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Viburnum prunifolium

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64405ae3b709d871631135
Scientific name Viburnum prunifolium
Authority L.
First published in Sp. Pl. : 268 (1753)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Viburnum pyrifolium Poir. Encycl. 8: 653 (1808)
Viburnum bushii Ashe J. Elisha Mitchell Sci. Soc. 40: 48 (1924)
Viburnum prunifolium var. bushii (Ashe) E.J.Palmer & Steyerm. Ann. Missouri Bot. Gard. 22: 651 (1935)
Viburnum prunifolium var. globosum Nash Bull. Torrey Bot. Club 20(2): 70. 1893 [15 Feb 1893]

Common names Top

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Language Common/alternative name
English black haw
English black haw viburnum
English blackhaw
English blackhaw viburnum
English stag bush
English sweet haw
Arabic أفلوس خوخي الورق
Arabic رباطية خوخية الورق
Cherokee ᎧᏂᎦ
Czech kalina višňolistá
Hungarian szilvalevelű bangita
Ukrainian Калина сливолиста
Chinese 李叶荚蒾
Chinese 莢迷花

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
  • Northern America
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Missouri
      • Oklahoma
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Michigan
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • West Virginia
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001290684
UNII 0QG66711UL
Flora of Alabama 1396
Cornell Woody Plants 276
USDA Plants VIPR
UConn 532
Tropicos 6000185
KEW urn:lsid:ipni.org:names:326270-2
The Plant List tro-6000185
Missouri Botanical Garden 278961
Open Tree Of Life 51715
NCBI Taxonomy 237954
Nature Serve 2.141845
IUCN Red List 88331553
IPNI 326270-2
iNaturalist 129977
GBIF 2888608
Freebase /m/02pxq75
WisFlora 5375
EPPO VIBPU
EOL 490017
USDA GRIN 41408
Wikipedia Viburnum_prunifolium

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
Radio Telemetry and Harmonic Radar Tracking of the Spotted Lanternfly, Lycorma delicatula (White) (Hemiptera: Fulgoridae) Siderhurst MS, Murman KM, Kaye KT, Wallace MS, Cooperband MF Insects 30-Dec-2023
PMCID:PMC10816356
doi:10.3390/insects15010017
PMID:38249023
Foraging Wild Edibles: Dietary Diversity in Expanded Food Systems Bellows AC, Raj S, Pitstick E, Potteiger MR, Diemont SA Nutrients 31-Oct-2023
PMCID:PMC10647252
doi:10.3390/nu15214630
PMID:37960283
Functional immune boosters; the herb or its dead microbiome? Antigenic TLR4 agonist MAMPs found in 65 medicinal roots and algae’s Mazzio E, Barnes A, Badisa R, Fierros-Romero G, Williams H, Council S, Soliman KF J Funct Foods 29-Jul-2023
PMCID:PMC10469438
doi:10.1016/j.jff.2023.105687
PMID:37654434
Breathing Fresh Air in the City: Implementing Avenue Trees as a Sustainable Solution to Reduce Particulate Pollution in Urban Agglomerations Mandal M, Popek R, Przybysz A, Roy A, Das S, Sarkar A Plants (Basel) 03-Apr-2023
PMCID:PMC10097214
doi:10.3390/plants12071545
PMID:37050171
Pharmacological Evaluation of Scopoletin in the Carbon Tetrachloride-Induced Hepatotoxicity Model in Wistar Rats Sharma S, Anand A, Bhatia A, Sharma V, Singh AK, Banerjee D, Patil AN J Pharm Bioallied Sci 17-Feb-2023
PMCID:PMC10084995
doi:10.4103/jpbs.jpbs_333_22
PMID:37051421
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
KCNQ5 activation by tannins mediates vasorelaxant effects of barks used in Native American botanical medicine Manville RW, Redford KE, van der Horst J, Hogenkamp DJ, Jepps TA, Abbott GW FASEB J 01-Sep-2022
PMCID:PMC9404676
doi:10.1096/fj.202200724R
PMID:35997997
Comparison of Herbal Medicines Used for Women’s Menstruation Diseases in Different Areas of the World Jiao M, Liu X, Ren Y, Wang Y, Cheng L, Liang Y, Li Y, Zhang T, Wang W, Mei Z Front Pharmacol 04-Feb-2022
PMCID:PMC8854496
doi:10.3389/fphar.2021.751207
PMID:35185533
Antispasmodic Potential of Medicinal Plants: A Comprehensive Review Rauf A, Akram M, Semwal P, Mujawah AA, Muhammad N, Riaz Z, Munir N, Piotrovsky D, Vdovina I, Bouyahya A, Adetunji CO, Shariati MA, Almarhoon ZM, Mabkhot YN, Khan H Oxid Med Cell Longev 11-Nov-2021
PMCID:PMC8601825
doi:10.1155/2021/4889719
PMID:34804367
Natural Coumarins: Exploring the Pharmacological Complexity and Underlying Molecular Mechanisms Sharifi-Rad J, Cruz-Martins N, López-Jornet P, Lopez EP, Harun N, Yeskaliyeva B, Beyatli A, Sytar O, Shaheen S, Sharopov F, Taheri Y, Docea AO, Calina D, Cho WC Oxid Med Cell Longev 23-Aug-2021
PMCID:PMC8440074
doi:10.1155/2021/6492346
PMID:34531939
Genus Viburnum: Therapeutic Potentialities and Agro-Food-Pharma Applications Sharifi-Rad J, Quispe C, Vergara CV, Kitic D, Kostic M, Armstrong L, Shinwari ZK, Khalil AT, Brdar-Jokanović M, Ljevnaić-Mašić B, Varoni EM, Iriti M, Leyva-Gómez G, Herrera-Bravo J, Salazar LA, Cho WC Oxid Med Cell Longev 16-Jul-2021
PMCID:PMC8310452
doi:10.1155/2021/3095514
PMID:34326915
Fungal Endophytes as Efficient Sources of Plant-Derived Bioactive Compounds and Their Prospective Applications in Natural Product Drug Discovery: Insights, Avenues, and Challenges Singh A, Singh DK, Kharwar RN, White JF, Gond SK Microorganisms 19-Jan-2021
PMCID:PMC7833388
doi:10.3390/microorganisms9010197
PMID:33477910
Chemical novelty facilitates herbivore resistance and biological invasions in some introduced plant species Sedio BE, Devaney JL, Pullen J, Parker GG, Wright SJ, Parker JD Ecol Evol 23-Jul-2020
PMCID:PMC7452787
doi:10.1002/ece3.6575
PMID:32884656
Novel Drug Targets with Traditional Herbal Medicines for Overcoming Endometriosis Ilhan M, Dereli FT, Akkol EK Curr Drug Deliv 01-Jun-2019
PMCID:PMC6637095
doi:10.2174/1567201816666181227112421
PMID:30588884
An Updated List of Neuromedicinal Plants of Pakistan, Their Uses, and Phytochemistry Khan AW, Khan AU, Shah SM, Ullah A, Faheem M, Saleem M Evid Based Complement Alternat Med 03-Mar-2019
PMCID:PMC6420976
doi:10.1155/2019/6191505
PMID:30941198

Phytochemical Profile Top

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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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane 11636 Click to see 380.70 unknown https://doi.org/10.1021/JA01453A027
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
Isovaleric Acid 10430 Click to see 102.13 unknown https://doi.org/10.1021/JA01453A027
https://doi.org/10.1002/JPS.3030351010
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Hexanoic Acid 8892 Click to see 116.16 unknown https://doi.org/10.1021/JA01453A027
Octanoic Acid 379 Click to see CCCCCCCC(=O)O 144.21 unknown https://doi.org/10.1021/JA01453A027
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(1S,4aS,6S,7S,7aS)-4-[[(2R,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-6-hydroxy-7-(hydroxymethyl)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl] 3-methylbutanoate 14109595 Click to see 504.50 unknown https://doi.org/10.1055/S-2006-960469
[(1S,4aS,7S,7aS)-4-[[(2R,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-7-(hydroxymethyl)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl] 3-methylbutanoate 14109593 Click to see CC(C)CC(=O)OC1C2C(CCC2C(=CO1)COC3C(C(C(C(O3)CO)O)O)OC(=O)C)CO 488.50 unknown https://doi.org/10.1055/S-2006-960469
[(1S,4aS,7S,7aS)-4-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxymethyl]-7-(hydroxymethyl)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl] 3-methylbutanoate 93473163 Click to see CC(C)CC(=O)OC1C2C(CCC2C(=CO1)COC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)CO 592.60 unknown https://doi.org/10.1055/S-2006-960469
[4-[[3-Acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-6-hydroxy-7-(hydroxymethyl)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl] 3-methylbutanoate 14109594 Click to see 504.50 unknown https://doi.org/10.1055/S-2006-960469
[4-[[3-Acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-7-(hydroxymethyl)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl] 3-methylbutanoate 14109592 Click to see CC(C)CC(=O)OC1C2C(CCC2C(=CO1)COC3C(C(C(C(O3)CO)O)O)OC(=O)C)CO 488.50 unknown https://doi.org/10.1055/S-2006-960469
[4-[[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3-(4-hydroxyphenyl)prop-2-enoyloxy]oxan-2-yl]oxymethyl]-7-(hydroxymethyl)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl] 3-methylbutanoate 74135936 Click to see CC(C)CC(=O)OC1C2C(CCC2C(=CO1)COC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)CO 592.60 unknown https://doi.org/10.1055/S-2006-960469
[6-Hydroxy-7-(hydroxymethyl)-4-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl] 3-methylbutanoate 4490287 Click to see 462.50 unknown https://doi.org/10.1055/S-2006-960469
Patrinoside 162135 Click to see CC(C)CC(=O)OC1C2C(CC(C2CO)O)C(=CO1)COC3C(C(C(C(O3)CO)O)O)O 462.50 unknown https://doi.org/10.1055/S-2006-960469
https://doi.org/10.1016/J.JEP.2009.03.021

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