Viburnum sieboldii - Unknown
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Internal ID UUID64405ae40a64a290588564
Scientific name Viburnum sieboldii
Authority Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi 2: 267 (1866)

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Viburnum sieboldii, also known as Siebold's viburnum, is a large shrub or small tree in the muskroot family, Adoxaceae. It has opposite, simple leaves and produces white flowers in the spring. This plant is native to East Asia and is commonly used as an ornamental plant in gardens and landscapes. It is also known for its medicinal properties, with its bark and roots being used in traditional medicine. Viburnum sieboldii is a popular choice for its attractive foliage and flowers, making it a valuable addition to any garden.

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No known synonyms.

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Language Common/alternative name
English siebold's arrowwood
Czech kalina sieboldova
Japanese ゴマギ
Chinese 毛叶荚迷
Chinese 毛葉莢迷

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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
  • Northern America
    • Northeastern U.S.A.
      • Connecticut
      • Massachusetts
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
    • Southeastern U.S.A.
      • Delaware
      • District Of Columbia
      • Kentucky
      • Maryland
      • Virginia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001290688
UNII WZI5PUR4YU
Cornell Woody Plants 281
USDA Plants VISI
UConn 538
Tropicos 6000192
KEW urn:lsid:ipni.org:names:149928-1
The Plant List tro-6000192
Missouri Botanical Garden 278964
Open Tree Of Life 383302
NCBI Taxonomy 61591
Nature Serve 2.137518
IPNI 149928-1
iNaturalist 170206
GBIF 2888597
Freebase /m/03d6b7_
EPPO VIBSI
EOL 488682
USDA GRIN 41428
Wikipedia Viburnum_sieboldii

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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Title Authors Publication Released IDs
Rapid Collection and Aptamer-Based Sensitive Electrochemical Detection of Soybean Rust Fungi Airborne Urediniospores Krivitsky V, Granot E, Avidor Y, Borberg E, Voegele RT, Patolsky F ACS Sens 28-Jan-2021
PMCID:PMC8023804
doi:10.1021/acssensors.0c02452
PMID:33507747
Taxonomy and phylogeny of the Erysiphe lonicerae complex (Helotiales, Erysiphaceae) on Lonicera spp. Bradshaw M, Braun U, Götz M, Takamatsu S Fungal Syst Evol 26-Nov-2020
PMCID:PMC8165964
doi:10.3114/fuse.2021.07.03
PMID:34124617
NGF-potentiating vibsane-type diterpenoids from Viburnum sieboldii. Kubo M, Kishimoto Y, Harada K, Hioki H, Fukuyama Y Bioorg Med Chem Lett 15-Apr-2010
doi:10.1016/J.BMCL.2010.02.085
PMID:20233658

