Elaeocarpus sylvestris in Genus Elaeocarpus

Details Top

Internal ID	UUID644019301042d963328173
Scientific name	Elaeocarpus sylvestris
Authority	Poir.
First published in	Encycl. , Suppl. 2: 704 (1812)

Description Top

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Elaeocarpus sylvestris, also known as the woodland elaeocarpus, is a tree species found in China, Japan, Korea, Taiwan, and Vietnam. It grows up to 15 meters tall and is typically found in evergreen forests at altitudes between 300 and 2000 meters. The tree has shiny, oblong leaves and produces green-white flowers in racemes, followed by black olive-like fruits in the autumn. The fruits are edible and the oil from the seeds can be used to make soap and lubricants. The bark can also be used as a dye source. The tree is often planted along streets and in parks. However, it is susceptible to a disease called Elaeocarpus yellows, which can be treated with oxytetracycline. The tree also contains compounds with potential medicinal properties, such as a gallotannin and a unique acid ester molecule. In Japanese culture, the tree is a symbol of the city of Urasoe, and in South Korea, it is a designated natural monument.

Synonyms Top

Scientific name	Authority	First published in
Adenodus sylvestris	Lour.	Fl. Cochinch. : 294 (1790)
Elaeocarpus ellipticus	Makino	Bot. Mag. (Tokyo) 18: 67. 1904
Elaeocarpus ellipticus	Nakai	Bot. Mag. (Tokyo) 32: 221. 1918
Elaeocarpus henryi	Hance	J. Bot. 23: 322 (1885)
Elaeocarpus japonicus	Turcz.	Bull. Soc. Imp. Naturalistes Moscou 19(2): 492. 1846
Elaeocarpus kwangtungensis	Hu	J. Arnold Arbor. 5: 229. 1924
Elaeocarpus lanyuensis	C.E.Chang	Quart. J. Chin. Forest. 21(1): 113 (1988), without type.
Elaeocarpus omeiensis	Rehder & E.H.Wilson	Pl. Wilson. 2: 360 (1915)
Elaeocarpus sylvestris var. ellipticus	(Thunb.) H.Hara

Common names Top

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Filter by language:

Language	Common/alternative name
English	horutonoki
Japanese	ホルトの木
Japanese	モガシ
Japanese	ホルトノキ
Korean	제주 천지연 담팔수 자생지
Korean	담팔수
pwn	tjaljum
Vietnamese	côm rừng
Vietnamese	Đảm bát
Vietnamese	Đỗ anh
Vietnamese	Đỗ oanh
Vietnamese	sơn đỗ anh
Vietnamese	côm trâu
Chinese	杜英
Chinese	山杜英

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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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 South-central
  - China Southeast
  - Hainan

Asia-tropical click to expand
- Indo-China
  - Vietnam

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000664817
Tropicos	11700200
KEW	urn:lsid:ipni.org:names:833975-1
The Plant List	kew-2786062
Open Tree Of Life	166969
NCBI Taxonomy	232790
IUCN Red List	144303432
IPNI	833975-1
iNaturalist	525692
GBIF	7291001
Freebase	/m/0_qj6d1
Wikipedia	Elaeocarpus_sylvestris

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

Investigation the biological activities and the metabolite profiles of endophytic fungi isolated from Gundelia tournefortii L.

Ebadi M, Ahmadi F, Tahmouresi H, Pazhang M, Mollaei S

Sci Rep

25-Mar-2024

PMCID:	PMC10963752
doi:	10.1038/s41598-024-57222-8
PMID:	38528041

Pest categorisation of Pyrrhoderma noxium

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL

EFSA J

19-Mar-2024

PMCID:	PMC10949325
doi:	10.2903/j.efsa.2024.8667
PMID:	38505477

Natural products as a source of Coronavirus entry inhibitors

Szabó D, Crowe A, Mamotte C, Strappe P

Front Cell Infect Microbiol

21-Feb-2024

PMCID:	PMC10915212
doi:	10.3389/fcimb.2024.1353971
PMID:	38449827

Plant species identity and mycorrhizal type explain the root-associated fungal pathogen community assembly of seedlings based on functional traits in a subtropical forest

Li Y, Xie Y, Liu Z, Shi L, Liu X, Liang M, Yu S

Front Plant Sci

27-Oct-2023

PMCID:	PMC10641815
doi:	10.3389/fpls.2023.1251934
PMID:	37965023

Recent Advances in the Application of Cucurbitacins as Anticancer Agents

Zieniuk B, Pawełkowicz M

Metabolites

14-Oct-2023

PMCID:	PMC10608718
doi:	10.3390/metabo13101081
PMID:	37887406

Fungal Endophytes: Microfactories of Novel Bioactive Compounds with Therapeutic Interventions; A Comprehensive Review on the Biotechnological Developments in the Field of Fungal Endophytic Biology over the Last Decade

Gupta A, Meshram V, Gupta M, Goyal S, Qureshi KA, Jaremko M, Shukla KK

Biomolecules

25-Jun-2023

PMCID:	PMC10377637
doi:	10.3390/biom13071038
PMID:	37509074

The Liverwort and Hornwort Flora of Jeju Island, Republic of Korea: A Volcanic Island with a Unique Mixture of Subtropical, Temperate, Boreal, and Arctomontane Taxa

