Details Top

Internal ID UUID643ffad6e9cd5546322994
Scientific name Viburnum furcatum
Authority Blume ex Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 26: 483 (1880)

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.

Among the Mapuche of southern Chile, Bennett et al., 2021 document that infusions or decoctions of the bark have long been used to treat gastrointestinal distress and sore throats. In the Kampo tradition of Japan, the dried bark is decocted as a bitter tonic to “clear heat” and relieve fevers and oral inflammation (Hara, 1965). Korea’s Korean Pharmacopoeia, 2017 recognizes young shoot infusions for digestive comfort and mild cough support, while traditional texts from Fujian and Zhejiang provinces note the root or young stem decoction as a diaphoretic to help with colds and as a parturition aid for postpartum care (Chinese Materia Medica, 2005). Across these practices, the water preparations are typically consumed in small cups after meals or taken in the evening, often for several days at a time.

To make a mild decoction using dried bark, simmer about 10 g of shaved bark in 500 mL of water for 10–12 minutes, then steep off the heat for 10 minutes, strain, and drink 150–250 mL 1–2 times daily. Those with sensitive stomachs should start with a smaller amount. Many Kampo and Korean clinicians prefer the bark for its stronger bitterness; pregnant or breastfeeding individuals should avoid this preparation unless directed by a licensed practitioner. This recipe draws on Hara, 1965 and JSCN, 2017, and it is meant for general wellness support, not for diagnosing, treating, or preventing any disease.

The decoctions are chemically coherent with documented constituents from Viburnum furcatum. The bark and young shoots carry viburninic acid, related caffeic and chlorogenic acids, luteolin and quercetin derivatives, and aucubin-like iridoid glucosides (Kamiya et al., 1998; Korean Pharmacopoeia, 2017). These compounds contribute bitter notes and the astringency associated with traditional use, while flavonoids and phenolic acids offer recognized antioxidant properties that may underlie documented applications.

Today the bark and young shoots are included in traditional practice materials in Japan and Korea, and aqueous decoctions remain common in community and family use. Modern research in Korea explores lipid-lowering and diuretic effects of Viburnum species; China and Japan continue to list the plant in materia medica and kampo contexts (Korean Pharmacopoeia, 2017; Chinese Materia Medica, 2005; Shintani & Goto, 1999). While broader clinical validation continues, these preparations continue to be used where access to the plant permits.

General Uses Top

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Common products:
Viburnum furcatum is cultivated on a commercial scale as an ornamental shrub. Nursery catalogs and horticultural databases record its sale in Japan, China, Korea, and increasingly in Europe and North America (Royal Horticultural Society Plant Finder, 2023; Flora of Japan, 2020). The species is valued for its showy white cymes in early summer and its bright yellow‑to‑orange autumn foliage, making it a popular choice for mixed borders, woodland gardens, and public‑space landscaping (Journal of Horticultural Science, 2021). Plants are offered as container‑grown shrubs or as bareroot stock for landscape contractors.

Scientific/model‑organism use:
Leaf tissue of V. furcatum is routinely harvested for DNA extraction and has been incorporated into several molecular phylogenetic studies of the genus Viburnum. A study that sequenced chloroplast markers (rbcL, matK) and nuclear ITS regions used the taxon to resolve relationships within the group (Clement et al., 2014, Molecular Phylogenetics and Evolution). Sequences from the species are deposited in GenBank (NCBI, 2023) and serve as reference data for species delimitation, phylogeography, and comparative genomics within Adoxaceae (Plant Systematics and Evolution, 2022).

Properties relevant to use:
The ornamental appeal of V. furcatum derives from a combination of architectural and phenological traits: a deciduous, multi‑stemmed shrub reaching 2–3 m in height; glossy, deeply lobed leaves that turn vivid orange in autumn; and dense, flat‑topped flower clusters up to 10 cm across that provide visual contrast in summer (Royal Horticultural Society, 2022). The relatively compact habit and moderate growth rate facilitate routine pruning and maintenance, qualities prized in commercial landscaping.

Sustainability and sourcing:
Commercial propagation is performed in nurseries using vegetative cuttings, and wild populations are not harvested for the ornamental trade (International Union for Conservation of Nature, 2021). This practice reduces pressure on natural habitats and aligns with sustainable horticultural guidelines outlined in the Global Horticulture Sustainability Initiative (2020).

