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

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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

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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

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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

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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.
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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Molecular insights into self-incompatibility systems: From evolution to breeding Zhang D, Li YY, Zhao X, Zhang C, Liu DK, Lan S, Yin W, Liu ZJ Plant Commun 16-Sep-2023
PMCID:PMC10873884
doi:10.1016/j.xplc.2023.100719
PMID:37718509
Improving Flavonoid Accumulation of Bioreactor-Cultured Adventitious Roots in Oplopanax elatus Using Yeast Extract Jin MY, Wang M, Wu XH, Fan MZ, Li HX, Guo YQ, Jiang J, Yin CR, Lian ML Plants (Basel) 30-May-2023
PMCID:PMC10255709
doi:10.3390/plants12112174
PMID:37299154
Phenotypic analysis of Longya-10 × pale flax hybrid progeny and identification of candidate genes regulating prostrate/erect growth in flax plants Qi Y, Wang L, Li W, Xie Y, Zhao W, Dang Z, Li W, Zhao L, Zhang J Front Plant Sci 06-Dec-2022
PMCID:PMC9763623
doi:10.3389/fpls.2022.1044415
PMID:36561460
Anchorage by seed mucilage prevents seed dislodgement in high surface flow: a mechanistic investigation Pan VS, Girvin C, LoPresti EF Ann Bot 24-Mar-2022
PMCID:PMC9292590
doi:10.1093/aob/mcac045
PMID:35325924
Scarlet Flax Linum grandiflorum (L.) In Vitro Cultures as a New Source of Antioxidant and Anti-Inflammatory Lignans Asad B, Khan T, Gul FZ, Ullah MA, Drouet S, Mikac S, Garros L, Ferrier M, Bose S, Munsch T, Tungmunnithum D, Lanoue A, Giglioli-Guivarc’h N, Hano C, Abbasi BH Molecules 27-Jul-2021
PMCID:PMC8348589
doi:10.3390/molecules26154511
PMID:34361665
Bumblebees can detect floral humidity Harrap MJ, Hempel de Ibarra N, Knowles HD, Whitney HM, Rands SA J Exp Biol 24-Jun-2021
PMCID:PMC8246344
doi:10.1242/jeb.240861
PMID:34161560
Chemical Diversity of Plant Cyanogenic Glycosides: An Overview of Reported Natural Products Yulvianti M, Zidorn C Molecules 30-Jan-2021
PMCID:PMC7866531
doi:10.3390/molecules26030719
PMID:33573160
Floral Humidity in Flowering Plants: A Preliminary Survey Harrap MJ, Hempel de Ibarra N, Knowles HD, Whitney HM, Rands SA Front Plant Sci 06-Mar-2020
PMCID:PMC7068853
doi:10.3389/fpls.2020.00249
PMID:32211004
Flower, seed, and fruit development in three Tunisian species of Polygonum: Implications for their taxonomy and evolution of distyly in Polygonaceae Mahmoudi M, Boughalleb F, Pellegrino G, Abdellaoui R, Nasri N PLoS One 10-Jan-2020
PMCID:PMC6953800
doi:10.1371/journal.pone.0227099
PMID:31923204
Cloning and functional analysis of the FAD2 gene family from desert shrub Artemisia sphaerocephala Miao X, Zhang L, Hu X, Nan S, Chen X, Fu H BMC Plant Biol 08-Nov-2019
PMCID:PMC6839233
doi:10.1186/s12870-019-2083-5
PMID:31703625
A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens Frey D, Moretti M Data Brief 23-May-2019
PMCID:PMC6545399
doi:10.1016/j.dib.2019.103982
PMID:31194048
Identification of a gene encoding polygalacturonase expressed specifically in short styles in distylous common buckwheat (Fagopyrum esculentum) Takeshima R, Nishio T, Komatsu S, Kurauchi N, Matsui K Heredity (Edinb) 10-May-2019
PMCID:PMC6781162
doi:10.1038/s41437-019-0227-x
PMID:31076649
The changing face of farmers’ home gardens: a diachronic analysis from Sillian (Eastern Tyrol, Austria) Vogl-Lukasser B, Vogl CR J Ethnobiol Ethnomed 29-Oct-2018
PMCID:PMC6205796
doi:10.1186/s13002-018-0262-3
PMID:30373655
GmMYB181, a Soybean R2R3-MYB Protein, Increases Branch Number in Transgenic Arabidopsis Yang H, Xue Q, Zhang Z, Du J, Yu D, Huang F Front Plant Sci 17-Jul-2018
PMCID:PMC6056663
doi:10.3389/fpls.2018.01027
PMID:30065741
Perennial Grass and Native Wildflowers: A Synergistic Approach to Habitat Management Xavier SS, Olson DM, Coffin AW, Strickland TC, Schmidt JM Insects 22-Sep-2017
PMCID:PMC5746787
doi:10.3390/insects8040104
PMID:28937651

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

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