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Flavonolignan

class of chemical compounds, any lignan condensed with a 2-aryl-1-benzopyran skeleton and its substituted derivatives

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Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionJan 15, 2026
Entity authorityQ3073502
Source-derived summary

Flavonolignans are natural phenols composed of a part flavonoid and a part phenylpropane.

Examples

Flavonolignans identified in Silybum marianum (milk thistle) silymarin complex include silibinin, silychristin, silydianin, dehydrosilybin, deoxysilycistin, deoxysilydianin, silandrin, silybinome, silyhermin and neosilyhermin and can be produced in vitro. Silibinin is found in the roots of S. marianum while silyamandin can be found in the fruit.

Hydnocarpin can be found naturally in Onopordon corymbosum and can be synthesised.

Scutellaprostin A, B, C, D, E and F can be isolated from Scutellaria prostrata and can also be synthesized.

Hydnowightin can be isolated from Hydnocarpus wightianus seeds.

Three flavonolignans derived from the flavone tricin have been isolated from the herb Avena sativa.

Palstatin has been isolated from the Amazon tree Hymeneae palustris.

Salcolin A and salcolin B can be found in Salsola collina.

Rhodiolin, the product of the oxidative coupling of coniferyl alcohol with the 7,8-dihydroxy grouping of the flavonol herbacetin, can be found in the rhizome of Rhodiola rosea.

Editorial summary

The public source identifies “Flavonolignan” as class of chemical compounds, any lignan condensed with a 2-aryl-1-benzopyran skeleton and its substituted derivatives. This brief keeps that definition visible, then builds a research path around Flavonolignan, class and chemical.

Editorial reviewUseful for establishing the present vocabulary of the subject while preserving a route back to the evidence on which that vocabulary rests. The current 160-word lead offers orientation but no explicit four-digit date, so chronology should not be assumed. The selected authority fields contribute no independent date. Its value is orientation rather than verdict, with Flavonolignan, class and chemical providing the first useful test.
Editorial analysis

Why this record matters

A short description can identify a subject without explaining its stakes. For “Flavonolignan”, the useful work is to connect “class of chemical compounds, any lignan condensed with a 2-aryl-1-benzopyran skeleton and its substituted derivatives” to the records capable of establishing context and consequence.

Evidence profile

The date and method of observation matter as much as the stated conclusion, especially where classification or consensus has changed. The source revision retrieved here is dated Jan 15, 2026. The linked authority identifier is Q3073502. None of the 0 selected statements returned an explicit reference.

Critical limits

Scientific names, classifications and consensus can change while older terminology persists in catalogues and historical literature. The lead is largely declarative, so disagreement and counter-evidence require a deliberate search beyond the opening account. Authority statements aid reconciliation but still require their own references, qualifiers and ranks to be checked.

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Primary datasets, specimen catalogues, standards bodies and the most recent peer-reviewed literature.

Three-step research path

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  2. Expand the search: follow Flavonolignan primary sources, Flavonolignan archive and Flavonolignan research across catalogues and specialist indexes.
  3. Test the account: compare the strongest cited source with the responsible institution’s current record and note any disagreement.

Questions for further research

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Source & attribution

This entry incorporates text from Flavonolignan” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.