pratensein (Q3401397)

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chemical compound

3'-hydroxybiochanin A
5,7,3'-trihydroxy-4'-methoxyisoflavone
3'-hydroxy-biochanin A
3',5,7-trihydroxy-4'-methoxyisoflavone
5,7-dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one

Language	Label	Description	Also known as
English	pratensein	chemical compound	3'-hydroxybiochanin A 5,7,3'-trihydroxy-4'-methoxyisoflavone 3'-hydroxy-biochanin A 3',5,7-trihydroxy-4'-methoxyisoflavone 5,7-dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one

Statements

type of chemical entity

0 references

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image of molecular model or crystal lattice model

Pratensein-3D-balls.png
2,000 × 1,017; 358 KB

ball-and-stick model

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300.063388 dalton

1 reference

language of work or name

UNII-D2CF8CJ6AP (English)

5 October 2016

chemical formula

C₁₆H₁₂O₆

1 reference

language of work or name

UNII-D2CF8CJ6AP (English)

5 October 2016

canonical SMILES

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

1 reference

language of work or name

UNII-D2CF8CJ6AP (English)

5 October 2016

Monopteryx inpae

1 reference

Isoflavone evolution in Monopteryx

Cicer arietinum

6 references

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

Flavonoids of some species of Cicer of the Central Asian flora

Cytochrome P450-dependent methylenedioxy bridge formation in Cicer arietinum

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

The distribution of isoflavonoids in cicer

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

Cicer mogoltavicum

1 reference

Isoflavonoids ofCiver mogoltavicum

Trifolium pratense

3 references

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

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

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

1 reference

The distribution of isoflavonoids in cicer

Cicer canariense

1 reference

The distribution of isoflavonoids in cicer

Cicer chorassanicum

1 reference

The distribution of isoflavonoids in cicer

1 reference

The distribution of isoflavonoids in cicer

Cicer echinospermum

1 reference

The distribution of isoflavonoids in cicer

1 reference

The distribution of isoflavonoids in cicer

Cicer macracanthum

1 reference

The distribution of isoflavonoids in cicer

Cicer microphyllum

1 reference

The distribution of isoflavonoids in cicer

Cicer nuristanicum

1 reference

The distribution of isoflavonoids in cicer

1 reference

The distribution of isoflavonoids in cicer

Cicer yamashitae

1 reference

The distribution of isoflavonoids in cicer

1 reference

Constituents of Useful Plants. IX. Constituents of Arachis hypogaea L.

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

Dermatophyllum secundiflorum

4 references

Isoflavonoids in roots of Sophora secundiflora

Flavonoids and isoflavonoids from Sophorae Flos improve glucose uptake in vitro

Isoflavanones in roots of Sophora secundiflora

Isoflavanones in roots of Sophora secundiflora

Cicer songaricum

1 reference

Flavonoids of Cicer songoricum

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

Cicer baldshuanicum

1 reference

Flavonoids of some species of Cicer of the Central Asian flora

Mucuna membranacea

1 reference

Chemical Constituents from Mucuna membranacea

1 reference

Antiplasmodial activity of isoflavones from Andira inermis

Bolusanthus speciosus

1 reference

Isoflavonoids from Bolusanthus speciosus (Bolus) Harms Leguminosae

Iris pseudacorus

1 reference

Isoflavonoids produced by Iris pseudacorus leaves treated with cupric chloride

Styphnolobium japonicum

2 references

Flavonoids and isoflavonoids from Sophorae Flos improve glucose uptake in vitro

Isoflavonoids in roots of Sophora secundiflora

Dalbergia sissoo

1 reference

Constituents of Dalbergia sissoo Roxb. leaves with osteogenic activity.

Ammopiptanthus mongolicus

1 reference

Three New Isoflavonoids from the Aerial Parts ofAmmopiptanthus mongolicus

Andira surinamensis

1 reference

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

Astragalus membranaceus

1 reference

Solvent effect in 1H NMR spectra of 3'-hydroxy-4'-methoxy isoflavonoids from Astragalus membranaceus var. mongholicus

Astragalus trimestris

1 reference

Solvent effect in 1H NMR spectra of 3'-hydroxy-4'-methoxy isoflavonoids from Astragalus membranaceus var. mongholicus

Astragalus mongholicus

1 reference

Solvent effect in 1H NMR spectra of 3'-hydroxy-4'-methoxy isoflavonoids from Astragalus membranaceus var. mongholicus

Cicer kopetdaghense

1 reference

Flavonoids of some species of Cicer of the Central Asian flora

Cicer anatolicum

1 reference

The distribution of isoflavonoids in cicer

1 reference

Effect of germination time on antioxidative activity and composition of yellow pea soluble free and polar soluble bound phenolic compounds

Cicer tragacanthoides

1 reference

Flavonoids of some species of Cicer of the Central Asian flora

Sophora koreensis

2 references

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

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

2 references

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

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

Commons category

Pratensein

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Identifiers

InChI=1S/C16H12O6/c1-21-13-3-2-8(4-11(13)18)10-7-22-14-6-9(17)5-12(19)15(14)16(10)20/h2-7,17-19H,1H3

1 reference

language of work or name

UNII-D2CF8CJ6AP (English)

5 October 2016

FPIOBTBNRZPWJW-UHFFFAOYSA-N

2 references

language of work or name

UNII-D2CF8CJ6AP (English)

5 October 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

language of work or name

pratensein (English)

5 October 2016

FPIOBTBNRZPWJW-UHFFFAOYSA-N

CAS Common Chemistry

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=2284-31-3

1 reference

language of work or name

Pratensein (English)

5 October 2016

2 references

language of work or name

UNII-D2CF8CJ6AP (English)

5 October 2016

matched by identifier from

FPIOBTBNRZPWJW-UHFFFAOYSA-N

Reaxys registry number

1293940

1 reference

language of work or name

pratensein (English)

5 October 2016

mapping relation type

2 references

language of work or name

pratensein (English)

5 October 2016

matched by identifier from

International Chemical Identifier

InChI=1S/C16H12O6/c1-21-13-3-2-8(4-11(13)18)10-7-22-14-6-9(17)5-12(19)15(14)16(10)20/h2-7,17-19H,1H3

1 reference

language of work or name

PRATENSEIN (English)

5 October 2016

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

FPIOBTBNRZPWJW-UHFFFAOYSA-N

UniChem compound ID

1 reference

DSSTox substance ID

2 references

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

matched by identifier from

FPIOBTBNRZPWJW-UHFFFAOYSA-N

DSSTOX compound identifier

0 references

875-677-6

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ECHA Substance Infocard ID

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Human Metabolome Database ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

FPIOBTBNRZPWJW-UHFFFAOYSA-N

3 references

language of work or name

pratensein (English)

5 October 2016

based on heuristic

inferred from InChIKey

matched by identifier from

FPIOBTBNRZPWJW-UHFFFAOYSA-N

2 references

Global Substance Registration System

language of work or name

PRATENSEIN (English)

5 October 2016

matched by identifier from

FPIOBTBNRZPWJW-UHFFFAOYSA-N

Probes And Drugs ID

0 references

1 reference

language of work or name

pratensein (English)

5 October 2016

0 references

0 references

Microsoft Academic ID

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Sitelinks

Wikipedia(7 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(1 entry)

commonswiki Category:Pratensein

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