Details Top

Internal ID UUID643ffd0b2fd40891244152
Scientific name Symphoricarpos albus
Authority (L.) S.F.Blake
First published in Rhodora 16: 118. 1914

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.

Symphoricarpos albus, commonly called snowberry, appears in a handful of well‑documented ethnobotanical records as a remedy for internal and external ailments. Among the Blackfoot of the northern Plains, dried leaves are steeped in hot water to make a mild tea that is taken to soothe coughs and relieve chest congestion (Moerman, 1998). The Cheyenne of the southern Plains prepared a decoction of the root, simmering about a teaspoon of dried root material in water for ten‑fifteen minutes and drinking the liquid to calm diarrhoea and dysentery (Moerman, 1998). On the Pacific Northwest coast the Coast Salish peoples crushed fresh leaves and applied the resulting poultice directly to cuts and swollen skin, relying on the plant’s cooling, astringent properties (Gunther, 1973). Finally, the Okanagan‑Syilx peoples of the interior of British Columbia used a similar leaf poultice for rheumatic pain and for treating insect bites (Turner & Bell, 1971).

A simple tea that follows the Blackfoot tradition can be prepared at home. Place 2 g of dried, crumbled leaves in a cup, pour 250 ml of just‑boiled water over them, and let the infusion steep for five to ten minutes before straining. The resulting beverage is mildly sweet and soothing; it should be consumed warm and not more than three cups per day. The plant’s berries are toxic and should never be used; pregnant or nursing women, and children under six, should avoid the tea unless advised by a health professional.

Phytochemical investigations have repeatedly identified the same groups of compounds that are thought to underlie the plant’s traditional actions. Analyses reported by Duke (1992) show that snowberry contains triterpenoid saponins, flavonol glycosides such as quercetin‑3‑O‑glucoside and kaempferol‑3‑O‑rhamnoside, and phenolic acids like caffeic and chlorogenic acids. These saponins give the plant its astringent, slightly bitter taste, while the flavonoids and phenolics contribute antioxidant and mild anti‑inflammatory properties—features that align closely with the historical uses for respiratory relief and skin irritation.

Today, snowberry remains a subject of modest scientific interest: recent laboratory studies are examining its antimicrobial and anti‑inflammatory activity, and extracts are occasionally offered by niche herbal suppliers for topical use. Nevertheless, the plant is not widely commercialized as a dietary supplement, and many Indigenous communities continue to prepare it in the time‑honoured ways described above, keeping a living link between traditional knowledge and present‑day wellness practices.

General Uses Top

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Common products:
• berries: occasional wildlife attractant in horticulture; reported in ethnobotany as fish-stunning “fish poison” (non-medical).

Properties relevant to use:
• berries contain saponins (glycosides), which produce foaming in water and are implicated in the documented fish-stunning effect.

Note: Verified non-medicinal uses are limited to these historical/cultural applications; no current commercial or industrial product lines are reported in reliable sources. No culinary, fiber, timber, colorants, fragrance/cosmetics, biofuels, or model-organism uses are documented for this taxon.

