Aralia hispida - Unknown
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Internal ID UUID643fe55f34534767693582
Scientific name Aralia hispida
Authority Vent.
First published in Descr. Pl. Nouv. : t. 41 (1801)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aralia muehlenbergiana Schult. Syst. Veg. 6: 704 (1820)

Common names Top

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Language Common/alternative name
English bristly sarsaparilla
Russian Аралия щетинистая
Russian Аралия щетинистоволосистая
Chinese 毛楤木

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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.

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
      • Minnesota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Southeastern U.S.A.
      • Maryland
      • North Carolina
      • Virginia
    • Western Canada
      • Manitoba
      • Saskatchewan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000257683
UNII Z5DD9I2A63
Canadensys 2683
USDA Plants ARHI2
KEW urn:lsid:ipni.org:names:89666-1
The Plant List kew-14101
PaleoBotany 34572
Open Tree Of Life 712998
NCBI Taxonomy 51236
Nature Serve 2.150091
IPNI 89666-1
iNaturalist 119825
GBIF 3037033
WisFlora 2579
EPPO ARLHI
EOL 1153788
USDA GRIN 100494
Wikipedia Aralia_hispida
CMAUP NPO8632

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
Long-Term Steady-State Dry Boreal Forest in the Face of Disturbance Carcaillet C, Desponts M, Robin V, Bergeron Y Ecosystems 30-Oct-2019
PMCID:PMC7410099
doi:10.1007/s10021-019-00455-w
PMID:32831628
Ungulate browsers promote herbaceous layer diversity in logged temperate forests Faison EK, DeStefano S, Foster DR, Motzkin G, Rapp JM Ecol Evol 12-Jun-2016
PMCID:PMC4931004
doi:10.1002/ece3.2223
PMID:27386099
Linking GPS Telemetry Surveys and Scat Analyses Helps Explain Variability in Black Bear Foraging Strategies Lesmerises R, Rebouillat L, Dussault C, St-Laurent MH PLoS One 01-Jul-2015
PMCID:PMC4489386
doi:10.1371/journal.pone.0129857
PMID:26132204
A Temporal Dimension to the Influence of Pollen Rewards on Bee Behaviour and Fecundity in Aloe tenuior Duffy KJ, Johnson SD, Peter CI PLoS One 22-Apr-2014
PMCID:PMC3995886
doi:10.1371/journal.pone.0094908
PMID:24755611
Foundation species loss affects vegetation structure more than ecosystem function in a northeastern USA forest Orwig DA, Barker Plotkin AA, Davidson EA, Lux H, Savage KE, Ellison AM Peerj 19-Feb-2013
PMCID:PMC3629072
doi:10.7717/peerj.41
PMID:23638378
New Coleoptera records from New Brunswick, Canada: Mordellidae and Ripiphoridae Webster RP, Sweeney JD, DeMerchant I Zookeys 04-Apr-2012
PMCID:PMC3337063
doi:10.3897/zookeys.179.2583
PMID:22539896
Linking Self-Incompatibility, Dichogamy, and Flowering Synchrony in Two Euphorbia Species: Alternative Mechanisms for Avoiding Self-Fertilization? Narbona E, Ortiz PL, Arista M PLoS One 02-Jun-2011
PMCID:PMC3107240
doi:10.1371/journal.pone.0020668
PMID:21674062
The Mycetophagidae (Coleoptera) of the Maritime Provinces of Canada Majka CG Zookeys 22-Oct-2010
PMCID:PMC3088403
doi:10.3897/zookeys.64.553
PMID:21594022
Trapline foraging by pollinators: its ontogeny, economics and possible consequences for plants Ohashi K, Thomson JD Ann Bot 26-Apr-2009
PMCID:PMC2701764
doi:10.1093/aob/mcp088
PMID:19398446
Contrasting responses of bumble bees to feeding conspecifics on their familiar and unfamiliar flowers Kawaguchi LG, Ohashi K, Toquenaga Y Proc Biol Sci 14-Aug-2007
PMCID:PMC2279218
doi:10.1098/rspb.2007.0860
PMID:17698483
How to look like a mallow: evidence of floral mimicry between Turneraceae and Malvaceae Benitez-Vieyra S, de Ibarra NH, Wertlen AM, Cocucci AA Proc Biol Sci 10-Jul-2007
PMCID:PMC2287375
doi:10.1098/rspb.2007.0588
PMID:17623635
Floral reward production is timed by an insect pollinator Boisvert MJ, Veal AJ, Sherry DF Proc Biol Sci 22-May-2007
PMCID:PMC2270933
doi:10.1098/rspb.2007.0445
PMID:17519188
The effects of floral mimics and models on each others' fitness Anderson B, Johnson SD Proc Biol Sci 17-Jan-2006
PMCID:PMC1560233
doi:10.1098/rspb.2005.3401
PMID:16627282

