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Sorbus decora

Sorbus decora - 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 UUID6440403a35fb7355212421
Scientific name Sorbus decora
Authority (Sarg.) C.K.Schneid.
First published in Bull. Herb. Boissier , sér. 2, 6: 313 (1906)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aucuparia subvestita Nieuwl. Amer. Midl. Naturalist 4: 175 (1915)
Sorbus americana var. sitchensis (Roem.) Sudw. Check List For. Trees U.S. : 133 (1927)
Sorbus americana var. decora Sarg. Man. Trees : 357 (1905)
Sorbus scopulina Hough Handbook of the trees of the Northern States and Canada ; 1907 241, f.280,281 1907
Sorbus americana Pursh Flora Americae septentrionalis ; 1814 341 1814
Sorbus sambucifolia Dippel Handbuch der Laubholzkunde ; 1889 368, f.191 1893
Sorbus dumosa House Annotated list of the ferns and flowering plants of New York State ; 1924 409 1924
Sorbus subvestita Rosend. & Butters Trees and shrubs of Minnesota ; 1928 195, f. 1928
Pyrus sambucifolia S.Watson & J.M.Coult. A manual of the botany of the Northern United States ; 1890 164 1890
Pyrus sitchensis B.L.Rob. & Fernald A manual of the botany of the Northern United States ; 1908 458 1908
Pyrus subvestita Farw. Amer. Midl. Naturalist 1930, xii. 122.
Pyrus dumosa Fernald Rhodora 23: 266 (1921)
Sorbus groenlandica (C.K.Schneid.) Á.Löve & D.Löve Univ. Colorado Stud., Ser. Biol. 17: 23 (1965)
Pyrus americana var. decora Sarg. Silva 14: 101 (1902)
Pyrus decora (Sarg.) Hyland Rhodora 45: 28 (1943)
Pyrus decora var. groenlandica (C.K.Schneid.) Fernald Rhodora 49: 233 (1947)
Sorbus decora var. groenlandica (C.K.Schneid.) G.N.Jones J. Arnold Arbor. 20: 30 (1939)

Common names Top

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Language Common/alternative name
English northern mountain ash
English dogberry
English northern mountain-ash
English showy mountain ash
English showy mountain-ash
Danish labrador-røn
Icelandic skrautreynir
Russian Рябина нарядная
Russian Рябина красивая
Chinese 装饰花楸

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
20°C x 2 weeks then 4°C x 16 weeks

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Eastern Canada
      • Labrador
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Minnesota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New York
      • Ohio
      • Pennsylvania
      • Vermont
    • Subarctic America
      • Greenland
      • Nunavut
    • Western Canada
      • Manitoba
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001015088
Canadensys 8965
USDA Plants SODE3
Tropicos 27800195
INPN 761882
KEW urn:lsid:ipni.org:names:240783-2
The Plant List rjp-6186
Missouri Botanical Garden 286371
Open Tree Of Life 426112
NCBI Taxonomy 765745
Nature Serve 2.961540
IUCN Red List 135957190
IPNI 240783-2
iNaturalist 54266
GBIF 3012350
Freebase /m/03nqdzc
WisFlora 5110
EPPO SOUDC
EOL 636876
Elurikkus 351043
USDA GRIN 35015
Wikipedia Sorbus_decora