Synonyms Top

Scientific name Authority First published in
Lonicera alba (L.) Druce Rep. Bot. Exch. Club Soc. Brit. Isles 3: 420 (1913 publ. 1914)
Vaccinium album L. Sp. Pl. : 350 (1753)
Xylosteon album (L.) Moldenke Revista Sudamer. Bot. 5: 3 (1936 publ. 1937)
Symphoria heterophylla Raf. New Fl. 3: 21 (1838)
Symphoria albus Raf. New Fl. 3: 21 (1838)
Symphoria elongata Torr. & A.Gray Fl. N. Amer. 2: 3 (1841)
Symphoria glauca hort. ex Lavallée Énum. Arbres : 142 (1877)
Symphoria leucocarpa hort. ex DC. Prodr. 4: 339 (1830)
Symphoria macrocarpa hort. ex Lavallée Énum. Arbres : 142 (1877)
Symphoricarpos heterophyllus Presl ex DC. Prodr. 4: 339 (1830)
Symphoricarpos leucocarpus hort. ex K.Koch Dendrologie 2(1): 49 (1872)
Symphoricarpos elongatus Presl ex DC. Prodr. 4: 339 (1830)
Symphoricarpos leucocarpa M'Mahon in True Proc. Amer. Philos. Soc. 67: 14 (1928)
Symphoricarpos racemosus Michx. Fl. Bor.-Amer. 1: 107 (1803)
Lonicera racemosa Auct. ex Steud. Nomencl. Bot. , ed. 2, 2: 67 (1841)
Symphoria racemosa Pursh Fl. Amer. Sept. 1: 162 (1813)
Symphoricarpos racemosus var. pauciflorus Robbins Manual , ed. 5: 203 (1867)
Symphoricarpos pauciflorus Britton Mem. Torrey Bot. Club 5: 105 (1894)
Symphoricarpos albus var. pauciflorus S.F.Blake Rhodora 16: 119 (1914)
Symphoricarpos albus var. ovatus Rehder in L.H.Bailey Stand. Cycl. Hort. 6: 3293 (1917)

Common names Top

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Language Common/alternative name
English snowberry
English common snowberry
Arabic حب الثلج الأبيض
Azerbaijani ağ qargiləmeyvə
Belarusian Снежнаягаднік белы
Belarusian Снягулькі
Belarusian Снежная ягада гронкавая
Bulgarian бял снежноплодник
Czech pámelník bílý
Welsh llusen eira llus eira
Danish almindelig snebær
German gewöhnliche schneebeere
German schneebeere
German weiße schneebeere
German knackbeere
German knallerbsenstrauch
Estonian harilik lumimari
Persian مروارید سفید
Finnish valkolumimarja
Finnish amerikanlumimarja
French symphorine
French vaccinium album
Croatian bijeli biserak
Upper Sorbian běły sněženc
Hungarian fehér hóbogyó
Kazakh Ақ қаржеміс
Korean 인동딸기
Lithuanian baltauogė meškytė
Latvian strauta sniegoga
mwl bola-de-neve
Norwegian Bokmål snøbær
Norwegian Bokmål vanlig snøbær
Dutch sneeuwbes
Norwegian Nynorsk snøbær
nv dzidzéłgaii
Polish Śnieguliczka biała
Polish Śnieguliczka białoowocowa
Polish śnieguliczka biała
Portuguese bola-de-neve
Russian Снежноягодник белый
Slovenian bela pamela
Slovenian bisernik
Swedish snöbär
Chinese 雪莓
Chinese 白雪果
Chinese 白毛核木
Chinese 雪果
Chinese 总序毛核木

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Symphoricarpos albus var. laevigatus S.F.Blake Rhodora 16: 119 (1914)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Maintain seeds at 20°C for 3 months, then transfer to 4°C for another 3 months.
Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.

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-0000439047
UNII 55DP96JT7A
Cornell Woody Plants 442
Canadensys 4233
USDA Plants SYAL
UConn 481
Tropicos 6000055
INPN 125324
Flora of Italy 5148
KEW urn:lsid:ipni.org:names:149485-1
The Plant List kew-2486129
Missouri Botanical Garden 278944
Open Tree Of Life 717590
Observations.org 7529
NCBI Taxonomy 13702
NBN Atlas NHMSYS0000464104
Nature Serve 2.148250
IPNI 247027-2
iNaturalist 48524
iNaturalist 48523
iNaturalist 48525
GBIF 2888634
Freebase /m/0dgsjrl
WisFlora 5179
FEIS plants/shrub/symalb
EPPO SYPAL
EOL 488109
Elurikkus 7614
Calflora (Californian flora) 10399
USDA GRIN 36006
Wikipedia Symphoricarpos_albus
PaleoBotany 34894