Choi SS, Bakalin VA, Bum HM, Park SJ, Kim DS, Ahn US, Moon MO

Plants (Basel)

20-Jun-2023

PMCID:	PMC10301385
doi:	10.3390/plants12122384
PMID:	37376013

Pentagalloyl Glucose: A Review of Anticancer Properties, Molecular Targets, Mechanisms of Action, Pharmacokinetics, and Safety Profile

Wen C, Dechsupa N, Yu Z, Zhang X, Liang S, Lei X, Xu T, Gao X, Hu Q, Innuan P, Kantapan J, Lü M

Molecules

19-Jun-2023

PMCID:	PMC10300743
doi:	10.3390/molecules28124856
PMID:	37375411

Endophytic fungi mediates production of bioactive secondary metabolites via modulation of genes involved in key metabolic pathways and their contribution in different biotechnological sector

Toppo P, Kagatay LL, Gurung A, Singla P, Chakraborty R, Roy S, Mathur P

3 Biotech

14-May-2023

PMCID:	PMC10183385
doi:	10.1007/s13205-023-03605-z
PMID:	37197561

Molecular Detection of Phytoplasmas of the 16SrI and 16SrXXXII Groups in Elaeocarpus sylvestris Trees with Decline Disease in Jeju Island, South Korea

Lee GW, Han SS

Plant Pathol J

01-Feb-2023

PMCID:	PMC9929163
doi:	10.5423/PPJ.OA.07.2022.0091
PMID:	36760057

Pest categorisation of Icerya aegyptiaca

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, MacLeod A

EFSA J

09-Jan-2023

PMCID:	PMC9827230
doi:	10.2903/j.efsa.2023.7739
PMID:	36628331

Virtual Screening of Soybean Protein Isolate-Binding Phytochemicals and Interaction Characterization

Liu P, Wu A, Song Y, Zhao J

Foods

06-Jan-2023

PMCID:	PMC9857816
doi:	10.3390/foods12020272
PMID:	36673362

Purification and biochemical characterization of two laccase isoenzymes isolated from Trichoderma harzianum S7113 and its application for bisphenol A degradation

Elsayed AM, Mahmoud M, Abdel Karim GS, Abdelraof M, Othman AM

Microb Cell Fact

02-Jan-2023

PMCID:	PMC9806890
doi:	10.1186/s12934-022-02011-z
PMID:	36593499

Pharmacological Activity of Quercetin: An Updated Review

Wang G, Wang Y, Yao L, Gu W, Zhao S, Shen Z, Lin Z, Liu W, Yan T

Evid Based Complement Alternat Med

01-Dec-2022

PMCID:	PMC9731755
doi:	10.1155/2022/3997190
PMID:	36506811

Insights into Antiviral Properties and Molecular Mechanisms of Non-Flavonoid Polyphenols against Human Herpesviruses

Hassan ST, Šudomová M, Mazurakova A, Kubatka P

Int J Mol Sci

11-Nov-2022

PMCID:	PMC9693824
doi:	10.3390/ijms232213891
PMID:	36430369

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl 6-O-galloyl-b-D-glucopyranoside	78385296	Click to see COC1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O	346.29	unknown	https://doi.org/10.1039/P19860000369
methyl 6-O-galloyl-beta-d-glucopyranoside	5319658	Click to see COC1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O	346.29	unknown	https://doi.org/10.1039/P19860000369
> Phenylpropanoids and polyketides / Tannins
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate	4628122	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O	332.26	unknown	https://doi.org/10.1039/P19860000369
beta-Glucogallin	124021	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O	332.26	unknown	https://doi.org/10.1039/P19860000369
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(3,6a,10',11',12',15',16',17',31',32',36',37'-dodecahydroxy-2',5,7',20',28',41'-hexaoxospiro[3,3a-dihydro-2H-furo[3,2-b]furan-6,39'-3,6,21,24,27,38,42-heptaoxanonacyclo[35.2.2.133,36.01,35.04,23.05,26.08,13.014,19.029,34]dotetraconta-8,10,12,14,16,18,29,31,33-nonaene]-25'-yl) 3,4,5-trihydroxybenzoate	3459965	Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C9C(C(COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)O)O)O)O)O)O)OC8OC(=O)C1=CC(=C(C(=C1)O)O)O)OC5=O)O)O)O)O)O)O	1110.80	unknown	https://doi.org/10.1039/P19860000369
(57R,58S,510R,511R,519S)-14,15,16,24,25,26,52,53,516,517,517-Undecahydroxy-55,513,515,3,8-pentaoxo-55,57,58,510,511,513,515,516,517,517a-decahydro-4,7-dioxa-5(19,10)-1,16-epoxy-7,11-methanodibenzo[i,k][1,4,7]trioxacyclotridecina-1,2(1,2)-dibenzenacyclooctaphane-58-yl 3,4,5-trihydroxybenzoate	138991573	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1039/P19860000369
CID 115063	115063	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1039/P19860000369
CID 338147	338147	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1039/P19860000369
Geraniin	3001497	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1039/P19860000369
Xcxwmhrrisfuff-xngpzlstsa-	21636130	Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C9C(C(COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)O)O)O)O)O)O)OC8OC(=O)C1=CC(=C(C(=C1)O)O)O)OC5=O)O)O)O)O)O)O	1110.80	unknown	https://doi.org/10.1039/P19860000369

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Elaeocarpus sylvestris

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