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
Anti-Diabetic Potential of Polyphenol-Rich Fruits from the Maleae Tribe—A Review of In Vitro and In Vivo Animal and Human Trials Rutkowska M, Olszewska MA Nutrients 28-Aug-2023
PMCID:PMC10489674
doi:10.3390/nu15173756
PMID:37686786
Nitrogen and sulfur deposition reductions projected to partially restore forest soil conditions in the US Northeast, while understory composition continues to shift with future climate change LeDuc SD, Clark CM, Phelan J, Belyazid S, Bennett M, Boaggio K, Buckley J, Cajka J, Jones P Water Air Soil Pollut 05-Sep-2022
PMCID:PMC9610802
doi:10.1007/s11270-022-05793-5
PMID:36312741
Terpenoid-Rich Extract of Dillenia indica L. Bark Displays Antidiabetic Action in Insulin-Resistant C2C12 Cells and STZ-Induced Diabetic Mice by Attenuation of Oxidative Stress Song BR, Alam MB, Lee SH Antioxidants (Basel) 23-Jun-2022
PMCID:PMC9312268
doi:10.3390/antiox11071227
PMID:35883721
Phytochemistry in the Ethnopharmacology of North and Central America Arnason JT, Harris CS, Guerrero-Analco JA Front Pharmacol 28-Feb-2022
PMCID:PMC8918843
doi:10.3389/fphar.2022.815742
PMID:35295322
A Multivariate Approach to Ethnopharmacology: Antidiabetic Plants of Eeyou Istchee Hall B, Rapinski M, Spoor D, Eid H, Saleem A, Arnason JT, Foster B, Cuerrier A, Haddad PS, Harris CS Front Pharmacol 18-Jan-2022
PMCID:PMC8808167
doi:10.3389/fphar.2021.511078
PMID:35126097
People and Plants in Nunatsiavut (Labrador, Canada): Examining Plants as a Foundational Aspect of Culture in the Subarctic Norton CH, Cuerrier A, Hermanutz L Econ Bot 01-Nov-2021
PMCID:PMC8888477
doi:10.1007/s12231-021-09530-7
PMID:35273405
Antidiabetic potential of the isolated fractions from the plants of Rosaceae family in streptozotocin-induced diabetic rats Bahrami G, Izadi B, Miraghaee SS, Mohammadi B, Hatami R, Sajadimajd S, Batooie N Res Pharm Sci 19-Aug-2021
PMCID:PMC8407159
doi:10.4103/1735-5362.323917
PMID:34522198
Gymnosporangium species on Malus: species delineation, diversity and host alternation Zhao P, Qi XH, Crous PW, Duan WJ, Cai L Persoonia 10-Jan-2020
PMCID:PMC8375348
doi:10.3767/persoonia.2020.45.03
PMID:34456372
Intestinal Saturated Long-Chain Fatty Acid, Glucose and Fructose Transporters and Their Inhibition by Natural Plant Extracts in Caco-2 Cells Schreck K, Melzig MF Molecules 06-Oct-2018
PMCID:PMC6222386
doi:10.3390/molecules23102544
PMID:30301205
Anti-apoptotic potential of several antidiabetic medicinal plants of the eastern James Bay Cree pharmacopeia in cultured kidney cells Li S, Pasquin S, Eid HM, Gauchat JF, Saleem A, Haddad PS BMC Complement Altern Med 30-Jan-2018
PMCID:PMC5789738
doi:10.1186/s12906-018-2104-1
PMID:29378549
Phytogeographic and genetic variation in Sorbus, a traditional antidiabetic medicine—adaptation in action in both a plant and a discipline Bailie A, Renaut S, Ubalijoro E, Guerrero-Analco JA, Saleem A, Haddad P, Arnason JT, Johns T, Cuerrier A PeerJ 03-Nov-2016
PMCID:PMC5101603
doi:10.7717/peerj.2645
PMID:27833811
Novel Approach to Identify Potential Bioactive Plant Metabolites: Pharmacological and Metabolomics Analyses of Ethanol and Hot Water Extracts of Several Canadian Medicinal Plants of the Cree of Eeyou Istchee Shang N, Saleem A, Musallam L, Walshe-Roussel B, Badawi A, Cuerrier A, Arnason JT, Haddad PS PLoS One 11-Aug-2015
PMCID:PMC4532419
doi:10.1371/journal.pone.0135721
PMID:26263160
A study of antioxidant activity, enzymatic inhibition and in vitro toxicity of selected traditional sudanese plants with anti-diabetic potential Hilmi Y, Abushama MF, Abdalgadir H, Khalid A, Khalid H BMC Complement Altern Med 07-May-2014
PMCID:PMC4017226
doi:10.1186/1472-6882-14-149
PMID:24885334
Investigating Wild Berries as a Dietary Approach to Reducing the Formation of Advanced Glycation Endproducts: Chemical Correlates of In Vitro Antiglycation Activity Harris CS, Cuerrier A, Lamont E, Haddad PS, Arnason JT, Bennett SA, Johns T Plant Foods Hum Nutr 22-Jan-2014
PMCID:PMC3930840
doi:10.1007/s11130-014-0403-3
PMID:24448675
The Action of Antidiabetic Plants of the Canadian James Bay Cree Traditional Pharmacopeia on Key Enzymes of Hepatic Glucose Homeostasis Nachar A, Vallerand D, Musallam L, Lavoie L, Badawi A, Arnason J, Haddad PS Evid Based Complement Alternat Med 24-Jun-2013
PMCID:PMC3707264
doi:10.1155/2013/189819
PMID:23864882

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
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
3,4,5-Trimethoxy-1,1'-biphenyl 46186838 Click to see COC1=CC(=CC(=C1OC)OC)C2=CC=CC=C2 244.28 unknown https://doi.org/10.1139/V62-170
Aucuparin 442508 Click to see COC1=CC(=CC(=C1O)OC)C2=CC=CC=C2 230.26 unknown https://doi.org/10.1139/V62-170
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-4,8a-bis(hydroxymethyl)-4,6a,6b,11,12,14b-hexamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 46939148 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)CO 458.70 unknown https://doi.org/10.1021/NP1003005
[(3S,4R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-4,8a-bis(hydroxymethyl)-4,6a,6b,11,12,14b-hexamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 46939046 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C)C2C1C)C)CO 620.90 unknown https://doi.org/10.1021/NP1003005
[3a,8-Bis(hydroxymethyl)-5a,5b,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 75244486 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)CO 620.90 unknown https://doi.org/10.1021/NP1003005
[4,8a-bis(hydroxymethyl)-4,6a,6b,11,12,14b-hexamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 75244485 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C)C2C1C)C)CO 620.90 unknown https://doi.org/10.1021/NP1003005
23-Hydroxybetulin 14605681 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)CO 458.70 unknown https://doi.org/10.1021/NP1003005
3,4-Dihydroxy-trans-cinnamic acid 23,28-dihydroxylupa-20(29)-ene-3beta-yl ester 46939047 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)CO 620.90 unknown https://doi.org/10.1021/NP1003005
3a,8-Bis(hydroxymethyl)-5a,5b,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 14605680 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)CO 458.70 unknown https://doi.org/10.1021/NP1003005
4,8a-bis(hydroxymethyl)-4,6a,6b,11,12,14b-hexamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 75244538 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)CO 458.70 unknown https://doi.org/10.1021/NP1003005
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP1003005
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/10.1021/NP1003005
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1021/NP1003005
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP1003005
Lup-20(29)-ene-3beta,28-diol 221023 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1021/NP1003005
Urs-12-en-3beta-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1021/NP1003005
Urs-12-ene-3,28-diol, (3beta)- 3266408 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1021/NP1003005
Uvaol 92802 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1021/NP1003005
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/NP1003005
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/NP1003005
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/NP1003005

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Collections Top

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