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Internal ID UUID6440483a9e349242383710
Scientific name Ilex goshiensis
Authority Hayata
First published in J. Coll. Sci. Imp. Univ. Tokyo 30(1): 54 (1911)

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Synonyms Top

Scientific name Authority First published in
Ilex hanceana f. rotundata Makino ex Yamam. Icon. Pl. Formosan., Suppl. 1: 34 1925
Ilex hanceana f. goshiensis Yamam. Sylvia 4: 105 1927

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Language Common/alternative name
Chinese 圓葉冬青
Chinese 海岛冬青
Chinese 圆叶冬青

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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 Southeast
      • Hainan
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001078619
USDA Plants ILGO2
Tropicos 2000499
KEW urn:lsid:ipni.org:names:83336-1
The Plant List tro-2000499
Open Tree Of Life 751410
NCBI Taxonomy 53203
IUCN Red List 147377723
IPNI 83336-1
iNaturalist 708966
GBIF 5533526
EOL 2907105
USDA GRIN 406980

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
The Chemical Structure of Neoilexonol Kazuyoshi YAGISHITA, Masaru NISHIMURA Oxford University Press (OUP) 30-Oct-2013
doi:10.1271/BBB1961.25.844
The Chemical Structure of Neoilexonol I. Kazuyoshi YAGISHITA, Masaru NISHIMURA Oxford University Press (OUP) 30-Oct-2013
doi:10.1271/BBB1961.25.517
Disturbance regimes, gap‐demanding trees and seed mass related to tree height in warm temperate rain forests worldwide Grubb PJ, Bellingham PJ, Kohyama TS, Piper FI, Valido A Biol Rev Camb Philos Soc 19-Mar-2013
PMCID:PMC7161821
doi:10.1111/brv.12029
PMID:23506298

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 10836206 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1271/BBB1961.25.844
10-Hydroxy-1,2,4a,6a,6b,9,9,12a-octamethyl-1,2,3,4,5,6,6a,7,8,8a,10,11,12,14b-tetradecahydropicen-13-one 74933427 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 440.70 unknown https://doi.org/10.1271/BBB1961.25.517
11-Oxo-alpha-amyrin 69166285 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 440.70 unknown https://doi.org/10.1271/BBB1961.25.517
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-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/10.1271/BBB1961.25.844

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