Elaeocarpus hainanensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Elaeocarpus hainanensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Elaeocarpus hainanensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID644019197e57b675815254
Scientific name Elaeocarpus hainanensis
Authority Oliv.
First published in Hooker's Icon. Pl. 25: t. 2462 (1896)

Description Top

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Synonyms Top

Scientific name Authority First published in
Elaeocarpus lacei Craib Bull. Misc. Inform. Kew 1925: 23 (1925)

Common names Top

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Language Common/alternative name
English hainan elaeocarpus
Chinese 水石榕
Chinese 水柳树
Chinese 海南胆八树

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Elaeocarpus hainanensis var. brachyphyllus Merr. Lingnan Sci. J. 5: 123. 1927 (1927)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
    • 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-0000664331
Tropicos 11700252
KEW urn:lsid:ipni.org:names:833840-1
The Plant List kew-2785601
Open Tree Of Life 1095783
NCBI Taxonomy 1082500
IPNI 833840-1
iNaturalist 359512
GBIF 4032315
EOL 2889327
USDA GRIN 461133

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
The complete chloroplast genome sequence of Melochia corchorifolia Linnaeus, 1753 (Sterculiaceae) Wang W, Wang X Mitochondrial DNA B Resour 24-Jan-2024
PMCID:PMC10810621
doi:10.1080/23802359.2024.2305711
PMID:38274854
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
Comparison of the chloroplast genomes and phylogenomic analysis of Elaeocarpaceae Wang Y, Xie Y, Jin J, Li J, Qiu X, Tong Y, Li Z, Zhang Z, Lai W PeerJ 09-May-2023
PMCID:PMC10178313
doi:10.7717/peerj.15322
PMID:37187516
Nonlinearity of root trait relationships and the root economics spectrum Kong D, Wang J, Wu H, Valverde-Barrantes OJ, Wang R, Zeng H, Kardol P, Zhang H, Feng Y Nat Commun 17-May-2019
PMCID:PMC6525182
doi:10.1038/s41467-019-10245-6
PMID:31101818
Patterns of ROS Accumulation in the Stigmas of Angiosperms and Visions into Their Multi-Functionality in Plant Reproduction Zafra A, Rejón JD, Hiscock SJ, Alché JD Front Plant Sci 05-Aug-2016
PMCID:PMC4974276
doi:10.3389/fpls.2016.01112
PMID:27547207
Seeds used for Bodhi beads in China Li F, Li J, Liu B, Zhuo J, Long C J Ethnobiol Ethnomed 30-Jan-2014
PMCID:PMC3914368
doi:10.1186/1746-4269-10-15
PMID:24479788
Terpenoids as potential chemopreventive and therapeutic agents in liver cancer Thoppil RJ, Bishayee A World J Hepatol 27-Sep-2011
PMCID:PMC3182282
doi:10.4254/wjh.v3.i9.228
PMID:21969877
Cytotoxic cucurbitane-type triterpenoids from Elaeocarpus hainanensis. Meng D, Qiang S, Lou L, Zhao W Planta Med 01-Nov-2008
doi:10.1055/S-2008-1081356
PMID:18937166

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 / Steroids and steroid derivatives / Cucurbitacins
17-(1,5-Dihydroxy-1,5-dimethyl-2-oxo-3-hexenyl)-2,16-dihydroxy-4,4,9,14-tetramethylestra-1,5-diene-3,11-dione 2888 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2C=C(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 514.60 unknown https://doi.org/10.1055/S-2008-1081356
17-(2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 2886 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 516.70 unknown https://doi.org/10.1055/S-2008-1081356
Cucurbitacin D 5281318 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 516.70 unknown https://doi.org/10.1055/S-2008-1081356
Cucurbitacin I 5281321 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2C=C(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 514.60 unknown https://doi.org/10.1055/S-2008-1081356

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