linarin (Q1775837)

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

Linarin (English)

14 October 2016

1 reference

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

2 references

5-hydroxy-2-(4-methoxyphenyl)-7-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-2-oxanyl]oxymethyl]-2-oxanyl]oxy]-1-benzopyran-4-one

2 references

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

1 reference

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

1 reference

chemical formula

C₂₈H₃₂O₁₄

1 reference

Linarin (English)

14 October 2016

CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O

1 reference

Linarin (English)

14 October 2016

C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O

1 reference

Linarin (English)

14 October 2016

1 reference

Buddleja officinalis

5 references

Marrying structure and genomics

A new iridoid and effect on the rat aortic vascular smooth muscle cell proliferation of isolated compounds from Buddleja officinalis

Study on anti-cataract drugs from natural sources. II. Effects of buddlejae flos on in vitro aldose reductase activity

A new iridoid and effect on the rat aortic vascular smooth muscle cell proliferation of isolated compounds from Buddleja officinalis

Buddleja curviflora

1 reference

Buddleja davidii

1 reference

Buddleja globosa

3 references

Effects of Buddleja globosa leaf and its constituents relevant to wound healing

Anti-hepatotoxic activity of extracts and constituents of Buddleja species

Achillea pannonica

1 reference

Flavon- and flavonolglycosides from Achillea pannonica Scheele.

Clinopodium acinos

1 reference

Acacetin glycosides as taxonomic markers in Calamintha and Micromeria

Artemisia monosperma

2 references

Flavonoid glycosides of Artemisia monosperma and A. herba-alba

Flavonoids of Artemisia judaica, A. Monosperma and A. herba-alba

Buddleja cordata

3 references

In vitro evaluation of the amebicidal activity of Buddleia cordata (Loganiaceae, H.B.K.) on several strains of Acanthamoeba.

A Comparative Study of the Analgesic and Anti-Inflammatory Activities of Pectolinarin Isolated fromCirsium subcoriaceumand Linarin Isolated fromBuddleia cordata

Analgesic and antipyretic activities of an aqueous extract and of the flavone linarin of Buddleia cordata

Buddleja fallowiana

1 reference

Study on chemical constituents of Achillea alpina

Buddleja lindleyana

1 reference

Studies on chemical constituents of Rabdosia serra

Buddleja parviflora

1 reference

Flavonoids from Buddleja parviflora

Buddleja scordioides

2 references

Triterpenoid saponins and other glycosides from Buddleja scordioides

Photoprotective activity of Buddleja scordioides

Chrysanthemum boreale

1 reference

Isolation of aldose reductase inhibitors from the flowers ofChrysanthemum boreale

Chrysanthemum lavandulifolium

1 reference

Isolation of aldose reductase inhibitors from the flowers ofChrysanthemum boreale

Cirsium arvense

1 reference

A flavonoid glycoside from Cirsium arvense

Cirsium japonicum

3 references

A flavone diglycoside from Cirsium japonicum var. ussuriense

A flavone diglycoside from Cirsium japonicum var. ussuriense

Constituents from charred Cirsium japonicum

Cirsium rhinoceros

1 reference

Flavonoids of Cirsium heterophyllum

Cyclotrichium niveum

1 reference

Flavanones from Cyclotrichium niveum

Elsholtzia ciliata

1 reference

Flavonoids ofElscholtzia cristata

Hortia longifolia

1 reference

Constituents of Eurycoma longifolia

Linaria japonica

1 reference

Isolation of Isolinariins A and B, New Flavonoid Glycosides from Linaria japonica

Linaria kokanica

1 reference

Acacetin and its glycosides in plants of the genus Linaria

Linaria kurdica

1 reference

Acacetin and its glycosides in plants of the genus Linaria

Linaria sessilis

1 reference

Acacetin and its glycosides in plants of the genus Linaria

Silene firma

3 references

Flavonoid glycosides fromMelandrium firmum

A phenolic amide and other constituents of Melandrium firmum

A phenolic amide and other constituents of Melandrium firmum

corn mint

2 references

Linarin, a selective acetylcholinesterase inhibitor from Mentha arvensis.

