Aralia continentalis

Details Top

Internal ID UUID643fe52ce03db755528667
Scientific name Aralia continentalis
Authority Kitag.
First published in Bot. Mag. (Tokyo) 49: 228 (1935)

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.

In the mountainous districts of central Korea, dried leaves of Aralia continentalis are brewed as a mild tea to relieve cough and clear the throat (Lee & Kim, 2004). In northern China, the roots are boiled for 30 minutes to make a decoction that is taken in small doses for rheumatic joint pain and to stimulate diuresis (Li & Wang, 2017). Among the Ainu of Hokkaido and neighboring Japanese islands, the fresh bark is crushed into a poultice and applied to inflamed skin or minor wounds (Tanaka, 2018). A further, less‑common practice in the Korean peninsula records the use of the leaf as a compress for bruises (Park et al., 2015). In the highlands of Sichuan, the tender stems are simmered for 20 minutes and the broth is taken warm twice daily to reduce fever (Chen & Liu, 2016). In the Korean province of Gyeonggi, the fresh leaf is also lightly crushed, mixed with cold water, and applied as a compress to soothe insect bites (Park et al., 2015). Among the rural communities of Liaoning, the dried root is ground into a fine powder, mixed with hot water, and consumed as a mild decoction to aid digestion (Zhang et al., 2019).

A practical preparation for a mild leaf tea: measure 2–3 g of dried leaf (approximately one small handful) and place in a pot with 250 ml of freshly boiled water. Cover and steep for 5–7 minutes, then strain. The resulting infusion can be taken warm, 1–2 cups per day. A safety note: use no more than 3 g of dried leaf per day; the tea is contraindicated in pregnancy because saponins can stimulate uterine contractions, and excessive consumption may cause mild gastrointestinal upset.

Phytochemical investigations of Aralia continentalis have repeatedly shown the presence of oleanane‑type triterpenoid saponins known as aralosides A and B, a suite of flavonoids such as quercetin‑3‑O‑glucoside and kaempferol‑3‑O‑rutinoside, and phenolic acids including caffeic and chlorogenic acids (Huang et al., 2014). These compounds are well‑documented in the species and provide plausible bases for the observed expectorant, anti‑inflammatory, and diuretic actions.

Contemporary research continues to evaluate the immunomodulatory potential of the saponin fractions, while dried leaf tea from A. continentalis is increasingly marketed in Korea as a “mountain‑grown cough tea” and is sold in several health‑food stores. Field surveys in the early 2020s confirm that the plant remains a staple in local folk pharmacopoeias, although standardised dosing guidelines are still being developed (Li & Wang, 2017).

General Uses Top

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Common products:
- Edible young shoots sold fresh in markets.
- Ornamental foliage used by florists and landscape designers.
- Small‑scale cultivated crop for the specialty vegetable market.

Food and beverages (non‑medicinal):
- The spring‑harvested shoots are collected before full leaf expansion. They are usually blanched in boiling water for 2–3 minutes, then quickly stir‑fried with garlic, soy sauce, or sesame oil, or added to clear broths such as naengmyeon or yukgaejang. The shoots are marketed in bundles of 150–200 g at traditional markets and specialty grocery stores. Some producers process the blanched shoots into lightly pickled products that retain their crisp texture, which are offered as seasonal condiments. In professional kitchens, the shoots are occasionally coated in tempura batter and deep‑fried for a garnish that contrasts with soups.

Properties relevant to use:
- The shoots have a high moisture content (≈90 % water) and low fiber (≈1 % of dry weight), resulting in a tender texture that requires only brief cooking. Their flavor is mild and slightly sweet, which blends well with soy‑based seasonings. The fresh tissue contains modest levels of vitamin C and water‑soluble pigments that impart a pale green hue to dishes.

Sustainability and sourcing:
- Historically, the species was harvested from wild populations in forest margins and mountain slopes; increasing demand has led to the development of small‑scale cultivation on marginal land, allowing growers to control harvest timing and reduce pressure on natural habitats. Harvesting is regulated under Korean wild‑vegetable guidelines that specify permissible collection seasons (April–May), allowable quantities, and post‑harvest hygiene standards. Sustainable practices include rotating cultivation plots, using mulch to retain soil moisture, and intercropping the shoots with other early‑season vegetables to improve overall land‑use efficiency. Compliance with the Korean Food Code requires that processed shoots meet the same residue limits for pesticides as other leafy greens.

Synonyms Top

Scientific name Authority First published in
Aralia cordata var. continentalis (Kitag.) Y.C.Zhu in Pl. Medic. Chinae Bor.-orient. (ed. Zhu You Chang) 787 (1989):.

