-4ead1b8467e6c5b1e6a8

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splash10-0006-0090000000-4c8290abea7d23440a13

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splash10-0006-0090000000-01f1a96e576e64bac413

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splash10-0006-0090000000-dac81021382eb3c0fcd2

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splash10-000i-0000900000-83fd5eadb77e8984bd25

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splash10-000i-0000900000-0905c32bf09edd5d431b

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splash10-000i-0000900000-695838d87a8b9d4c76c0

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splash10-014i-0000900000-ad8baf73ea6a3e189d21

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splash10-0a4i-0090000000-ebb40f663cd4f7c62b9d

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splash10-0a4i-0090000000-d54e9a1ee9a3a57569ab

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splash10-0a4i-0090000000-7345d94dfce25c5ddab0

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splash10-0a4i-0090000000-64b58fe578c34aae023a

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splash10-0a4i-0190000000-3bb2d8555d8ee711e50f

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splash10-014i-0000900000-96b3f34c7edaccc9fc6e

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splash10-014i-0000900000-b453bc2c290416360a50

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splash10-0uxr-0090600000-03aab88939b342719e35

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splash10-0udi-0090000000-93ba9f1fa4c2df2964bf

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splash10-0udi-0090000000-fd290a7113bf8b50734b

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splash10-03di-0000092000-84a513c4afef1602030f

0 references

splash10-03di-0000900000-a8a90b48831795fcef5b

0 references

splash10-0w29-0090800000-71336b3ac56112e89965

0 references

DSSTox substance ID

DTXSID00862180

1 reference

EC number

611-245-3

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

Daidzin (English)

CAS no.: 552-66-9 (English)

ECHA Substance Infocard ID

100.107.506

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

Daidzin (English)

CAS no.: 552-66-9 (English)

MeSH descriptor ID

C013908

1 reference

Medical Subject Headings

14 March 2018

1 reference

Human Metabolome Database ID

HMDB0033991

2 references

based on heuristic

inferred from InChIKey

http://kanaya.naist.jp/knapsack_jsp/information.jsp?sname=C_ID&word=C00002518

KNApSAcK ID

C00002518

1 reference

reference URL

UNII

4R2X91A5M5

1 reference

0 references

1 reference

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

Serbo-Croatian Wikipedia

0 references

0 references

0 references

Microsoft Academic ID

0 references

1 reference

26 January 2022

UMLS CUI

C0057091

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata