Food and beverages (non-medicinal):
Ripe fruits are eaten fresh or cooked in East Asia, notably in Japan and Korea, where they are consumed locally as a minor wild edible. No specialized industrial food products derived from Viburnum wrightii are documented.
Properties relevant to use:
Fruit pulp is fleshy and sweet, supporting straightforward consumption.

Synonyms Top

Scientific name	Authority	First published in
Viburnum hessei	Koehne	Gartenflora 58: 91 (1909)

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	ミヤマガマズミ
Russian	Калина Райта
Chinese	浙皖荚蒾

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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No forms added yet.

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

Northern America click to expand
- Northeastern U.S.A.
  - Massachusetts

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001290804
USDA Plants	VIWR
UConn	527
Tropicos	6000439
KEW	urn:lsid:ipni.org:names:150014-1
The Plant List	tro-6000439
Open Tree Of Life	857961
Observations.org	150630
NCBI Taxonomy	349481
IPNI	150014-1
GBIF	3856130
EPPO	VIBWR
EOL	7018964
Elurikkus	426353
USDA GRIN	41446
Plantarium	40353

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 complete chloroplast genome of Viburnum dilatatum (Adoxaceae)

Wang X, Zhang X, Li D, Hou J, Sheng L, Sun G, Zhu L, Chen Z

Mitochondrial DNA B Resour

22-Mar-2021

PMCID:	PMC7995874
doi:	10.1080/23802359.2021.1891988
PMID:	33796714

The complete chloroplast genome sequence of Viburnum erosum (Adoxaceae)

Park J, Choi YG, Yun N, Xi H, Min J, Kim Y, Oh SH

Mitochondrial DNA B Resour

30-Sep-2019

PMCID:	PMC7707357
doi:	10.1080/23802359.2019.1667919
PMID:	33365955

Redescription of Takahashia citricola Kuwana, 1909, and its transfer to the genus Pulvinaria Targioni Tozzetti (Coccoidea, Coccidae)

Tanaka H

Zookeys

28-Aug-2012

PMCID:	PMC3433700
doi:	10.3897/zookeys.217.3405
PMID:	22977340

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

Studies on the Constituents of Viburnum Species. VIII. .GAMMA.-Lactone Glycosides from the Leaves of Viburnum wrightii MIQ.

Koichi MACHIDA, Masao KIKUCHI

Pharmaceutical Society of Japan

08-Dec-2011

doi:	10.1248/CPB.42.1388

Studies on the Constituents of Viburnum Species. On Phenolic Glycosides from the Leaves of Viburnum wrightii MIQ.

