prunetin (Q7253051)

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chemical compound

4',5-dihydroxy-7-methoxyisoflavone
5-hydroxy-3-(4-hydroxyphenyl)-7-methoxychromen-4-one
4',5-dihydroxy-7-methoxygenistein
7-O-methyl-genistein
5-hydroxy-3-(4-hydroxyphenyl)-7-methoxy-4-benzopyrone
5-hydroxy-3-(4-hydroxyphenyl)-7-methoxy-4H-1-benzopyran-4-one
5,4'-dihydroxy-7-methoxyisoflavone
padmakastein
prunusetin

Language	Label	Description	Also known as
English	prunetin	chemical compound	4',5-dihydroxy-7-methoxyisoflavone 5-hydroxy-3-(4-hydroxyphenyl)-7-methoxychromen-4-one 4',5-dihydroxy-7-methoxygenistein 7-O-methyl-genistein 5-hydroxy-3-(4-hydroxyphenyl)-7-methoxy-4-benzopyrone 5-hydroxy-3-(4-hydroxyphenyl)-7-methoxy-4H-1-benzopyran-4-one 5,4'-dihydroxy-7-methoxyisoflavone padmakastein prunusetin

Statements

type of chemical entity

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chemical structure

Prunetin.svg
685 × 315; 14 KB

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image of molecular model or crystal lattice model

Prunetin-3D-balls.png
2,000 × 1,029; 341 KB

ball-and-stick model

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284.068473 dalton

1 reference

language of work or name

Prunetin (English)

3 October 2016

chemical formula

C₁₆H₁₂O₅

1 reference

language of work or name

Prunetin (English)

3 October 2016

canonical SMILES

COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)O)O

1 reference

language of work or name

Prunetin (English)

3 October 2016

Trifolium pratense

3 references

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

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

New genistein monogalactoside from the aerial part of Trifolium pratense

3 references

Flavonoid variation in the leaves of Glycyrrhiza glabra

Flavonoids of Glycyrrhiza glabra

Flavonoids of Glycyrrhiza glabra

Cladrastis platycarpa

1 reference

A New Pterocarpan from the Heartwood of Cladrastis platycarpa

Achlys triphylla

1 reference

Four flavonol glycosides from Achlys triphylla

Derris laxiflora

2 references

Two New Flavanones and Two New Chalcones from the Root of Derris laxiflora BENTH.

Three New Flavonoids, 3'-Methoxylupinifolin, Laxifolin, and Isolaxifolin from the Roots of Derris laxiflora BENTH.

3 references

Amorphane Sesquiterpenes from a Marine Streptomyces sp.1

Amorphane sesquiterpenes from a marine Streptomyces sp.

Amorphane sesquiterpenes from a marine Streptomyces sp.

2 references

Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa

Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa

Myristica malabarica

3 references

An isoflavone from Myristica malabarica

An isoflavone from Myristica malabarica

An isoflavone from Myristica malabarica

Ochna calodendron

2 references

Triflavonoids of Ochna calodendron

Triflavonoids of Ochna calodendron

3 references

Antioxidant polyphenols from tart cherries (Prunus cerasus).

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

2 references

Andinermals A-C, antiplasmodial constituents from Andira inermis

Antiplasmodial activity of isoflavones from Andira inermis

Butea monosperma

2 references

Constituents of the stem bark from <em>Butea monosperama</em> (Leguminosae)

Osteogenic activity of constituents from Butea monosperma

Dalbergia sissoo

1 reference

Phytochemical and Pharmacological Studies of Dalbergia sissoo Growing in Egypt

Glycyrrhiza pallidiflora

2 references

Structures of Prenylated Dihydrochalcone, Gancaonin J and Homoisoflavonone, Gancaonin K from Glycyrrhiza pallidiflora

Structures of Prenylated Dihydrochalcone, Gancaonin J and Homoisoflavonone, Gancaonin K from Glycyrrhiza pallidiflora

1 reference

Aphanomyces euteiches zoospore attractant isolated from pea root ; Prunetin.

Pterocarpus soyauxii

1 reference

Flavonoid analogues from Pterocarpus species

Crotalaria lachnophora

2 references

Antimicrobial isopropenyl-dihydrofuranoisoflavones from Crotalaria lachnophora

Antimicrobial isopropenyl-dihydrofuranoisoflavones from Crotalaria lachnophora

Neolitsea daibuensis

2 references

Secondary metabolites from the roots of Neolitsea daibuensis and their anti-inflammatory activity

Secondary metabolites from the roots of Neolitsea daibuensis and their anti-inflammatory activity

Dalbergia odorifera

1 reference

Liquid chromatography/electrospray ionization mass spectrometry for the characterization of twenty-three flavonoids in the extract of Dalbergia odorifera

