Elaeocarpus sylvestris - Unknown
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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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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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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan

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
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
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
Biogeography and Ecological Differentiation of Pseudasphondylia gall midges (Diptera: Cecidomyiidae) Distributed in Taiwan and Japan, with Description of a New Species P. kiwiphila sp. nov. and the Southernmost Record of P. elaeocarpi Lin SF, Tokuda M, Tung GS, Pan LY, Kim W, Yukawa J, Yang MM Zool Stud 11-Oct-2022
PMCID:PMC9745572
doi:10.6620/ZS.2022.61-39
PMID:36568810
The phenomenon of red and yellow autumn leaves: Hypotheses, agreements and disagreements Lev‐Yadun S J Evol Biol 16-Aug-2022
PMCID:PMC9804425
doi:10.1111/jeb.14069
PMID:35975328
Investigation of the inhibition effect of 1,2,3,4,6-pentagalloyl-β-D-glucose on gastric cancer cells based on a network pharmacology approach and experimental validation Bi JH, Jiang YH, Ye SJ, Wu MR, Yi Y, Wang HX, Wang LM Front Oncol 03-Aug-2022
PMCID:PMC9383036
doi:10.3389/fonc.2022.934958
PMID:35992839

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
> 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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