(Q27106177)

Cirsiliol (English)

5 October 2016

C₁₇H₁₄O₇

1 reference

Cirsiliol (English)

5 October 2016

COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC

1 reference

Cirsiliol (English)

5 October 2016

Lantana montevidensis

2 references

The methoxylated flavones eupatorin and cirsiliol induce CYP1 enzyme expression in MCF7 cells.

Antiproliferative constituents in plants 10. Flavones from the leaves of Lantana montevidensis Briq. and consideration of structure-activity relationship

Calanticaria greggii

1 reference

Flavonoids of Viguiera series Brevifoliae

Sideritis ochroleuca

1 reference

External and vacuolar flavonoids from ibero-North African Sideritis species. A chemosystematic approach

Sideritis hirsuta

1 reference

External and vacuolar flavonoids from ibero-North African Sideritis species. A chemosystematic approach

Sideritis jahandiezii

1 reference

External and vacuolar flavonoids from ibero-North African Sideritis species. A chemosystematic approach

Sideritis briquetiana

1 reference

External and vacuolar flavonoids from ibero-North African Sideritis species. A chemosystematic approach

Achillea kotschyi

1 reference

Distribution of externally accumulated flavonoid aglycones within the Achillea nobilis group

Lantana fucata

1 reference

Phenylethanoid glycosides from Lantana fucata with in vitro anti-inflammatory activity.

Salvia columbariae

2 references

[Flavones from Salvia officinalis L. 22. Components of Salvia off. L]

Salvia dorrii

2 references

[Flavones from Salvia officinalis L. 22. Components of Salvia off. L]

Salvia granitica

2 references

[Flavones from Salvia officinalis L. 22. Components of Salvia off. L]

Salvia guaranitica

4 references

Cirsiliol and caffeic acid ethyl ester, isolated from Salvia guaranitica, are competitive ligands for the central benzodiazepine receptors

Sedative and hypnotic properties of Salvia guaranitica St. Hil. and of its active principle, Cirsiliol.

[Flavones from Salvia officinalis L. 22. Components of Salvia off. L]

Salvia hypoleuca

2 references

[Flavones from Salvia officinalis L. 22. Components of Salvia off. L]

Salvia macrosiphon

2 references

[Flavones from Salvia officinalis L. 22. Components of Salvia off. L]

Salvia stenophylla

2 references

[Flavones from Salvia officinalis L. 22. Components of Salvia off. L]

Salvia verbenaca

2 references

[Flavones from Salvia officinalis L. 22. Components of Salvia off. L]

Achillea ageratum

1 reference

Germacranes and flavonoids from Achillea ageratum

Achillea millefolium

1 reference

A sesquiterpene lactone from Achillea millefolium subsp. Millefolium

Achillea setacea

1 reference

Leaf flavonoids of the Achillea Millefolium group part II: Distribution patterns of free aglycones in leaf exudates

Fridericia platyphylla

1 reference

Foliar epicuticular wax of Arrabidaea brachypoda: flavonoids and antifungal activity

Artemisia annua

1 reference

Methoxylated flavones and coumarins from Artemisia annua

Artemisia xanthochloa

1 reference

Flavanoids ofArtemisia xanthochroa

Baccharis flabellata

1 reference

A diterpene and flavonoids of Baccharis flabellata

Baccharis genistelloides

1 reference

Studies on the constituents of Baccharis genistelloides.

Centaurea sinaica

1 reference

Guaianolides from Centaurea sinaica

Centaurea urvillei

1 reference

Cytotoxic Flavones From Centaurea urvillei

Ferula aucheri

1 reference

Dorema aucheri, the first umbelliferous plant found to produce exudate flavonoids

Isodon japonicus

1 reference

Taibaijaponicains C and D: two new diterpenoids from Isodon japonica

Isodon tenuifolius

1 reference

Three New ent-Kauranoids from Isodon phyllostachys

Leucocyclus formosus

1 reference

Flavonoid Aglycones in the Leaf Exudate of the Genus Leucocyclus (Compositae)

Aloysia citrodora

1 reference

Flavonoids from Lippia citriodora

Lycopus europaeus

1 reference

Flavones from the aerial parts of Lycopus europaeus

Passiflora menispermifolia

1 reference

C-Glycosylflavonoids and Other Compounds From Passiflora cyanea, P. oerstedii and P. menispermifolia

Isodon angustifolius

1 reference

Crystal Structure of a 1:1 Complex of Natural Diterpenoids: Absolute Configurations and Unambiguous NMR Spectral Assignments of Neoangustifolin and Epinodosinol

Isodon rubescens

1 reference

Structure and Bonding

Salvia lineata

1 reference

Clerodane diterpenoids of Salvia lineata

Salvia montbretii

1 reference

Triterpenoids from the aerial parts of Salvia montbretii

Salvia rhyacophila

1 reference

Clerodane and aromatic seco-clerodane diterpenoids from salvia rhyacophua.

