Eleutherococcus sieboldianus in Genus Eleutherococcus

Details Top

Internal ID	UUID6440390fe75f0797729101
Scientific name	Eleutherococcus sieboldianus
Authority	(Makino) Koidz.
First published in	Acta Phytotax. Geobot. 8: 52 (1939)

Description Top

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Eleutherococcus sieboldianus, also known as the five-fingered aralia or fiveleaf aralia, is a flowering plant belonging to the Araliaceae family. It is originally from Anhui province in China, but has been introduced to other countries such as Korea, Japan, and the United States. There is also a variegated variety of this plant that grows up to 8 feet tall.

Synonyms Top

Scientific name	Authority	First published in
Aralia pentaphylla	Thunb.	Fl. Jap. (Thunberg) 128. 1784 [Aug 1784]
Acanthopanax pentaphyllus var. variegatus	(G.Nicholson) Rehder	Stand. Cycl. Hort. 1: 11 1900
Acanthopanax sieboldianus	Makino	Bot. Mag. (Tokyo) 12: 10 (1898)
Eleutherococcus pentaphyllus	Nakai	Chosen Shokubutsu 1: 420 (1914)
Eleutherococcus sieboldianus f. variegatus	(G.Nicholson) S.Y.Hu	J. Arnold Arbor. 61: 110 (1980)
Aralia pentaphylla var. variegata	G.Nicholson	Ill. Dict. Gard. 1: 104. 1884
Acanthopanax sieboldianus var. variegatus	(G.Nicholson) Rehder	J. Arnold Arbor. 7: 243 (1926)
Eleutherococcus japonicus var. variegata	(G.Nicholson) Nakai	J. Arnold Arbor. 5: 11 (1924)

Common names Top

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Filter by language:

Language	Common/alternative name
English	fiveleaf aralia
English	five-fingered aralia
English	five-leaved aralia
Danish	finger-aralie
Danish	finger-aralie (eleutherococcus sieboldianus)
Danish	almindelig tornaralie
German	siebolds fingeraralie
Japanese	hime-ukogi
Japanese	ukogi
Japanese	ウコギ
Japanese	ヒメウコギ
Korean	오가나무
Swedish	japansk stickaralia
Chinese	百骑大栗树
Chinese	异株五加

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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 click to expand
- China
  - China Southeast
- Eastern Asia
  - Japan
  - Korea

Northern America click to expand
- North-central U.S.A.
  - Illinois
- Northeastern U.S.A.
  - Connecticut
  - Massachusetts
  - New Hampshire
  - New York
  - Pennsylvania
  - West Virginia
- Southeastern U.S.A.
  - Kentucky
  - Maryland
- Southwestern U.S.A.
  - Utah

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000948129
Cornell Woody Plants	393
Canadensys	29944
UConn	12
Tropicos	2200802
KEW	urn:lsid:ipni.org:names:90437-1
The Plant List	kew-66488
PFAF	Eleutherococcus sieboldianus
Open Tree Of Life	513396
NCBI Taxonomy	257409
IPNI	90437-1
iNaturalist	144021
GBIF	3035473
EOL	1145571
USDA GRIN	409414
Wikipedia	Eleutherococcus_sieboldianus

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

Modelling and targeting mitochondrial protein tyrosine phosphatase 1: a computational approach

Ragunathan V, Chithra K, Shivanika C, Sudharsan MS

In Silico Pharmacol

17-Jan-2022

PMCID:	PMC8762535
doi:	10.1007/s40203-022-00119-z
PMID:	35111562

Integrating structure-based machine learning and co-evolution to investigate specificity in plant sesquiterpene synthases

Durairaj J, Melillo E, Bouwmeester HJ, Beekwilder J, de Ridder D, van Dijk AD

PLoS Comput Biol

22-Mar-2021

PMCID:	PMC8016262
doi:	10.1371/journal.pcbi.1008197
PMID:	33750949

Nigella A ameliorates inflammation and intestinal flora imbalance in DSS induced colitis mice

