Viburnum furcatum
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
Suggest a correction!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).
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Japanese | オオカメノキ |
Germination/Propagation Top
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No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Asia-temperate click to expand
-
Eastern Asia
- Japan
- Korea
-
Russian Far East
- Kuril Islands
- Sakhalin
-
Eastern Asia
Links to other databases Top
Suggest others/fix!| 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)!
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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 |
|---|---|---|---|---|---|
| > 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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |