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Viburnum mathewsii

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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 UUID64405ae43c70f681663467
Scientific name Viburnum mathewsii
Authority (Oerst.) Killip & A.C.Sm.
First published in Bull. Torrey Bot. Club 57: 253 (1930 publ. 1931)

Description Top

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Synonyms Top

Scientific name Authority First published in
Oreinotinus mathewsii Oerst. Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1860: 291 (1861)
Viburnum fur Graebn. Bot. Jahrb. Syst. 37: 434 (1906)

Common names Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001290697
Tropicos 6000243
KEW urn:lsid:ipni.org:names:264916-2
The Plant List tro-6000243
Open Tree Of Life 6061104
IPNI 264916-2
GBIF 3855950

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)!
Title Authors Publication Released IDs
The Revised Structure of Furcation, a Component of Leaves of <i>Viburnum furcatum</i> Blume Tsunao Hase, Tetsuo Iwagawa Oxford University Press (OUP) 26-Jul-2006
doi:10.1246/BCSJ.55.3663
Three iridoid glycosides from Viburnum furcatum T Hase Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81125-5

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
4-Allylphenol 68148 Click to see C=CCC1=CC=C(C=C1)O 134.17 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin palmitate 10394654 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
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Furcatin 442789 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

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