Andira surinamensis

1 reference

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

1 reference

Osteogenic activity of constituents from Butea monosperma

Flemingia macrophylla

1 reference

Neuroprotective flavonoids from Flemingia macrophylla

1 reference

Phenolic constituents of Iris milesii rhizomes

Millettia erythrocalyx

2 references

New flavones from Millettia erythrocalyx

Flavonoids from the roots of Millettia erythrocalyx

Pterocarpus angolensis

4 references

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

An isoflavone from Pterocarpus santalinus

354. The chemistry of extractives from hardwoods. Part VII. Constituents of muninga, the heartwood of pterocarpus angolensis. B : 2 : 4-dihydroxyphenyl 1-p-methoxyphenylethyl ketone (angolensin)

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

Genista tridentata

2 references

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

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

Prunus armeniaca

3 references

Antioxidant polyphenols from tart cherries (Prunus cerasus).

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

Dalbergia coromandeliana

1 reference

Coromandelin, a New Isoflavone Apioglucoside from the Leaves of Dalbergia coromandeliana

Arabidopsis thaliana

1 reference

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

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.).

Dermatophyllum secundiflorum

1 reference

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

Styphnolobium japonicum

1 reference

A new coumaronochromone from Sophora japonica

Prunus cerasoides

1 reference

Puddumin-A, a New Flavanone Glucoside from Prunus cerasoides

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

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

Prunus serrulata

1 reference

A note on the components of the bark ofPrunus puddum

physically interacts with

Aldehyde dehydrogenase 2 family member

subject has role

enzyme inhibitor

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

language of work or name

17 August 2016

has characteristic

1 reference

Commons category

Prunetin

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Identifiers

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

1 reference

language of work or name

Prunetin (English)

3 October 2016

KQMVAGISDHMXJJ-UHFFFAOYSA-N

2 references

language of work or name

Prunetin (English)

3 October 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

language of work or name

prunetin (English)

3 October 2016

KQMVAGISDHMXJJ-UHFFFAOYSA-N

CAS Common Chemistry

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=552-59-0

1 reference

language of work or name

Prunetin (English)

3 October 2016

2 references

language of work or name

Prunetin (English)

3 October 2016

matched by identifier from

KQMVAGISDHMXJJ-UHFFFAOYSA-N

Reaxys registry number

292155

1 reference

language of work or name

prunetin (English)

3 October 2016

mapping relation type

2 references

language of work or name

prunetin (English)

3 October 2016

matched by identifier from

International Chemical Identifier

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

1 reference

language of work or name

PRUNETIN (English)

3 October 2016

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

KQMVAGISDHMXJJ-UHFFFAOYSA-N

UniChem compound ID

1 reference

MassBank accession ID

MSBNK-BS-BS003052

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MSBNK-BS-BS003053

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MSBNK-BS-BS003054

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MSBNK-BS-BS003055

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MSBNK-BS-BS003056

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splash10-0159-0090000000-a85c6c3392aa2541b48c

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splash10-001i-0090000000-11b97ad586d2e24e7115

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splash10-014r-0090000000-fb797f4684174e26b1d0

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splash10-014i-0090000000-6db4d2441911d696b121

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splash10-03di-1932800000-7ba8925a2b1306b10b50

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splash10-01k0-0090000000-0cec22133db876cbe6e4

0 references

splash10-0udi-0190000000-b6ecb3ccb54bdeacbe00

0 references

DSSTox substance ID

2 references

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

matched by identifier from

KQMVAGISDHMXJJ-UHFFFAOYSA-N

DSSTOX compound identifier

0 references

209-018-5

1 reference

Global Substance Registration System

language of work or name

PRUNETIN (English)

3 October 2016

ECHA Substance Infocard ID

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

5-hydroxy-3-(4-hydroxyphenyl)-7-methoxy-4-benzopyrone (English)

CAS no.: 552-59-0 (English)

Guide to Pharmacology Ligand ID

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

language of work or name

prunetin (English)

3 October 2016

Human Metabolome Database ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

KQMVAGISDHMXJJ-UHFFFAOYSA-N

3 references

language of work or name

prunetin (English)

3 October 2016

based on heuristic

inferred from InChIKey

matched by identifier from

KQMVAGISDHMXJJ-UHFFFAOYSA-N

2 references

Global Substance Registration System

language of work or name

PRUNETIN (English)

3 October 2016

matched by identifier from

KQMVAGISDHMXJJ-UHFFFAOYSA-N

Probes And Drugs ID

0 references

1 reference

language of work or name

prunetin (English)

3 October 2016

0 references

1 reference

Freebase Data Dumps

publication date

28 October 2013

Microsoft Academic ID

0 references

Sitelinks

Wikipedia(7 entries)

azbwiki پرونتین
enwiki Prunetin
eowiki Prunetino
fawiki پرونتین
plwiki Prunetyna
shwiki Prunetin
srwiki Prunetin

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:Prunetin

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