ononin (Q7094502)

3-(4-methoxyphenyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

Ononin (English)

5 October 2016

2 references

3-(4-methoxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

2 references

3-(4-methoxyphenyl)-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

2 references

3-(4-methoxyphenyl)-7-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

1 reference

3-(4-methoxyphenyl)-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

1 reference

chemical formula

C₂₂H₂₂O₉

1 reference

Ononin (English)

5 October 2016

COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O

1 reference

Ononin (English)

5 October 2016

COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O

1 reference

Chemical analysis of Radix Astragali (Huangqi) in China: a comparison with its adulterants and seasonal variations

Ononin (English)

5 October 2016

1 reference

Astragalus hoantchy

1 reference

Chemical analysis of Radix Astragali (Huangqi) in China: a comparison with its adulterants and seasonal variations

Astragalus lehmannianus

1 reference

Chemical analysis of Radix Astragali (Huangqi) in China: a comparison with its adulterants and seasonal variations

Astragalus lepsensis

1 reference

Chemical analysis of Radix Astragali (Huangqi) in China: a comparison with its adulterants and seasonal variations

Astragalus membranaceus

4 references

Chemical analysis of Radix Astragali (Huangqi) in China: a comparison with its adulterants and seasonal variations

Flavonoids and phenol carboxylic acids in the oriental medicinal plant Astragalus membranaceus acclimated in Poland.

Liquid chromatography-electrospray ionization mass spectrometry study of the flavonoids of the roots of Astragalus mongholicus and A. membranaceus

Micellar electrokinetic chromatography for the quantitative analysis of flavonoids in the radix of Astragalus membranaceus var. mongholicus

Astragalus propinquus

1 reference

Chemical analysis of Radix Astragali (Huangqi) in China: a comparison with its adulterants and seasonal variations

Astragalus sieversianus

1 reference

Chemical analysis of Radix Astragali (Huangqi) in China: a comparison with its adulterants and seasonal variations

Cicer arietinum

5 references

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

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

Cicer flexuosum

1 reference

Flavonoids of some species of Cicer of the Central Asian flora

Cicer mogoltavicum

1 reference

Isoflavonoids ofCiver mogoltavicum

Cicer pungens

1 reference

Flavonoids of some species of Cicer of the Central Asian flora

Cicer songaricum

2 references

Flavonoids of Cicer songoricum

Flavonoids of Cicer songoricum

soybean

3 references

Flavonoids ofGlycine hispida

Isoflavone glucoside stress metabolites of soybean leaves

Flavonoids ofGlycine hispida

liquorice

3 references

Chemical studies of Chinese licorice-roots. I. Elucidation of five new flavonoid constituents from the roots of Glycyrrhiza glabra L. collected in Xinjiang

Flavonoid constituents from Glycyrrhiza glabra hairy root cultures

Flavonoid constituents from Glycyrrhiza glabra hairy root cultures

Glycyrrhiza pallidiflora

3 references

Flavonoids and isoflavonoids of chemotaxonomic significance from Glycyrrhiza pallidiflora (Leguminosae)

Flavonoids from Glycyrrhiza pallidiflora hairy root cultures

Flavonoids from Glycyrrhiza pallidiflora hairy root cultures

Glycyrrhiza uralensis

3 references

Saponin and sapogenol. L. On the constituents of the roots of Glycyrrhiza uralensis Fischer from Xinjiang, China. Chemical structures of licorice-saponin L3 and isoliquiritin apioside

Flavonoid glycosides of the roots of Glycyrrhiza uralensis

Inhibition of neuraminidase activity by polyphenol compounds isolated from the roots of Glycyrrhiza uralensis

Hedysarum polybotrys

3 references

Chemical analysis of Radix Astragali (Huangqi) in China: a comparison with its adulterants and seasonal variations

Studies on the constituents of Hedysarum polybotrys Hand.-Mazz.

Studies on the constituents of Hedysarum polybotrys Hand.-Mazz.

