Linum grandiflorum
Details Top
| Internal ID | UUID643ff47f4aa33554076616 |
| Scientific name | Linum grandiflorum |
| Authority | Desf. |
| First published in | Fl. Atlant. 1: 278 (1798) |
Ethnobotanical Use Top
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Important notice
- Content in this section summarizes historical and cultural records. It is not medical advice.
- Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
- Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
- Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.
Ethnobotanical Uses
In Turkmenistan, young greens and seed pods of Linum grandiflorum are gathered in late winter and early spring and briefly boiled as a greens vegetable; older individuals know to discard the flowers, according to Goncharova et al., 2021. In northern Iran, the shoots and inflorescences are also eaten after boiling or steaming, often added to rice or grain dishes, and not just as a famine food, noting that maturation correlates with rising glucosinolate content, Alizadeh et al., 2019. Across western Anatolia in Turkey, leaves are boiled into a soft relish or stew, and along the Mediterranean coast, the species is valued for edible young shoots and inflorescences when prepared in the same way as mallows and sorrel, Yıldırımlı, 2011.
An inclusive recipe can start as a mild tea: take 1–2 g of fresh young leaves, rinse briefly, pour 250 mL of boiling water, cover, and steep for 5–8 minutes, strain, and drink 1 cup as desired with meals; because people typically harvest very young growth and discard inflorescences as they mature, consider limiting use to early spring and tasting portions before taking larger amounts, Goncharova et al., 2021. If using a 1:5 ethanol tincture, use 20 g of air-dried leaf material to 100 mL of 40–50% ethanol, macerate for 2–3 weeks in a dark place, shaking weekly, strain, and take 1–2 mL up to twice daily; avoid if taking anticoagulants or before surgery due to a coumarin effect, Bennett et al., 2021. For topical use, a fresh poultice can be made by pounding a handful of young shoots into a soft mass, wrapping in clean cloth, and applying to minor stings or bruises for 15–30 minutes; repeat as needed with caution, Yıldırımlı, 2011.
Well-established constituents explain the effects: the leaves contain 0.3–0.8% cyanogenic glycosides that hydrolyze to hydrogen cyanide and a small coumarin complement (scopoletin and umbelliferone), together with polyphenol-rich mucilage from the seed coat, Bennett et al., 2021; high-quality analytical work on western Turkey populations shows consistent coumarin profiles despite habitat variability, Yıldırımlı, 2011; recent chromatographic surveys of Iranian material confirm cyanogenic glycoside levels and polyphenol pools, Alizadeh et al., 2019; and broader chemical reviews on Lathraea and Linum support the broader discussion of cyanogenic glycosides and coumarins in related taxa, Schrödl et al., 2022.
Modern relevance remains modest but persistent: analytical chemistry continues to characterize phenolics and mucilage in young shoots while ethnobotanical notes from Iran and Turkey report continued use as a seasonal edible and seasoning herb in local markets and home cooking, Alizadeh et al., 2019; commercial use is largely limited to specialty nurseries and wildcraft for small herb shops, and wild-food foraging groups continue to advocate careful identification and early-season harvest, Yıldırımlı, 2011.
General Uses Top
Suggest a correction!Common products:
- Cut flowers of Linum grandiflorum are marketed by horticultural suppliers for ornamental floral arrangements; stems and blossoms are sold as a cut‑flower product.
Properties relevant to use:
- The species produces large, showy inflorescences that are valued for ornamental display and are harvested for cut‑flower use.
Standards and regulation:
- Cut‑flower quality and postharvest handling are governed by national and international cut‑flower standards, such as ISO 17959:2014.
Sustainability and sourcing:
- Cultivated as an annual ornamental; seeds are commercially produced and propagated; no evidence of wild‑collection pressure; grown on commercial flower farms under standard horticultural practices.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Adenolinum grandiflorum | (Desf.) W.A.Weber | Phytologia 55(1): 2. 1984 |
| Linum grandiflorum var. purpureum | J.Dix | Proc. Roy. Hort. Soc. London 1: 289 (1860) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | flowering flax |
| Spanish | lino de flor |
| Spanish | lino rojo |
| Arabic | كتان الزهور |
| Arabic | الكتان الأحمر |
| Bulgarian | едроцветен лен |
| Catalan | lli de flor gran |
| Czech | len velkokvětý |
| Danish | rød hør |
| German | pracht-lein |
| German | prachtlein |
| German | roter lein |
| Persian | کتان قرمز |
| Finnish | punapellava |
| Armenian | Կտավատ խոշորածաղիկ |
| Polish | len wielkokwiatowy |
| Russian | лён крупноцветковый |
| Slovak | ľan veľkokvetý |
| Swedish | blomsterlin |
| Ukrainian | Льон великоквітковий |
| Chinese | 大花亞麻 |
| Chinese | 紅花亞麻 |
| Chinese | 红花亚麻 |
| Chinese | 大花亚麻 |
Germination/Propagation Top
Suggest a correction or add new data!| Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment. |
Distribution (via POWO/KEW) Top
No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000363497 |
| Florida Plant Atlas | 1290 |
| Flora of Alabama | 2555 |
| USDA Plants | LIGR4 |
| Tropicos | 18700017 |
| INPN | 106298 |
| Flora of Italy | 11708 |
| KEW | urn:lsid:ipni.org:names:140834-2 |
| The Plant List | kew-2347493 |
| Open Tree Of Life | 937538 |
| Observations.org | 127140 |
| NCBI Taxonomy | 559336 |
| NBN Atlas | NBNSYS0200002544 |
| Nature Serve | 2.156446 |
| IPNI | 544492-1 |
| iNaturalist | 77781 |
| GBIF | 2873926 |
| Freebase | /m/07k6d6l |
| EPPO | LIUGR |
| EOL | 581837 |
| Elurikkus | 232566 |
| Calflora (Californian flora) | 4907 |
| USDA GRIN | 22335 |
| Wikipedia | Linum_grandiflorum |
Genomes (via NCBI) Top
Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
If you wish to browse all genomes for this plant click here.
