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Elaeocarpus chinensis

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440190f7ad83017010804
Scientific name Elaeocarpus chinensis
Authority Hook.f. ex Benth.
First published in Fl. Hongk. : 43 (1861)

Description Top

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Synonyms Top

Scientific name Authority First published in
Elaeocarpus integripetalus Gagnep. Notul. Syst. (Paris) 11: 6. 1943
Friesia chinensis Gardner & Champ. Hooker's J. Bot. Kew Gard. Misc. 1: 243 (1849)

Common names Top

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Language Common/alternative name
Chinese 盐匏藤果
Chinese 中华杜英
Chinese 华杜英
Chinese 高山望
Chinese 桃榅
Chinese 羊屎乌
Chinese 中華杜英
Chinese 一种维管植物

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000664130
Tropicos 11700282
KEW urn:lsid:ipni.org:names:833794-1
The Plant List kew-2785414
Open Tree Of Life 514558
NCBI Taxonomy 1008905
IUCN Red List 147617201
IPNI 833794-1
iNaturalist 633723
GBIF 5833757

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
Strategies for the discovery of potential anticancer agents from plants collected from Southeast Asian tropical rainforests as a case study de Blanco EJ, Addo EM, Rakotondraibe HL, Soejarto DD, Kinghorn AD Nat Prod Rep 19-Jul-2023
PMCID:PMC10524867
doi:10.1039/d2np00080f
PMID:37194649
“Realistic strategies” and neutral processes drive the community assembly based on leaf functional traits in a subtropical evergreen broad‐leaved forest Zhao L, Xiang W, Li J, Liu W, Hu Y, Wu H, Zhang Y, Cheng X, Wang W, Wang W, Ouyang S Ecol Evol 17-Sep-2022
PMCID:PMC9482003
doi:10.1002/ece3.9323
PMID:36177111
Effects of enemy exclusion on biodiversity–productivity relationships in a subtropical forest experiment Huang Y, Schuldt A, Hönig L, Yang B, Liu X, Bruelheide H, Ma K, Schmid B, Niklaus PA J Ecol 20-Jun-2022
PMCID:PMC9544039
doi:10.1111/1365-2745.13940
PMID:36250130
Tree diversity and functional leaf traits drive herbivore‐associated microbiomes in subtropical China Li Y, Chesters D, Wang M, Wubet T, Schuldt A, Anttonen P, Guo P, Chen J, Zhou Q, Zhang N, Ma K, Bruelheide H, Wu C, Zhu C Ecol Evol 31-Mar-2021
PMCID:PMC8207151
doi:10.1002/ece3.7434
PMID:34141209
Seasonal variations in group leaf characteristics in species with red young leaves Zhang TJ, Tian XS, Liu XT, Huang XD, Peng CL Sci Rep 11-Nov-2019
PMCID:PMC6848096
doi:10.1038/s41598-019-52753-x
PMID:31712569
Natural Product Triterpenoids and Their Semi-synthetic Derivatives with Potential Anticancer Activity Ren Y, Douglas Kinghorn A Planta Med 18-Jan-2019
PMCID:PMC6639164
doi:10.1055/a-0832-2383
PMID:30658371
Linking Xylem Hydraulic Conductivity and Vulnerability to the Leaf Economics Spectrum—A Cross-Species Study of 39 Evergreen and Deciduous Broadleaved Subtropical Tree Species Kröber W, Zhang S, Ehmig M, Bruelheide H PLoS One 25-Nov-2014
PMCID:PMC4244042
doi:10.1371/journal.pone.0109211
PMID:25423316
Assay Development for the Discovery of Semaphorin 3B Inducing Agents from Natural Product Sources Yong Y, Pan L, Ren Y, Fatima N, Ahmed S, Chang LC, Zhang X, Kinghorn AD, Swanson SM, Carcache de Blanco EJ Fitoterapia 10-Jul-2014
PMCID:PMC4196688
doi:10.1016/j.fitote.2014.07.004
PMID:25016954
Investigation of Vietnamese plants for potential anticancer agents Pérez LB, Still PC, Naman CB, Ren Y, Pan L, Chai HB, Carcache de Blanco EJ, Ninh TN, Van Thanh B, Swanson SM, Soejarto DD, Kinghorn AD Phytochem Rev 28-Jan-2014
PMCID:PMC4225705
doi:10.1007/s11101-014-9335-7
PMID:25395897
Natural Compounds as Potential Treatments of NF2-Deficient Schwannoma and Meningioma: Cucurbitacin D and Goyazensolide Spear SA, Burns SS, Oblinger JL, Ren Y, Pan L, Kinghorn AD, Welling DB, Chang LS Otol Neurotol 01-Oct-2013
PMCID:PMC4334125
doi:10.1097/MAO.0b013e3182956169
PMID:23928514
Isolation, structure elucidation, and biological evaluation of 16,23-epoxycucurbitacin constituents from Eleaocarpus chinensis L Pan, Y Yong, Y Deng, DD Lantvit, TN Ninh, H Chai, EJ Carcache de Blanco, DD Soejarto, SM Swanson, AD Kinghorn Georg Thieme Verlag KG 30-Aug-2012
doi:10.1055/S-0032-1320924
Isolation, Structure Elucidation, and Biological Evaluation of 16,23-Epoxycucurbitacin Constituents from Eleaocarpus chinensis Pan L, Yong Y, Deng Y, Lantvit DD, Ninh TN, Chai H, de Blanco EJ, Soejarto DD, Swanson SM, Kinghorn AD J Nat Prod 12-Jan-2012
PMCID:PMC3311738
doi:10.1021/np200879p
PMID:22239601

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-0032-1320924
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-0032-1320924
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-0032-1320924
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-0032-1320924

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