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Viburnum wrightii

Viburnum wrightii - Unknown
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Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64405ae8f1f1c998830772
Scientific name Viburnum wrightii
Authority Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi 2: 267 (1866)

Description Top

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Synonyms Top

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

Common names Top

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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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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
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Kuril Islands
      • Sakhalin

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

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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
> 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 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
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 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
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
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80358-1
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 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
24-Ethylcholest-5-en-3beta-ol 22012 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
> 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 C1C(C2(C(=O)OC3C2(OCC3O)OC4C(C(C(C(O4)CO)O)O)O)OC1=O)C5=CC=C(C=C5)O 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 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
[(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 C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)O)O)O)O 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 C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)O)O)O)O 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 C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O 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 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
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 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
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 CC(=O)OC1C(C(C(OC1OC2=CC=C(C=C2)O)CO)O)O 314.29 unknown https://doi.org/10.1248/CPB.41.248
coumaroyl(-2)Glc(b)-O-Ph(4-OH) 163191119 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
coumaroyl(3-OH)(-4)Glc(b)-O-Ph(4-OH) 10388193 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O 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 C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)O)O)O)O 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 C1=CC(=CC=C1C=CC(=O)O)O 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 C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 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 C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 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
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(00)80358-1

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