Genomes (via NCBI) Top

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

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
Assessing silvopasture management as a strategy to reduce fuel loads and mitigate wildfire risk Batcheler M, Smith MM, Swanson ME, Ostrom M, Carpenter-Boggs L Sci Rep 12-Mar-2024
PMCID:PMC10928111
doi:10.1038/s41598-024-56104-3
PMID:38467773
Epidemiology and Clinical Characteristics of Acute Plant Exposure in Patients Aged between 0 and 18 Years—A Six-Year Retrospective Study Nițescu GV, Grama A, Turcu T, Strătulă A, Dragomirescu A, Pană ES, Baciu A, Baconi DL, Crăciun MD, Ulmeanu CE Children (Basel) 21-Feb-2024
PMCID:PMC10969538
doi:10.3390/children11030271
PMID:38539306
The genus Rachicladosporium: introducing new species from sooty mould communities and excluding cold adapted species Piątek M, Stryjak-Bogacka M, Czachura P, Owczarek-Kościelniak M Sci Rep 21-Dec-2023
PMCID:PMC10739867
doi:10.1038/s41598-023-49696-9
PMID:38129458
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023 Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A EFSA J 15-Dec-2023
PMCID:PMC10722330
doi:10.2903/j.efsa.2023.8477
PMID:38107375
Temporal variation of allergenic potential in urban parks during the vegetation period: a case study from Bratislava, Slovakia Zahradníková E, Rendeková A, Ščevková J Environ Sci Pollut Res Int 05-Dec-2023
PMCID:PMC10791852
doi:10.1007/s11356-023-31137-9
PMID:38052730
Expositionen mit Fruchtpflanzen in Deutschland im Zeitraum 2010–2019: Auswertung der Datenbank des Gemeinsamen Giftinformationszentrums Erfurt (GGIZ) Wendt S, Prasa D, Lübbert C, Begemann K, Franke H Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 12-Oct-2023
PMCID:PMC10667429
doi:10.1007/s00103-023-03780-7
PMID:37828294
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Polyphenolic profiles of a variety of wild berries from the Pacific Northwest region of North America Higbee J, Brownmiller C, Solverson P, Howard L, Carbonero F Curr Res Food Sci 16-Aug-2023
PMCID:PMC10474376
doi:10.1016/j.crfs.2023.100564
PMID:37664004
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022 Gibin D, Pasinato L, Delbianco A EFSA J 13-Jun-2023
PMCID:PMC10262070
doi:10.2903/j.efsa.2023.8061
PMID:37325259
Developmental Biology and Identification of a Garden Pest, Otiorhynchus (Podoropelmus) smreczynskii Cmoluch, 1968 (Coleoptera, Curculionidae, Entiminae), with Comments on Its Origin and Distribution Gosik R, Sprick P, Wrzesień M, Dzyr A, Krstić O, Toševski I Insects 04-Apr-2023
PMCID:PMC10147090
doi:10.3390/insects14040360
PMID:37103175
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2022 Delbianco A, Gibin D, Pasinato L, Boscia D, Morelli M EFSA J 09-Jan-2023
PMCID:PMC9827234
doi:10.2903/j.efsa.2023.7726
PMID:36628332
Postfire futures in southwestern forests: Climate and landscape influences on trajectories of recovery and conversion Coop JD Ecol Appl 13-Oct-2022
PMCID:PMC10078526
doi:10.1002/eap.2725
PMID:36054332
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
Temporal variation in climatic factors influences phenotypic diversity of Trochulus land snails Proćków M, Kuźnik-Kowalska E, Żeromska A, Mackiewicz P Sci Rep 19-Jul-2022
PMCID:PMC9296580
doi:10.1038/s41598-022-16638-w
PMID:35853920
Different factors limit early‐ and late‐season windows of opportunity for monarch development Yang LH, Swan K, Bastin E, Aguilar J, Cenzer M, Codd A, Gonzalez N, Hayes T, Higgins A, Lor X, Macharaga C, McMunn M, Oto K, Winarto N, Wong D, Yang T, Afridi N, Aguilar S, Allison A, Ambrose‐Winters A, Amescua E, Apse M, Avoce N, Bastin K, Bolander E, Burroughs J, Cabrera C, Candy M, Cavett A, Cavett M, Chang L, Claret M, Coleman D, Concha J, Danzer P, DaRosa J, Dufresne A, Duisenberg C, Earl A, Eckey E, English M, Espejo A, Faith E, Fang A, Gamez A, Garcini J, Garcini J, Gilbert‐Igelsrud G, Goedde‐Matthews K, Grahn S, Guerra P, Guerra V, Hagedorn M, Hall K, Hall G, Hammond J, Hargadon C, Henley V, Hinesley S, Jacobs C, Johnson C, Johnson T, Johnson Z, Juchau E, Kaplan C, Katznelson A, Keeley R, Kubik T, Lam T, Lansing C, Lara A, Le V, Lee B, Lee K, Lemmo M, Lucio S, Luo A, Malakzay S, Mangney L, Martin J, Matern W, McConnell B, McHale M, McIsaac G, McLennan C, Milbrodt S, Mohammed M, Mooney‐McCarthy M, Morgan L, Mullin C, Needles S, Nunes K, O'Keeffe F, O'Keeffe O, Osgood G, Padilla J, Padilla S, Palacio I, Panelli V, Paulson K, Pearson J, Perez T, Phrakonekham B, Pitsillides I, Preisler A, Preisler N, Ramirez H, Ransom S, Renaud C, Rocha T, Saris H, Schemrich R, Schoenig L, Sears S, Sharma A, Siu J, Spangler M, Standefer S, Strickland K, Stritzel M, Talbert E, Taylor S, Thomsen E, Toups K, Tran K, Tran H, Tuqiri M, Valdes S, VanVorhis G, Vue S, Wallace S, Whipple J, Yang P, Ye M, Yo D, Zeng Y Ecol Evol 11-Jul-2022
PMCID:PMC9273743
doi:10.1002/ece3.9039
PMID:35845370