Koichi MACHIDA, Masao KIKUCHI

Pharmaceutical Society of Japan

08-Dec-2011

doi:	10.1248/CPB.41.248

Covalent interaction of ascorbic acid with natural products

Kesinger NG, Stevens JF

Phytochemistry

28-Oct-2009

PMCID:	PMC2787919
doi:	10.1016/j.phytochem.2009.09.028
PMID:	19875138

A phenol alloside from viburnum wrightii

Tetsuo Iwagawa, Hideo Takahashi, Kiyotaka Munesada, Tsunao Hase

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)80358-1

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(3R)-3-[(3S,3aR,6S,6aR)-3,6-dihydroxy-5-oxo-6a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,3a-dihydro-2H-furo[3,2-b]furan-6-yl]-3-(4-hydroxyphenyl)propanoic acid	10391341	Click to see	502.40	unknown	https://doi.org/10.1248/CPB.42.1388
3-[3,6-dihydroxy-5-oxo-6a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,3a-dihydro-2H-furo[3,2-b]furan-6-yl]-3-(4-hydroxyphenyl)propanoic acid	78111521	Click to see C1C(C2C(O1)(C(C(=O)O2)(C(CC(=O)O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	502.40	unknown	https://doi.org/10.1248/CPB.42.1388
methyl (3R)-3-[(3S,3aR,6S,6aR)-3,6-dihydroxy-5-oxo-6a-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,3a-dihydro-2H-furo[3,2-b]furan-6-yl]-3-(4-hydroxyphenyl)propanoate	162901295	Click to see	516.40	unknown	https://doi.org/10.1248/CPB.42.1388
methyl 3-[3,6-dihydroxy-5-oxo-6a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,3a-dihydro-2H-furo[3,2-b]furan-6-yl]-3-(4-hydroxyphenyl)propanoate	78111452	Click to see COC(=O)CC(C1=CC=C(C=C1)O)C2(C(=O)OC3C2(OCC3O)OC4C(C(C(C(O4)CO)O)O)O)O	516.40	unknown	https://doi.org/10.1248/CPB.42.1388
> 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)80358-1
Alpha-Amyrin	73170	Click to see	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)80358-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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)80358-1
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(00)80358-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3S,3aR,4'R,6R,6aR)-3-hydroxy-4'-(4-hydroxyphenyl)-6a-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[3,3a-dihydro-2H-furo[3,2-b]furan-6,5'-oxolane]-2',5-dione	162850294	Click to see	484.40	unknown	https://doi.org/10.1248/CPB.42.1388
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol	7576924	Click to see	272.25	unknown	https://doi.org/10.1016/S0031-9422(00)80358-1
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl (Z)-3-(4-hydroxyphenyl)prop-2-enoate	10002084	Click to see	418.40	unknown	https://doi.org/10.1248/CPB.41.248
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(4-hydroxyphenoxy)oxan-3-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate	10432153	Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(OC2OC3=CC=C(C=C3)O)CO)O)O)O	418.40	unknown	https://doi.org/10.1248/CPB.41.248
[3,4,5-Trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	85088698	Click to see	418.40	unknown	https://doi.org/10.1248/CPB.41.248
[4,5-Dihydroxy-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate	85129014	Click to see	434.40	unknown	https://doi.org/10.1248/CPB.41.248
[4,5-Dihydroxy-6-(hydroxymethyl)-2-(4-hydroxyphenoxy)oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate	85141334	Click to see	418.40	unknown	https://doi.org/10.1248/CPB.41.248
2-(Hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol	346	Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O	272.25	unknown	https://doi.org/10.1016/S0031-9422(00)80358-1
6-O-Acetylarbutin	14542705	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC=C(C=C2)O)O)O)O	314.29	unknown	https://doi.org/10.1016/S0031-9422(00)80358-1
6-O-Caffeoylarbutin	15689808	Click to see	434.40	unknown	https://doi.org/10.1248/CPB.41.248
Arbutin	440936	Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O	272.25	unknown	https://doi.org/10.1016/S0031-9422(00)80358-1
beta-D-Glucopyranoside, 4-hydroxyphenyl, 2-acetate	162851636	Click to see	314.29	unknown	https://doi.org/10.1248/CPB.41.248
coumaroyl(-2)Glc(b)-O-Ph(4-OH)	163191119	Click to see	418.40	unknown	https://doi.org/10.1248/CPB.41.248
coumaroyl(3-OH)(-4)Glc(b)-O-Ph(4-OH)	10388193	Click to see	434.40	unknown	https://doi.org/10.1248/CPB.41.248
coumaroyl(3-OH)(-6)All(b)-O-Ph(4-OH)	15689809	Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O	434.40	unknown	https://doi.org/10.1248/CPB.41.248
Robustaside A	26263971	Click to see	418.40	unknown	https://doi.org/10.1248/CPB.41.248
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
P-Coumaric Acid	637542	Click to see	164.16	unknown	https://doi.org/10.1016/S0031-9422(00)80358-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(2-oxochromen-7-yl)oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	10096901	Click to see	486.40	unknown	https://doi.org/10.1248/CPB.41.248
[3,4,5-Trihydroxy-6-(2-oxochromen-7-yl)oxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	162886755	Click to see	486.40	unknown	https://doi.org/10.1248/CPB.41.248
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
13-(3,4-dihydroxyphenyl)-7-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5-(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol	14586201	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC=C(C=C9)O)O)O)O)C1=CC(=C(C=C1)O)O)O	848.80	unknown	https://doi.org/10.1248/CPB.41.248
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	https://doi.org/10.1016/S0031-9422(00)80358-1

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Viburnum wrightii

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top