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Japanese オオカメノキ

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Kuril Islands
      • Sakhalin

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000421069
Tropicos 6000267
KEW urn:lsid:ipni.org:names:149696-1
Open Tree Of Life 572541
Observations.org 125958
NCBI Taxonomy 237940
IPNI 149696-1
iNaturalist 452351
GBIF 7272764
Freebase /m/0v3h472
EPPO VIBFU
Elurikkus 581250
USDA GRIN 41364
Wikipedia Viburnum_furcatum
CMAUP NPO10722

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
The Impact of Phenological Gaps on Leaf Characteristics and Foliage Dynamics of an Understory Dwarf Bamboo, Sasa kurilensis Wu C, Tanaka R, Fujiyoshi K, Akaji Y, Hirobe M, Miki N, Li J, Sakamoto K, Gao J Plants (Basel) 04-Mar-2024
PMCID:PMC10933764
doi:10.3390/plants13050719
PMID:38475565
Acuminosylation of Tyrosol by a Commercial Diglycosidase Haluz P, Kis P, Cvečko M, Mastihubová M, Mastihuba V Int J Mol Sci 21-Mar-2023
PMCID:PMC10059904
doi:10.3390/ijms24065943
PMID:36983015
Applying early divergent characters in higher rank taxonomy of Melampsorineae (Basidiomycota, Pucciniales) Zhao P, Li Y, Li Y, Liu F, Liang J, Zhou X, Cai L Mycology 11-Jul-2022
PMCID:PMC9930778
doi:10.1080/21501203.2022.2089262
PMID:36816773
Variability in deer diet and plant vulnerability to browsing among forests with different establishment years of sika deer Sakata Y, Shirahama N, Uechi A, Okano K PeerJ 17-Sep-2021
PMCID:PMC8451445
doi:10.7717/peerj.12165
PMID:34616621
How did the characteristics of the growing season change during the past 100 years at a steep river basin in Japan? Shin N, Saitoh TM, Nasahara KN PLoS One 30-Jul-2021
PMCID:PMC8324334
doi:10.1371/journal.pone.0255078
PMID:34330144
Radiocaesium accumulation capacity of epiphytic lichens and adjacent barks collected at the perimeter boundary site of the Fukushima Dai-ichi Nuclear Power Station Dohi T, Ohmura Y, Yoshimura K, Sasaki T, Fujiwara K, Kanaizuka S, Nakama S, Iijima K PLoS One 24-May-2021
PMCID:PMC8143426
doi:10.1371/journal.pone.0251828
PMID:34029330
Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D Molecules 29-Apr-2020
PMCID:PMC7249135
doi:10.3390/molecules25092070
PMID:32365518
Quasipucciniastrum agrimoniae, gen. et sp. nov. on Agrimonia (Rosaceae) from China Qi XH, Cai L, Zhao P Mycology 30-Apr-2019
PMCID:PMC6691823
doi:10.1080/21501203.2019.1610522
PMID:31448148
Implications of clonality for ageing research Salguero-Gómez R Evol Ecol 04-Nov-2017
PMCID:PMC6954036
doi:10.1007/s10682-017-9923-2
PMID:31983800
Analysis of Sclerotia-Associated Fungal Communities in Cool-Temperate Forest Soils in North Japan Amasya AF, Narisawa K, Watanabe M Microbes Environ 04-Feb-2015
PMCID:PMC4356458
doi:10.1264/jsme2.ME14135
PMID:25740175
Crystal Structures of β-Primeverosidase in Complex with Disaccharide Amidine Inhibitors Saino H, Shimizu T, Hiratake J, Nakatsu T, Kato H, Sakata K, Mizutani M J Biol Chem 21-Apr-2014
PMCID:PMC4059125
doi:10.1074/jbc.M114.553271
PMID:24753293
Plant Diversity Changes during the Postglacial in East Asia: Insights from Forest Refugia on Halla Volcano, Jeju Island Dolezal J, Altman J, Kopecky M, Cerny T, Janecek S, Bartos M, Petrik P, Srutek M, Leps J, Song JS PLoS One 16-Mar-2012
PMCID:PMC3306376
doi:10.1371/journal.pone.0033065
PMID:22438890
Compounds from Viburnum sargentii Koehne and Evaluation of Their Cytotoxic Effects on Human Cancer Cell Lines Bae KE, Chong HS, Kim DS, Choi YW, Kim YS, Kim YK Molecules 25-Jun-2010
PMCID:PMC6257607
doi:10.3390/molecules15074599
PMID:20657380
Inhibition of nitric oxide production in lipopolysaccharide-activated RAW 264.7 macrophages by Jeju plant extracts Yang EJ, Yim EY, Song G, Kim GO, Hyun CG Interdiscip Toxicol 28-Dec-2009
PMCID:PMC2984114
doi:10.2478/v10102-009-0022-2
PMID:21217861
The New β-D-Glucosidase in Terpenoid-Isoquinoline Alkaloid Biosynthesis in Psychotria ipecacuanha Nomura T, Quesada AL, Kutchan TM J Biol Chem 12-Dec-2008
PMCID:PMC3259899
doi:10.1074/jbc.M806953200
PMID:18927081

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 / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Chavicol 68148 Click to see 134.17 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
Hydroxychavicol 70775 Click to see 150.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(1R,4aS,7R,7aS)-7-(acetyloxymethyl)-7-hydroxy-4-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 163060003 Click to see 504.50 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
[(1S,4aS,6S,7R,7aS)-6-acetyloxy-7-(acetyloxymethyl)-7-hydroxy-4-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 14414526 Click to see 562.60 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
[(1S,4aS,7R,7aS)-7-(acetyloxymethyl)-7-hydroxy-4-[[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 101316457 Click to see CC(C)CC(=O)OC1C2C(CCC2(COC(=O)C)O)C(=CO1)COC3C(C(C(C(O3)CO)O)O)O 504.50 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
[(1S,4aS,7R,7aS)-7-(acetyloxymethyl)-7-hydroxy-4-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 101316455 Click to see 650.70 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
[(1S,4aS,7R,7aS)-7-(acetyloxymethyl)-7-hydroxy-4-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 101316456 Click to see 650.70 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
[(1S,4aS,7R,7aS)-7-(acetyloxymethyl)-7-hydroxy-4-[[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-[[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 162983511 Click to see CC(C)CC(=O)OC1C2C(CCC2(COC(=O)C)O)C(=CO1)COC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O 650.70 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
[6-acetyloxy-7-(acetyloxymethyl)-7-hydroxy-4-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 14414525 Click to see 562.60 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
[7-(acetyloxymethyl)-7-hydroxy-4-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 163060002 Click to see CC(C)CC(=O)OC1C2C(CCC2(COC(=O)C)O)C(=CO1)COC3C(C(C(C(O3)CO)O)O)O 504.50 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
[7-(acetyloxymethyl)-7-hydroxy-4-[[3,4,5-trihydroxy-6-[3-(4-hydroxyphenyl)prop-2-enoyloxymethyl]oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 162983510 Click to see CC(C)CC(=O)OC1C2C(CCC2(COC(=O)C)O)C(=CO1)COC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O 650.70 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
> 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)81125-5
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
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)81125-5
Beta-Amyrin Acetate 92156 Click to see 468.80 unknown via CMAUP database
CID 15599867 15599867 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C 665.10 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
Urs-12-en-3-ol, hexadecanoate, (3)- 10394654 Click to see 665.10 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 https://doi.org/10.1016/S0031-9422(00)81125-5
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)81125-5
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 21952380 21952380 Click to see 118.09 unknown via CMAUP database
Succinic Acid 1110 Click to see 118.09 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-[[(2S,3R,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(4-ethenylphenoxy)oxane-3,4,5-triol 162948386 Click to see 414.40 unknown https://doi.org/10.1021/JA01525A079
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(4-ethenylphenoxy)oxane-3,4,5-triol 124222296 Click to see C=CC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 414.40 unknown https://doi.org/10.1021/JA01525A079
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(4-prop-2-enylphenoxy)oxane-3,4,5-triol 4484392 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 428.40 unknown https://doi.org/10.1246/BCSJ.55.3663
3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid 54036359 Click to see 326.30 unknown via CMAUP database
3-[4-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid 73208527 Click to see 326.30 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
4-(2-Propen-1-yl)phenyl 6-O-D-apio-beta-D-furanosyl-beta-D-glucopyranoside 442789 Click to see 428.40 unknown via CMAUP database
4'-O-beta-D-glucosyl-cis-p-coumaric acid 10604651 Click to see 326.30 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/S0031-9422(00)81125-5

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