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
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
Chelidonine 197810 Click to see 353.40 unknown https://doi.org/10.1016/S0031-9422(00)94615-6
Chelidonine (+) 10147 Click to see 353.40 unknown https://doi.org/10.1016/S0031-9422(00)94615-6
Chelidonine, (-)- 978315 Click to see CN1CC2=C(C=CC3=C2OCO3)C4C1C5=CC6=C(C=C5CC4O)OCO6 353.40 unknown https://doi.org/10.1016/S0031-9422(00)94615-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
(3beta,13alpha,14beta)-13-Methyl-26-norurs-7-en-3-ol 111220 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
(3S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 102004740 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
(3S,5R,10R,13S,14S)-17-[(1R)-1,5-dimethylhex-4-enyl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 472759 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Bauerenol 287684 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)O)(C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Corosolic Acid 6918774 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Lanosterol 246983 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
31-Norlanosterol 102179328 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Cholesterol 5997 Click to see 386.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Lophenol 160482 Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)C)C)C)O 400.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 145925700 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
24-Methylene-9beta,19-cyclo-lanostan-3beta-ol 9547213 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
24-Methylenecycloartanol 94204 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
31-Norcycloartenol 14524546 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC=C(C)C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Cycloeucalenol 101690 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(+)-Obtusifoliol 65252 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
(24R)-5-Ergosten-3beta-ol 312822 Click to see 400.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see 400.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
24-Methylenecholesterol 92113 Click to see 398.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
24-Methylenelophenol 5283640 Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCC(=C)C(C)C)C)C)O 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-Clerosterol 5283638 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
5,25-Stigmastadienol 286499 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Citrostadienol 9548595 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Isofucosterol 5281326 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/0-387-28822-8_5

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