Maackia amurensis

5 references

A prenylated flavanone from roots of Maackia amurensis subsp. Buergeri

Isoflavonoids of the bark and leaves ofMaackia amurensis

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

Isoflavonoids of the bark and leaves ofMaackia amurensis

A prenylated flavanone from roots of Maackia amurensis subsp. Buergeri

Ononis arvensis

1 reference

Phenolic compounds of Ononis arvensis. I

Ononis speciosa

1 reference

Resorcinol derivatives and other components of Ononis speciosa

Pluchea lanceolata

2 references

Allelopathic potential of the phenolics from the roots of Pluchea lanceolata

Formononetin 7-O-glucoside (ononin), an additional growth inhibitor in soils associated with the weed,Pluchea lanceolata (DC) C.B. Clarke (Asteraceae)

Sophora flavescens

1 reference

Activity of Ku Shen compounds againstStaphylococcus aureus andStreptococcus mutans

mountain clover

1 reference

Flavonoids of Trifolium montanum

Trifolium polyphyllum

1 reference

Flavonoids fromTrifolium polyphyllum

Trifolium aureum

2 references

Flavonoids ofTrifolium strepens

Flavonoids ofTrifolium strepens

Vigna radiata

1 reference

Flavonoids of Phaseolus aureus

Wisteria brachybotrys

4 references

Isoflavones from the gall and wood of Wisteria brachybotrys

Studies on inhibitors of skin tumor promotion, III. Inhibitory effects of isoflavonoids from Wisteria brachybotrys on Epstein-Barr virus activation

Studies on inhibitors of skin tumor promotion, III. Inhibitory effects of isoflavonoids from Wisteria brachybotrys on Epstein-Barr virus activation

Isoflavones from the gall and wood of Wisteria brachybotrys

Ammopiptanthus mongolicus

2 references

Three New Isoflavonoids from the Aerial Parts ofAmmopiptanthus mongolicus

Chemical study of plants of the mongolian flora isoflavones of Ammopiptanthus mongolicus

Amorpha fruticosa

1 reference

Isoflavone glycosides from the bark of Amorpha fruticosa

Butea frondosa

1 reference

Osteogenic activity of constituents from Butea monosperma

Caragana conferta

1 reference

Caragisides A - C, New Isoflavone Glucosides from Caragana conferta with Inhibition of Platelet Aggregation

Mucuna birdwoodiana

1 reference

Two new isoflavone glycosides from Mucuna birdwoodiana

Podocytisus caramanicus

1 reference

Effect of 7-O-beta-D-glucopyranosylchrysin and its aglycone chrysin isolated from Podocytisus caramanicus on estrogen receptor alpha transcriptional activity

Styphnolobium japonicum

1 reference

A new isoflavone glycoside from the stem bark of Sophora japonica

Thermopsis alterniflora

1 reference

Flavonoids of Thermopsis alterniflora

Thermopsis lupinoides

1 reference

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

reversed clover

1 reference

Flavonoids from Trifolium resupinatum var. microcephalum

Trifolium subterraneum

2 references

Bioactive Isoflavonols and Other Components fromTrifolium subterraneum

The acylated isoflavone glycosides from subterranean clover and red clover

Xanthium strumarium

1 reference

New thiazinediones and other components from Xanthium strumarium

Chesneya mongolica

1 reference

Three New Isoflavonoids from the Aerial Parts ofAmmopiptanthus mongolicus

Thermopsis californica

1 reference

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

Trifolium incarnatum

1 reference

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

Trifolium repens

1 reference

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

Cicer bijugum

1 reference

Cicer canariense

1 reference

Cicer chorassanicum

1 reference

Cicer cuneatum

1 reference

Cicer echinospermum

1 reference

Cicer pinnatifidum

1 reference

Cicer judaicum

1 reference

Cicer macracanthum

1 reference

Cicer microphyllum

1 reference

Cicer nuristanicum

1 reference

Cicer oxyodon

1 reference

Cicer reticulatum

1 reference

Cicer yamashitae

1 reference

Astragalus austrosibiricus

1 reference

Chemical analysis of Radix Astragali (Huangqi) in China: a comparison with its adulterants and seasonal variations

Cicer kopetdaghense

1 reference

Flavonoids of some species of Cicer of the Central Asian flora

Thermopsis lanceolata

1 reference

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

Butea monosperma

2 references

Osteogenic activity of constituents from Butea monosperma

Bioactive flavonoids of the flowers of Butea monosperma

Pueraria montana var. lobata

1 reference

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

Sophora tonkinensis var. tonkinensis

1 reference

A new pterocarpan, (-)-maackiain sulfate, from the roots of Sophora subprostrata

Cicer anatolicum

1 reference

Ononis spinosa

3 references

Spinonin, a novel glycoside from Ononis spinosa subsp. leiosperma.

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

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

Trifolium pratense

6 references

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

Determination of isoflavone glucoside malonates in Trifolium pratense L. (red clover) extracts: quantification and stability studies.