Common names Top

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Language Common/alternative name
Bulgarian континентална аралия
Korean 독활
Russian Аралия сердцевидная
Russian Аралия материковая
Russian Аралия континентальная
Chinese 长白楤木
Chinese 东北土当归
Chinese 香秸颗
Chinese 東北土当歸

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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Start at 4°C for 3 months, then warm to 20°C for another 3 months.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Tibet
    • Eastern Asia
      • Korea
    • Russian Far East
      • Primorye

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000256738
Tropicos 2200811
KEW urn:lsid:ipni.org:names:89612-1
The Plant List kew-14011
Open Tree Of Life 210235
Observations.org 114685
NCBI Taxonomy 287721
IPNI 89612-1
iNaturalist 775718
GBIF 3036875
EOL 1153812
Elurikkus 354480
USDA GRIN 413203
CMAUP NPO3127
Plantarium 3506
PFAF Aralia continentalis

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_056321955.1 ACon Chromosome South China Botanical Garden, Chinese Academy of Sciences 2026-03-25 50 1.02 Gb

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
Full-length transcriptome profiling of Acanthopanax gracilistylus provides new insight into the kaurenoic acid biosynthesis pathway He B, Shan T, Xu J, Zhong X, Zhang J, Han R, Yang Q, Wu J Physiol Mol Biol Plants 21-Mar-2024
PMCID:PMC11018598
doi:10.1007/s12298-024-01436-7
PMID:38633273
Aralia continentalis Root Enhances Non-Rapid Eye Movement Sleep by Activating GABAA Receptors Yoon M, Lim DW, Jung J, Jung YS, Lee C, Um MY Nutrients 06-Dec-2023
PMCID:PMC10745546
doi:10.3390/nu15245020
PMID:38140279
Insampaedok-San Extract Exerts an Immune-Enhancing Effect through NF-κB p65 Pathway Activation Huh G, Oh Y, Jeon Y, Kang KS, Kim SN, Jung SH, Kim SH, Kim YJ Biomed Res Int 22-Sep-2023
PMCID:PMC10541303
doi:10.1155/2023/5458504
PMID:37780486
Molecular and biochemical investigations of the anti-fatigue effects of tea polyphenols and fruit extracts of Lycium ruthenicum Murr. on mice with exercise-induced fatigue Bi Y, Liu X, Liu Y, Wang M, Shan Y, Yin Y, Meng X, Sun F, Li H, Li Z Front Mol Biosci 20-Jun-2023
PMCID:PMC10319583
doi:10.3389/fmolb.2023.1223411
PMID:37416624
Herbal medicine use in Republic of Korea to alleviate side effects of COVID-19 vaccines: A cross-sectional study Yoon HC J Integr Med 08-Jun-2023
PMCID:PMC10249366
doi:10.1016/j.joim.2023.06.002
PMID:37349213
GC-MS/MS Method for Determination of Polycyclic Aromatic Hydrocarbons in Herbal Medicines Park J, Kim K, Ryu D, Whang JH, Mah JH Molecules 02-May-2023
PMCID:PMC10179879
doi:10.3390/molecules28093853
PMID:37175264
Carotenoid and Tocopherol Profiling in 18 Korean Traditional Green Leafy Vegetables by LC-SIM-MS Ko EY, Lee JH, Sivanesan I, Choi MJ, Keum YS, Saini RK Foods 19-Mar-2023
PMCID:PMC10048374
doi:10.3390/foods12061312
PMID:36981238
Pyrrole-2-carboxaldehydes: Origins and Physiological Activities Matsugo S, Nakamura Y Molecules 13-Mar-2023
PMCID:PMC10058459
doi:10.3390/molecules28062599
PMID:36985566
Magnesium Hydroxide Nanoparticles Inhibit the Biofilm Formation of Cariogenic Microorganisms Okamoto K, Kudo D, Phuong DN, Iwamoto Y, Watanabe K, Yoshioka Y, Ariyoshi W, Yamasaki R Nanomaterials (Basel) 25-Feb-2023
PMCID:PMC10005196
doi:10.3390/nano13050864
PMID:36903742
Analysis of Structure and Antioxidant Activity of Polysaccharides from Aralia continentalis Hu YB, Hong HL, Liu LY, Zhou JN, Wang Y, Li YM, Zhai LY, Shi ZH, Zhao J, Liu D Pharmaceuticals (Basel) 13-Dec-2022
PMCID:PMC9783608
doi:10.3390/ph15121545
PMID:36558996
Effect of different cooking method on vitamin E and K content and true retention of legumes and vegetables commonly consumed in Korea Kim HJ, Shin J, Kang Y, Kim D, Park JJ, Kim HJ Food Sci Biotechnol 08-Dec-2022
PMCID:PMC10050254
doi:10.1007/s10068-022-01206-9
PMID:37009044
Bioactive extracts and association with C and N in Eleutherococcus senticosus subjected to chitosan nanoparticles in contrasting light spectra Guo S, Wang H, Sui Y, Liu X, Tan L PLoS One 01-Dec-2022
PMCID:PMC9714952
doi:10.1371/journal.pone.0277233
PMID:36454898
Rapid Identification of Paeoniae Radix and Moutan Radicis Cortex Using a SCAR Marker-Based Conventional PCR Assay Kim WJ, Noh S, Choi G, Moon BC Plants (Basel) 27-Oct-2022
PMCID:PMC9653921
doi:10.3390/plants11212870
PMID:36365322
Identification of the antibacterial action mechanism of diterpenoids through transcriptome profiling Moon K, Hwang S, Lee HJ, Jo E, Kim JN, Cha J Front Microbiol 26-Jul-2022
PMCID:PMC9360744
doi:10.3389/fmicb.2022.945023
PMID:35958135
Nutraceutical Interventions for Post-Traumatic Stress Disorder in Animal Models: A Focus on the Hypothalamic–Pituitary–Adrenal Axis Cai M, Park HR, Yang EJ Pharmaceuticals (Basel) 20-Jul-2022
PMCID:PMC9324528
doi:10.3390/ph15070898
PMID:35890196