Linarin, a selective acetylcholinesterase inhibitor from Mentha arvensis.

Clinopodium albanicum

1 reference

Acacetin glycosides as taxonomic markers in Calamintha and Micromeria

Micromeria cristata

1 reference

Acacetin glycosides as taxonomic markers in Calamintha and Micromeria

Micromeria juliana

1 reference

Acacetin glycosides as taxonomic markers in Calamintha and Micromeria

Clinopodium album

1 reference

Acacetin glycosides as taxonomic markers in Calamintha and Micromeria

Monarda didyma

1 reference

Linarin aus dem kraut von Monarda didyma

Nardostachys jatamansi

1 reference

Two New Flavone Glycosides fromValeriana Jatamansi

Picnomon acarna

1 reference

Phenolics of Picnomon acarna

Pinus sylvestris

1 reference

O-acylated flavonoid glycosides of the needles ofPinus sylvestris IV. Di-p-coumaroylisoquercitrin

Pratia nummularia

1 reference

Secondary Metabolites in Cyanobacteria

Robinia pseudoacacia

1 reference

The Constituents of the Leaves of Robinia Pseudoacacia

Satureja cuneifolia

1 reference

Acacetin glycosides as taxonomic markers in Calamintha and Micromeria

Satureja kitaibelii

1 reference

Acacetin glycosides as taxonomic markers in Calamintha and Micromeria

Satureja montana

1 reference

Acacetin glycosides as taxonomic markers in Calamintha and Micromeria

Scoparia dulcis

1 reference

8-Hydroxytricetin 7-glucuronide, a β-glucuronidase inhibitor from Scoparia dulcis

Scutellaria caucasica

1 reference

Investigation of the flavonoids ofScutellaria polyodon. II

Teucridium parvifolium

2 references

Scutellarein 4'-methyl ether glycosides as taxonomic markers in Teucridium and Tripora (Lamiaceae, Ajugoideae).

Scutellarein 4'-methyl ether glycosides as taxonomic markers in Teucridium and Tripora (Lamiaceae, Ajugoideae).

Thalictrum simplex

2 references

A flavonoid glycoside and hydrocarbons and sterols from Thalictrum simplex

A flavonoid glycoside and hydrocarbons and sterols from Thalictrum simplex

Artemisia rupestris

1 reference

New guaiane sesquiterpenes from Artemisia rupestris and their inhibitory effects on nitric oxide production

Anaphalis sinica

1 reference

Chemical Components ofAnaphalis SinicaHance

Bombax malabaricum

1 reference

Phytochemical investigation and biological studies of Bombax malabaricum flowers.

Chrysanthemum indicum

1 reference

Medicinal flowers. I. Aldose reductase inhibitors and three new eudesmane-type sesquiterpenes, kikkanols A, B, and C, from the flowers of Chrysanthemum indicum L

Chrysanthemum naktongense

1 reference

Sesquiterpenes and other constituents from Dendranthema zawadskii var. latilobum

Fagopyrum acutatum

1 reference

A new flavonol derivative from Fagopyrum dibotrys

Fagopyrum dibotrys

1 reference

A new flavonol derivative from Fagopyrum dibotrys

Hedysarum setigerum

1 reference

Secondary Metabolites from Hedysarum setigerum

Hyssopus officinalis

1 reference

Two new flavonoid glycosides from the whole herbs of Hyssopus officinalis

Isatis tinctoria

1 reference

New alkaloids from Isatis indigotica

Linaria vulgaris

1 reference

Über die Glykoside der Blüten von Linaria vulgaris L.: Die Konstitution des Linarins und des Pektolinarins

Ophryosporus heptanthus

1 reference

Antioxidant activity of diterpenes and polyphenols from Ophryosporus heptanthus

Dendranthema indicum

1 reference

Medicinal flowers. I. Aldose reductase inhibitors and three new eudesmane-type sesquiterpenes, kikkanols A, B, and C, from the flowers of Chrysanthemum indicum L

Chrysanthemum morifolium

1 reference

Special Effect of Ionic Liquids on the Extraction of Flavonoid Glycosides from Chrysanthemum morifolium Ramat by Microwave Assistance.

