Details Top

Internal ID UUID644010cace784435263441
Scientific name Chenopodium foliosum
Authority Asch.
First published in Fl. Brandenburg : 572 (1864)

Ethnobotanical Use Top

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General Uses Top

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Food and beverages (non-medicinal):
The plant produces small, juicy fruits that are consumed as a fresh fruit; they are also used in jams, desserts, and traditional fermented beverages (e.g., kisses or honey cake fillings). Reports describe a mildly sweet to slightly tart flavor and sometimes note a mild “raw” or “leafy” note that can be reduced by brief heat or processing. Regional cuisines report combining C. foliosum fruits with other berries and syrups, in which the mucilaginous pulp contributes to a viscous mouthfeel.

Colorants and tanning:
Berries yield anthocyanins that give purple–magenta coloration in acidic media and blue–green hues under alkaline conditions; the plant is used as a natural coloring agent in foods and beverages. The leaf sheaths yield a yellow/brown dye that has been used on textile fibers; β-sitosterol is present in plant tissues. There is no documented traditional or industrial tannin extraction.

Fragrance and cosmetics:
Fresh leaves have been described as having a mild, herbaceous aroma; leaves and berries have been used in perfumery in combination with other herbs. Extracts have been tested for cosmetic applications as potential fragrance components; no commercial-scale adoption is reported.

Scientific/model-organism use:
C. foliosum is used as a comparative model in studies of the evolution of betalain biosynthesis in Caryophyllales. Molecular phylogenies and population-level studies have clarified relationships among C. album, C. quinoa, and C. foliosum, and an available dataset is used to identify ecological and genetic factors driving adaptation. The species is cited in genomic comparisons of betalain pathways; no reference genome for C. foliosum is reported.

Ornamental and horticultural:
cultivars are grown as ornamental climbers for their purple-red fruits and foliage; cut branches and garlands are used in floral arrangements. The plant’s low-water tolerance supports landscape uses in drier sites.

Standards and regulation:
As a novel or minor fruit/leaf food, some jurisdictions require pre-market assessment for food use and exclude unverified health claims. Dye uses for textiles are not regulated beyond standard colorfastness standards. No ISO/ASTM specifications exist for C. foliosum products; national rules for novel foods or cosmetics may apply where relevant.

Sustainability and sourcing:
Harvesting from wild populations is conducted in parts of the Mediterranean; concerns have been raised about overharvesting in some regions, leading to recommendations for managed cultivation. Cropping methods focus on propagation from seed and support production without irrigation in semi-arid soils.

Synonyms Top

Scientific name Authority First published in
Morocarpus foliosus Moench Methodus (Moench) 342. 1794 [4 May 1794]
Blitum korshinskyi Litv. Trudy Bot. Muz. Imp. Akad. Nauk 7: 76 (1910)
Blitum virgatum L. Sp. Pl. : 4 (1753)
Chenopodium blitum F.Muell. Addit. Princip. Timber Trees & Sel. Pl. : 11 (1874)
Chenopodium korshinskyi Litv. Trav. Mus. Bot. Acad. Petersb. vii. 77 (1910).
Chenopodium virgatum (L.) Ambrosi Fl. Tirolo Mer. 2: 179. 1857
Chenopodium foliosum var. virgatum (L.) Maire & Weiller in Fl. Afr. Nord 8: 43 1962
Monocarpus foliosus Moench Methodus 342 1794
Chenopodium korshinskyi (Litv.) Minkw. Rastit. Turkestana 332 1915
Chenopodium blitum Hook.f. Gen. Pl. 3: 52 1880

Common names Top

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Language Common/alternative name
English leafy goosefoot
English strawberry goosefoot
Czech merlík listnatý
German durchblätterter erdbeerspinat
German erdbeerspinat
Estonian vits-hanemalts
Finnish marjasavikka
French épinard-fraise en baguette
Upper Sorbian Łopjenata pólšica
Latvian lapainā balanda
Norwegian Bokmål bærmelde
Dutch rode aardbeispinazie
Russian Марь многолистная
Swedish bärmålla
Chinese 球花藜

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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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-0000601286
Canadensys 4507
USDA Plants CHFO2
Tropicos 7200031
KEW urn:lsid:ipni.org:names:164938-1
The Plant List kew-2717327
NBN Atlas NBNSYS0200003524
Nature Serve 2.155885
IPNI 164938-1
iNaturalist 76273
GBIF 3083844
WisFlora 7162
EOL 586713
Elurikkus 3674
Calflora (Californian flora) 1973
USDA GRIN 10187
CMAUP NPO25532

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-Lyoniresinol 3alpha-O-beta-D-glucopyranoside 10483388 Click to see 582.60 unknown via CMAUP database
(2R,3R,4R,5R,6S)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-methyloxane-3,4,5-triol 71477642 Click to see 566.60 unknown via CMAUP database
Aviculin 10391477 Click to see 506.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-2,3-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 10055182 Click to see 664.80 unknown via CMAUP database
Trachelosperogenin A1, >=95% (LC/MS-ELSD) 21637743 Click to see 680.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
((1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta(a)chrysen-9-yl) (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 12149208 Click to see 588.90 unknown via CMAUP database
(+)-Erythrodiol 101761 Click to see 442.70 unknown via CMAUP database
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(2R,3R,4R,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-2,3,12-trihydroxy-4,6a,6b,11,12,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 69569684 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)O 518.70 unknown via CMAUP database
(2R,3R,4R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-2,3-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 10029042 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1)C)C(=O)O)C 502.70 unknown via CMAUP database
[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate 101756120 Click to see 588.90 unknown via CMAUP database
23-Hydroxybetulin 14605681 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)CO 458.70 unknown via CMAUP database
3-O-(E)-p-Coumaroylbetulin 12086730 Click to see 588.90 unknown via CMAUP database
Alphitolic acid 12305768 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)O 472.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulin caffeate 10153267 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)CO 604.90 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3,4,5-Trimethoxyphenyl beta-D-glucopyranoside 636454 Click to see 346.33 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 7-O-glucoside 10095180 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
7-hydroxy-3-(4-hydroxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14583643 Click to see 432.40 unknown via CMAUP database
Genistin 5281377 Click to see 432.40 unknown via CMAUP database

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