Salvia tonalensis

1 reference

Languidulane, clerodane and secoclerodane diterpenes from Salvia tonalensis

Sideritis algarviensis

1 reference

A chemotaxonomical study of some portuguese Sideritis species

Sideritis angustifolia

2 references

A chemotaxonomical study of some portuguese Sideritis species

Verification of Sideritis incana X S. angustifolia hybrids by flavonoid analysis

Sideritis arborescens

1 reference

A chemotaxonomical study of some portuguese Sideritis species

Sideritis leucantha

2 references

An HPLC study of flavones from some Spanish Sideritis species

Seasonal Variation of Free Flavone Aglycones from Sideritis leucantha (Lamiaceae)

Teucrium chamaedrys

1 reference

Steroidal compounds from Teucrium chamaedrys subsp. Chamaedrys

Teucrium divaricatum

1 reference

Rearranged abietane diterpenes from Teucrium divaricatum subsp. Villosum

Teucrium kotschyanum

1 reference

Neo-clerodane diterpenoids from Teucrium kotschyanum

Teucrium lepicephalum

1 reference

Neo-clerodane diterpenoids from teucrium lepicephalum and teucrium buxifolium

Teucrium montanum

1 reference

Neo-clerodane diterpenoids from teucrium montanum

Teucrium nudicaule

1 reference

BioactiveNeo-Clerodane Diterpenoids TowardTenebrio MolitorLarvae fromTeucrium nudicauleH. andBaccharis spicata(Lam.) Beill

Teucrium oliverianum

1 reference

Neocleordane Diterpenoids and Their Artifacts from Teucrium olivarianum

Teucrium polium

2 references

A chlorine-containing and two 17β-neo-clerodane diterpenoids from Teucrium polium subsp. Vincentinum

Methylated Flavones fromTeucrium polium

Teucrium stocksianum

1 reference

Methylated Flavones ofTeucrium stocksianum

Teucrium yemense

1 reference

Neo-clerodane diterpenoids from Teucrium yemense

Thymus herba-barona

1 reference

Free flavonoid aglycones from Thymus herba barona and its monoterpenoid chemotypes

Wilkesia hobdyi

1 reference

Nonpolar flavonoids of Wilkesia and Argyroxiphium

Phyla nodiflora

1 reference

HPLC-fingerprints and antioxidant constituents of Phyla nodiflora.

Achillea millefolium var. millefolium

1 reference

A sesquiterpene lactone from Achillea millefolium subsp. Millefolium

Brickellia dentata

1 reference

Flavonoids from Brickellia chlorolepis and B. dentata

African blue basil

1 reference

Distribution of 8-oxygenated leaf-surface flavones in the genus Ocimum

Salvia limbata

1 reference

Flavones and rosmarinic acid from Salvia limbata

Salvia officinalis

3 references

[Flavones from Salvia officinalis L. 22. Components of Salvia off. L]

Neo-clerodane and languidulane diterpenoids from Salvia sousae and S. karwinskii

Clerodane-type diterpenoids from Salvia sousae

Hydnora johannis

1 reference

Antibacterial activity, cytotoxicity and chemical constituents of Hydnora johannis roots

Sideritis maireana

1 reference

External and vacuolar flavonoids from ibero-North African Sideritis species. A chemosystematic approach

Hydnora abyssinica

1 reference

Antibacterial activity, cytotoxicity and chemical constituents of Hydnora johannis roots

Pisum sativum

1 reference

Microwave drying effects on drying kinetics, bioactive compounds and antioxidant activity of green peas (Pisum sativum L.)

Baccharis venosa

1 reference

Studies on the constituents of Baccharis genistelloides.

Baccharis sagittalis

1 reference

Studies on the constituents of Baccharis genistelloides.

Centaurea raphanina

1 reference

Cytotoxic Flavones From Centaurea urvillei

Ocimum americanum

1 reference

Chemical profiling of Ocimum americanum using external flavonoids

Identifiers

InChI

InChI=1S/C17H14O7/c1-22-14-7-13-15(16(21)17(14)23-2)11(20)6-12(24-13)8-3-4-9(18)10(19)5-8/h3-7,18-19,21H,1-2H3

1 reference

Cirsiliol (English)

5 October 2016

2 references

Cirsiliol (English)

5 October 2016

ChEBI release 2020-09-01

2 references

cirsiliol (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=34334-69-5

9 April 2021

1 reference

Cirsiliol (English)

5 October 2016

2 references

English

Cirsiliol (English)

5 October 2016

Reaxys registry number

1354524

1 reference

cirsiliol (English)

5 October 2016

mapping relation type

2 references

English

cirsiliol (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C17H14O7/c1-22-14-7-13-15(16(21)17(14)23-2)11(20)6-12(24-13)8-3-4-9(18)10(19)5-8/h3-7,18-19,21H,1-2H3

1 reference

CIRSILIOL (English)

5 October 2016

2 references

inferred from InChIKey

MSBNK-Univ_Toyama-TY000127

1 reference

MassBank accession ID

0 references

MSBNK-Univ_Toyama-TY000211

0 references

SPLASH

splash10-056r-0009105000-cde208d24f6729ce75b8

0 references

splash10-0089-0698000000-805c80c3eb0013604024

0 references

DSSTox substance ID

DTXSID60187907

2 references

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

DSSTOX compound identifier

0 references

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.237.002

27 December 2018

ECHA Substance Infocard ID

[No public or meaningful name is available] (English)

quotation

CAS no.: 34334-69-5 (English)

100.237.002

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.237.002

27 December 2018

Human Metabolome Database ID

[No public or meaningful name is available] (English)

quotation

CAS no.: 34334-69-5 (English)

HMDB0250275

2 references

based on heuristic

inferred from InChIKey

3 references

cirsiliol (English)

5 October 2016

inferred from InChIKey

UNII

8W4Y5JK3XE

1 reference

0 references

1 reference