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Elaeocarpus mastersii

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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 UUID6440192109a4c464890528
Scientific name Elaeocarpus mastersii
Authority King
First published in J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 60: 139 (1891)

Description Top

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Synonyms Top

Scientific name Authority First published in
Monocera cyrtostachya Miq. Fl. Ned. Ind., Eerste Bijv. 3: 408. 1861

Common names Top

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Language Common/alternative name
Chinese 马来杜英

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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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

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Database ID/link to page
World Flora Online wfo-0000664497
Tropicos 100329475
KEW urn:lsid:ipni.org:names:833881-1
The Plant List kew-2785758
Open Tree Of Life 5748808
NCBI Taxonomy 1526293
IUCN Red List 135889368
IPNI 833881-1
iNaturalist 707876
GBIF 4031115
EOL 5408083

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
Benefits of tropical peatland rewetting for subsidence reduction and forest regrowth: results from a large-scale restoration trial Hooijer A, Vernimmen R, Mulyadi D, Triantomo V, Hamdani, Lampela M, Agusti R, Page SE, Doloksaribu J, Setiawan I, Suratmanto B, Swarup S Sci Rep 10-May-2024
PMCID:PMC11087581
doi:10.1038/s41598-024-60462-3
PMID:38729962
Phytochemicals from Bark Extracts and Their Applicability in the Synthesis of Thermosetting Polymers: An Overview Szmechtyk T, Małecka M Materials (Basel) 30-Apr-2024
PMCID:PMC11084627
doi:10.3390/ma17092123
PMID:38730929
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
Ellagic acid derivatives and cytotoxic cucurbitacins from Elaeocarpus mastersii. Ito A, Chai HB, Lee D, Kardono LB, Riswan S, Farnsworth NR, Cordell GA, Pezzuto JM, Kinghorn AD Phytochemistry 01-Sep-2002
doi:10.1016/S0031-9422(02)00232-7
PMID:12169311

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
(2S,3R,8S,9R,10R,13R,14S,16R,17R)-17-[(E,2R)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 68103154 Click to see CC1(C(C(CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)C=CC(C)(C)O)O)O)C)C)C)O)O)C 518.70 unknown https://doi.org/10.1016/S0031-9422(02)00232-7
(8S,9R,10S,13R,14S)-17-[(2R)-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 138113434 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/10.1016/S0031-9422(02)00232-7
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/10.1016/S0031-9422(02)00232-7
Cucurbitacin F 5281320 Click to see CC1(C(C(CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)C=CC(C)(C)O)O)O)C)C)C)O)O)C 518.70 unknown https://doi.org/10.1016/S0031-9422(02)00232-7
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2S,3R,4R,5S,6S)-3-acetyloxy-5-hydroxy-2-[(14-hydroxy-6,13-dimethoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-7-yl)oxy]-6-methyloxan-4-yl] acetate 11071799 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C4=C2OC(=O)C5=CC(=C(C(=C54)OC3=O)O)OC)OC)OC(=O)C)OC(=O)C)O 560.50 unknown https://doi.org/10.1016/S0031-9422(02)00232-7
[3-Acetyloxy-2-[(6,14-dihydroxy-13-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-7-yl)oxy]-5-hydroxy-6-methyloxan-4-yl] acetate 21159147 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C4=C2OC(=O)C5=CC(=C(C(=C54)OC3=O)O)OC)O)OC(=O)C)OC(=O)C)O 546.40 unknown https://doi.org/10.1016/S0031-9422(02)00232-7
[3-Acetyloxy-5-hydroxy-2-[(14-hydroxy-6,13-dimethoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-7-yl)oxy]-6-methyloxan-4-yl] acetate 85388516 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C4=C2OC(=O)C5=CC(=C(C(=C54)OC3=O)O)OC)OC)OC(=O)C)OC(=O)C)O 560.50 unknown https://doi.org/10.1016/S0031-9422(02)00232-7

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