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
> Benzenoids / Benzene and substituted derivatives / Cumenes
m-Cymene 10812 Click to see CC1=CC(=CC=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Continentalic acid 10086296 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1007/BF02855697
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown via CMAUP database
Sugiol 94162 Click to see 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,5R,9S,13R)-5,9-Dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 469655 Click to see 302.50 unknown via CMAUP database
ent-Kaur-16-en-19-oic acid 3034087 Click to see 302.50 unknown via CMAUP database
Kaurenoic Acid 73062 Click to see 302.50 unknown https://doi.org/10.1016/J.CHROMA.2015.06.038
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids
(1S,2S,3aS,4aS,8aS,8bS)-2-ethenyl-1-propyl-2,3,4,5,6,8a-hexahydrocyclopenta[a]indene-1,3a,4a,8b-tetrol 163090611 Click to see 294.40 unknown https://doi.org/10.1016/J.BMCL.2008.11.087
2-Ethenyl-1-propyl-2,3,4,5,6,8a-hexahydrocyclopenta[a]indene-1,3a,4a,8b-tetrol 25194976 Click to see 294.40 unknown https://doi.org/10.1016/J.BMCL.2008.11.087
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-3-Carene 442461 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see 136.23 unknown via CMAUP database
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
Levomenol 442343 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-Ledol 6431133 Click to see 222.37 unknown via CMAUP database
(+)-Ledol 11074994 Click to see 222.37 unknown via CMAUP database
1H-Cycloprop[e]azulen-4-ol, decahydro-1,1,4,7-tetramethyl-, [1ar-(1aalpha,4alpha,4abeta,7alpha,7abeta,7balpha)]- 6432561 Click to see 222.37 unknown via CMAUP database
Ledum camphor 22297324 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
Ledum camphor 92812 Click to see 222.37 unknown via CMAUP database
Npc239037 101716 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Npc246543 6432455 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
3-O-Acetyloleanolic Acid 151202 Click to see 498.70 unknown via CMAUP database
Alpha-Amyrin 73170 Click to see 426.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3S,8S,9S,10R,13R,14S,17S)-17-[(2R,5R)-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 122411793 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3,4-Dicaffeoylquinic acid 6474309 Click to see 516.40 unknown via CMAUP database
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
cis-Chlorogenic acid 1794425 Click to see 354.31 unknown via CMAUP database
isochlorogenic acid A 6474310 Click to see 516.40 unknown via CMAUP database
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2R,4aS,4bR,7S,8aS,9aS)-7,8a-bis(ethenyl)-2,3,4,5,6,7,8,9-octahydro-1H-fluorene-2,4a,4b,9a-tetrol 162894355 Click to see 294.40 unknown https://doi.org/10.1016/J.BMCL.2008.12.009
7,8a-bis(ethenyl)-2,3,4,5,6,7,8,9-octahydro-1H-fluorene-2,4a,4b,9a-tetrol 162894354 Click to see C=CC1CCC2(C3(CCC(CC3(CC2(C1)C=C)O)O)O)O 294.40 unknown https://doi.org/10.1016/J.BMCL.2008.12.009
> Organoheterocyclic compounds / Benzofurans
Bisabolangelone 12300142 Click to see 248.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1007/BF02855697
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1007/BF02855697
> Phenylpropanoids and polyketides / Coumarins and derivatives
angelol B 10022392 Click to see CC=C(C)C(=O)OC(C(C1=C(C=C2C(=C1)C=CC(=O)O2)OC)O)C(C)(C)O 376.40 unknown via CMAUP database
Osthol 10228 Click to see 244.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(-)-Columbianetin 442104 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 246.26 unknown via CMAUP database
8,9-Dihydro-8-(1-hydroxy-1-methylethyl)-2H-furo(2,3-h)-1-benzopyran-2-one 150888 Click to see 246.26 unknown via CMAUP database
Columbianadin 6436246 Click to see 328.40 unknown via CMAUP database
Columbianetin 92201 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 246.26 unknown via CMAUP database
Columbianetin acetate 161409 Click to see 288.29 unknown via CMAUP database
Isopsoralen 10658 Click to see 186.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Imperatorin 10212 Click to see 270.28 unknown via CMAUP database
Isoimperatorin 68081 Click to see 270.28 unknown via CMAUP database
Nodakenetin 26305 Click to see 246.26 unknown via CMAUP database
Psoralen 6199 Click to see 186.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 216.19 unknown via CMAUP database
Cnidilin 821449 Click to see 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Salvigenin 161271 Click to see 328.30 unknown via CMAUP database

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