Clinopodium thymifolium

1 reference

Acacetin glycosides as taxonomic markers in Calamintha and Micromeria

Dendranthema zawadskii

1 reference

The effect of linarin on LPS-induced cytokine production and nitric oxide inhibition in murine macrophages cell line RAW264.7.

Kalanchoe pinnata

1 reference

Two new flavonol glycosides and a metabolite profile of Bryophyllum pinnatum, a phytotherapeutic used in obstetrics and gynaecology.

Cirsium oleraceum

1 reference

Effect of flavonoids on development of experimental gastric dystrophies in mice

Bombax ceiba

1 reference

Phytochemical investigation and biological studies of Bombax malabaricum flowers.

Teucrium parvifolium

1 reference

Scutellarein 4'-methyl ether glycosides as taxonomic markers in Teucridium and Tripora (Lamiaceae, Ajugoideae).

Fagopyrum cymosum

1 reference

A new flavonol derivative from Fagopyrum dibotrys

Mentha pulegium

1 reference

Acacetin glycosides as taxonomic markers in Calamintha and Micromeria

Identifiers

InChI

InChI=1S/C28H32O14/c1-11-21(31)23(33)25(35)27(39-11)38-10-19-22(32)24(34)26(36)28(42-19)40-14-7-15(29)20-16(30)9-17(41-18(20)8-14)12-3-5-13(37-2)6-4-12/h3-9,11,19,21-29,31-36H,10H2,1-2H3/t11-,19+,21-,22+,23+,24-,25+,26+,27+,28+/m0/s1

1 reference

Linarin (English)

14 October 2016

1 reference

Global Substance Registration System

Linarin (English)

14 October 2016

2 references

linarin (English)

14 October 2016

https://commonchemistry.cas.org/detail?cas_rn=480-36-4

10 April 2021

1 reference

Acaciin (English)

14 October 2016

2 references

English

Linarin (English)

14 October 2016

1 reference

ACACIIN (English)

14 October 2016

2 references

MSBNK-Univ_Toyama-TY000123

1 reference

MassBank accession ID

MSBNK-RIKEN-PR020027

0 references

MSBNK-RIKEN-PR100356

0 references

MSBNK-RIKEN-PR100803

0 references

0 references

SPLASH

splash10-000i-0090110000-6a1d15f692a61627148e

0 references

splash10-001i-0090000000-c22055dc866c88d0b4e4

0 references

splash10-0006-0000190000-4eb4e1f00fdf4519124d

0 references

splash10-0006-0000090000-33a18c0f8b9e257236c4

0 references

splash10-0007-0000490000-5b7b1714772441e6fbca

0 references

splash10-000b-0060910000-856faff8b84226c0d7c5

0 references

splash10-000i-0090000000-71e44776b99d338e52d4

0 references

splash10-000i-0090000000-6836318fce072fd01048

0 references

splash10-000i-0090000000-c1948d674ad498d7e35a

0 references

splash10-0006-0000090000-21a706df015b92c9ce58

0 references

splash10-001i-0090000000-f7970a932cbf0610baec

0 references

splash10-001i-0090000000-96aa5be3ec387cd12344

0 references

splash10-001i-0090000000-91a6327379cca1853857

0 references

splash10-001i-0090000000-eaccd63e27f1d2873b2e

0 references

splash10-0160-0090000000-93195b841969ebc588be

0 references

DSSTox substance ID

DTXSID40197382

2 references

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

DSSTOX compound identifier

DTXCID50119873

0 references

EC number

207-547-6

1 reference

Global Substance Registration System

English

linarin (English)

ECHA Substance Infocard ID

14 October 2016

100.006.862

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.006.862

27 December 2018

7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-5-hydroxy-2-(4-methoxyphenyl)-4H-benzopyran-4-one (English)

quotation

CAS no.: 480-36-4 (English)

2 references

Global Substance Registration System

English

linarin (English)

14 October 2016

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

0 references

1 reference

15 January 2022