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Viburnum furcatum

Viburnum furcatum - Unknown
Part: Unknown
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 UUID643ffad6e9cd5546322994
Scientific name Viburnum furcatum
Authority Blume ex Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 26: 483 (1880)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Japanese オオカメノキ

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-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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Applying early divergent characters in higher rank taxonomy of Melampsorineae (Basidiomycota, Pucciniales) Zhao P, Li Y, Li Y, Liu F, Liang J, Zhou X, Cai L Mycology 11-Jul-2022
PMCID:PMC9930778
doi:10.1080/21501203.2022.2089262
PMID:36816773
Variability in deer diet and plant vulnerability to browsing among forests with different establishment years of sika deer Sakata Y, Shirahama N, Uechi A, Okano K PeerJ 17-Sep-2021
PMCID:PMC8451445
doi:10.7717/peerj.12165
PMID:34616621
How did the characteristics of the growing season change during the past 100 years at a steep river basin in Japan? Shin N, Saitoh TM, Nasahara KN PLoS One 30-Jul-2021
PMCID:PMC8324334
doi:10.1371/journal.pone.0255078
PMID:34330144
Radiocaesium accumulation capacity of epiphytic lichens and adjacent barks collected at the perimeter boundary site of the Fukushima Dai-ichi Nuclear Power Station Dohi T, Ohmura Y, Yoshimura K, Sasaki T, Fujiwara K, Kanaizuka S, Nakama S, Iijima K PLoS One 24-May-2021
PMCID:PMC8143426
doi:10.1371/journal.pone.0251828
PMID:34029330
Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D Molecules 29-Apr-2020
PMCID:PMC7249135
doi:10.3390/molecules25092070
PMID:32365518
Quasipucciniastrum agrimoniae, gen. et sp. nov. on Agrimonia (Rosaceae) from China Qi XH, Cai L, Zhao P Mycology 30-Apr-2019
PMCID:PMC6691823
doi:10.1080/21501203.2019.1610522
PMID:31448148
Implications of clonality for ageing research Salguero-Gómez R Evol Ecol 04-Nov-2017
PMCID:PMC6954036
doi:10.1007/s10682-017-9923-2
PMID:31983800
Analysis of Sclerotia-Associated Fungal Communities in Cool-Temperate Forest Soils in North Japan Amasya AF, Narisawa K, Watanabe M Microbes Environ 04-Feb-2015
PMCID:PMC4356458
doi:10.1264/jsme2.ME14135
PMID:25740175
Crystal Structures of β-Primeverosidase in Complex with Disaccharide Amidine Inhibitors Saino H, Shimizu T, Hiratake J, Nakatsu T, Kato H, Sakata K, Mizutani M J Biol Chem 21-Apr-2014
PMCID:PMC4059125
doi:10.1074/jbc.M114.553271
PMID:24753293
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
Compounds from Viburnum sargentii Koehne and Evaluation of Their Cytotoxic Effects on Human Cancer Cell Lines Bae KE, Chong HS, Kim DS, Choi YW, Kim YS, Kim YK Molecules 25-Jun-2010
PMCID:PMC6257607
doi:10.3390/molecules15074599
PMID:20657380
Inhibition of nitric oxide production in lipopolysaccharide-activated RAW 264.7 macrophages by Jeju plant extracts Yang EJ, Yim EY, Song G, Kim GO, Hyun CG Interdiscip Toxicol 28-Dec-2009
PMCID:PMC2984114
doi:10.2478/v10102-009-0022-2
PMID:21217861
The New β-D-Glucosidase in Terpenoid-Isoquinoline Alkaloid Biosynthesis in Psychotria ipecacuanha Nomura T, Quesada AL, Kutchan TM J Biol Chem 12-Dec-2008
PMCID:PMC3259899
doi:10.1074/jbc.M806953200
PMID:18927081
Analysis of rice glycosyl hydrolase family 1 and expression of Os4bglu12 β-glucosidase Opassiri R, Pomthong B, Onkoksoong T, Akiyama T, Esen A, Ketudat Cairns JR BMC Plant Biol 29-Dec-2006
PMCID:PMC1781453
doi:10.1186/1471-2229-6-33
PMID:17196101
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

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 via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
4-Allylbenzene-1,2-diol 70775 Click to see C=CCC1=CC(=C(C=C1)O)O 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 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,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 CC(C)CC(=O)OC1C2C(CC(C2(COC(=O)C)O)OC(=O)C)C(=CO1)COC3C(C(C(C(O3)CO)O)O)O 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
Furcatoside A 101316455 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
Furcatoside B 101316456 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
Furcatoside C 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
Suspensolide A 14414526 Click to see CC(C)CC(=O)OC1C2C(CC(C2(COC(=O)C)O)OC(=O)C)C(=CO1)COC3C(C(C(C(O3)CO)O)O)O 562.60 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(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 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
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)81125-5
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 via CMAUP database
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 CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown via CMAUP database
beta-Ursolic acid 220774 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)81125-5
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
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)81125-5
> 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)81125-5
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)81125-5
Beta-Sitosterol 222284 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
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
Succinic Acid 1110 Click to see C(CC(=O)O)C(=O)O 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 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-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 C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 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 C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
4'-O-beta-D-glucosyl-cis-p-coumaric acid 10604651 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
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 via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/S0031-9422(00)81125-5
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)81125-5

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