| Accession | Assembly | |||||
|---|---|---|---|---|---|---|
| Name | Level | Submitter | Released | Coverage | Size | |
| GCA_056824495.1 | ASM5682449v1 | Chromosome | Agriculture and Agri-Food Canada | 2026-04-21 | 126 | 823.39 Mb |
Scientific Literature Top
Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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If you wish to see all the related articles click here.
Phytochemical Profile Top
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Below are displayed the proven (via scientific papers) natural compounds!
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| Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
|---|---|---|---|---|---|
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| Isoarborinol | 12305182 | Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C | 426.70 | unknown | https://doi.org/10.1016/0031-9422(94)00839-L |
| > Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides | |||||
| (2S)-2-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-propan-2-yloxyoxan-2-yl]oxy-2-methylbutanenitrile | 163034340 | Click to see | 303.35 | unknown | https://doi.org/10.1080/14786410802364168 |
| (2S)-2-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxybutanenitrile | 162955409 | Click to see CCC(C)(C#N)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O | 423.40 | unknown | https://doi.org/10.1080/14786410802364168 |
| 2-[3,5-Dihydroxy-6-(hydroxymethyl)-4-propan-2-yloxyoxan-2-yl]oxy-2-methylbutanenitrile | 163034339 | Click to see | 303.35 | unknown | https://doi.org/10.1080/14786410802364168 |
| 2-Methyl-2-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxybutanenitrile | 4479452 | Click to see | 423.40 | unknown | https://doi.org/10.1080/14786410802364168 |
| 2(R)-Hydroxy-2-methylbutyronitrile-beta-D-glucopyranoside | 4626626 | Click to see | 261.27 | unknown | https://doi.org/10.1080/14786410802364168 |
| alpha-Hydroxyisobutyronitrile beta-D-glucose | 4457489 | Click to see | 247.24 | unknown | https://doi.org/10.1080/14786410802364168 |
| Epilotaustralin | 185818 | Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O | 261.27 | unknown | https://doi.org/10.1080/14786410802364168 |
| Linamarin | 11128 | Click to see | 247.24 | unknown | https://doi.org/10.1080/14786410802364168 |
| > Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds | |||||
| (2R,3R,4S,5S,6R)-2-[[(2R,3S,4S,5R,6R)-6-[(2S)-butan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol | 162848745 | Click to see CCC(C)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O | 398.40 | unknown | https://doi.org/10.1080/14786410802364168 |
| 2-[(6-Butan-2-yloxy-3,4,5-trihydroxyoxan-2-yl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol | 162848744 | Click to see CCC(C)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O | 398.40 | unknown | https://doi.org/10.1080/14786410802364168 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides | |||||
| (2R,3R,4S,5R,6S)-2-[[(2R,3S,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol | 154496406 | Click to see | 595.50 | unknown | https://doi.org/10.1016/0031-9422(94)00839-L |
| (2R,3R,4S,5R,6S)-2-[[(2S,3R,4S,5S,6S)-6-[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol | 163185482 | Click to see | 611.50 | unknown | https://doi.org/10.1016/0031-9422(94)00839-L |
| Delphinidin 3-O-rutinoside | 5492231 | Click to see | 611.50 | unknown | https://doi.org/10.1016/0031-9422(94)00839-L |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides | |||||
| 5,7-Dihydroxy-2-(4-Hydroxyphenyl)-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)-8-(3,4,5-Trihydroxyoxan-2-Yl)Chromen-4-One | 3550102 | Click to see | 564.50 | unknown | https://doi.org/10.1080/14786410802364168 |
| 5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)-6-(3,4,5-trihydroxyoxan-2-yl)chromen-4-one | 13644660 | Click to see | 564.50 | unknown | https://doi.org/10.1080/14786410802364168 |
| Vicenin 1 | 13644663 | Click to see | 564.50 | unknown | https://doi.org/10.1080/14786410802364168 |
| Vicenin 2 | 3084407 | Click to see | 594.50 | unknown | https://doi.org/10.1080/14786410802364168 |
| Vicenin 2 | 442664 | Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O | 594.50 | unknown | https://doi.org/10.1080/14786410802364168 |
| Vicenin 3 | 185958 | Click to see | 564.50 | unknown | https://doi.org/10.1080/14786410802364168 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| [(2R,3S,4S,5R,6R)-6-[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate | 163188022 | Click to see | 786.70 | unknown | https://doi.org/10.1080/14786410802364168 |
| [6-[2-[2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate | 162842319 | Click to see | 786.70 | unknown | https://doi.org/10.1080/14786410802364168 |
| Luteolin 7-galactoside | 5291488 | Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O | 448.40 | unknown | https://doi.org/10.1080/14786410802364168 |
| Luteolin 7-O-glucoside | 5280637 | Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O | 448.40 | unknown | https://doi.org/10.1080/14786410802364168 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |