(Q3459109)

Isosakuranetin (English)

5 October 2016

2 references

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₁₆H₁₄O₅

1 reference

Isosakuranetin (English)

20 November 2016

canonical SMILES

COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O

1 reference

Isosakuranetin (English)

20 November 2016

isomeric SMILES

COC1=CC=C(C=C1)[C@@H]2CC(=O)C3=C(C=C(C=C3O2)O)O

1 reference

Isosakuranetin (English)

20 November 2016

found in taxon

Populus grandidentata

2 references

Chemotaxonomy of section Leuce poplars by GC-MS of bud exudate

Bud exudate composition of Populus tremuloides

Populus tremula

1 reference

Chemotaxonomy of section Leuce poplars by GC-MS of bud exudate

Populus tremuloides

2 references

Chemotaxonomy of section Leuce poplars by GC-MS of bud exudate

Bud exudate composition of Populus tremuloides

Populus tristis

1 reference

Analysis of Phenolics of Bud Exudate of Populus tristis by GC/MS

Populus laurifolia

1 reference

Notes: Analysis of Phenolics of Bud Exudate of Populus laurifolia by GC-MS

Populus koreana

1 reference

Analysis of Phenolics of Bud Exudates of Populus koreana, Populus maximowiczii and Populus suaveolens by GC-MS

Populus suaveolens

1 reference

Analysis of Phenolics of Bud Exudates of Populus koreana, Populus maximowiczii and Populus suaveolens by GC-MS

Populus maximowiczii

1 reference

Analysis of Phenolics of Bud Exudates of Populus koreana, Populus maximowiczii and Populus suaveolens by GC-MS

Populus cathayana

1 reference

Analysis of Phenolics of Bud Exudates of Populus cathayana and Populus szechuanica by GC-MS

Populus szechuanica

1 reference

Analysis of Phenolics of Bud Exudates of Populus cathayana and Populus szechuanica by GC-MS

Chromolaena odorata

6 references

Antimycobacterial activity and cytotoxicity of flavonoids from the flowers of Chromolaena odorata

Exudate flavonoids in a tropical weed, Chromolaena odorata (L.) R. M. King et H. Robinson

Chemical constituents from Polygonatum odoratum

Flavonoid glycosides from Chromolaena odorata leaves and their in vitro cytotoxic activity

Platelet-activating factor (PAF) receptor binding antagonist activity of the methanol extracts and isolated flavonoids from Chromolaena odorata (L.) King and Robinson

Flavonoids from Eupatorium odoratum with Death Receptor 5 Promoter Enhancing Activity

Piper crassinervium

1 reference

Benzoic acid derivatives from Piper species and their fungitoxic activity against Cladosporium cladosporioides and C. sphaerospermum

Artemisia campestris

4 references

A cadinane derivative from Artemisia crithmifolia

Chromones and flavanones from artemisia campestris subsp. maritima

Flavonoids from Artemisia campestris ssp. glutinosa

Chromones and flavanones from artemisia campestris subsp. maritima

Artemisia xanthochloa

1 reference

Prenylated coumarates from Artemisia xanthochroa

Baccharis dracunculifolia

2 references

Studies on the constituents from the aerial part of Baccharis dracunculifolia DC. II.

In vitro antileishmanial, antiplasmodial and cytotoxic activities of phenolics and triterpenoids from Baccharis dracunculifolia D. C. (Asteraceae).

Baccharis pingraea

1 reference

Diterpene glycosides and other constituents from argentinian baccharis species

Baccharis salicifolia

2 references

Sesqui- and diterpenes from Baccharis species

Diterpene glycosides and other constituents from argentinian baccharis species

Baccharis vaccinioides

1 reference

Flavonoids and Terpenoids from the Exudates of Some Baccharis Species

Calceolaria hypericina

1 reference

Phenylpropanoid glycosides from Calceolaria hypericina

Clinopodium laxiflorum

1 reference

Constituents of the Whole Herb ofClinoponium laxiflorum

Clinopodium umbrosum

1 reference

Constituents ofClinopodium Umbrosum

Commiphora socotrana

1 reference

7-O-methylaloeresin A--a new chromone glycoside from Commiphora socotrana

Cyclotrichium niveum

1 reference

Flavanones from Cyclotrichium niveum

Diplostephium cinereum

1 reference

Flavonoids in the trichome tesinous exudate from Diplosthepium cinereum

Dolichlasium lagascae

1 reference

α-Isocedrene derivatives, 5-methyl coumarins and other constituents from the subtribe nassauviinae of the compositae

Eriodictyon californicum

1 reference

Isolation of potential cancer chemopreventive agents from Eriodictyon californicum

Heteroplexis microcephala

1 reference

Chemical constituents of Heteroplexis micocephala.