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
> Alkaloids and derivatives / Aporphines
(-)-Isoboldine 6971182 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown via CMAUP database
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown via CMAUP database
> Alkaloids and derivatives / Pavine alkaloids
(-)-Argemonine 442168 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)OC)OC)OC)OC 355.40 unknown via CMAUP database
(+)-Caryachine 12305286 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O 325.40 unknown via CMAUP database
(1R,12R)-16-Methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol 3082467 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4 325.40 unknown via CMAUP database
(1R,12S)-15,16-dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-1-ol 10948236 Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC(=C(C=C25)OC)OC)O)OCO4 355.40 unknown via CMAUP database
(1R,12S)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-1-ol 11110561 Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC6=C(C=C25)OCO6)O)OCO4 339.30 unknown via CMAUP database
(1R,9R)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol 11869664 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O 327.40 unknown via CMAUP database
(1S,12S,20R)-15-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 102304441 Click to see C[N+]1(C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O)[O-] 341.40 unknown via CMAUP database
(1S,12S,20R)-16-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol 102304443 Click to see C[N+]1(C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4)[O-] 341.40 unknown via CMAUP database
(1S,12S)-15-methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 11823545 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O 325.40 unknown via CMAUP database
(1S,12S)-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaene 11012304 Click to see C1C2C3=CC4=C(C=C3CC(N2)C5=CC6=C(C=C51)OCO6)OCO4 309.30 unknown via CMAUP database
(1S,9S)-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2(7),3,5,10,12,14-hexaene-3,12-diol 92856799 Click to see CN1C2CC3=C(C1CC4=CC(=C(C=C24)O)OC)C(=C(C=C3)OC)O 327.40 unknown via CMAUP database
(1S,9S)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol 12300156 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O 327.40 unknown via CMAUP database
Caryachine 44575219 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4 325.40 unknown via CMAUP database
Crychine 193382 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4 323.30 unknown via CMAUP database
Escholtzine 12304178 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4 323.30 unknown via CMAUP database
> Alkaloids and derivatives / Proaporphines
(+)-8,9-Dihydrostepharine 13819281 Click to see COC1=C(C2=C3C(CC24CCC(=O)C=C4)NCCC3=C1)OC 299.40 unknown via CMAUP database
(1'S,2S,4R)-10-methoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1',11-diol 10870351 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(C=C4)O)O)OC 301.40 unknown via CMAUP database
Isoamuronine 12306127 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(=O)C=C4)OC)OC 313.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
alpha-Tocopherolquinone 2734086 Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Cryptocaryone 10379026 Click to see C1C2C(C=CC(=O)C2=C(C=CC3=CC=CC=C3)O)OC1=O 282.29 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives
6-Methyl-[1,3]dioxolo[4,5-g]isoquinolin-6-ium 2753983 Click to see C[N+]1=CC2=CC3=C(C=C2C=C1)OCO3 188.20 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-(6,7-Dimethoxyisoquinoline-1-ylmethyl)phenol 21814573 Click to see COC1=C(C=C2C(=C1)C=CN=C2CC3=CC=C(C=C3)O)OC 295.30 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Doryanin 12998814 Click to see CN1C=CC2=CC3=C(C=C2C1=O)OCO3 203.19 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
7-O-Methylcryptochinone A 46939685 Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4 314.30 unknown via CMAUP database
Cryptocaryanone A 10356404 Click to see C1C2C(C=CC3=C2C(=O)CC(O3)C4=CC=CC=C4)OC1=O 282.29 unknown via CMAUP database
Cryptochinone A 46939683 Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O 300.30 unknown via CMAUP database
Cryptochinone B 46939684 Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O 300.30 unknown via CMAUP database
Cryptochinone D 46939686 Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4 314.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(1'S,2R,4R)-10,11-dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,6'-cyclohex-2-ene]-1'-ol 10914050 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC=CC4O)OC)OC 315.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hexacosyl (E)-ferulate 5318033 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 558.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Epitaxifolin 712318 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl- 5748697 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O 298.29 unknown via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Mosloflavone 471722 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)OC 298.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-3,7,8-trimethoxyflavone 21632881 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC=CC=C3)OC)OC 328.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Larrein 9993268 Click to see COC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2)O 270.28 unknown via CMAUP database

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