Hu X, Xu N, Yang X, Hu X, Zheng Y, Zhang Q

AMB Express

04-Oct-2020

PMCID:	PMC7533278
doi:	10.1186/s13568-020-01114-3
PMID:	33011900

The effect of Opuntia ficus‐indica juice supplementation on oxidative stress, cardiovascular parameters, and biochemical markers following yo‐yo Intermittent recovery test

Khouloud A, Abedelmalek S, Chtourou H, Souissi N

Food Sci Nutr

06-Dec-2017

PMCID:	PMC5849923
doi:	10.1002/fsn3.529
PMID:	29564091

Effects of Flavonoids and Triterpene Analogues from Leaves of Eleutherococcus sieboldianus (Makino) Koidz. ‘Himeukogi’ in 3T3-L1 Preadipocytes

Nishina A, Itagaki M, Suzuki Y, Koketsu M, Ninomiya M, Sato D, Suzuki T, Hayakawa S, Kuroda M, Kimura H

Molecules

22-Apr-2017

PMCID:	PMC6154646
doi:	10.3390/molecules22040671
PMID:	28441735

The Hidden World within Plants: Ecological and Evolutionary Considerations for Defining Functioning of Microbial Endophytes

Hardoim PR, van Overbeek LS, Berg G, Pirttilä AM, Compant S, Campisano A, Döring M, Sessitsch A

Microbiol Mol Biol Rev

01-Jul-2015

PMCID:	PMC4488371
doi:	10.1128/MMBR.00050-14
PMID:	26136581

The Blood Lactate Increase in High Intensity Exercise Is Depressed by Acanthopanax sieboldianus

Kato M, Kurakane S, Nishina A, Park J, Chang H

Nutrients

16-Oct-2013

PMCID:	PMC3820064
doi:	10.3390/nu5104134
PMID:	24135965

Triterpene glycosides from leaves ofAcanthopanax sieboldianus introduced to Ukraine and Crimea

V. I. Grishkovets, A. M. Pyatygin, V. Ya. Chirva

Springer Science and Business Media LLC

14-Nov-2005

doi:	10.1007/BF02238349

Saponins from leaves of Acanthopanax sieboldianus.

Sawada H, Miyakoshi M, Isoda S, Ida Y, Shoji J

Phytochemistry

01-Nov-1993

doi:	10.1016/S0031-9422(00)90727-1
PMID:	7764238

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[6-[[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 10-[3-[3,5-dihydroxy-6-methyl-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	56671047	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1353.50	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
Cussonoside A	171596	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)O)C)(C)C)O)O)O)CO)O)O)O	943.10	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
HuzhangosideB	13880086	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1337.50	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
Kalopanaxsaponin B	11491905	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1221.40	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1 https://doi.org/10.1007/BF02238349
Kalopanaxsaponin B;Glycoside L-H2; Hederoside H1	3874518	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1221.40	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
Olean-12-en-28-oic acid, 3-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-alpha-L-arabinopyranosyl]oxy]-23-hydroxy-, O-6-deoxy-alpha-L-mannopyranosyl-(1.fwdarw.4)-O-beta-D-glucopyranosyl-(1.fwdarw.6)-beta-D-glucopyranosyl ester, (3beta,4alpha)-	73297	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1221.40	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1 https://doi.org/10.1007/BF02238349
Sieboldianoside A	57393816	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1353.50	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
Sieboldianoside B	192585	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1337.50	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1 https://doi.org/10.1007/BF02238349
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	21637697	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
(4aS,6bR,9S,10S,12aR)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	6325965	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
10-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	267360	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)O)O	751.00	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
alpha-Hederin	73296	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)O)O	751.00	unknown	https://doi.org/10.1007/BF02238349 https://doi.org/10.1016/S0031-9422(00)90727-1
CID 15625347	15625347	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
Presapogenin CP4	13880090	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	867.10	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
Presapogenin-CP4	21637703	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	867.10	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
Sapindoside B	161686	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	12313332	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1
Kaempferol-3-O-rutinoside	5318767	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(00)90727-1

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Eleutherococcus sieboldianus

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top