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 acid esters
[(E)-2-[(1R,2R,8S,10R,12S)-8-methyl-2,10-bis(2-oxopropyl)-3,11-dioxatricyclo[6.3.1.01,5]dodec-5-en-12-yl]ethenyl] 3-methylbut-2-enoate 162983703 Click to see CC(=CC(=O)OC=CC1C2(CC=C3C1(C(OC3)CC(=O)C)OC(C2)CC(=O)C)C)C 416.50 unknown https://doi.org/10.1016/J.BMCL.2010.02.085
2-[8-Methyl-2,10-bis(2-oxopropyl)-3,11-dioxatricyclo[6.3.1.01,5]dodec-5-en-12-yl]ethenyl 3-methylbut-2-enoate 75225886 Click to see CC(=CC(=O)OC=CC1C2(CC=C3C1(C(OC3)CC(=O)C)OC(C2)CC(=O)C)C)C 416.50 unknown https://doi.org/10.1016/J.BMCL.2010.02.085
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(E)-2-[(1R,2R,7R)-5-(hydroxymethyl)-2-[(E)-4-methoxy-4-methylpent-2-enyl]-2-methyl-6-oxo-7-(2-oxopropyl)cyclohept-4-en-1-yl]ethenyl] 3-methylbut-2-enoate 163056865 Click to see CC(=CC(=O)OC=CC1C(C(=O)C(=CCC1(C)CC=CC(C)(C)OC)CO)CC(=O)C)C 446.60 unknown https://doi.org/10.1016/J.BMCL.2010.02.085
[(E)-2-[(1R,2R,7S)-5-(hydroxymethyl)-2-[(E)-4-methoxy-4-methylpent-2-enyl]-2-methyl-6-oxo-7-(2-oxopropyl)cyclohept-4-en-1-yl]ethenyl] 3-methylbut-2-enoate 163056864 Click to see CC(=CC(=O)OC=CC1C(C(=O)C(=CCC1(C)CC=CC(C)(C)OC)CO)CC(=O)C)C 446.60 unknown https://doi.org/10.1016/J.BMCL.2010.02.085
2-[5-(Hydroxymethyl)-2-(4-methoxy-4-methylpent-2-enyl)-2-methyl-6-oxo-7-(2-oxopropyl)cyclohept-4-en-1-yl]ethenyl 3-methylbut-2-enoate 75225901 Click to see CC(=CC(=O)OC=CC1C(C(=O)C(=CCC1(C)CC=CC(C)(C)OC)CO)CC(=O)C)C 446.60 unknown https://doi.org/10.1016/J.BMCL.2010.02.085
> Organoheterocyclic compounds / Furofurans
(8Z)-neovibsanin M 46884910 Click to see CC(=CC(=O)OC=CC1C(CC=C2C13C(CC(O3)(C)OC)OC2)(C)CC=CC(C)(C)OC)C 460.60 unknown https://doi.org/10.1016/J.BMCL.2010.02.085
2-[2-methoxy-8-(4-methoxy-4-methylpent-2-enyl)-2,8-dimethyl-3a,5,7,9-tetrahydro-3H-furo[2,3-i][2]benzofuran-9-yl]ethenyl 3-methylbut-2-enoate 75225900 Click to see CC(=CC(=O)OC=CC1C(CC=C2C13C(CC(O3)(C)OC)OC2)(C)CC=CC(C)(C)OC)C 460.60 unknown https://doi.org/10.1016/J.BMCL.2010.02.085
Neovibsanin A 46866590 Click to see CC(=CCCC1(CC=C2COC3C2(C1C=COC(=O)C=C(C)C)OC(C3)(C)OC)C)C 430.60 unknown https://doi.org/10.1016/J.BMCL.2010.02.085
Neovibsanin B 25259221 Click to see CC(=CCCC1(CC=C2COC3C2(C1C=COC(=O)C=C(C)C)OC(C3)(C)OC)C)C 430.60 unknown https://doi.org/10.1016/J.BMCL.2010.02.085
neovibsanin L 46866589 Click to see CC(=CC(=O)OC=CC1C(CC=C2C13C(CC(O3)(C)OC)OC2)(C)CC=CC(C)(C)OC)C 460.60 unknown https://doi.org/10.1016/J.BMCL.2010.02.085
neovibsanin M 46866492 Click to see CC(=CC(=O)OC=CC1C(CC=C2C13C(CC(O3)(C)OC)OC2)(C)CC=CC(C)(C)OC)C 460.60 unknown https://doi.org/10.1016/J.BMCL.2010.02.085
> Phenylpropanoids and polyketides / Isochromanequinones / Benzoisochromanequinones
(1R,3S,4R)-4-hydroxy-9-methoxy-1,3-dimethyl-3,4-dihydro-1H-benzo[g]isochromene-5,10-dione 162993454 Click to see CC1C(C2=C(C(O1)C)C(=O)C3=C(C2=O)C=CC=C3OC)O 288.29 unknown https://doi.org/10.1016/J.BMCL.2010.02.085

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