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

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

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

The acylated isoflavone glycosides from subterranean clover and red clover

Cicer tragacanthoides

1 reference

Flavonoids of some species of Cicer of the Central Asian flora

Astragalus trimestris

4 references

Flavonoids and phenol carboxylic acids in the oriental medicinal plant Astragalus membranaceus acclimated in Poland.

Chemical analysis of Radix Astragali (Huangqi) in China: a comparison with its adulterants and seasonal variations

Liquid chromatography-electrospray ionization mass spectrometry study of the flavonoids of the roots of Astragalus mongholicus and A. membranaceus

Micellar electrokinetic chromatography for the quantitative analysis of flavonoids in the radix of Astragalus membranaceus var. mongholicus

Astragalus mongholicus

4 references

Flavonoids and phenol carboxylic acids in the oriental medicinal plant Astragalus membranaceus acclimated in Poland.

Chemical analysis of Radix Astragali (Huangqi) in China: a comparison with its adulterants and seasonal variations

Liquid chromatography-electrospray ionization mass spectrometry study of the flavonoids of the roots of Astragalus mongholicus and A. membranaceus

Micellar electrokinetic chromatography for the quantitative analysis of flavonoids in the radix of Astragalus membranaceus var. mongholicus

Baptisia australis

1 reference

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

Deguelia scandens

1 reference

Isoflavone glycosides from Derris scandens

Identifiers

InChI

InChI=1S/C22H22O9/c1-28-12-4-2-11(3-5-12)15-10-29-16-8-13(6-7-14(16)18(15)24)30-22-21(27)20(26)19(25)17(9-23)31-22/h2-8,10,17,19-23,25-27H,9H2,1H3/t17-,19-,20+,21-,22-/m1/s1

1 reference

Ononin (English)

5 October 2016

2 references

Ononin (English)

5 October 2016

ChEBI release 2020-09-01

2 references

ononin (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=486-62-4

10 April 2021

1 reference

Ononin (English)

5 October 2016

2 references

English

title

Ononin (English)

retrieved

5 October 2016

Reaxys registry number

63067

1 reference

ononin (English)

5 October 2016

mapping relation type

2 references

English

title

ononin (English)

retrieved

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C22H22O9/c1-28-12-4-2-11(3-5-12)15-10-29-16-8-13(6-7-14(16)18(15)24)30-22-21(27)20(26)19(25)17(9-23)31-22/h2-8,10,17,19-23,25-27H,9H2,1H3/t17-,19-,20+,21-,22-/m1/s1

1 reference

ONONIN (English)

5 October 2016

2 references

splash10-014i-0090000000-73d57a2194a7712e79d1

1 reference

MassBank accession ID

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MSBNK-IPB_Halle-PB000745

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MSBNK-IPB_Halle-PB000746

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MSBNK-IPB_Halle-PB000781

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MSBNK-IPB_Halle-PB000782

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SPLASH

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splash10-014i-0090000000-496bc7f7d879774e97c3

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splash10-0gb9-0290000000-7668bb15644a7d8dc6f5

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splash10-001i-0000900000-c2d377d0b3d5d4de46a7

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splash10-014i-0090000000-fe72c6473532677b1425

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splash10-0gb9-0090100000-7c95282ec7095806ed5e

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splash10-0uxr-0090000000-ec827988d17ba7072dd0

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splash10-03di-0009000000-32224e82894f6f52341e

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splash10-014i-0091000000-0b8b699e053575b227f0

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splash10-001i-0000900000-8d92f94429b532d770ca

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splash10-014i-0090000000-422db14def1e9c6051a5

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splash10-014i-0090000000-4b795f781362c4e194b5

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splash10-014i-0090000000-4062d54bc295b78e3a14

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splash10-014i-0090000000-35348bf7e7685f7378f8

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splash10-014i-0090000000-e46dec2f65176dcbe76d

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splash10-014i-0190000000-8c26edd0fe5581b30b45

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splash10-014i-0090000000-78dd16aeabbde194ce8d

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splash10-014i-0090500000-f70bd611448779e8cc15

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splash10-014i-0090000000-f3127b96ec2ef7f4022a

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DSSTox substance ID

DTXSID70964089

1 reference

DSSTOX compound identifier

DTXCID501391801

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Human Metabolome Database ID

0 references

1 reference

Global Substance Registration System

ononin (English)

5 October 2016

2 references

UNII

Z0Z637970U

English

title

ONONIN (English)

retrieved

5 October 2016

0 references

1 reference