Hypenia salzmannii

1 reference

(−)-Salzol, an isopimarane diterpene, and a chalcone from Hyptis salzmanii

Lycium bridgesii

1 reference

9-acetoxynerolidol from Phrodus bridgesii

Phrodus bridgesii

1 reference

9-acetoxynerolidol from Phrodus bridgesii

Plazia daphnoides

1 reference

Diterpenes and 5-methyl coumarin derivatives from Gypothamnium pinifolium and Plazia daphnoides

Proustia cuneifolia

1 reference

Coumarins and guaianolides from further chilean representatives of the subtribe nassauviinae

Prunus domestica

1 reference

Dihydroflavonols from Prunus domestica

Tanacetum sibiricum

1 reference

Flavonoids from Tanacetum vulgare flowers

Wyethia angustifolia

1 reference

Flavonoids of Wyethia angustifolia and W. helenioides

Wyethia glabra

1 reference

Flavonoids from Wyethia glabra

Wyethia helenioides

1 reference

Flavonoids of Wyethia angustifolia and W. helenioides

Baccharis leptocephala

1 reference

Diterpenes from Baccharis species

Piper marginatum

1 reference

Chemical constituents from Piper marginatum Jacq. (Piperaceae)—antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435)

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

Vitex quinata

1 reference

Phytochemical and Bioactivity Studies on Constituents of the Leaves of Vitex Quinata

Ageratina altissima

1 reference

Flavonoids from Eupatorium odoratum with Death Receptor 5 Promoter Enhancing Activity

Rosmarinus officinalis

1 reference

Phytochemical Profiling of Flavonoids, Phenolic Acids, Terpenoids, and Volatile Fraction of a Rosemary (Rosmarinus officinalis L.) Extract.

Prunus serrulata var. pubescens

1 reference

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

Citrus × paradisi

1 reference

Phenolic composition of various tissues of rutaceae species

Prunus avium

1 reference

Analysis of glycosylated flavonoids extracted from sweet-cherry stems, as antibacterial agents against pathogenic Escherichia coli isolates.

mandarin orange

1 reference

Discrimination of Citrus reticulata Blanco and Citrus reticulata 'Chachi' as well as the Citrus reticulata 'Chachi' within different storage years using ultra high performance liquid chromatography quadrupole/time-of-flight mass spectrometry based m

Citrus × deliciosa

1 reference

Discrimination of Citrus reticulata Blanco and Citrus reticulata 'Chachi' as well as the Citrus reticulata 'Chachi' within different storage years using ultra high performance liquid chromatography quadrupole/time-of-flight mass spectrometry based m

Populus trichocarpa

1 reference

Analysis of Phenolics of Bud Exudate of Populus tristis by GC/MS

Baccharis glutinosa

1 reference

Diterpene glycosides and other constituents from argentinian baccharis species

Xanthorrhoea preissii

1 reference

Some Constituents of the Resins of Xanthorrhoea preissii, australis and hastile

Xanthorrhoea australis

1 reference

Some Constituents of the Resins of Xanthorrhoea preissii, australis and hastile

Xanthorrhoea resinosa

1 reference

Some Constituents of the Resins of Xanthorrhoea preissii, australis and hastile

Identifiers

InChI

InChI=1S/C16H14O5/c1-20-11-4-2-9(3-5-11)14-8-13(19)16-12(18)6-10(17)7-15(16)21-14/h2-7,14,17-18H,8H2,1H3/t14-/m0/s1

1 reference

Isosakuranetin (English)

HMUJXQRRKBLVOO-AWEZNQCLSA-N

20 November 2016

InChIKey

2 references

Isosakuranetin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

480-43-3

2 references

Global Substance Registration System

UNII

U02X7TF8UA

isosakuranetin (English)

HMUJXQRRKBLVOO-AWEZNQCLSA-N

20 November 2016

InChIKey

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=480-43-3

1 reference

Isosakuranetin (English)

20 November 2016

1 reference

Isosakuranetin (English)

20 November 2016

Reaxys registry number

91627

1 reference

4'-methoxy-5,7-dihydroxyflavanone (English)

5 October 2016

ChEBI ID

27552

mapping relation type

1 reference

ISOSAKUTANETIN (English)

20 November 2016

1 reference

splash10-01vo-0490000000-41dadf703a87dca8bf84

ISOSAKUTANETIN (English)

20 November 2016

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

splash10-01vo-0490000000-901a287fd594fc9be735

0 references

splash10-0a4i-0190000000-999a218aa8042d2b6615

0 references

splash10-000i-0090000000-1a2a0e0133be7ea80b28

0 references

splash10-000i-0290000000-2551fc2983ce9ad034b8

0 references

splash10-0w29-0920000000-a6201b219da74be69430

0 references

splash10-0udi-0900000000-934741bc378aad093370

0 references

splash10-0udi-1900000000-a9d38a40865ddbd0ebc8

0 references

splash10-0udi-5900000000-6a07c0cf09c4310d725c

0 references

splash10-0udi-0920000000-d759e31423bd2dfc30bb

0 references

splash10-01vo-0490000000-7c431bd61a47a6f62c6b

0 references

DSSTox substance ID

DTXSID60963980

0 references

DSSTOX compound identifier

DTXCID701391702

0 references

EC number

207-551-8

1 reference

Global Substance Registration System

UNII

U02X7TF8UA

isosakuranetin (English)

ECHA Substance Infocard ID

20 November 2016

100.006.866

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.006.866

27 December 2018

Guide to Pharmacology Ligand ID

(S)-2,3-dihydro-5,7-dihydroxy-2-(4-methoxyphenyl)-4-benzopyrone (English)

quotation

CAS no.: 480-43-3 (English)

10299

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

5 February 2021

1 reference

Global Substance Registration System

4'-methoxy-5,7-dihydroxyflavanone (English)

5 October 2016

1 reference

UNII

U02X7TF8UA